ATF6 (activating transcription factor 6) - Rat Genome Database

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Gene: ATF6 (activating transcription factor 6) Homo sapiens
Analyze
Symbol: ATF6
Name: activating transcription factor 6
RGD ID: 1313517
HGNC Page HGNC:791
Description: Enables several functions, including DNA-binding transcription activator activity, RNA polymerase II-specific; identical protein binding activity; and protein heterodimerization activity. Involved in several processes, including positive regulation of ATF6-mediated unfolded protein response; positive regulation of transcription by RNA polymerase II; and visual perception. Acts upstream of or within positive regulation of autophagy. Located in Golgi apparatus; RNA polymerase II transcription regulator complex; and endoplasmic reticulum membrane. Implicated in achromatopsia 7.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: ACHM7; activating transcription factor 6 alpha; ATF6-alpha; ATF6A; ATP6alpha; cAMP-dependent transcription factor ATF-6 alpha; cyclic AMP-dependent transcription factor ATF-6 alpha; DKFZp686P2194; FLJ21663
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381161,766,320 - 161,964,070 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1161,766,298 - 161,977,574 (+)EnsemblGRCh38hg38GRCh38
GRCh371161,736,110 - 161,933,860 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361160,002,708 - 160,195,476 (+)NCBINCBI36Build 36hg18NCBI36
Build 341158,467,741 - 158,660,510NCBI
Celera1134,839,502 - 135,032,269 (+)NCBICelera
Cytogenetic Map1q23.3NCBI
HuRef1132,980,970 - 133,178,653 (+)NCBIHuRef
CHM1_11163,157,827 - 163,355,630 (+)NCBICHM1_1
T2T-CHM13v2.01161,110,648 - 161,308,347 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(+)-catechin  (EXP)
(+)-schisandrin B  (ISO)
(1->4)-beta-D-glucan  (ISO)
(R)-lipoic acid  (ISO)
(S)-nicotine  (ISO)
1,10-phenanthroline  (EXP)
1,2-dimethylhydrazine  (ISO)
15-acetyldeoxynivalenol  (EXP)
17alpha-ethynylestradiol  (ISO)
17beta-estradiol  (ISO)
1H-pyrazole  (ISO)
2,2',4,4'-Tetrabromodiphenyl ether  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2,4-dichlorophenol  (ISO)
2-amino-2-deoxy-D-glucopyranose  (EXP,ISO)
2-hydroxypropanoic acid  (EXP)
3,3',4,4',5-pentachlorobiphenyl  (ISO)
3,4-methylenedioxymethamphetamine  (ISO)
3-acetyldeoxynivalenol  (EXP,ISO)
3-chloropropane-1,2-diol  (EXP,ISO)
3-isobutyl-1-methyl-7H-xanthine  (EXP)
3H-1,2-dithiole-3-thione  (ISO)
4-amino-2,6-dinitrotoluene  (ISO)
4-Hydroxybenzophenone  (ISO)
4-hydroxynon-2-enal  (ISO)
4-phenylbutyric acid  (EXP,ISO)
5-fluorouracil  (EXP)
6-chloro-2,3,4,9-tetrahydro-1H-carbazole-1-carboxamide  (ISO)
6-propyl-2-thiouracil  (ISO)
abamectin  (ISO)
acetamide  (ISO)
acrylamide  (ISO)
aflatoxin B1  (ISO)
agomelatine  (ISO)
aldehydo-D-glucosamine  (EXP,ISO)
aldehydo-D-glucose  (EXP,ISO)
all-trans-retinoic acid  (EXP,ISO)
allopurinol  (EXP)
amiodarone  (ISO)
antimony trichloride  (ISO)
antirheumatic drug  (EXP)
apigenin  (ISO)
aristolochic acid A  (EXP)
arsenite(3-)  (EXP,ISO)
arsenous acid  (EXP,ISO)
atazanavir sulfate  (EXP)
atorvastatin calcium  (ISO)
atrazine  (ISO)
BAPTA  (EXP)
benzo[a]pyrene  (EXP,ISO)
benzo[a]pyrene diol epoxide I  (EXP)
beta-D-glucosamine  (EXP,ISO)
bilirubin IXalpha  (EXP,ISO)
bis(2-ethylhexyl) phthalate  (ISO)
bisphenol A  (EXP,ISO)
bisphenol F  (EXP)
boric acid  (EXP)
brefeldin A  (ISO)
Butylparaben  (EXP)
C.I. Natural Red 20  (ISO)
C60 fullerene  (ISO)
cadmium atom  (ISO)
cadmium dichloride  (EXP,ISO)
calcitriol  (EXP)
cantharidin  (EXP)
casticin  (EXP)
chenodeoxycholic acid  (EXP)
chloroacetic acid  (ISO)
Chloroacetonitrile  (ISO)
chlorogenic acid  (ISO)
chlorpyrifos  (ISO)
chromium(6+)  (ISO)
chrysazin  (EXP)
cobalt dichloride  (ISO)
cocaine  (ISO)
crocidolite asbestos  (EXP)
curcumin  (EXP,ISO)
cyclosporin A  (EXP,ISO)
cypermethrin  (ISO)
cyproconazole  (ISO)
D-glucose  (EXP,ISO)
D-penicillamine  (EXP)
dapagliflozin  (ISO)
DDE  (EXP)
decabromodiphenyl ether  (ISO)
demethoxycurcumin  (EXP)
deoxycholic acid  (EXP)
deoxynivalenol  (EXP,ISO)
dexamethasone  (EXP)
diarsenic trioxide  (EXP,ISO)
dibutyl phthalate  (ISO)
dicrotophos  (EXP)
dioscin  (ISO)
dioxygen  (ISO)
diquat  (ISO)
disodium selenite  (EXP)
dorsomorphin  (ISO)
doxorubicin  (EXP,ISO)
endosulfan  (ISO)
epoxiconazole  (ISO)
ethanol  (ISO)
fenofibrate  (ISO)
ferrostatin-1  (ISO)
fipronil  (ISO)
fisetin  (EXP)
FR900359  (EXP)
fructose  (ISO)
fulvestrant  (EXP)
furan  (ISO)
Fusarenone X  (EXP)
gadolinium trichloride  (ISO)
gentamycin  (ISO)
geraniol  (EXP)
ginsenoside Rg1  (EXP)
glucose  (EXP,ISO)
glutathione  (ISO)
glycochenodeoxycholic acid  (EXP)
glycocholic acid  (EXP)
glycodeoxycholic acid  (EXP)
glycyrrhetinate  (ISO)
glycyrrhetinic acid  (ISO)
gold atom  (EXP)
gold(0)  (EXP)
Guanabenz  (ISO)
GW 4064  (ISO)
hesperidin  (ISO)
hexadecanoic acid  (EXP,ISO)
hydroquinone  (EXP)
Ibutilide  (ISO)
indometacin  (EXP)
ivermectin  (ISO)
ketamine  (ISO)
KN-93  (ISO)
L-glutamic acid  (ISO)
L-serine  (EXP)
lead diacetate  (ISO)
letrozole  (ISO)
lipoic acid  (ISO)
lipopolysaccharide  (EXP)
luteolin  (EXP)
LY294002  (ISO)
lycopene  (ISO)
manganese atom  (EXP)
manganese(0)  (EXP)
manganese(II) chloride  (EXP,ISO)
melatonin  (ISO)
menadione  (EXP)
metformin  (ISO)
methamphetamine  (EXP,ISO)
methapyrilene  (ISO)
methoxychlor  (ISO)
methylmercury chloride  (ISO)
methylseleninic acid  (EXP)
metyrapone  (EXP)
minocycline  (ISO)
mono(2-ethylhexyl) phthalate  (ISO)
N(4)-hydroxycytidine  (ISO)
N-acetyl-L-cysteine  (EXP,ISO)
N-benzyloxycarbonyl-L-leucyl-L-leucyl-L-leucinal  (EXP)
N-hexadecanoylsphingosine  (ISO)
N-methyl-4-phenylpyridinium  (ISO)
naltrexone  (EXP)
nefazodone  (EXP)
nelfinavir  (EXP)
nickel atom  (ISO)
nickel sulfate  (ISO)
nicotine  (ISO)
nilotinib  (EXP)
Nivalenol  (EXP)
Nonidet P-40  (EXP)
Norbinaltorphimine  (EXP)
ochratoxin A  (EXP)
oleic acid  (EXP,ISO)
oxaliplatin  (ISO)
Pachymic acid  (EXP)
paclitaxel  (ISO)
paracetamol  (ISO)
paraquat  (EXP,ISO)
Pendulone  (EXP)
perfluorobutyric acid  (EXP)
perfluorooctane-1-sulfonic acid  (ISO)
perfluorooctanoic acid  (EXP)
perhexiline  (EXP)
phenethyl caffeate  (ISO)
poly(guanylic acid)  (ISO)
potassium dichromate  (ISO)
procymidone  (ISO)
propiconazole  (ISO)
psoralen  (EXP)
pyocyanine  (ISO)
pyrazinecarboxamide  (EXP)
quercetin  (EXP,ISO)
quercetin 3-O-beta-D-glucofuranoside  (ISO)
quercetin 3-O-beta-D-glucopyranoside  (ISO)
rac-lactic acid  (EXP)
reactive oxygen species  (ISO)
Repaglinide  (ISO)
resveratrol  (EXP,ISO)
rifampicin  (EXP)
Riluzole  (EXP)
rimonabant  (EXP)
roflumilast  (ISO)
rotenone  (EXP,ISO)
Salinomycin  (EXP)
salubrinal  (ISO)
saquinavir  (EXP)
serpentine asbestos  (EXP)
Shikonin  (ISO)
silicon dioxide  (ISO)
simvastatin  (ISO)
sirolimus  (EXP)
sodium arsenite  (EXP,ISO)
sodium dichromate  (ISO)
sodium fluoride  (ISO)
SR 144528  (EXP)
streptozocin  (ISO)
sulindac  (EXP)
tacrolimus hydrate  (ISO)
tauroursodeoxycholic acid  (EXP,ISO)
tetrachloromethane  (ISO)
thapsigargin  (EXP,ISO)
thioacetamide  (ISO)
thymoquinone  (EXP)
Tiron  (ISO)
titanium dioxide  (ISO)
tributylstannane  (EXP)
Tributyltin oxide  (ISO)
trichloroethene  (ISO)
triclocarban  (EXP)
triclosan  (EXP)
trimellitic anhydride  (ISO)
triphenyl phosphate  (ISO)
Triptolide  (ISO)
troglitazone  (EXP,ISO)
tungsten  (ISO)
tunicamycin  (EXP,ISO)
valproic acid  (EXP)
vildagliptin  (ISO)
vincristine  (ISO)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. Cellular communication network factor 1 (CCN1) knockdown exerts a protective effect for hepatic ischemia/reperfusion injury by deactivating the MEK/ERK pathway. Liu H, etal., Clin Res Hepatol Gastroenterol. 2021 Sep;45(5):101737. doi: 10.1016/j.clinre.2021.101737. Epub 2021 Jun 16.
3. Naltrexone changes the expression of lipid metabolism-related proteins in the endoplasmic reticulum stress induced hepatic steatosis in mice. Moslehi A, etal., Clin Exp Pharmacol Physiol. 2017 Feb;44(2):207-212. doi: 10.1111/1440-1681.12695.
4. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
5. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
6. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
7. RGD HPO Phenotype Annotation Pipeline RGD automated import pipeline for human HPO-to-gene-to-disease annotations
8. The impact of the unfolded protein response on human disease. Wang S and Kaufman RJ, J Cell Biol. 2012 Jun 25;197(7):857-67. doi: 10.1083/jcb.201110131.
9. LncRNA H19 inhibits ER stress induced apoptosis and improves diabetic cardiomyopathy by regulating PI3K/AKT/mTOR axis. Wang S, etal., Aging (Albany NY). 2022 Aug 30;14(16):6809-6828. doi: 10.18632/aging.204256. Epub 2022 Aug 30.
10. Endoplasmic reticulum stress and neurodegeneration in rats neonatally infected with borna disease virus. Williams BL and Lipkin WI, J Virol. 2006 Sep;80(17):8613-26. doi: 10.1128/JVI.00836-06.
11. MTORC1 coordinates the autophagy and apoptosis signaling in articular chondrocytes in osteoarthritic temporomandibular joint. Yang H, etal., Autophagy. 2020 Feb;16(2):271-288. doi: 10.1080/15548627.2019.1606647. Epub 2019 Apr 21.
Additional References at PubMed
PMID:2516827   PMID:8889548   PMID:9271374   PMID:9837962   PMID:10564271   PMID:10866666   PMID:11158310   PMID:11163209   PMID:11256944   PMID:11287625   PMID:11483355   PMID:11779464  
PMID:11805088   PMID:11821395   PMID:11909875   PMID:12014989   PMID:12076252   PMID:12097557   PMID:12477932   PMID:12713871   PMID:12782636   PMID:12805554   PMID:12949534   PMID:14699159  
PMID:14752510   PMID:14765107   PMID:14973138   PMID:15063770   PMID:15299016   PMID:15342556   PMID:15489334   PMID:15598891   PMID:15899857   PMID:16196087   PMID:16236796   PMID:16469704  
PMID:16505252   PMID:16710414   PMID:17092596   PMID:17101776   PMID:17327457   PMID:17440018   PMID:17442311   PMID:17522056   PMID:17686766   PMID:17765680   PMID:18022401   PMID:18635891  
PMID:18650380   PMID:18840095   PMID:19122331   PMID:19274049   PMID:19304306   PMID:19420237   PMID:19543265   PMID:19667116   PMID:19693772   PMID:19722195   PMID:19723703   PMID:19772629  
PMID:19822759   PMID:19913121   PMID:20102225   PMID:20160352   PMID:20219975   PMID:20301591   PMID:20628086   PMID:20732420   PMID:20800603   PMID:20936779   PMID:21106748   PMID:21131360  
PMID:21150130   PMID:21211013   PMID:21329801   PMID:21329806   PMID:21345978   PMID:21355074   PMID:21385877   PMID:21454619   PMID:21521793   PMID:21809331   PMID:21832049   PMID:21841196  
PMID:21873635   PMID:21976666   PMID:21988832   PMID:22013072   PMID:22013210   PMID:22099811   PMID:22102412   PMID:22146569   PMID:22268729   PMID:22354938   PMID:22577136   PMID:22682248  
PMID:22872700   PMID:22917505   PMID:22956602   PMID:23011799   PMID:23037953   PMID:23382691   PMID:23661758   PMID:23864652   PMID:23924739   PMID:24043630   PMID:24177270   PMID:24240056  
PMID:24269637   PMID:24302549   PMID:24636989   PMID:24664756   PMID:24726443   PMID:25135476   PMID:25241909   PMID:25302688   PMID:25409632   PMID:25444553   PMID:25450523   PMID:25593314  
PMID:25609649   PMID:25675914   PMID:25754093   PMID:25976933   PMID:26029869   PMID:26063662   PMID:26186194   PMID:26261584   PMID:26707144   PMID:26752648   PMID:26925648   PMID:27085326  
PMID:27117871   PMID:27238082   PMID:27461470   PMID:27563820   PMID:27590344   PMID:28028229   PMID:28105371   PMID:28157699   PMID:28473536   PMID:28514442   PMID:28611215   PMID:28629319  
PMID:28747345   PMID:28803844   PMID:28812650   PMID:28884228   PMID:28958904   PMID:29061306   PMID:29117863   PMID:29180619   PMID:29386036   PMID:29395067   PMID:29440509   PMID:29483204  
PMID:29512699   PMID:29513927   PMID:29568061   PMID:29601799   PMID:29851562   PMID:29987050   PMID:30063110   PMID:30063920   PMID:30084354   PMID:30086303   PMID:30287689   PMID:30639234  
PMID:30717233   PMID:30944250   PMID:31029032   PMID:31035281   PMID:31073040   PMID:31105062   PMID:31227689   PMID:31237654   PMID:31312025   PMID:31368601   PMID:31500833   PMID:31506423  
PMID:31536960   PMID:31852864   PMID:31871319   PMID:31884629   PMID:31900015   PMID:31926341   PMID:32046286   PMID:32138230   PMID:32234634   PMID:32271167   PMID:32409323   PMID:32514126  
PMID:32614325   PMID:32724472   PMID:32788342   PMID:32877691   PMID:32905769   PMID:33109440   PMID:33397415   PMID:33545068   PMID:33545358   PMID:33599179   PMID:33686769   PMID:33919712  
PMID:33957083   PMID:33960419   PMID:33961781   PMID:34079125   PMID:34186245   PMID:34432599   PMID:34561305   PMID:34623328   PMID:34664059   PMID:34851146   PMID:35089606   PMID:35271311  
PMID:35338505   PMID:35696571   PMID:35883579   PMID:35914814   PMID:36149636   PMID:36377459   PMID:36696173   PMID:37209959   PMID:37314749   PMID:37376599   PMID:37407995   PMID:37715829  
PMID:38015761  


Genomics

Comparative Map Data
ATF6
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381161,766,320 - 161,964,070 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1161,766,298 - 161,977,574 (+)EnsemblGRCh38hg38GRCh38
GRCh371161,736,110 - 161,933,860 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361160,002,708 - 160,195,476 (+)NCBINCBI36Build 36hg18NCBI36
Build 341158,467,741 - 158,660,510NCBI
Celera1134,839,502 - 135,032,269 (+)NCBICelera
Cytogenetic Map1q23.3NCBI
HuRef1132,980,970 - 133,178,653 (+)NCBIHuRef
CHM1_11163,157,827 - 163,355,630 (+)NCBICHM1_1
T2T-CHM13v2.01161,110,648 - 161,308,347 (+)NCBIT2T-CHM13v2.0
Atf6
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391170,532,026 - 170,696,414 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1170,532,243 - 170,695,340 (-)EnsemblGRCm39 Ensembl
GRCm381170,704,457 - 170,868,585 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1170,704,674 - 170,867,771 (-)EnsemblGRCm38mm10GRCm38
MGSCv371172,634,588 - 172,797,902 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361172,541,132 - 172,710,564 (-)NCBIMGSCv36mm8
Celera1173,146,825 - 173,324,073 (-)NCBICelera
Cytogenetic Map1H3NCBI
cM Map176.96NCBI
Atf6
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81385,460,312 - 85,639,959 (-)NCBIGRCr8
mRatBN7.21382,927,579 - 83,106,381 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1382,930,034 - 83,107,177 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1385,558,613 - 85,732,374 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01386,852,287 - 87,025,840 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01384,083,880 - 84,257,664 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01389,053,457 - 89,242,531 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1389,055,983 - 89,242,443 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01393,668,054 - 93,854,918 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41386,543,773 - 86,718,970 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11386,559,136 - 86,734,174 (-)NCBI
Celera1382,588,612 - 82,760,829 (-)NCBICelera
Cytogenetic Map13q24NCBI
Atf6
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495546214,357,945 - 14,548,543 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495546214,352,956 - 14,553,299 (-)NCBIChiLan1.0ChiLan1.0
ATF6
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2187,820,564 - 88,020,287 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1187,484,878 - 87,688,569 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01137,178,629 - 137,382,256 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11140,977,750 - 141,181,837 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1140,977,750 - 141,176,725 (+)Ensemblpanpan1.1panPan2
ATF6
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.13820,705,167 - 20,903,852 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl3820,709,038 - 20,903,814 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha3820,758,598 - 20,956,710 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.03820,788,925 - 20,987,730 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl3820,788,924 - 20,987,623 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.13820,761,253 - 20,959,710 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.03821,114,892 - 21,313,427 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.03821,406,602 - 21,593,774 (-)NCBIUU_Cfam_GSD_1.0
Atf6
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_0244050587,651,241 - 7,833,831 (+)NCBIHiC_Itri_2
SpeTri2.0NW_004937131170,649 - 183,942 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ATF6
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl488,591,288 - 88,805,304 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1488,591,279 - 88,806,156 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2496,614,364 - 96,821,004 (-)NCBISscrofa10.2Sscrofa10.2susScr3
ATF6
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1202,112,819 - 2,304,063 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl202,117,982 - 2,304,027 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660381,151,751 - 1,344,350 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Atf6
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_004624826190,131 - 412,197 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_004624826189,899 - 412,540 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in ATF6
360 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_007348.3(ATF6):c.159+1609G>T single nucleotide variant Lung cancer [RCV000089848] Chr1:161779929 [GRCh38]
Chr1:161749719 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.3(ATF6):c.1322A>G (p.Tyr441Cys) single nucleotide variant Lung cancer [RCV000089849] Chr1:161851724 [GRCh38]
Chr1:161821514 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.3(ATF6):c.1720-2348T>C single nucleotide variant Lung cancer [RCV000089850] Chr1:161909948 [GRCh38]
Chr1:161879738 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.809T>C (p.Val270Ala) single nucleotide variant not provided [RCV001229495] Chr1:161802172 [GRCh38]
Chr1:161771962 [GRCh37]
Chr1:1q23.3
uncertain significance
GRCh38/hg38 1q23.2-24.1(chr1:159479887-166895086)x1 copy number loss See cases [RCV000051172] Chr1:159479887..166895086 [GRCh38]
Chr1:159449677..166864323 [GRCh37]
Chr1:157716301..165130947 [NCBI36]
Chr1:1q23.2-24.1
pathogenic
GRCh38/hg38 1q23.1-25.1(chr1:157747246-176021247)x3 copy number gain See cases [RCV000051854] Chr1:157747246..176021247 [GRCh38]
Chr1:157717036..175990383 [GRCh37]
Chr1:155983660..174257006 [NCBI36]
Chr1:1q23.1-25.1
pathogenic
GRCh38/hg38 1q23.3-24.2(chr1:160789732-168617494)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053913]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053913]|See cases [RCV000053913] Chr1:160789732..168617494 [GRCh38]
Chr1:160759522..168586732 [GRCh37]
Chr1:159026146..166853356 [NCBI36]
Chr1:1q23.3-24.2
pathogenic
GRCh38/hg38 1q23.3-25.1(chr1:161740907-173965154)x1 copy number loss See cases [RCV000053914] Chr1:161740907..173965154 [GRCh38]
Chr1:161710697..173934292 [GRCh37]
Chr1:159977321..172200915 [NCBI36]
Chr1:1q23.3-25.1
pathogenic
NM_007348.3(ATF6):c.949C>T (p.Arg317Ter) single nucleotide variant Malignant melanoma [RCV000059968] Chr1:161819672 [GRCh38]
Chr1:161789462 [GRCh37]
Chr1:160056086 [NCBI36]
Chr1:1q23.3
not provided
NM_007348.4(ATF6):c.484+3A>C single nucleotide variant not provided [RCV001312750] Chr1:161791540 [GRCh38]
Chr1:161761330 [GRCh37]
Chr1:1q23.3
uncertain significance
GRCh38/hg38 1q21.2-25.2(chr1:149854269-180267197)x3 copy number gain See cases [RCV000143515] Chr1:149854269..180267197 [GRCh38]
Chr1:149825831..180236332 [GRCh37]
Chr1:148092455..178502955 [NCBI36]
Chr1:1q21.2-25.2
pathogenic
NM_007348.4(ATF6):c.82+5G>T single nucleotide variant Achromatopsia 7 [RCV000191035]|not provided [RCV001093017] Chr1:161766447 [GRCh38]
Chr1:161736237 [GRCh37]
Chr1:1q23.3
pathogenic
NM_007348.4(ATF6):c.353del (p.Pro118fs) deletion Achromatopsia 7 [RCV000191036] Chr1:161784094 [GRCh38]
Chr1:161753884 [GRCh37]
Chr1:1q23.3
pathogenic
NM_007348.4(ATF6):c.1533+1G>C single nucleotide variant Achromatopsia 7 [RCV000191038] Chr1:161853324 [GRCh38]
Chr1:161823114 [GRCh37]
Chr1:1q23.3
pathogenic
NM_007348.4(ATF6):c.797dup (p.Pro266_Asn267insTer) duplication Achromatopsia 7 [RCV000191039] Chr1:161802157..161802158 [GRCh38]
Chr1:161771947..161771948 [GRCh37]
Chr1:1q23.3
pathogenic
NM_007348.4(ATF6):c.1110dup (p.Val371fs) duplication Achromatopsia 7 [RCV000191040] Chr1:161821081..161821082 [GRCh38]
Chr1:161790871..161790872 [GRCh37]
Chr1:1q23.3
pathogenic
NM_007348.4(ATF6):c.1187+5G>C single nucleotide variant Achromatopsia 7 [RCV000191037] Chr1:161821166 [GRCh38]
Chr1:161790956 [GRCh37]
Chr1:1q23.3
pathogenic
NM_007348.3:c.355_356dupG duplication Achromatopsia 7 [RCV000201242] Chr1:1q23.3 pathogenic
NM_007348.3(ATF6):c.355dup duplication Achromatopsia 7 [RCV000190367] Chr1:161791406..161791407 [GRCh38]
Chr1:161761196..161761197 [GRCh37]
Chr1:1q23.3
pathogenic
NM_007348.4(ATF6):c.970C>T (p.Arg324Cys) single nucleotide variant ATF6-related condition [RCV003390920]|Achromatopsia 7 [RCV000190368]|not provided [RCV001390414] Chr1:161819693 [GRCh38]
Chr1:161789483 [GRCh37]
Chr1:1q23.3
pathogenic
ATF6, IVS12, G-C, +1 single nucleotide variant ACHROMATOPSIA 7 [RCV000190369]|Achromatopsia 7 [RCV000190369] Chr1:1q23.3 pathogenic
ATF6, 1-BP DUP, 797C duplication ACHROMATOPSIA 7 [RCV000190370]|Achromatopsia 7 [RCV000190370] Chr1:1q23.3 pathogenic
ATF6, 1-BP DUP, 1110A duplication ACHROMATOPSIA 7 [RCV000190371]|Achromatopsia 7 [RCV000190371] Chr1:1q23.3 pathogenic
NM_007348.4(ATF6):c.1699T>A (p.Tyr567Asn) single nucleotide variant Achromatopsia 7 [RCV000190372] Chr1:161863292 [GRCh38]
Chr1:161833082 [GRCh37]
Chr1:1q23.3
pathogenic
NM_007348.4(ATF6):c.1784del (p.Leu595fs) deletion Achromatopsia 7 [RCV000723355] Chr1:161912359 [GRCh38]
Chr1:161882149 [GRCh37]
Chr1:1q23.3
likely pathogenic
GRCh37/hg19 1q23.3-25.3(chr1:161676893-184071723)x1 copy number loss See cases [RCV000447098] Chr1:161676893..184071723 [GRCh37]
Chr1:1q23.3-25.3
pathogenic
NM_007348.4(ATF6):c.1018G>C (p.Ala340Pro) single nucleotide variant Macular dystrophy [RCV000505004] Chr1:161819741 [GRCh38]
Chr1:161789531 [GRCh37]
Chr1:1q23.3
likely pathogenic
NM_007348.4(ATF6):c.417dup (p.Asn140Ter) duplication Achromatopsia [RCV000504633] Chr1:161791469..161791470 [GRCh38]
Chr1:161761259..161761260 [GRCh37]
Chr1:1q23.3
likely pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3 copy number gain See cases [RCV000510383] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684) copy number gain See cases [RCV000510926] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44
pathogenic
NM_007348.4(ATF6):c.1224T>A (p.Ser408Arg) single nucleotide variant Inborn genetic diseases [RCV003281424] Chr1:161846485 [GRCh38]
Chr1:161816275 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.920T>G (p.Leu307Arg) single nucleotide variant Inborn genetic diseases [RCV003246434] Chr1:161819643 [GRCh38]
Chr1:161789433 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.3(ATF6):c.160dup (p.Glu54Glyfs) duplication Achromatopsia [RCV000608330] Chr1:161781910..161781911 [GRCh38]
Chr1:161751700..161751701 [GRCh37]
Chr1:1q23.3
pathogenic
GRCh37/hg19 1q23.3(chr1:161469309-162517412)x3 copy number gain not provided [RCV000684667] Chr1:161469309..162517412 [GRCh37]
Chr1:1q23.3
uncertain significance
GRCh37/hg19 1q23.3(chr1:161726804-161867948)x1 copy number loss not provided [RCV000684668] Chr1:161726804..161867948 [GRCh37]
Chr1:1q23.3
uncertain significance
GRCh37/hg19 1p36.33-q44(chr1:47851-249228449)x3 copy number gain not provided [RCV000736295] Chr1:47851..249228449 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:82154-249218992)x3 copy number gain not provided [RCV000736305] Chr1:82154..249218992 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1q23.2-25.2(chr1:159815642-177026983)x1 copy number loss not provided [RCV000736717] Chr1:159815642..177026983 [GRCh37]
Chr1:1q23.2-25.2
pathogenic
NM_007348.4(ATF6):c.1108A>T (p.Lys370Ter) single nucleotide variant not provided [RCV000760796] Chr1:161821082 [GRCh38]
Chr1:161790872 [GRCh37]
Chr1:1q23.3
pathogenic
NM_007348.4(ATF6):c.496A>C (p.Thr166Pro) single nucleotide variant not provided [RCV001053648] Chr1:161792135 [GRCh38]
Chr1:161761925 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.199A>G (p.Met67Val) single nucleotide variant Achromatopsia 7 [RCV000986451]|not provided [RCV001518516] Chr1:161781951 [GRCh38]
Chr1:161751741 [GRCh37]
Chr1:1q23.3
benign
NM_007348.4(ATF6):c.1617G>C (p.Gly539=) single nucleotide variant not provided [RCV000904971] Chr1:161863210 [GRCh38]
Chr1:161833000 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.688+10C>G single nucleotide variant not provided [RCV000922876] Chr1:161792337 [GRCh38]
Chr1:161762127 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1311C>T (p.Asn437=) single nucleotide variant not provided [RCV000926061] Chr1:161846572 [GRCh38]
Chr1:161816362 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.47G>T (p.Ser16Ile) single nucleotide variant not provided [RCV000904801] Chr1:161766407 [GRCh38]
Chr1:161736197 [GRCh37]
Chr1:1q23.3
benign|likely benign
NM_007348.4(ATF6):c.326A>G (p.Asp109Gly) single nucleotide variant not provided [RCV001040662] Chr1:161784068 [GRCh38]
Chr1:161753858 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.237A>G (p.Gln79=) single nucleotide variant not provided [RCV001070412] Chr1:161781989 [GRCh38]
Chr1:161751779 [GRCh37]
Chr1:1q23.3
likely benign|uncertain significance
NM_007348.4(ATF6):c.1714C>G (p.Arg572Gly) single nucleotide variant not provided [RCV001066654] Chr1:161863307 [GRCh38]
Chr1:161833097 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.804C>T (p.His268=) single nucleotide variant not provided [RCV000952458] Chr1:161802167 [GRCh38]
Chr1:161771957 [GRCh37]
Chr1:1q23.3
benign
NM_007348.4(ATF6):c.1416C>T (p.Asn472=) single nucleotide variant not provided [RCV000900202] Chr1:161851818 [GRCh38]
Chr1:161821608 [GRCh37]
Chr1:1q23.3
benign
NM_007348.4(ATF6):c.715A>G (p.Thr239Ala) single nucleotide variant not provided [RCV000948569]|not specified [RCV001700515] Chr1:161802078 [GRCh38]
Chr1:161771868 [GRCh37]
Chr1:1q23.3
benign
NM_007348.4(ATF6):c.999G>T (p.Gly333=) single nucleotide variant not provided [RCV000909157] Chr1:161819722 [GRCh38]
Chr1:161789512 [GRCh37]
Chr1:1q23.3
likely benign
GRCh37/hg19 1q23.2-25.1(chr1:160369890-175796325) copy number loss not provided [RCV000767779] Chr1:160369890..175796325 [GRCh37]
Chr1:1q23.2-25.1
pathogenic
NM_007348.4(ATF6):c.511del (p.Ile171fs) deletion Achromatopsia 7 [RCV000985102] Chr1:161792144 [GRCh38]
Chr1:161761934 [GRCh37]
Chr1:1q23.3
likely pathogenic
NM_007348.4(ATF6):c.316C>T (p.Arg106Trp) single nucleotide variant not provided [RCV001053818] Chr1:161784058 [GRCh38]
Chr1:161753848 [GRCh37]
Chr1:1q23.3
uncertain significance
GRCh37/hg19 1q23.3(chr1:160744174-162583871)x3 copy number gain not provided [RCV000849025] Chr1:160744174..162583871 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.494T>A (p.Leu165Gln) single nucleotide variant not provided [RCV001210868] Chr1:161792133 [GRCh38]
Chr1:161761923 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.709C>T (p.Gln237Ter) single nucleotide variant Achromatopsia 7 [RCV000986452]|not provided [RCV001869334] Chr1:161802072 [GRCh38]
Chr1:161771862 [GRCh37]
Chr1:1q23.3
pathogenic
NM_007348.4(ATF6):c.452A>G (p.Asp151Gly) single nucleotide variant not provided [RCV001237065] Chr1:161791505 [GRCh38]
Chr1:161761295 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1880_1882del (p.His627_Ile628delinsLeu) deletion not provided [RCV001224348] Chr1:161958521..161958523 [GRCh38]
Chr1:161928311..161928313 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1522C>T (p.Arg508Cys) single nucleotide variant not provided [RCV001233630] Chr1:161853312 [GRCh38]
Chr1:161823102 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.935G>A (p.Arg312His) single nucleotide variant not provided [RCV001241574] Chr1:161819658 [GRCh38]
Chr1:161789448 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.27C>T (p.Gly9=) single nucleotide variant not provided [RCV001238275] Chr1:161766387 [GRCh38]
Chr1:161736177 [GRCh37]
Chr1:1q23.3
likely benign|uncertain significance
NM_007348.4(ATF6):c.742G>A (p.Val248Ile) single nucleotide variant not provided [RCV001225362] Chr1:161802105 [GRCh38]
Chr1:161771895 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1592C>G (p.Thr531Ser) single nucleotide variant not provided [RCV001210432] Chr1:161860265 [GRCh38]
Chr1:161830055 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.484+1G>T single nucleotide variant Achromatopsia [RCV001195419]|not provided [RCV001378682] Chr1:161791538 [GRCh38]
Chr1:161761328 [GRCh37]
Chr1:1q23.3
likely pathogenic
NM_007348.4(ATF6):c.1325A>G (p.Asp442Gly) single nucleotide variant not provided [RCV001202563] Chr1:161851727 [GRCh38]
Chr1:161821517 [GRCh37]
Chr1:1q23.3
uncertain significance
GRCh37/hg19 1q23.1-24.2(chr1:157321299-167391423)x1 copy number loss not provided [RCV000848773] Chr1:157321299..167391423 [GRCh37]
Chr1:1q23.1-24.2
pathogenic
NM_007348.4(ATF6):c.1190_1191insTTTTT (p.Met397fs) insertion Achromatopsia 7 [RCV000986453] Chr1:161846450..161846451 [GRCh38]
Chr1:161816240..161816241 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1191G>T (p.Met397Ile) single nucleotide variant Achromatopsia 7 [RCV000986454] Chr1:161846452 [GRCh38]
Chr1:161816242 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1523G>A (p.Arg508His) single nucleotide variant not provided [RCV001229347] Chr1:161853313 [GRCh38]
Chr1:161823103 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.435G>A (p.Ala145=) single nucleotide variant not provided [RCV001245763] Chr1:161791488 [GRCh38]
Chr1:161761278 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.360G>A (p.Glu120=) single nucleotide variant not provided [RCV000954072]|not specified [RCV001699475] Chr1:161791413 [GRCh38]
Chr1:161761203 [GRCh37]
Chr1:1q23.3
benign|likely benign
NM_007348.4(ATF6):c.248-9G>A single nucleotide variant not provided [RCV000902077] Chr1:161783981 [GRCh38]
Chr1:161753771 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1602C>T (p.Ile534=) single nucleotide variant not provided [RCV000885720] Chr1:161860275 [GRCh38]
Chr1:161830065 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1508A>G (p.Asn503Ser) single nucleotide variant not provided [RCV001201556] Chr1:161853298 [GRCh38]
Chr1:161823088 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1333G>A (p.Val445Ile) single nucleotide variant not provided [RCV001213085] Chr1:161851735 [GRCh38]
Chr1:161821525 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.425T>C (p.Leu142Pro) single nucleotide variant not provided [RCV001245612] Chr1:161791478 [GRCh38]
Chr1:161761268 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.289T>C (p.Ser97Pro) single nucleotide variant not provided [RCV001241705] Chr1:161784031 [GRCh38]
Chr1:161753821 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.833C>T (p.Ala278Val) single nucleotide variant not provided [RCV000891047] Chr1:161802196 [GRCh38]
Chr1:161771986 [GRCh37]
Chr1:1q23.3
benign
NM_007348.4(ATF6):c.1434-3T>A single nucleotide variant Achromatopsia 7 [RCV000986455]|not provided [RCV001513111] Chr1:161853221 [GRCh38]
Chr1:161823011 [GRCh37]
Chr1:1q23.3
benign
NM_007348.4(ATF6):c.861C>T (p.Ser287=) single nucleotide variant not provided [RCV000890665] Chr1:161802224 [GRCh38]
Chr1:161772014 [GRCh37]
Chr1:1q23.3
benign
NM_007348.4(ATF6):c.406G>A (p.Gly136Ser) single nucleotide variant not provided [RCV001053489] Chr1:161791459 [GRCh38]
Chr1:161761249 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1997C>G (p.Pro666Arg) single nucleotide variant not provided [RCV001064406] Chr1:161958638 [GRCh38]
Chr1:161928428 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1187+3A>G single nucleotide variant not provided [RCV001246548] Chr1:161821164 [GRCh38]
Chr1:161790954 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.17G>T (p.Gly6Val) single nucleotide variant not provided [RCV001065735] Chr1:161766377 [GRCh38]
Chr1:161736167 [GRCh37]
Chr1:1q23.3
conflicting interpretations of pathogenicity|uncertain significance
NM_007348.4(ATF6):c.1403A>C (p.Gln468Pro) single nucleotide variant not provided [RCV001214001] Chr1:161851805 [GRCh38]
Chr1:161821595 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1249C>A (p.His417Asn) single nucleotide variant not provided [RCV001233396] Chr1:161846510 [GRCh38]
Chr1:161816300 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.67C>T (p.Leu23=) single nucleotide variant not provided [RCV001246987] Chr1:161766427 [GRCh38]
Chr1:161736217 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.355-3C>T single nucleotide variant not provided [RCV001049799] Chr1:161791405 [GRCh38]
Chr1:161761195 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.149A>G (p.Asn50Ser) single nucleotide variant not provided [RCV001208580] Chr1:161778310 [GRCh38]
Chr1:161748100 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1533+5G>A single nucleotide variant not provided [RCV001233876] Chr1:161853328 [GRCh38]
Chr1:161823118 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1954C>T (p.Pro652Ser) single nucleotide variant Inborn genetic diseases [RCV003243411]|not provided [RCV001039052] Chr1:161958595 [GRCh38]
Chr1:161928385 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1493GAA[1] (p.Arg499del) microsatellite not provided [RCV001210997] Chr1:161853281..161853283 [GRCh38]
Chr1:161823071..161823073 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1175A>G (p.Tyr392Cys) single nucleotide variant not provided [RCV001201629] Chr1:161821149 [GRCh38]
Chr1:161790939 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.702G>T (p.Leu234Phe) single nucleotide variant not provided [RCV001870693] Chr1:161802065 [GRCh38]
Chr1:161771855 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.245C>T (p.Thr82Ile) single nucleotide variant not provided [RCV001204436] Chr1:161781997 [GRCh38]
Chr1:161751787 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1679G>A (p.Arg560His) single nucleotide variant not provided [RCV001231287] Chr1:161863272 [GRCh38]
Chr1:161833062 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.679C>T (p.Pro227Ser) single nucleotide variant not provided [RCV001205101] Chr1:161792318 [GRCh38]
Chr1:161762108 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1237A>T (p.Asn413Tyr) single nucleotide variant not provided [RCV001233664] Chr1:161846498 [GRCh38]
Chr1:161816288 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.761C>T (p.Pro254Leu) single nucleotide variant not provided [RCV001040998] Chr1:161802124 [GRCh38]
Chr1:161771914 [GRCh37]
Chr1:1q23.3
uncertain significance
NC_000001.11:g.(?_161819633)_(161821161_?)dup duplication not provided [RCV001032936] Chr1:161789423..161790951 [GRCh37]
Chr1:1q23.3
likely pathogenic
NM_007348.4(ATF6):c.2011T>C (p.Ter671Gln) single nucleotide variant not provided [RCV001240049] Chr1:161958652 [GRCh38]
Chr1:161928442 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.3G>T (p.Met1Ile) single nucleotide variant Achromatopsia 7 [RCV001255912] Chr1:161766363 [GRCh38]
Chr1:161736153 [GRCh37]
Chr1:1q23.3
pathogenic
NM_007348.4(ATF6):c.950G>A (p.Arg317Gln) single nucleotide variant Achromatopsia 7 [RCV001255911] Chr1:161819673 [GRCh38]
Chr1:161789463 [GRCh37]
Chr1:1q23.3
likely pathogenic
NM_007348.4(ATF6):c.854A>G (p.Lys285Arg) single nucleotide variant Achromatopsia 7 [RCV001255913] Chr1:161802217 [GRCh38]
Chr1:161772007 [GRCh37]
Chr1:1q23.3
likely pathogenic
NM_007348.4(ATF6):c.77A>G (p.Asp26Gly) single nucleotide variant not provided [RCV001303900] Chr1:161766437 [GRCh38]
Chr1:161736227 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.308C>T (p.Ser103Leu) single nucleotide variant not provided [RCV001304785] Chr1:161784050 [GRCh38]
Chr1:161753840 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.682A>G (p.Thr228Ala) single nucleotide variant not provided [RCV001308521] Chr1:161792321 [GRCh38]
Chr1:161762111 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.863T>A (p.Val288Glu) single nucleotide variant not provided [RCV001326235] Chr1:161802226 [GRCh38]
Chr1:161772016 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.82+5G>A single nucleotide variant not provided [RCV001317723] Chr1:161766447 [GRCh38]
Chr1:161736237 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.859T>C (p.Ser287Pro) single nucleotide variant not provided [RCV001308760] Chr1:161802222 [GRCh38]
Chr1:161772012 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1441C>T (p.His481Tyr) single nucleotide variant not provided [RCV001301783] Chr1:161853231 [GRCh38]
Chr1:161823021 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.563C>G (p.Ala188Gly) single nucleotide variant not provided [RCV001340550] Chr1:161792202 [GRCh38]
Chr1:161761992 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1070G>A (p.Arg357Gln) single nucleotide variant not provided [RCV001343460] Chr1:161819793 [GRCh38]
Chr1:161789583 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.688+4C>G single nucleotide variant not provided [RCV001307071] Chr1:161792331 [GRCh38]
Chr1:161762121 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.901G>A (p.Gly301Ser) single nucleotide variant Inborn genetic diseases [RCV003166744]|not provided [RCV001306485] Chr1:161802264 [GRCh38]
Chr1:161772054 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1354A>T (p.Met452Leu) single nucleotide variant not provided [RCV001363175] Chr1:161851756 [GRCh38]
Chr1:161821546 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1284C>G (p.Asp428Glu) single nucleotide variant not provided [RCV001327033] Chr1:161846545 [GRCh38]
Chr1:161816335 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.923G>A (p.Arg308Lys) single nucleotide variant not provided [RCV001349468] Chr1:161819646 [GRCh38]
Chr1:161789436 [GRCh37]
Chr1:1q23.3
uncertain significance
NC_000001.10:g.(?_130980840)_(248900000_?)dup duplication Gastrointestinal stromal tumor [RCV001300221]|Parathyroid carcinoma [RCV001341077] Chr1:130980840..248900000 [GRCh37]
Chr1:1q12-44
uncertain significance
NM_007348.4(ATF6):c.696G>A (p.Thr232=) single nucleotide variant not provided [RCV001414262] Chr1:161802059 [GRCh38]
Chr1:161771849 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.754G>A (p.Ala252Thr) single nucleotide variant not provided [RCV001371967] Chr1:161802117 [GRCh38]
Chr1:161771907 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.593T>C (p.Val198Ala) single nucleotide variant not provided [RCV001346305] Chr1:161792232 [GRCh38]
Chr1:161762022 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1103G>T (p.Arg368Met) single nucleotide variant not provided [RCV001339696] Chr1:161821077 [GRCh38]
Chr1:161790867 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.721G>A (p.Val241Ile) single nucleotide variant not provided [RCV001318564] Chr1:161802084 [GRCh38]
Chr1:161771874 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.13G>A (p.Ala5Thr) single nucleotide variant not provided [RCV001322938] Chr1:161766373 [GRCh38]
Chr1:161736163 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1719+17A>G single nucleotide variant not provided [RCV001345797] Chr1:161863329 [GRCh38]
Chr1:161833119 [GRCh37]
Chr1:1q23.3
likely benign|uncertain significance
NM_007348.4(ATF6):c.805G>A (p.Val269Met) single nucleotide variant not provided [RCV001346573] Chr1:161802168 [GRCh38]
Chr1:161771958 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.677C>A (p.Ala226Glu) single nucleotide variant Achromatopsia 7 [RCV001333648] Chr1:161792316 [GRCh38]
Chr1:161762106 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.881A>G (p.Gln294Arg) single nucleotide variant not provided [RCV001347375] Chr1:161802244 [GRCh38]
Chr1:161772034 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.431C>T (p.Ser144Leu) single nucleotide variant not provided [RCV001314921] Chr1:161791484 [GRCh38]
Chr1:161761274 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1132G>C (p.Val378Leu) single nucleotide variant not provided [RCV001372934] Chr1:161821106 [GRCh38]
Chr1:161790896 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1718G>A (p.Arg573Lys) single nucleotide variant not provided [RCV001300902] Chr1:161863311 [GRCh38]
Chr1:161833101 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.434C>T (p.Ala145Val) single nucleotide variant not provided [RCV001362063] Chr1:161791487 [GRCh38]
Chr1:161761277 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1925G>C (p.Arg642Thr) single nucleotide variant Inborn genetic diseases [RCV003298579]|not provided [RCV001363634] Chr1:161958566 [GRCh38]
Chr1:161928356 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1961C>A (p.Ala654Glu) single nucleotide variant not provided [RCV001363852] Chr1:161958602 [GRCh38]
Chr1:161928392 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.748C>T (p.Pro250Ser) single nucleotide variant not provided [RCV001296701] Chr1:161802111 [GRCh38]
Chr1:161771901 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1946T>G (p.Phe649Cys) single nucleotide variant not provided [RCV001373366] Chr1:161958587 [GRCh38]
Chr1:161928377 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.403T>C (p.Tyr135His) single nucleotide variant not provided [RCV001366867] Chr1:161791456 [GRCh38]
Chr1:161761246 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.585C>G (p.Asn195Lys) single nucleotide variant Inborn genetic diseases [RCV002543694]|not provided [RCV001316382] Chr1:161792224 [GRCh38]
Chr1:161762014 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1648A>G (p.Arg550Gly) single nucleotide variant Inborn genetic diseases [RCV003246933]|not provided [RCV001358950] Chr1:161863241 [GRCh38]
Chr1:161833031 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.512T>A (p.Ile171Asn) single nucleotide variant not provided [RCV001338375] Chr1:161792151 [GRCh38]
Chr1:161761941 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1018G>A (p.Ala340Thr) single nucleotide variant not provided [RCV001315748] Chr1:161819741 [GRCh38]
Chr1:161789531 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1520C>A (p.Thr507Asn) single nucleotide variant not provided [RCV001317353] Chr1:161853310 [GRCh38]
Chr1:161823100 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.41C>A (p.Pro14His) single nucleotide variant not provided [RCV001365842] Chr1:161766401 [GRCh38]
Chr1:161736191 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1229G>A (p.Ser410Asn) single nucleotide variant Inborn genetic diseases [RCV002543127]|not provided [RCV001305251] Chr1:161846490 [GRCh38]
Chr1:161816280 [GRCh37]
Chr1:1q23.3
likely benign|uncertain significance
NM_007348.4(ATF6):c.136T>C (p.Leu46=) single nucleotide variant not provided [RCV001469306] Chr1:161778297 [GRCh38]
Chr1:161748087 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1805-4G>A single nucleotide variant not provided [RCV001495565] Chr1:161958442 [GRCh38]
Chr1:161928232 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1092A>G (p.Ser364=) single nucleotide variant not provided [RCV001438604] Chr1:161819815 [GRCh38]
Chr1:161789605 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.994C>T (p.Leu332=) single nucleotide variant not provided [RCV001464755] Chr1:161819717 [GRCh38]
Chr1:161789507 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.270T>C (p.Pro90=) single nucleotide variant Achromatopsia 7 [RCV001553924]|not provided [RCV001510281] Chr1:161784012 [GRCh38]
Chr1:161753802 [GRCh37]
Chr1:1q23.3
benign
NM_007348.4(ATF6):c.309G>A (p.Ser103=) single nucleotide variant Achromatopsia 7 [RCV001553925]|not provided [RCV001510282] Chr1:161784051 [GRCh38]
Chr1:161753841 [GRCh37]
Chr1:1q23.3
benign
NM_007348.4(ATF6):c.485-4C>G single nucleotide variant not provided [RCV001431241] Chr1:161792120 [GRCh38]
Chr1:161761910 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1335T>G (p.Val445=) single nucleotide variant not provided [RCV001468240] Chr1:161851737 [GRCh38]
Chr1:161821527 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1554A>G (p.Ser518=) single nucleotide variant not provided [RCV001522604] Chr1:161860227 [GRCh38]
Chr1:161830017 [GRCh37]
Chr1:1q23.3
benign
NM_007348.4(ATF6):c.384G>A (p.Gln128=) single nucleotide variant not provided [RCV001470476] Chr1:161791437 [GRCh38]
Chr1:161761227 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1805-8G>A single nucleotide variant not provided [RCV001478591] Chr1:161958438 [GRCh38]
Chr1:161928228 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.159+14A>G single nucleotide variant not provided [RCV001519110] Chr1:161778334 [GRCh38]
Chr1:161748124 [GRCh37]
Chr1:1q23.3
benign
NM_007348.4(ATF6):c.1337C>G (p.Ser446Ter) single nucleotide variant not provided [RCV001380306] Chr1:161851739 [GRCh38]
Chr1:161821529 [GRCh37]
Chr1:1q23.3
pathogenic
NM_007348.4(ATF6):c.1491A>G (p.Ser497=) single nucleotide variant not provided [RCV001426828] Chr1:161853281 [GRCh38]
Chr1:161823071 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.777T>C (p.Ala259=) single nucleotide variant not provided [RCV001411046] Chr1:161802140 [GRCh38]
Chr1:161771930 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1767A>G (p.Pro589=) single nucleotide variant not provided [RCV001419637] Chr1:161912343 [GRCh38]
Chr1:161882133 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.156G>A (p.Thr52=) single nucleotide variant not provided [RCV001408859] Chr1:161778317 [GRCh38]
Chr1:161748107 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1960G>A (p.Ala654Thr) single nucleotide variant not provided [RCV001394040] Chr1:161958601 [GRCh38]
Chr1:161928391 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1534-10A>C single nucleotide variant not provided [RCV001498895] Chr1:161860197 [GRCh38]
Chr1:161829987 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1533+8T>C single nucleotide variant not provided [RCV001495728] Chr1:161853331 [GRCh38]
Chr1:161823121 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.469C>T (p.Pro157Ser) single nucleotide variant not provided [RCV001510284] Chr1:161791522 [GRCh38]
Chr1:161761312 [GRCh37]
Chr1:1q23.3
benign
NM_007348.4(ATF6):c.105C>T (p.Leu35=) single nucleotide variant Achromatopsia 7 [RCV001553870]|not provided [RCV001510280] Chr1:161778266 [GRCh38]
Chr1:161748056 [GRCh37]
Chr1:1q23.3
benign
NM_007348.4(ATF6):c.385A>G (p.Met129Val) single nucleotide variant not provided [RCV001515991] Chr1:161791438 [GRCh38]
Chr1:161761228 [GRCh37]
Chr1:1q23.3
benign
NM_007348.4(ATF6):c.159+12C>T single nucleotide variant not provided [RCV001503540] Chr1:161778332 [GRCh38]
Chr1:161748122 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1485C>G (p.Thr495=) single nucleotide variant not provided [RCV001516454] Chr1:161853275 [GRCh38]
Chr1:161823065 [GRCh37]
Chr1:1q23.3
benign
NM_007348.4(ATF6):c.689-5C>T single nucleotide variant not provided [RCV001497164] Chr1:161802047 [GRCh38]
Chr1:161771837 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.485-9T>C single nucleotide variant not provided [RCV001496942] Chr1:161792115 [GRCh38]
Chr1:161761905 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.681C>T (p.Pro227=) single nucleotide variant not provided [RCV001471283] Chr1:161792320 [GRCh38]
Chr1:161762110 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.59T>C (p.Phe20Ser) single nucleotide variant not provided [RCV001523512] Chr1:161766419 [GRCh38]
Chr1:161736209 [GRCh37]
Chr1:1q23.3
benign
NM_007348.4(ATF6):c.355-7G>C single nucleotide variant not provided [RCV001478368] Chr1:161791401 [GRCh38]
Chr1:161761191 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.819A>G (p.Val273=) single nucleotide variant not provided [RCV001504773] Chr1:161802182 [GRCh38]
Chr1:161771972 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1719+8C>A single nucleotide variant not provided [RCV001523160] Chr1:161863320 [GRCh38]
Chr1:161833110 [GRCh37]
Chr1:1q23.3
benign
NM_007348.4(ATF6):c.433G>C (p.Ala145Pro) single nucleotide variant not provided [RCV001510283] Chr1:161791486 [GRCh38]
Chr1:161761276 [GRCh37]
Chr1:1q23.3
benign
NM_007348.4(ATF6):c.579A>G (p.Gln193=) single nucleotide variant not provided [RCV001432513] Chr1:161792218 [GRCh38]
Chr1:161762008 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1896A>G (p.Ser632=) single nucleotide variant Achromatopsia 7 [RCV001553926]|not provided [RCV001517526] Chr1:161958537 [GRCh38]
Chr1:161928327 [GRCh37]
Chr1:1q23.3
benign
NM_007348.4(ATF6):c.1804+19G>A single nucleotide variant not provided [RCV001511758] Chr1:161912399 [GRCh38]
Chr1:161882189 [GRCh37]
Chr1:1q23.3
benign
NM_007348.4(ATF6):c.957C>T (p.Ser319=) single nucleotide variant not provided [RCV001485450] Chr1:161819680 [GRCh38]
Chr1:161789470 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1719+9A>G single nucleotide variant not provided [RCV001485458] Chr1:161863321 [GRCh38]
Chr1:161833111 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1782G>A (p.Val594=) single nucleotide variant not provided [RCV001471800] Chr1:161912358 [GRCh38]
Chr1:161882148 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.484+1G>A single nucleotide variant not provided [RCV001379608] Chr1:161791538 [GRCh38]
Chr1:161761328 [GRCh37]
Chr1:1q23.3
likely pathogenic
NM_007348.4(ATF6):c.1095+17C>G single nucleotide variant not provided [RCV001518232] Chr1:161819835 [GRCh38]
Chr1:161789625 [GRCh37]
Chr1:1q23.3
benign
NM_007348.4(ATF6):c.1983T>C (p.Val661=) single nucleotide variant not provided [RCV001424449] Chr1:161958624 [GRCh38]
Chr1:161928414 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1108A>G (p.Lys370Glu) single nucleotide variant Inborn genetic diseases [RCV003275445] Chr1:161821082 [GRCh38]
Chr1:161790872 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1649G>C (p.Arg550Thr) single nucleotide variant not provided [RCV001907880] Chr1:161863242 [GRCh38]
Chr1:161833032 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.247+6T>C single nucleotide variant not provided [RCV001968420] Chr1:161782005 [GRCh38]
Chr1:161751795 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.317G>C (p.Arg106Pro) single nucleotide variant not provided [RCV002024753] Chr1:161784059 [GRCh38]
Chr1:161753849 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1605-5T>G single nucleotide variant not provided [RCV001895729] Chr1:161863193 [GRCh38]
Chr1:161832983 [GRCh37]
Chr1:1q23.3
likely benign|uncertain significance
NM_007348.4(ATF6):c.1372C>G (p.Pro458Ala) single nucleotide variant not provided [RCV001913678] Chr1:161851774 [GRCh38]
Chr1:161821564 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.565G>A (p.Ala189Thr) single nucleotide variant not provided [RCV001970619] Chr1:161792204 [GRCh38]
Chr1:161761994 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.966G>C (p.Gln322His) single nucleotide variant not provided [RCV001929965] Chr1:161819689 [GRCh38]
Chr1:161789479 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1549G>A (p.Gly517Ser) single nucleotide variant not provided [RCV001873977] Chr1:161860222 [GRCh38]
Chr1:161830012 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.662T>C (p.Ile221Thr) single nucleotide variant not provided [RCV001949959] Chr1:161792301 [GRCh38]
Chr1:161762091 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.422G>A (p.Ser141Asn) single nucleotide variant not provided [RCV001988545] Chr1:161791475 [GRCh38]
Chr1:161761265 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1127G>A (p.Arg376Gln) single nucleotide variant not provided [RCV001986540] Chr1:161821101 [GRCh38]
Chr1:161790891 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.367T>G (p.Leu123Val) single nucleotide variant not provided [RCV002021780] Chr1:161791420 [GRCh38]
Chr1:161761210 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1096-18T>A single nucleotide variant not provided [RCV001986015] Chr1:161821052 [GRCh38]
Chr1:161790842 [GRCh37]
Chr1:1q23.3
uncertain significance
GRCh37/hg19 1q23.2-24.1(chr1:160417296-166197042) copy number loss not specified [RCV002053658] Chr1:160417296..166197042 [GRCh37]
Chr1:1q23.2-24.1
pathogenic
NM_007348.4(ATF6):c.1981G>A (p.Val661Ile) single nucleotide variant not provided [RCV001985517] Chr1:161958622 [GRCh38]
Chr1:161928412 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.563C>T (p.Ala188Val) single nucleotide variant not provided [RCV001872884] Chr1:161792202 [GRCh38]
Chr1:161761992 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1661A>G (p.Asp554Gly) single nucleotide variant not provided [RCV002044546] Chr1:161863254 [GRCh38]
Chr1:161833044 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.505A>G (p.Lys169Glu) single nucleotide variant not provided [RCV001912546] Chr1:161792144 [GRCh38]
Chr1:161761934 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.497C>T (p.Thr166Ile) single nucleotide variant not provided [RCV001984868] Chr1:161792136 [GRCh38]
Chr1:161761926 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1532A>G (p.Gln511Arg) single nucleotide variant not provided [RCV001911114] Chr1:161853322 [GRCh38]
Chr1:161823112 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1393C>A (p.Pro465Thr) single nucleotide variant not provided [RCV001983692] Chr1:161851795 [GRCh38]
Chr1:161821585 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1289C>T (p.Ser430Leu) single nucleotide variant not provided [RCV001966707] Chr1:161846550 [GRCh38]
Chr1:161816340 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.7G>T (p.Glu3Ter) single nucleotide variant not provided [RCV001949324] Chr1:161766367 [GRCh38]
Chr1:161736157 [GRCh37]
Chr1:1q23.3
pathogenic
NM_007348.4(ATF6):c.494T>C (p.Leu165Pro) single nucleotide variant not provided [RCV001890656] Chr1:161792133 [GRCh38]
Chr1:161761923 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1748A>G (p.His583Arg) single nucleotide variant not provided [RCV001928068] Chr1:161912324 [GRCh38]
Chr1:161882114 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.884G>C (p.Ser295Thr) single nucleotide variant not provided [RCV001894548] Chr1:161802247 [GRCh38]
Chr1:161772037 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.760C>T (p.Pro254Ser) single nucleotide variant not provided [RCV001927490] Chr1:161802123 [GRCh38]
Chr1:161771913 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1327C>G (p.His443Asp) single nucleotide variant not provided [RCV001985203] Chr1:161851729 [GRCh38]
Chr1:161821519 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.269C>A (p.Pro90His) single nucleotide variant not provided [RCV002022434] Chr1:161784011 [GRCh38]
Chr1:161753801 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.281C>G (p.Ser94Cys) single nucleotide variant not provided [RCV001983684] Chr1:161784023 [GRCh38]
Chr1:161753813 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.535A>G (p.Ile179Val) single nucleotide variant not provided [RCV002038448] Chr1:161792174 [GRCh38]
Chr1:161761964 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.680C>G (p.Pro227Arg) single nucleotide variant not provided [RCV002048072] Chr1:161792319 [GRCh38]
Chr1:161762109 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.82+1G>T single nucleotide variant not provided [RCV002016015] Chr1:161766443 [GRCh38]
Chr1:161736233 [GRCh37]
Chr1:1q23.3
likely pathogenic
NM_007348.4(ATF6):c.1434-14A>G single nucleotide variant not provided [RCV001963390] Chr1:161853210 [GRCh38]
Chr1:161823000 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1146G>A (p.Met382Ile) single nucleotide variant not provided [RCV002001365] Chr1:161821120 [GRCh38]
Chr1:161790910 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.199A>T (p.Met67Leu) single nucleotide variant not provided [RCV002001420] Chr1:161781951 [GRCh38]
Chr1:161751741 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1299T>G (p.Ile433Met) single nucleotide variant not provided [RCV001930543] Chr1:161846560 [GRCh38]
Chr1:161816350 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1319+17C>G single nucleotide variant not provided [RCV001963626] Chr1:161846597 [GRCh38]
Chr1:161816387 [GRCh37]
Chr1:1q23.3
likely benign|uncertain significance
NM_007348.4(ATF6):c.159+4del deletion not provided [RCV001877265] Chr1:161778323 [GRCh38]
Chr1:161748113 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.920_931del (p.Leu307_Gln310del) deletion not provided [RCV001993580] Chr1:161819641..161819652 [GRCh38]
Chr1:161789431..161789442 [GRCh37]
Chr1:1q23.3
uncertain significance
NC_000001.10:g.(?_161748014)_(161748130_?)dup duplication not provided [RCV002050881] Chr1:161748014..161748130 [GRCh37]
Chr1:1q23.3
likely pathogenic
NM_007348.4(ATF6):c.502A>G (p.Lys168Glu) single nucleotide variant not provided [RCV002031603] Chr1:161792141 [GRCh38]
Chr1:161761931 [GRCh37]
Chr1:1q23.3
uncertain significance
NC_000001.10:g.(?_161816219)_(162040092_?)dup duplication not provided [RCV001932872] Chr1:161816219..162040092 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1450C>G (p.Arg484Gly) single nucleotide variant not provided [RCV001956040] Chr1:161853240 [GRCh38]
Chr1:161823030 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1319+2T>C single nucleotide variant not provided [RCV001974443] Chr1:161846582 [GRCh38]
Chr1:161816372 [GRCh37]
Chr1:1q23.3
likely pathogenic
NM_007348.4(ATF6):c.1208G>A (p.Arg403Lys) single nucleotide variant not provided [RCV001867765] Chr1:161846469 [GRCh38]
Chr1:161816259 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1275G>T (p.Glu425Asp) single nucleotide variant not provided [RCV002014824] Chr1:161846536 [GRCh38]
Chr1:161816326 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.840C>G (p.Ser280Arg) single nucleotide variant not provided [RCV001922290] Chr1:161802203 [GRCh38]
Chr1:161771993 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1618A>G (p.Ser540Gly) single nucleotide variant not provided [RCV001980527] Chr1:161863211 [GRCh38]
Chr1:161833001 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1306A>G (p.Lys436Glu) single nucleotide variant not provided [RCV001934925] Chr1:161846567 [GRCh38]
Chr1:161816357 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1237A>C (p.Asn413His) single nucleotide variant not provided [RCV002049427] Chr1:161846498 [GRCh38]
Chr1:161816288 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.987A>C (p.Glu329Asp) single nucleotide variant not provided [RCV001999470] Chr1:161819710 [GRCh38]
Chr1:161789500 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1093G>A (p.Glu365Lys) single nucleotide variant not provided [RCV002030028] Chr1:161819816 [GRCh38]
Chr1:161789606 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1262T>C (p.Phe421Ser) single nucleotide variant not provided [RCV001997884] Chr1:161846523 [GRCh38]
Chr1:161816313 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.41C>T (p.Pro14Leu) single nucleotide variant not provided [RCV001998509] Chr1:161766401 [GRCh38]
Chr1:161736191 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1912C>T (p.Arg638Ter) single nucleotide variant not provided [RCV002047468] Chr1:161958553 [GRCh38]
Chr1:161928343 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1340A>G (p.Asn447Ser) single nucleotide variant not provided [RCV002028848] Chr1:161851742 [GRCh38]
Chr1:161821532 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.160-8A>G single nucleotide variant not provided [RCV001991965] Chr1:161781904 [GRCh38]
Chr1:161751694 [GRCh37]
Chr1:1q23.3
uncertain significance
NC_000001.10:g.(?_158581054)_(162750036_?)dup duplication Autoimmune interstitial lung disease-arthritis syndrome [RCV001918952]|not provided [RCV001918953] Chr1:158581054..162750036 [GRCh37]
Chr1:1q23.1-23.3
uncertain significance|no classifications from unflagged records
NM_007348.4(ATF6):c.415T>G (p.Ser139Ala) single nucleotide variant not provided [RCV001979585] Chr1:161791468 [GRCh38]
Chr1:161761258 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1356G>A (p.Met452Ile) single nucleotide variant Inborn genetic diseases [RCV002548142]|not provided [RCV002018038] Chr1:161851758 [GRCh38]
Chr1:161821548 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.695C>T (p.Thr232Met) single nucleotide variant Inborn genetic diseases [RCV002573449]|not provided [RCV001998174] Chr1:161802058 [GRCh38]
Chr1:161771848 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.257T>C (p.Ile86Thr) single nucleotide variant not provided [RCV002015097] Chr1:161783999 [GRCh38]
Chr1:161753789 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1720-15_1720-9del deletion not provided [RCV001880421] Chr1:161912276..161912282 [GRCh38]
Chr1:161882066..161882072 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.40C>T (p.Pro14Ser) single nucleotide variant not provided [RCV002046450] Chr1:161766400 [GRCh38]
Chr1:161736190 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.694A>G (p.Thr232Ala) single nucleotide variant not provided [RCV002029287] Chr1:161802057 [GRCh38]
Chr1:161771847 [GRCh37]
Chr1:1q23.3
uncertain significance
NC_000001.10:g.(?_161645027)_(161772082_?)dup duplication not provided [RCV001883368] Chr1:161645027..161772082 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1805-13T>G single nucleotide variant not provided [RCV002013012] Chr1:161958433 [GRCh38]
Chr1:161928223 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.910-13T>C single nucleotide variant not provided [RCV002076389] Chr1:161819620 [GRCh38]
Chr1:161789410 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.160-18C>T single nucleotide variant not provided [RCV002190704] Chr1:161781894 [GRCh38]
Chr1:161751684 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1158A>G (p.Ala386=) single nucleotide variant not provided [RCV002128528] Chr1:161821132 [GRCh38]
Chr1:161790922 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1320-14C>T single nucleotide variant not provided [RCV002169210] Chr1:161851708 [GRCh38]
Chr1:161821498 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.485-4C>T single nucleotide variant not provided [RCV002206204] Chr1:161792120 [GRCh38]
Chr1:161761910 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1221T>A (p.Pro407=) single nucleotide variant not provided [RCV002109535] Chr1:161846482 [GRCh38]
Chr1:161816272 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.248-20C>T single nucleotide variant not provided [RCV002085695] Chr1:161783970 [GRCh38]
Chr1:161753760 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1319+18T>C single nucleotide variant not provided [RCV002089446] Chr1:161846598 [GRCh38]
Chr1:161816388 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1434-11A>G single nucleotide variant not provided [RCV002168608] Chr1:161853213 [GRCh38]
Chr1:161823003 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1410A>G (p.Leu470=) single nucleotide variant not provided [RCV002209988] Chr1:161851812 [GRCh38]
Chr1:161821602 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.759G>A (p.Gln253=) single nucleotide variant not provided [RCV002170659] Chr1:161802122 [GRCh38]
Chr1:161771912 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.321A>G (p.Ser107=) single nucleotide variant not provided [RCV002116627] Chr1:161784063 [GRCh38]
Chr1:161753853 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1299T>C (p.Ile433=) single nucleotide variant not provided [RCV002208024] Chr1:161846560 [GRCh38]
Chr1:161816350 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.247+13T>C single nucleotide variant not provided [RCV002175075] Chr1:161782012 [GRCh38]
Chr1:161751802 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1959C>T (p.Pro653=) single nucleotide variant not provided [RCV002172766] Chr1:161958600 [GRCh38]
Chr1:161928390 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1317C>T (p.Tyr439=) single nucleotide variant not provided [RCV002173554] Chr1:161846578 [GRCh38]
Chr1:161816368 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.15T>C (p.Ala5=) single nucleotide variant not provided [RCV002080682] Chr1:161766375 [GRCh38]
Chr1:161736165 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1320-33_1320-18del deletion not provided [RCV002146143] Chr1:161851689..161851704 [GRCh38]
Chr1:161821479..161821494 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1536T>G (p.Gly512=) single nucleotide variant not provided [RCV002095506] Chr1:161860209 [GRCh38]
Chr1:161829999 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.66G>A (p.Arg22=) single nucleotide variant not provided [RCV002115355] Chr1:161766426 [GRCh38]
Chr1:161736216 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1206C>T (p.Ser402=) single nucleotide variant not provided [RCV002132682] Chr1:161846467 [GRCh38]
Chr1:161816257 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.83-19T>C single nucleotide variant not provided [RCV002116617] Chr1:161778225 [GRCh38]
Chr1:161748015 [GRCh37]
Chr1:1q23.3
benign
NM_007348.4(ATF6):c.1833A>G (p.Glu611=) single nucleotide variant not provided [RCV002172107] Chr1:161958474 [GRCh38]
Chr1:161928264 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.462C>T (p.Val154=) single nucleotide variant not provided [RCV002113660] Chr1:161791515 [GRCh38]
Chr1:161761305 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1113C>G (p.Val371=) single nucleotide variant not provided [RCV002149895] Chr1:161821087 [GRCh38]
Chr1:161790877 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1534-11T>A single nucleotide variant not provided [RCV002138752] Chr1:161860196 [GRCh38]
Chr1:161829986 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1604+11G>A single nucleotide variant not provided [RCV002218408] Chr1:161860288 [GRCh38]
Chr1:161830078 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.588C>T (p.Ser196=) single nucleotide variant not provided [RCV002218754] Chr1:161792227 [GRCh38]
Chr1:161762017 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.333T>C (p.Tyr111=) single nucleotide variant not provided [RCV002216980] Chr1:161784075 [GRCh38]
Chr1:161753865 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1319+8G>A single nucleotide variant not provided [RCV002139319] Chr1:161846588 [GRCh38]
Chr1:161816378 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.248-14T>G single nucleotide variant not provided [RCV002177750] Chr1:161783976 [GRCh38]
Chr1:161753766 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.354+12del deletion not provided [RCV002139679] Chr1:161784108 [GRCh38]
Chr1:161753898 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.123T>C (p.Thr41=) single nucleotide variant not provided [RCV002202614] Chr1:161778284 [GRCh38]
Chr1:161748074 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1926G>A (p.Arg642=) single nucleotide variant not provided [RCV002082330] Chr1:161958567 [GRCh38]
Chr1:161928357 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.705G>C (p.Leu235=) single nucleotide variant not provided [RCV002161332] Chr1:161802068 [GRCh38]
Chr1:161771858 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1604+17G>A single nucleotide variant not provided [RCV002199458] Chr1:161860294 [GRCh38]
Chr1:161830084 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1720-14T>C single nucleotide variant not provided [RCV002154209] Chr1:161912282 [GRCh38]
Chr1:161882072 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.957C>A (p.Ser319=) single nucleotide variant not provided [RCV002155003] Chr1:161819680 [GRCh38]
Chr1:161789470 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1980C>T (p.His660=) single nucleotide variant not provided [RCV002164286] Chr1:161958621 [GRCh38]
Chr1:161928411 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.423T>C (p.Ser141=) single nucleotide variant not provided [RCV002175437] Chr1:161791476 [GRCh38]
Chr1:161761266 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1008G>A (p.Ala336=) single nucleotide variant not provided [RCV002201835] Chr1:161819731 [GRCh38]
Chr1:161789521 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.83-9T>C single nucleotide variant not provided [RCV002221059] Chr1:161778235 [GRCh38]
Chr1:161748025 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.689-4G>A single nucleotide variant not provided [RCV002183041] Chr1:161802048 [GRCh38]
Chr1:161771838 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1604+12C>G single nucleotide variant not provided [RCV002199183] Chr1:161860289 [GRCh38]
Chr1:161830079 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.441A>G (p.Pro147=) single nucleotide variant not provided [RCV002161669] Chr1:161791494 [GRCh38]
Chr1:161761284 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.159+16G>A single nucleotide variant not provided [RCV002177160] Chr1:161778336 [GRCh38]
Chr1:161748126 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.864G>A (p.Val288=) single nucleotide variant not provided [RCV002157852] Chr1:161802227 [GRCh38]
Chr1:161772017 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.900C>T (p.Val300=) single nucleotide variant not provided [RCV002216646] Chr1:161802263 [GRCh38]
Chr1:161772053 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1805-18G>A single nucleotide variant not provided [RCV002154177] Chr1:161958428 [GRCh38]
Chr1:161928218 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1805-16A>G single nucleotide variant not provided [RCV002203223] Chr1:161958430 [GRCh38]
Chr1:161928220 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.159+16_159+17delinsAA indel not provided [RCV002159528] Chr1:161778336..161778337 [GRCh38]
Chr1:161748126..161748127 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1095+18G>A single nucleotide variant not provided [RCV002156409] Chr1:161819836 [GRCh38]
Chr1:161789626 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1095+17C>T single nucleotide variant not provided [RCV002141579] Chr1:161819835 [GRCh38]
Chr1:161789625 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.300T>C (p.Tyr100=) single nucleotide variant not provided [RCV002158690] Chr1:161784042 [GRCh38]
Chr1:161753832 [GRCh37]
Chr1:1q23.3
likely benign
NC_000001.10:g.(?_161279609)_(161751809_?)dup duplication Charcot-Marie-Tooth disease, type I [RCV003111375] Chr1:161279609..161751809 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.62A>G (p.His21Arg) single nucleotide variant not provided [RCV002297688] Chr1:161766422 [GRCh38]
Chr1:161736212 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1312A>T (p.Ser438Cys) single nucleotide variant Inborn genetic diseases [RCV003305021] Chr1:161846573 [GRCh38]
Chr1:161816363 [GRCh37]
Chr1:1q23.3
uncertain significance
GRCh37/hg19 1q23.3(chr1:161924068-164761399)x1 copy number loss not provided [RCV002474557] Chr1:161924068..164761399 [GRCh37]
Chr1:1q23.3
likely pathogenic
NM_007348.4(ATF6):c.463A>G (p.Thr155Ala) single nucleotide variant not provided [RCV002296272] Chr1:161791516 [GRCh38]
Chr1:161761306 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.700T>G (p.Leu234Val) single nucleotide variant not provided [RCV002296289] Chr1:161802063 [GRCh38]
Chr1:161771853 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.4G>C (p.Gly2Arg) single nucleotide variant not provided [RCV002299178] Chr1:161766364 [GRCh38]
Chr1:161736154 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1209G>T (p.Arg403Ser) single nucleotide variant not provided [RCV002303194] Chr1:161846470 [GRCh38]
Chr1:161816260 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.158A>G (p.Tyr53Cys) single nucleotide variant not provided [RCV002861640] Chr1:161778319 [GRCh38]
Chr1:161748109 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1393C>T (p.Pro465Ser) single nucleotide variant not provided [RCV002617911] Chr1:161851795 [GRCh38]
Chr1:161821585 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.364G>T (p.Asp122Tyr) single nucleotide variant not provided [RCV002755819] Chr1:161791417 [GRCh38]
Chr1:161761207 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.347A>G (p.His116Arg) single nucleotide variant not provided [RCV002816272] Chr1:161784089 [GRCh38]
Chr1:161753879 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1740T>C (p.Ala580=) single nucleotide variant not provided [RCV002774929] Chr1:161912316 [GRCh38]
Chr1:161882106 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1095+7G>A single nucleotide variant not provided [RCV002771479] Chr1:161819825 [GRCh38]
Chr1:161789615 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.99T>C (p.Ala33=) single nucleotide variant not provided [RCV002617742] Chr1:161778260 [GRCh38]
Chr1:161748050 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1777A>G (p.Ile593Val) single nucleotide variant Inborn genetic diseases [RCV002688222] Chr1:161912353 [GRCh38]
Chr1:161882143 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.21T>C (p.Val7=) single nucleotide variant not provided [RCV002994922] Chr1:161766381 [GRCh38]
Chr1:161736171 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1468C>T (p.His490Tyr) single nucleotide variant not provided [RCV002843160] Chr1:161853258 [GRCh38]
Chr1:161823048 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1690G>A (p.Asp564Asn) single nucleotide variant not provided [RCV002662951] Chr1:161863283 [GRCh38]
Chr1:161833073 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1548G>C (p.Gln516His) single nucleotide variant not provided [RCV002952694] Chr1:161860221 [GRCh38]
Chr1:161830011 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.566C>T (p.Ala189Val) single nucleotide variant not provided [RCV002796814] Chr1:161792205 [GRCh38]
Chr1:161761995 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1183A>G (p.Met395Val) single nucleotide variant not provided [RCV003020978] Chr1:161821157 [GRCh38]
Chr1:161790947 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.33G>A (p.Met11Ile) single nucleotide variant not provided [RCV002572178] Chr1:161766393 [GRCh38]
Chr1:161736183 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1903C>T (p.Pro635Ser) single nucleotide variant not provided [RCV002735093] Chr1:161958544 [GRCh38]
Chr1:161928334 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1294_1296delinsTAC (p.Gly432Tyr) indel not provided [RCV003035794] Chr1:161846555..161846557 [GRCh38]
Chr1:161816345..161816347 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1154T>C (p.Leu385Ser) single nucleotide variant not provided [RCV002912982] Chr1:161821128 [GRCh38]
Chr1:161790918 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.484+10T>A single nucleotide variant not provided [RCV003020394] Chr1:161791547 [GRCh38]
Chr1:161761337 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1320A>G (p.Arg440=) single nucleotide variant not provided [RCV003038189] Chr1:161851722 [GRCh38]
Chr1:161821512 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.654A>G (p.Gln218=) single nucleotide variant not provided [RCV002636709] Chr1:161792293 [GRCh38]
Chr1:161762083 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1221T>C (p.Pro407=) single nucleotide variant not provided [RCV002640115] Chr1:161846482 [GRCh38]
Chr1:161816272 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1188-13T>C single nucleotide variant not provided [RCV002760714] Chr1:161846436 [GRCh38]
Chr1:161816226 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.939_941del (p.Met313del) deletion not provided [RCV002824981] Chr1:161819660..161819662 [GRCh38]
Chr1:161789450..161789452 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.222G>A (p.Trp74Ter) single nucleotide variant not provided [RCV002820245] Chr1:161781974 [GRCh38]
Chr1:161751764 [GRCh37]
Chr1:1q23.3
pathogenic
NM_007348.4(ATF6):c.219T>C (p.Ile73=) single nucleotide variant not provided [RCV002760849] Chr1:161781971 [GRCh38]
Chr1:161751761 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.484+20C>A single nucleotide variant not provided [RCV002639232] Chr1:161791557 [GRCh38]
Chr1:161761347 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.61C>T (p.His21Tyr) single nucleotide variant Inborn genetic diseases [RCV003250588]|not provided [RCV002785403] Chr1:161766421 [GRCh38]
Chr1:161736211 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1621G>A (p.Glu541Lys) single nucleotide variant not provided [RCV002706131] Chr1:161863214 [GRCh38]
Chr1:161833004 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.364G>A (p.Asp122Asn) single nucleotide variant not provided [RCV002820935] Chr1:161791417 [GRCh38]
Chr1:161761207 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.420T>C (p.Asn140=) single nucleotide variant not provided [RCV003043554] Chr1:161791473 [GRCh38]
Chr1:161761263 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1374A>G (p.Pro458=) single nucleotide variant not provided [RCV002745342] Chr1:161851776 [GRCh38]
Chr1:161821566 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1632G>A (p.Val544=) single nucleotide variant not provided [RCV003085017] Chr1:161863225 [GRCh38]
Chr1:161833015 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.404A>G (p.Tyr135Cys) single nucleotide variant Inborn genetic diseases [RCV002919436] Chr1:161791457 [GRCh38]
Chr1:161761247 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1450C>T (p.Arg484Ter) single nucleotide variant not provided [RCV003043318] Chr1:161853240 [GRCh38]
Chr1:161823030 [GRCh37]
Chr1:1q23.3
pathogenic
NM_007348.4(ATF6):c.17G>C (p.Gly6Ala) single nucleotide variant not provided [RCV003059828] Chr1:161766377 [GRCh38]
Chr1:161736167 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1763_1770dup (p.Met591fs) duplication not provided [RCV002667744] Chr1:161912336..161912337 [GRCh38]
Chr1:161882126..161882127 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.629C>T (p.Thr210Met) single nucleotide variant not provided [RCV002597064] Chr1:161792268 [GRCh38]
Chr1:161762058 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1916A>C (p.Asp639Ala) single nucleotide variant not provided [RCV003041667] Chr1:161958557 [GRCh38]
Chr1:161928347 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1535G>A (p.Gly512Asp) single nucleotide variant not provided [RCV002576386] Chr1:161860208 [GRCh38]
Chr1:161829998 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.910-1G>T single nucleotide variant not provided [RCV002918147] Chr1:161819632 [GRCh38]
Chr1:161789422 [GRCh37]
Chr1:1q23.3
likely pathogenic
NM_007348.4(ATF6):c.1434-14A>T single nucleotide variant not provided [RCV003040404] Chr1:161853210 [GRCh38]
Chr1:161823000 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.605C>A (p.Thr202Asn) single nucleotide variant not provided [RCV003057562] Chr1:161792244 [GRCh38]
Chr1:161762034 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.376A>G (p.Ser126Gly) single nucleotide variant Inborn genetic diseases [RCV002929456] Chr1:161791429 [GRCh38]
Chr1:161761219 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1019C>T (p.Ala340Val) single nucleotide variant not provided [RCV003022658] Chr1:161819742 [GRCh38]
Chr1:161789532 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1606A>G (p.Arg536Gly) single nucleotide variant not provided [RCV002711748] Chr1:161863199 [GRCh38]
Chr1:161832989 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1094A>T (p.Glu365Val) single nucleotide variant not provided [RCV003040754] Chr1:161819817 [GRCh38]
Chr1:161789607 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.426C>G (p.Leu142=) single nucleotide variant not provided [RCV002642497] Chr1:161791479 [GRCh38]
Chr1:161761269 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.106G>A (p.Gly36Ser) single nucleotide variant not provided [RCV002928399] Chr1:161778267 [GRCh38]
Chr1:161748057 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1320A>C (p.Arg440Ser) single nucleotide variant not provided [RCV002663613] Chr1:161851722 [GRCh38]
Chr1:161821512 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1893G>A (p.Ser631=) single nucleotide variant not provided [RCV002594340] Chr1:161958534 [GRCh38]
Chr1:161928324 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1482G>A (p.Arg494=) single nucleotide variant not provided [RCV003039713] Chr1:161853272 [GRCh38]
Chr1:161823062 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.434C>A (p.Ala145Glu) single nucleotide variant not provided [RCV002632059] Chr1:161791487 [GRCh38]
Chr1:161761277 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1957C>T (p.Pro653Ser) single nucleotide variant not provided [RCV002631934] Chr1:161958598 [GRCh38]
Chr1:161928388 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.45dup (p.Ser16Ter) duplication not provided [RCV002676577] Chr1:161766401..161766402 [GRCh38]
Chr1:161736191..161736192 [GRCh37]
Chr1:1q23.3
pathogenic
NM_007348.4(ATF6):c.909+5G>A single nucleotide variant not provided [RCV002941912] Chr1:161802277 [GRCh38]
Chr1:161772067 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.137T>C (p.Leu46Ser) single nucleotide variant Inborn genetic diseases [RCV003167567]|not provided [RCV002649841] Chr1:161778298 [GRCh38]
Chr1:161748088 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1319+19A>G single nucleotide variant not provided [RCV002600622] Chr1:161846599 [GRCh38]
Chr1:161816389 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1534-14_1534-11del deletion not provided [RCV003029308] Chr1:161860184..161860187 [GRCh38]
Chr1:161829974..161829977 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.575C>T (p.Thr192Ile) single nucleotide variant not provided [RCV002833070] Chr1:161792214 [GRCh38]
Chr1:161762004 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.847A>C (p.Asn283His) single nucleotide variant not provided [RCV003030884] Chr1:161802210 [GRCh38]
Chr1:161772000 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1283A>G (p.Asp428Gly) single nucleotide variant not provided [RCV003029788] Chr1:161846544 [GRCh38]
Chr1:161816334 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1937_1939del (p.Asn646del) deletion not provided [RCV002580035] Chr1:161958576..161958578 [GRCh38]
Chr1:161928366..161928368 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.303A>C (p.Ser101=) single nucleotide variant not provided [RCV002835343] Chr1:161784045 [GRCh38]
Chr1:161753835 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.248-11A>G single nucleotide variant not provided [RCV002577329] Chr1:161783979 [GRCh38]
Chr1:161753769 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1319+13G>A single nucleotide variant not provided [RCV002650181] Chr1:161846593 [GRCh38]
Chr1:161816383 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1096-12C>A single nucleotide variant not provided [RCV003028733] Chr1:161821058 [GRCh38]
Chr1:161790848 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.802C>G (p.His268Asp) single nucleotide variant Inborn genetic diseases [RCV002831345] Chr1:161802165 [GRCh38]
Chr1:161771955 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1189A>G (p.Met397Val) single nucleotide variant Inborn genetic diseases [RCV002647033]|not provided [RCV002653924] Chr1:161846450 [GRCh38]
Chr1:161816240 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1744A>G (p.Thr582Ala) single nucleotide variant not provided [RCV002833841] Chr1:161912320 [GRCh38]
Chr1:161882110 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.88G>A (p.Ala30Thr) single nucleotide variant not provided [RCV003045161] Chr1:161778249 [GRCh38]
Chr1:161748039 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.386T>G (p.Met129Arg) single nucleotide variant Inborn genetic diseases [RCV002934579] Chr1:161791439 [GRCh38]
Chr1:161761229 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1813A>G (p.Ile605Val) single nucleotide variant not provided [RCV002811889] Chr1:161958454 [GRCh38]
Chr1:161928244 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1667T>C (p.Phe556Ser) single nucleotide variant not provided [RCV002630963] Chr1:161863260 [GRCh38]
Chr1:161833050 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1007C>T (p.Ala336Val) single nucleotide variant not provided [RCV002633268] Chr1:161819730 [GRCh38]
Chr1:161789520 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.155C>T (p.Thr52Met) single nucleotide variant not provided [RCV002583068] Chr1:161778316 [GRCh38]
Chr1:161748106 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.418A>G (p.Asn140Asp) single nucleotide variant not provided [RCV002725395] Chr1:161791471 [GRCh38]
Chr1:161761261 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.276A>G (p.Pro92=) single nucleotide variant not provided [RCV002605430] Chr1:161784018 [GRCh38]
Chr1:161753808 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.355-13T>C single nucleotide variant not provided [RCV002589411] Chr1:161791395 [GRCh38]
Chr1:161761185 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.909+4A>T single nucleotide variant not provided [RCV002635513] Chr1:161802276 [GRCh38]
Chr1:161772066 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.635T>C (p.Met212Thr) single nucleotide variant not provided [RCV002653929] Chr1:161792274 [GRCh38]
Chr1:161762064 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.485-7dup duplication not provided [RCV002609935] Chr1:161792112..161792113 [GRCh38]
Chr1:161761902..161761903 [GRCh37]
Chr1:1q23.3
benign
NM_007348.4(ATF6):c.1626A>G (p.Leu542=) single nucleotide variant not provided [RCV002721358] Chr1:161863219 [GRCh38]
Chr1:161833009 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1267G>C (p.Ala423Pro) single nucleotide variant Inborn genetic diseases [RCV003300322] Chr1:161846528 [GRCh38]
Chr1:161816318 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.797C>T (p.Pro266Leu) single nucleotide variant Inborn genetic diseases [RCV003340186] Chr1:161802160 [GRCh38]
Chr1:161771950 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1600A>G (p.Ile534Val) single nucleotide variant Inborn genetic diseases [RCV003360534] Chr1:161860273 [GRCh38]
Chr1:161830063 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1232C>G (p.Pro411Arg) single nucleotide variant Inborn genetic diseases [RCV003344928] Chr1:161846493 [GRCh38]
Chr1:161816283 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.661A>G (p.Ile221Val) single nucleotide variant Inborn genetic diseases [RCV003374529] Chr1:161792300 [GRCh38]
Chr1:161762090 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.1479A>G (p.Glu493=) single nucleotide variant not provided [RCV003570462] Chr1:161853269 [GRCh38]
Chr1:161823059 [GRCh37]
Chr1:1q23.3
likely benign
GRCh37/hg19 1q23.1-23.3(chr1:158001058-162858285)x1 copy number loss not provided [RCV003483944] Chr1:158001058..162858285 [GRCh37]
Chr1:1q23.1-23.3
likely pathogenic
NM_007348.4(ATF6):c.1141G>T (p.Val381Leu) single nucleotide variant not provided [RCV003409211] Chr1:161821115 [GRCh38]
Chr1:161790905 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_007348.4(ATF6):c.83-12C>A single nucleotide variant not provided [RCV003686759] Chr1:161778232 [GRCh38]
Chr1:161748022 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.206G>A (p.Trp69Ter) single nucleotide variant not provided [RCV003547335] Chr1:161781958 [GRCh38]
Chr1:161751748 [GRCh37]
Chr1:1q23.3
pathogenic
NM_007348.4(ATF6):c.1330del (p.Ser444fs) deletion not provided [RCV003547341] Chr1:161851731 [GRCh38]
Chr1:161821521 [GRCh37]
Chr1:1q23.3
pathogenic
NM_007348.4(ATF6):c.1164A>T (p.Ile388=) single nucleotide variant not provided [RCV003688263] Chr1:161821138 [GRCh38]
Chr1:161790928 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.732A>G (p.Gln244=) single nucleotide variant not provided [RCV003660245] Chr1:161802095 [GRCh38]
Chr1:161771885 [GRCh37]
Chr1:1q23.3
likely benign
NM_007348.4(ATF6):c.1278A>T (p.Ala426=) single nucleotide variant not provided [RCV003546074] Chr1:161846539 [GRCh38]
Chr1:161816329 [GRCh37]
Chr1:1q23.3
likely benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2170
Count of miRNA genes:1063
Interacting mature miRNAs:1285
Transcripts:ENST00000367942, ENST00000476437
Prediction methods:Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region
RH69585  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371161,861,741 - 161,861,956UniSTSGRCh37
Build 361160,128,365 - 160,128,580RGDNCBI36
Celera1134,965,147 - 134,965,362RGD
Cytogenetic Map1q22-q23UniSTS
HuRef1133,106,639 - 133,106,854UniSTS
GeneMap99-GB4 RH Map1576.33UniSTS
WI-13539  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371161,932,818 - 161,932,967UniSTSGRCh37
Build 361160,199,442 - 160,199,591RGDNCBI36
Celera1135,036,229 - 135,036,378RGD
Cytogenetic Map1q22-q23UniSTS
HuRef1133,177,611 - 133,177,760UniSTS
GeneMap99-GB4 RH Map1596.62UniSTS
GeneMap99-GB4 RH Map1590.96UniSTS
Whitehead-RH Map1733.6UniSTS
AL034282  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371161,769,652 - 161,769,834UniSTSGRCh37
Build 361160,036,276 - 160,036,458RGDNCBI36
Celera1134,873,060 - 134,873,242RGD
Cytogenetic Map1q22-q23UniSTS
HuRef1133,014,584 - 133,014,766UniSTS
RH78635  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371161,817,580 - 161,817,748UniSTSGRCh37
Build 361160,084,204 - 160,084,372RGDNCBI36
Celera1134,920,986 - 134,921,154RGD
Cytogenetic Map1q22-q23UniSTS
HuRef1133,062,485 - 133,062,653UniSTS
GeneMap99-GB4 RH Map1596.42UniSTS
RH68768  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371161,933,670 - 161,933,807UniSTSGRCh37
Build 361160,200,294 - 160,200,431RGDNCBI36
Celera1135,037,081 - 135,037,218RGD
Cytogenetic Map1q22-q23UniSTS
HuRef1133,178,463 - 133,178,600UniSTS
GeneMap99-GB4 RH Map1576.12UniSTS
REN67335  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,012,186 - 116,012,426UniSTSGRCh37
GRCh371161,802,942 - 161,803,182UniSTSGRCh37
Build 361160,069,566 - 160,069,806RGDNCBI36
Celera1134,906,348 - 134,906,588RGD
Celera7110,819,550 - 110,819,790UniSTS
Cytogenetic Map1q22-q23UniSTS
HuRef7110,378,478 - 110,378,718UniSTS
HuRef1133,047,847 - 133,048,087UniSTS
CRA_TCAGchr7v27115,407,581 - 115,407,821UniSTS
G16275  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371161,775,080 - 161,775,255UniSTSGRCh37
Build 361160,041,704 - 160,041,879RGDNCBI36
Celera1134,878,488 - 134,878,663RGD
Cytogenetic Map1q22-q23UniSTS
HuRef1133,020,012 - 133,020,187UniSTS
STS-H29771  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371161,858,200 - 161,858,310UniSTSGRCh37
Build 361160,124,824 - 160,124,934RGDNCBI36
Celera1134,961,606 - 134,961,716RGD
Cytogenetic Map1q22-q23UniSTS
HuRef1133,103,098 - 133,103,208UniSTS
GeneMap99-GB4 RH Map1591.17UniSTS
RH69812  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371161,917,208 - 161,917,326UniSTSGRCh37
Build 361160,183,832 - 160,183,950RGDNCBI36
Celera1135,020,625 - 135,020,743RGD
Cytogenetic Map1q22-q23UniSTS
HuRef1133,162,118 - 133,162,236UniSTS
GeneMap99-GB4 RH Map1577.37UniSTS
SHGC-32839  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371161,928,360 - 161,928,494UniSTSGRCh37
Build 361160,194,984 - 160,195,118RGDNCBI36
Celera1135,031,777 - 135,031,911RGD
Cytogenetic Map1q22-q23UniSTS
HuRef1133,173,159 - 133,173,293UniSTS
Stanford-G3 RH Map16198.0UniSTS
GeneMap99-GB4 RH Map1590.23UniSTS
Whitehead-RH Map1720.2UniSTS
NCBI RH Map11441.4UniSTS
GeneMap99-G3 RH Map16154.0UniSTS
D8S2278  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map3p25.3-p24.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map10q11UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map12q21.31UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map7q34-q35UniSTS
Cytogenetic MapXp22.1UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map4q34.1UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map2p23.1UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map12p12.3UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map15q22.1UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map14q22UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map13q11UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map14q12-q13UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map4q31UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map15q15-q21.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map17q22-q23.2UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic MapXq26.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map3p12.1UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map12q14.3-q15UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map3q28UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map19q13.13UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map21q21.1UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1p13-p12UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map10q21.1UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map14q31UniSTS
D11S3114  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map15q11.2-q21.3UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map9q21.12UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map7q21.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map11q13.1-q13.2UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map12p12.2-p11.2UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map10q11.1-q24UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map7q31.1-q31.3UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic MapXq13.1-q21.1UniSTS
Cytogenetic Map20pter-q12UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map15q21-q22UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map1q41-q42.2UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map9p23UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map2q37.2UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map1q31-q32UniSTS
Cytogenetic Map6q24.1UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map3p26.1-p25.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map17q24-q25UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic MapXq21UniSTS
Cytogenetic Map6p12UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic Map19qUniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map22q12.3-q13.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map2q34UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map9p22.3UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map4p12UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map19q11UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map1p32.2-p32.1UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map4q13.2UniSTS
Cytogenetic Map4q31.23UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map14q24.2UniSTS
sY3084  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map6q22.33UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map7q11.2UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map18q22.1UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map4q27UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map14q22UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map1p35.3-p33UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map15q15-q21.1UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map18p11.3-p11.2UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map13q13.3UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapXq21.3UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map4p16UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map18p11.22UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map13q32.1UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map14q32.1UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map3q12.3UniSTS
L18426  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map20q13.1UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map10p11UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map2p23.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map8p23-p22UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map17q21-q22UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map13q11UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map2p25UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map1p21.3UniSTS
Cytogenetic Map19q13.13UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map17q22-q23.2UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map12q24.1-q24.3UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map9p24.2UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map1p32UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map6q25.1-q26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17q23.1UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map1q41-q42.2UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map11p11.11UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map21q22.1UniSTS
Cytogenetic Map4q25-q27UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map7p14.2UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map18p11.22UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map21q21.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map12p12.3UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map22q12UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map1p13-p12UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map10q21.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map20p11.21UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map16p13.13-p13.12UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map1p13.1UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map14q22-q24UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map10q11UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map12q21.31UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map9p21.1UniSTS
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map13q14.1-q14.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17p13.1-p12UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map10q23-q24UniSTS
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Cytogenetic Map17q11-q21UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map3p26.1-p25.1UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map6q16.3UniSTS
Cytogenetic Map17q24-q25UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic MapXq27.1UniSTS
Cytogenetic Map8q12.3UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map2q21.2UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map18q12.3UniSTS
Cytogenetic Map18p11.3UniSTS
Cytogenetic Map17q11.1UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map13q12.3UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map12q14UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map2q32-q34UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map6q23-q24UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map6p12.3-p11.2UniSTS
Cytogenetic Map6q16.1-q16.3UniSTS
Cytogenetic Map22q11UniSTS
Cytogenetic Map7q31.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3q25.2UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map22q12-q13UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map1q24.3UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2p16.2UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map1q23UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map11q13.3UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map11q12.1UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map8p21UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map10q26.1UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q33-q34UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map13q32UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map5q22UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map3p26.3UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map12q24.23UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic MapXp22.31UniSTS
Cytogenetic MapXp21.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3q24UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map14q11.2-q12UniSTS
Cytogenetic Map3p24UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map4p13-p12UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS
D1S1425  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map8q12.1UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map6q25.2-q25.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map2p23-p22UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic Map2p11.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map2p12-p11.2UniSTS
Cytogenetic Map3q11.1UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map1p21.3UniSTS
Cytogenetic Map1q32.2UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map18p11.3-p11.2UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map21p11.1UniSTS
Cytogenetic Map12q24.31-q24.32UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map12p12.2-p11.2UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map17q22-q23.2UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map7q31.1-q31.3UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map3p21.1-p14.2UniSTS
Cytogenetic Map2p24UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map12q24.32UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map15q11-q12UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map15q21.1-q21.2UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map12p13.33UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map4q31.21UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map10p15-p14UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q13.1-q13.2UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map3q12.1UniSTS
Cytogenetic Map15q24-q25UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map6pter-p12.1UniSTS
Cytogenetic Map6q16UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map11q23.1-q23.2UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map16q24.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic MapXq21.1UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 1974 1930 1399 403 1624 260 3616 965 1567 323 1359 1597 156 1154 2078 4
Low 465 1061 327 221 327 205 740 1232 2167 96 101 16 19 1 50 710 1 2
Below cutoff

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_029773 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001410890 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_007348 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011509308 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011509309 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011509310 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047449542 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054335215 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054335216 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054335217 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054335218 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB015856 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB208929 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC243424 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC244129 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF005887 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF088035 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK025316 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK290498 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL359541 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL391825 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL450995 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC014969 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC071997 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM683233 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BP380917 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX538263 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471067 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068277 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

RefSeq Acc Id: ENST00000367942   ⟹   ENSP00000356919
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,766,320 - 161,964,070 (+)Ensembl
RefSeq Acc Id: ENST00000476437
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,840,075 - 161,860,244 (+)Ensembl
RefSeq Acc Id: ENST00000679833   ⟹   ENSP00000505321
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,766,356 - 161,865,955 (+)Ensembl
RefSeq Acc Id: ENST00000679853   ⟹   ENSP00000506149
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,766,309 - 161,962,101 (+)Ensembl
RefSeq Acc Id: ENST00000679886   ⟹   ENSP00000506559
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,766,320 - 161,959,632 (+)Ensembl
RefSeq Acc Id: ENST00000680180
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,766,321 - 161,888,547 (+)Ensembl
RefSeq Acc Id: ENST00000680462   ⟹   ENSP00000505583
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,766,321 - 161,865,955 (+)Ensembl
RefSeq Acc Id: ENST00000680481   ⟹   ENSP00000505919
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,766,321 - 161,958,854 (+)Ensembl
RefSeq Acc Id: ENST00000680633   ⟹   ENSP00000505371
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,766,322 - 161,792,288 (+)Ensembl
RefSeq Acc Id: ENST00000680688   ⟹   ENSP00000504865
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,766,298 - 161,959,632 (+)Ensembl
RefSeq Acc Id: ENST00000681001   ⟹   ENSP00000506145
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,766,320 - 161,959,658 (+)Ensembl
RefSeq Acc Id: ENST00000681036   ⟹   ENSP00000505474
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,766,564 - 161,959,658 (+)Ensembl
RefSeq Acc Id: ENST00000681169   ⟹   ENSP00000505455
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,766,320 - 161,959,632 (+)Ensembl
RefSeq Acc Id: ENST00000681187
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,766,321 - 161,887,436 (+)Ensembl
RefSeq Acc Id: ENST00000681492   ⟹   ENSP00000506139
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,766,320 - 161,958,997 (+)Ensembl
RefSeq Acc Id: ENST00000681541   ⟹   ENSP00000506087
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,766,515 - 161,959,658 (+)Ensembl
RefSeq Acc Id: ENST00000681557   ⟹   ENSP00000506229
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,766,342 - 161,959,658 (+)Ensembl
RefSeq Acc Id: ENST00000681738   ⟹   ENSP00000505025
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,766,311 - 161,977,574 (+)Ensembl
RefSeq Acc Id: ENST00000681779
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,766,311 - 161,936,523 (+)Ensembl
RefSeq Acc Id: ENST00000681801   ⟹   ENSP00000505998
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,766,311 - 161,975,373 (+)Ensembl
RefSeq Acc Id: ENST00000681912   ⟹   ENSP00000505875
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,766,342 - 161,959,651 (+)Ensembl
RefSeq Acc Id: NM_001410890   ⟹   NP_001397819
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381161,766,320 - 161,964,070 (+)NCBI
T2T-CHM13v2.01161,110,648 - 161,308,347 (+)NCBI
RefSeq Acc Id: NM_007348   ⟹   NP_031374
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381161,766,320 - 161,964,070 (+)NCBI
GRCh371161,736,034 - 161,933,860 (+)NCBI
Build 361160,002,708 - 160,195,476 (+)NCBI Archive
HuRef1132,980,970 - 133,178,653 (+)NCBI
CHM1_11163,157,827 - 163,355,630 (+)NCBI
T2T-CHM13v2.01161,110,648 - 161,308,347 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011509308   ⟹   XP_011507610
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381161,766,320 - 161,964,070 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011509309   ⟹   XP_011507611
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381161,766,320 - 161,964,070 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011509310   ⟹   XP_011507612
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381161,766,320 - 161,866,730 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047449542   ⟹   XP_047305498
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381161,766,320 - 161,892,191 (+)NCBI
RefSeq Acc Id: XM_054335215   ⟹   XP_054191190
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01161,110,648 - 161,308,347 (+)NCBI
RefSeq Acc Id: XM_054335216   ⟹   XP_054191191
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01161,110,648 - 161,308,347 (+)NCBI
RefSeq Acc Id: XM_054335217   ⟹   XP_054191192
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01161,110,648 - 161,211,020 (+)NCBI
RefSeq Acc Id: XM_054335218   ⟹   XP_054191193
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01161,110,648 - 161,238,530 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001397819 (Get FASTA)   NCBI Sequence Viewer  
  NP_031374 (Get FASTA)   NCBI Sequence Viewer  
  XP_011507610 (Get FASTA)   NCBI Sequence Viewer  
  XP_011507611 (Get FASTA)   NCBI Sequence Viewer  
  XP_011507612 (Get FASTA)   NCBI Sequence Viewer  
  XP_047305498 (Get FASTA)   NCBI Sequence Viewer  
  XP_054191190 (Get FASTA)   NCBI Sequence Viewer  
  XP_054191191 (Get FASTA)   NCBI Sequence Viewer  
  XP_054191192 (Get FASTA)   NCBI Sequence Viewer  
  XP_054191193 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAB64434 (Get FASTA)   NCBI Sequence Viewer  
  AAH14969 (Get FASTA)   NCBI Sequence Viewer  
  AAH71997 (Get FASTA)   NCBI Sequence Viewer  
  BAA34722 (Get FASTA)   NCBI Sequence Viewer  
  BAD92166 (Get FASTA)   NCBI Sequence Viewer  
  BAF83187 (Get FASTA)   NCBI Sequence Viewer  
  EAW90694 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000356919
  ENSP00000356919.3
  ENSP00000504865
  ENSP00000504865.1
  ENSP00000505025.1
  ENSP00000505321.1
  ENSP00000505371.1
  ENSP00000505455.1
  ENSP00000505474.1
  ENSP00000505583
  ENSP00000505583.1
  ENSP00000505875.1
  ENSP00000505919.1
  ENSP00000505998.1
  ENSP00000506087.1
  ENSP00000506139.1
  ENSP00000506145.1
  ENSP00000506149
  ENSP00000506149.1
  ENSP00000506229.1
  ENSP00000506559.1
GenBank Protein P18850 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_031374   ⟸   NM_007348
- Peptide Label: isoform 1
- UniProtKB: Q6IPB5 (UniProtKB/Swiss-Prot),   Q5VW62 (UniProtKB/Swiss-Prot),   O15139 (UniProtKB/Swiss-Prot),   Q9UEC9 (UniProtKB/Swiss-Prot),   P18850 (UniProtKB/Swiss-Prot),   A8K383 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011507610   ⟸   XM_011509308
- Peptide Label: isoform X1
- UniProtKB: A0A7P0Z421 (UniProtKB/TrEMBL),   A8K383 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011507611   ⟸   XM_011509309
- Peptide Label: isoform X2
- UniProtKB: A8K383 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011507612   ⟸   XM_011509310
- Peptide Label: isoform X3
- UniProtKB: A0A7P0T8R5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000356919   ⟸   ENST00000367942
RefSeq Acc Id: ENSP00000505998   ⟸   ENST00000681801
RefSeq Acc Id: ENSP00000505321   ⟸   ENST00000679833
RefSeq Acc Id: ENSP00000506087   ⟸   ENST00000681541
RefSeq Acc Id: ENSP00000505455   ⟸   ENST00000681169
RefSeq Acc Id: ENSP00000505875   ⟸   ENST00000681912
RefSeq Acc Id: ENSP00000505371   ⟸   ENST00000680633
RefSeq Acc Id: ENSP00000506145   ⟸   ENST00000681001
RefSeq Acc Id: ENSP00000504865   ⟸   ENST00000680688
RefSeq Acc Id: ENSP00000506149   ⟸   ENST00000679853
RefSeq Acc Id: ENSP00000505919   ⟸   ENST00000680481
RefSeq Acc Id: ENSP00000505474   ⟸   ENST00000681036
RefSeq Acc Id: ENSP00000506559   ⟸   ENST00000679886
RefSeq Acc Id: ENSP00000505583   ⟸   ENST00000680462
RefSeq Acc Id: ENSP00000506139   ⟸   ENST00000681492
RefSeq Acc Id: ENSP00000505025   ⟸   ENST00000681738
RefSeq Acc Id: ENSP00000506229   ⟸   ENST00000681557
RefSeq Acc Id: XP_047305498   ⟸   XM_047449542
- Peptide Label: isoform X4
- UniProtKB: A0A7P0T8R5 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001397819   ⟸   NM_001410890
- Peptide Label: isoform 2
- UniProtKB: A0A7P0TAF2 (UniProtKB/TrEMBL),   A8K383 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054191190   ⟸   XM_054335215
- Peptide Label: isoform X1
- UniProtKB: A0A7P0Z421 (UniProtKB/TrEMBL),   A8K383 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054191191   ⟸   XM_054335216
- Peptide Label: isoform X2
- UniProtKB: A8K383 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054191193   ⟸   XM_054335218
- Peptide Label: isoform X4
- UniProtKB: A0A7P0T8R5 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054191192   ⟸   XM_054335217
- Peptide Label: isoform X3
- UniProtKB: A0A7P0T8R5 (UniProtKB/TrEMBL)
Protein Domains
bZIP

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-P18850-F1-model_v2 AlphaFold P18850 1-670 view protein structure

Promoters
RGD ID:6784678
Promoter ID:HG_KWN:5888
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:OTTHUMT00000060304,   OTTHUMT00000083586,   OTTHUMT00000083587,   UC001GBQ.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361160,001,761 - 160,002,947 (+)MPROMDB
RGD ID:6851140
Promoter ID:EP73367
Type:multiple initiation site
Name:HS_ATF6
Description:Activating transcription factor 6.
SO ACC ID:SO:0000170
Source:EPD (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:NEDO full length human cDNA sequencing project.; Oligo-capping
Position:
Human AssemblyChrPosition (strand)Source
Build 361160,002,738 - 160,002,798EPD
RGD ID:6784575
Promoter ID:HG_KWN:5891
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell
Transcripts:UC001GBS.2
Position:
Human AssemblyChrPosition (strand)Source
Build 361160,198,886 - 160,199,386 (+)MPROMDB
RGD ID:6857910
Promoter ID:EPDNEW_H2120
Type:initiation region
Name:ATF6_1
Description:activating transcription factor 6
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381161,766,320 - 161,766,380EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:791 AgrOrtholog
COSMIC ATF6 COSMIC
Ensembl Genes ENSG00000118217 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000367942 ENTREZGENE
  ENST00000367942.4 UniProtKB/Swiss-Prot
  ENST00000679833.1 UniProtKB/TrEMBL
  ENST00000679853 ENTREZGENE
  ENST00000679853.1 UniProtKB/TrEMBL
  ENST00000679886.1 UniProtKB/TrEMBL
  ENST00000680462 ENTREZGENE
  ENST00000680462.1 UniProtKB/TrEMBL
  ENST00000680481.1 UniProtKB/TrEMBL
  ENST00000680633.1 UniProtKB/TrEMBL
  ENST00000680688 ENTREZGENE
  ENST00000680688.1 UniProtKB/TrEMBL
  ENST00000681001.1 UniProtKB/TrEMBL
  ENST00000681036.1 UniProtKB/TrEMBL
  ENST00000681169.1 UniProtKB/TrEMBL
  ENST00000681492.1 UniProtKB/TrEMBL
  ENST00000681541.1 UniProtKB/TrEMBL
  ENST00000681557.1 UniProtKB/TrEMBL
  ENST00000681738.1 UniProtKB/Swiss-Prot
  ENST00000681801.1 UniProtKB/Swiss-Prot
  ENST00000681912.1 UniProtKB/TrEMBL
Gene3D-CATH 1.20.5.170 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000118217 GTEx
HGNC ID HGNC:791 ENTREZGENE
Human Proteome Map ATF6 Human Proteome Map
InterPro bZIP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  bZIP_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:22926 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 22926 ENTREZGENE
OMIM 605537 OMIM
PANTHER ATF6, ISOFORM C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR46164:SF1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam bZIP_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA25091 PharmGKB
PROSITE BZIP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  BZIP_BASIC UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART BRLZ UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF57959 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A7P0T8R5 ENTREZGENE, UniProtKB/TrEMBL
  A0A7P0T8Y1_HUMAN UniProtKB/TrEMBL
  A0A7P0T992_HUMAN UniProtKB/TrEMBL
  A0A7P0T9H5_HUMAN UniProtKB/TrEMBL
  A0A7P0T9V3_HUMAN UniProtKB/TrEMBL
  A0A7P0TAB8_HUMAN UniProtKB/TrEMBL
  A0A7P0TAD1_HUMAN UniProtKB/TrEMBL
  A0A7P0TAF2 ENTREZGENE, UniProtKB/TrEMBL
  A0A7P0TAH1_HUMAN UniProtKB/TrEMBL
  A0A7P0TAI7_HUMAN UniProtKB/TrEMBL
  A0A7P0TB89_HUMAN UniProtKB/TrEMBL
  A0A7P0Z421 ENTREZGENE, UniProtKB/TrEMBL
  A0A7P0Z4I7_HUMAN UniProtKB/TrEMBL
  A8K383 ENTREZGENE, UniProtKB/TrEMBL
  ATF6A_HUMAN UniProtKB/Swiss-Prot
  O15139 ENTREZGENE
  P18850 ENTREZGENE
  Q5VW62 ENTREZGENE
  Q6IPB5 ENTREZGENE
  Q9UEC9 ENTREZGENE
UniProt Secondary O15139 UniProtKB/Swiss-Prot
  Q5VW62 UniProtKB/Swiss-Prot
  Q6IPB5 UniProtKB/Swiss-Prot
  Q9UEC9 UniProtKB/Swiss-Prot