CHEK1 (checkpoint kinase 1) - Rat Genome Database

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Gene: CHEK1 (checkpoint kinase 1) Homo sapiens
Analyze
Symbol: CHEK1
Name: checkpoint kinase 1
RGD ID: 732292
HGNC Page HGNC:1925
Description: Enables histone H3T11 kinase activity and protein domain specific binding activity. Involved in several processes, including cellular response to mechanical stimulus; peptidyl-threonine phosphorylation; and regulation of cell cycle process. Located in several cellular components, including centrosome; chromosome, telomeric region; and nuclear lumen. Part of protein-containing complex. Implicated in pancreatic cancer.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: cell cycle checkpoint kinase; checkpoint kinase-1; Checkpoint, S. pombe, homolog of, 1; CHK1; CHK1 checkpoint homolog; Chk1-S; OZEMA21; serine/threonine-protein kinase Chk1
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh3811125,625,136 - 125,681,124 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl11125,625,163 - 125,676,255 (+)EnsemblGRCh38hg38GRCh38
GRCh3711125,495,031 - 125,546,150 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 3611125,001,547 - 125,030,847 (+)NCBINCBI36Build 36hg18NCBI36
Build 3411125,001,546 - 125,030,847NCBI
Celera11122,655,346 - 122,706,400 (+)NCBICelera
Cytogenetic Map11q24.2NCBI
HuRef11121,436,397 - 121,487,529 (+)NCBIHuRef
CHM1_111125,381,155 - 125,432,283 (+)NCBICHM1_1
T2T-CHM13v2.011125,653,757 - 125,709,785 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(+)-schisandrin B  (ISO)
(S)-naringenin  (EXP)
1,1-dichloroethene  (ISO)
1,3-dinitrobenzene  (ISO)
17alpha-ethynylestradiol  (ISO)
17beta-estradiol  (EXP,ISO)
17beta-hydroxy-17-methylestra-4,9,11-trien-3-one  (EXP)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
2,6-di-tert-butyl-4-methylphenol  (ISO)
2-methylcholine  (EXP)
3,3',4,4',5-pentachlorobiphenyl  (ISO)
3,3',5-triiodo-L-thyronine  (EXP)
3,4-methylenedioxymethamphetamine  (ISO)
3-methyladenine  (EXP)
4-hydroxynon-2-enal  (ISO)
4-methoxy-TEMPO  (EXP)
4-nitrophenol  (ISO)
4-nonylphenol  (EXP)
4-tert-Octylphenol  (EXP)
5,7-dihydroxy-4'-methoxyflavone  (EXP)
5-aza-2'-deoxycytidine  (EXP)
5-fluorouracil  (EXP,ISO)
6-(cyclohexylmethoxy)-5-nitrosopyrimidine-2,4-diamine  (EXP)
6-propyl-2-thiouracil  (ISO)
7,12-dimethyltetraphene  (ISO)
acrolein  (EXP)
acrylamide  (ISO)
aflatoxin B1  (EXP)
all-trans-retinoic acid  (EXP,ISO)
amitrole  (ISO)
ammonium chloride  (ISO)
anthocyanin  (EXP)
anthracene-1,8,9-triol  (ISO)
antimycin A  (EXP)
aphidicolin  (ISO)
aristolochic acid A  (EXP)
arsenite(3-)  (EXP)
arsenous acid  (EXP,ISO)
artesunate  (EXP)
atrazine  (EXP)
auraptene  (EXP)
azathioprine  (EXP)
benzo[a]pyrene  (EXP,ISO)
benzo[a]pyrene diol epoxide I  (EXP,ISO)
berberine  (EXP)
biphenyl-4-amine  (EXP)
bis(2-chloroethyl) sulfide  (EXP)
bis(2-ethylhexyl) phthalate  (EXP)
bisphenol A  (EXP,ISO)
Brevetoxin B  (EXP)
busulfan  (EXP)
cadmium atom  (EXP)
cadmium dichloride  (EXP)
caffeine  (EXP,ISO)
camptothecin  (EXP,ISO)
cannabidiol  (EXP)
carbamazepine  (EXP)
carmustine  (EXP)
catechol  (ISO)
cefaloridine  (ISO)
chlorpyrifos  (ISO)
cholic acid  (ISO)
choline  (EXP,ISO)
ciprofloxacin  (ISO)
cisplatin  (EXP,ISO)
clofarabine  (EXP)
clofibrate  (ISO)
cobalt dichloride  (EXP)
copper atom  (EXP,ISO)
copper(0)  (EXP,ISO)
copper(II) sulfate  (EXP)
corosolic acid  (EXP)
coumarin  (EXP)
coumestrol  (EXP)
crocidolite asbestos  (EXP)
curcumin  (EXP)
CX-5461  (EXP)
cyclosporin A  (EXP,ISO)
cylindrospermopsin  (EXP)
Decamethylcyclopentasiloxane  (EXP)
deguelin  (EXP)
Diallyl sulfide  (EXP)
diarsenic trioxide  (EXP,ISO)
dibutyl phthalate  (ISO)
diclofenac  (EXP)
dicrotophos  (EXP)
diepoxybutane  (ISO)
diethyl sulfate  (EXP)
digitoxin  (EXP)
dioscin  (EXP)
doxorubicin  (EXP,ISO)
Echimidine  (EXP)
Enterolactone  (EXP)
entinostat  (EXP)
epoxiconazole  (ISO)
equol  (EXP)
estragole  (ISO)
etoposide  (EXP)
fenofibrate  (ISO)
fenpyroximate  (EXP)
fisetin  (EXP)
flavonoids  (ISO)
floxuridine  (EXP)
flumequine  (ISO)
folic acid  (EXP,ISO)
FR900359  (EXP)
furan  (ISO)
furazolidone  (EXP)
furosemide  (ISO)
genistein  (EXP)
geraniol  (EXP)
glyphosate  (EXP)
Goe 6976  (EXP)
gold atom  (EXP)
gold(0)  (EXP)
GW 4064  (EXP)
hexamethylcyclotrisiloxane  (EXP)
hydrogen peroxide  (EXP)
hydroxyurea  (EXP,ISO)
indole-3-methanol  (ISO)
irinotecan  (EXP)
iron dichloride  (ISO)
iron trichloride  (ISO)
isoflurane  (ISO)
kaempferol  (ISO)
L-methionine  (ISO)
Lasiocarpine  (EXP)
lead diacetate  (ISO)
lead(0)  (EXP)
leflunomide  (ISO)
leptomycin B  (EXP)
lovastatin  (EXP,ISO)
MeIQx  (ISO)
melphalan  (EXP)
menadione  (EXP)
metformin  (EXP)
methapyrilene  (ISO)
methimazole  (ISO)
methotrexate  (EXP,ISO)
methyl isocyanate  (ISO)
methylmercury chloride  (ISO)
Mezerein  (ISO)
mifepristone  (ISO)
mitomycin C  (EXP)
monocrotaline  (EXP)
N-acetyl-L-cysteine  (EXP,ISO)
N-benzyloxycarbonyl-L-leucyl-L-leucyl-L-leucinal  (ISO)
N-methyl-N'-nitro-N-nitrosoguanidine  (EXP)
N-nitrosodiethylamine  (ISO)
nickel atom  (EXP)
nimustine  (EXP)
nocodazole  (EXP)
NORCANTHARIDIN  (EXP)
O-methyleugenol  (ISO)
ochratoxin A  (EXP,ISO)
octamethylcyclotetrasiloxane  (EXP)
olaparib  (EXP)
oxaliplatin  (ISO)
oxfendazole  (ISO)
ozone  (ISO)
p-anisidine  (ISO)
p-tert-Amylphenol  (EXP)
paclitaxel  (EXP,ISO)
paracetamol  (EXP,ISO)
paraquat  (ISO)
perfluorooctane-1-sulfonic acid  (ISO)
PF-00477736  (EXP)
phenobarbital  (ISO)
PhIP  (EXP)
phorbol 13-acetate 12-myristate  (ISO)
pirinixic acid  (ISO)
platinum  (EXP)
platinum(0)  (EXP)
pregnenolone 16alpha-carbonitrile  (ISO)
progesterone  (ISO)
promethazine  (ISO)
propiconazole  (ISO)
Ptaquiloside  (EXP)
pyrimidifen  (EXP)
quercetin  (EXP,ISO)
quizartinib  (EXP)
resveratrol  (EXP,ISO)
RGFP966  (EXP)
riddelliine  (EXP)
rimonabant  (EXP)
romidepsin  (EXP)
rotenone  (EXP)
saccharin  (ISO)
selinexor  (EXP)
silver(1+) nitrate  (EXP)
sodium arsenite  (EXP)
sodium nitrite  (ISO)
stavudine  (ISO)
sterigmatocystin  (EXP)
styrene oxide  (ISO)
succimer  (ISO)
sulfadimethoxine  (ISO)
sunitinib  (EXP)
tamoxifen  (ISO)
temozolomide  (EXP)
tert-butyl hydroperoxide  (EXP)
testosterone  (ISO)
tetrachloromethane  (ISO)
thapsigargin  (EXP)
thioacetamide  (ISO)
titanium dioxide  (ISO)
topotecan  (ISO)
trichostatin A  (EXP)
trimellitic anhydride  (ISO)
triphenyl phosphate  (EXP)
troglitazone  (EXP)
tungsten  (ISO)
usnic acid  (EXP)
valproic acid  (EXP)
vemurafenib  (EXP)
versicolorin A  (EXP)
wortmannin  (EXP)
Xanthatin  (EXP)
zearalenone  (ISO)
zidovudine  (EXP)
zinc dichloride  (ISO)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. Met proto-oncogene and insulin-like growth factor binding protein 3 overexpression correlates with metastatic ability in well-differentiated pancreatic endocrine neoplasms. Hansel DE, etal., Clin Cancer Res. 2004 Sep 15;10(18 Pt 1):6152-8.
3. The radioresistance to killing of A1-5 cells derives from activation of the Chk1 pathway. Hu B, etal., J Biol Chem. 2001 May 25;276(21):17693-8. Epub 2001 Mar 7.
4. Modes of p53 regulation. Kruse JP and Gu W, Cell. 2009 May 15;137(4):609-22. doi: 10.1016/j.cell.2009.04.050.
5. The complexity of p53 stabilization and activation. Lavin MF and Gueven N, Cell Death Differ. 2006 Jun;13(6):941-50.
6. Single-nucleotide polymorphisms of DNA damage response genes are associated with overall survival in patients with pancreatic cancer. Okazaki T, etal., Clin Cancer Res. 2008 Apr 1;14(7):2042-8.
7. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
8. PID Annotation Import Pipeline Pipeline to import Pathway Interaction Database annotations from NCI into RGD
9. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
10. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:8889549   PMID:9278511   PMID:9278512   PMID:9382850   PMID:9765199   PMID:10557092   PMID:10608806   PMID:10673501   PMID:10681541   PMID:10717241   PMID:10761933   PMID:10859164  
PMID:11016625   PMID:11252893   PMID:11329013   PMID:11333986   PMID:11390642   PMID:11535615   PMID:11551930   PMID:11709713   PMID:11799067   PMID:11821419   PMID:11836499   PMID:11896572  
PMID:11912127   PMID:12062056   PMID:12150968   PMID:12244092   PMID:12399544   PMID:12446774   PMID:12477932   PMID:12588868   PMID:12660173   PMID:12676583   PMID:12676925   PMID:12676962  
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PMID:18550533   PMID:18566216   PMID:18614046   PMID:18632613   PMID:18642443   PMID:18671143   PMID:18676680   PMID:18698031   PMID:18723495   PMID:18820127   PMID:18950845   PMID:18983824  
PMID:19060337   PMID:19064565   PMID:19064572   PMID:19091954   PMID:19119425   PMID:19124506   PMID:19170196   PMID:19177015   PMID:19223857   PMID:19242509   PMID:19270516   PMID:19275579  
PMID:19276361   PMID:19330022   PMID:19401701   PMID:19453842   PMID:19473886   PMID:19477924   PMID:19487575   PMID:19546241   PMID:19570909   PMID:19584159   PMID:19593445   PMID:19615254  
PMID:19625176   PMID:19628579   PMID:19690177   PMID:19692168   PMID:19694479   PMID:19714462   PMID:19716789   PMID:19743875   PMID:19778378   PMID:19828454   PMID:19837665   PMID:19838212  
PMID:19843865   PMID:19861535   PMID:19903823   PMID:19931269   PMID:20029092   PMID:20053681   PMID:20068082   PMID:20090422   PMID:20123862   PMID:20146081   PMID:20159774   PMID:20233725  
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PMID:20616048   PMID:20639859   PMID:20644561   PMID:20716119   PMID:20719863   PMID:20731661   PMID:20805465   PMID:20932473   PMID:20940144   PMID:20969866   PMID:21034966   PMID:21051833  
PMID:21118956   PMID:21145461   PMID:21154811   PMID:21171266   PMID:21173116   PMID:21179472   PMID:21212274   PMID:21301228   PMID:21383502   PMID:21389083   PMID:21401699   PMID:21440578  
PMID:21502314   PMID:21532626   PMID:21557990   PMID:21566061   PMID:21615992   PMID:21628425   PMID:21680529   PMID:21680713   PMID:21752283   PMID:21803008   PMID:21832049   PMID:21845734  
PMID:21858151   PMID:21873635   PMID:21907702   PMID:21921034   PMID:21988832   PMID:21995812   PMID:22024163   PMID:22044003   PMID:22080164   PMID:22106282   PMID:22134241   PMID:22159421  
PMID:22184239   PMID:22203733   PMID:22231448   PMID:22357623   PMID:22401965   PMID:22433954   PMID:22435685   PMID:22469983   PMID:22505024   PMID:22529391   PMID:22553144   PMID:22556425  
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PMID:33168956   PMID:33197893   PMID:33306668   PMID:33503415   PMID:33504652   PMID:33542435   PMID:33556369   PMID:33663378   PMID:33729478   PMID:33744317   PMID:33789090   PMID:33820915  
PMID:33910274   PMID:33948904   PMID:33961781   PMID:34058013   PMID:34090465   PMID:34188037   PMID:34189442   PMID:34237211   PMID:34320214   PMID:34372559   PMID:34373451   PMID:34509474  
PMID:34597346   PMID:34663432   PMID:34668620   PMID:34768043   PMID:34782371   PMID:34882011   PMID:35048968   PMID:35142956   PMID:35150405   PMID:35231158   PMID:35271311   PMID:35286657  
PMID:35302600   PMID:35439318   PMID:35673965   PMID:35955683   PMID:36215168   PMID:36307841   PMID:36311753   PMID:36555509   PMID:36671510   PMID:36736316   PMID:36841324   PMID:36919124  
PMID:36931259   PMID:37167062   PMID:37393021   PMID:37499664   PMID:37715382   PMID:37762228   PMID:37773176   PMID:37866880   PMID:38036565   PMID:38047473   PMID:38266782   PMID:38578830  
PMID:38588804   PMID:38803224  


Genomics

Comparative Map Data
CHEK1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh3811125,625,136 - 125,681,124 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl11125,625,163 - 125,676,255 (+)EnsemblGRCh38hg38GRCh38
GRCh3711125,495,031 - 125,546,150 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 3611125,001,547 - 125,030,847 (+)NCBINCBI36Build 36hg18NCBI36
Build 3411125,001,546 - 125,030,847NCBI
Celera11122,655,346 - 122,706,400 (+)NCBICelera
Cytogenetic Map11q24.2NCBI
HuRef11121,436,397 - 121,487,529 (+)NCBIHuRef
CHM1_111125,381,155 - 125,432,283 (+)NCBICHM1_1
T2T-CHM13v2.011125,653,757 - 125,709,785 (+)NCBIT2T-CHM13v2.0
Chek1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39936,619,935 - 36,637,897 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl936,619,778 - 36,638,361 (-)EnsemblGRCm39 Ensembl
GRCm38936,708,482 - 36,726,658 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl936,708,482 - 36,727,065 (-)EnsemblGRCm38mm10GRCm38
MGSCv37936,516,067 - 36,534,243 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36936,458,153 - 36,476,298 (-)NCBIMGSCv36mm8
Celera933,911,337 - 33,929,618 (-)NCBICelera
Cytogenetic Map9A4NCBI
cM Map920.67NCBI
Chek1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8844,609,417 - 44,629,867 (-)NCBIGRCr8
mRatBN7.2836,420,565 - 36,443,477 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl836,420,569 - 36,441,009 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx840,429,698 - 40,450,231 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0838,712,754 - 38,733,290 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0836,575,640 - 36,596,176 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0839,181,162 - 39,201,588 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl839,181,163 - 39,243,882 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0839,184,020 - 39,204,446 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4837,954,322 - 37,974,748 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1837,963,088 - 37,983,514 (-)NCBI
Celera838,000,251 - 38,020,582 (+)NCBICelera
Cytogenetic Map8q22NCBI
Chek1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0NW_00495541226,627,606 - 26,650,554 (+)NCBIChiLan1.0ChiLan1.0
CHEK1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v29126,315,104 - 126,366,201 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan111127,420,236 - 127,470,688 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v011120,446,352 - 120,478,207 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.111124,359,218 - 124,410,385 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl11124,359,218 - 124,390,981 (+)Ensemblpanpan1.1panPan2
CHEK1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.158,878,511 - 8,910,626 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl58,879,147 - 8,907,669 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha58,923,479 - 8,955,720 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.058,821,650 - 8,853,260 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl58,821,983 - 8,853,208 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.158,890,756 - 8,922,634 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.058,860,679 - 8,892,710 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.058,897,288 - 8,929,731 (-)NCBIUU_Cfam_GSD_1.0
Chek1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024404947107,757,062 - 107,779,783 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049367432,005,851 - 2,026,587 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049367432,004,535 - 2,027,287 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
CHEK1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl952,753,528 - 52,790,700 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1952,759,224 - 52,790,878 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2958,411,395 - 58,444,086 (+)NCBISscrofa10.2Sscrofa10.2susScr3
CHEK1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11116,768,141 - 116,809,557 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1116,767,944 - 116,801,371 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660439,201,283 - 9,302,468 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Chek1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046249271,610,878 - 1,643,409 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046249271,609,404 - 1,643,409 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in CHEK1
59 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 11q23.3-25(chr11:116851395-134998513)x3 copy number gain See cases [RCV000050331] Chr11:116851395..134998513 [GRCh38]
Chr11:116722111..134868407 [GRCh37]
Chr11:116227321..134373617 [NCBI36]
Chr11:11q23.3-25
pathogenic
GRCh38/hg38 11q24.2-25(chr11:124155723-134998513)x1 copy number loss See cases [RCV000050865] Chr11:124155723..134998513 [GRCh38]
Chr11:124026430..134868407 [GRCh37]
Chr11:123531640..134373617 [NCBI36]
Chr11:11q24.2-25
pathogenic
GRCh38/hg38 11q23.3-25(chr11:119433909-134998513)x1 copy number loss See cases [RCV000050905] Chr11:119433909..134998513 [GRCh38]
Chr11:119304619..134868407 [GRCh37]
Chr11:118809829..134373617 [NCBI36]
Chr11:11q23.3-25
pathogenic
GRCh38/hg38 11q23.3-25(chr11:118789765-134998513)x3 copy number gain See cases [RCV000051213] Chr11:118789765..134998513 [GRCh38]
Chr11:118660474..134868407 [GRCh37]
Chr11:118165684..134373617 [NCBI36]
Chr11:11q23.3-25
pathogenic
GRCh38/hg38 11q23.3-25(chr11:119215032-134998654)x1 copy number loss See cases [RCV000052715] Chr11:119215032..134998654 [GRCh38]
Chr11:119085742..134868548 [GRCh37]
Chr11:118590952..134373758 [NCBI36]
Chr11:11q23.3-25
pathogenic
GRCh38/hg38 11q23.3-25(chr11:120507265-134576266)x1 copy number loss See cases [RCV000052716] Chr11:120507265..134576266 [GRCh38]
Chr11:120377974..134446160 [GRCh37]
Chr11:119883184..133951370 [NCBI36]
Chr11:11q23.3-25
pathogenic
GRCh38/hg38 11q22.1-25(chr11:100348599-135040246)x3 copy number gain See cases [RCV000053638] Chr11:100348599..135040246 [GRCh38]
Chr11:100219331..134910140 [GRCh37]
Chr11:99724541..134415350 [NCBI36]
Chr11:11q22.1-25
pathogenic
GRCh38/hg38 11q23.3-25(chr11:120236432-135040246)x3 copy number gain See cases [RCV000053643] Chr11:120236432..135040246 [GRCh38]
Chr11:120107141..134910140 [GRCh37]
Chr11:119612351..134415350 [NCBI36]
Chr11:11q23.3-25
pathogenic
GRCh38/hg38 11q24.1-25(chr11:123753493-134998513)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053645]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053645]|See cases [RCV000053645] Chr11:123753493..134998513 [GRCh38]
Chr11:123624201..134868407 [GRCh37]
Chr11:123129411..134373617 [NCBI36]
Chr11:11q24.1-25
pathogenic
NM_001114121.2(CHEK1):c.1054C>T (p.His352Tyr) single nucleotide variant Malignant melanoma [RCV000062168] Chr11:125644221 [GRCh38]
Chr11:125514116 [GRCh37]
Chr11:125019326 [NCBI36]
Chr11:11q24.2
not provided
GRCh38/hg38 11q24.2-25(chr11:124205225-134998526)x1 copy number loss See cases [RCV000134731] Chr11:124205225..134998526 [GRCh38]
Chr11:124075932..134868420 [GRCh37]
Chr11:123581142..134373630 [NCBI36]
Chr11:11q24.2-25
pathogenic
GRCh38/hg38 11q24.1-25(chr11:123799938-134998526)x1 copy number loss See cases [RCV000134708] Chr11:123799938..134998526 [GRCh38]
Chr11:123670646..134868420 [GRCh37]
Chr11:123175856..134373630 [NCBI36]
Chr11:11q24.1-25
pathogenic
GRCh38/hg38 11q23.3-25(chr11:116851372-134998526)x3 copy number gain See cases [RCV000134064] Chr11:116851372..134998526 [GRCh38]
Chr11:116722088..134868420 [GRCh37]
Chr11:116227298..134373630 [NCBI36]
Chr11:11q23.3-25
pathogenic
GRCh38/hg38 11q24.1-24.2(chr11:122182443-125957977)x1 copy number loss See cases [RCV000136594] Chr11:122182443..125957977 [GRCh38]
Chr11:122053151..125827872 [GRCh37]
Chr11:121558361..125333082 [NCBI36]
Chr11:11q24.1-24.2
pathogenic
GRCh38/hg38 11q24.2-25(chr11:125241472-134998513)x1 copy number loss See cases [RCV000136612] Chr11:125241472..134998513 [GRCh38]
Chr11:125111368..134868407 [GRCh37]
Chr11:124616578..134373617 [NCBI36]
Chr11:11q24.2-25
pathogenic
GRCh38/hg38 11q23.3-25(chr11:116868935-135075271)x3 copy number gain See cases [RCV000137453] Chr11:116868935..135075271 [GRCh38]
Chr11:116739651..134945165 [GRCh37]
Chr11:116244861..134450377 [NCBI36]
Chr11:11q23.3-25
pathogenic|conflicting data from submitters
GRCh38/hg38 11q23.2-25(chr11:112864326-131189315)x3 copy number gain See cases [RCV000137582] Chr11:112864326..131189315 [GRCh38]
Chr11:112832130..131059210 [GRCh37]
Chr11:112240259..130564420 [NCBI36]
Chr11:11q23.2-25
pathogenic
GRCh38/hg38 11q24.1-25(chr11:121780459-135075271)x1 copy number loss See cases [RCV000138014] Chr11:121780459..135075271 [GRCh38]
Chr11:121651167..134945165 [GRCh37]
Chr11:121156377..134450377 [NCBI36]
Chr11:11q24.1-25
pathogenic
GRCh38/hg38 11q24.2-25(chr11:124940059-135075271)x1 copy number loss See cases [RCV000138675] Chr11:124940059..135075271 [GRCh38]
Chr11:124809955..134945165 [GRCh37]
Chr11:124315165..134450377 [NCBI36]
Chr11:11q24.2-25
pathogenic|likely benign
GRCh38/hg38 11q23.3-25(chr11:120515759-135075271)x1 copy number loss See cases [RCV000138373] Chr11:120515759..135075271 [GRCh38]
Chr11:120386468..134945165 [GRCh37]
Chr11:119891678..134450377 [NCBI36]
Chr11:11q23.3-25
pathogenic
GRCh38/hg38 11q23.3-25(chr11:116806268-135075271)x3 copy number gain See cases [RCV000138307] Chr11:116806268..135075271 [GRCh38]
Chr11:116676984..134945165 [GRCh37]
Chr11:116182194..134450377 [NCBI36]
Chr11:11q23.3-25
pathogenic
GRCh38/hg38 11q24.1-25(chr11:123963074-135075271)x1 copy number loss See cases [RCV000138544] Chr11:123963074..135075271 [GRCh38]
Chr11:123833781..134945165 [GRCh37]
Chr11:123338991..134450377 [NCBI36]
Chr11:11q24.1-25
pathogenic
GRCh38/hg38 11q23.3-24.2(chr11:117333952-127709156)x3 copy number gain See cases [RCV000139362] Chr11:117333952..127709156 [GRCh38]
Chr11:117204668..127579051 [GRCh37]
Chr11:116709878..127084261 [NCBI36]
Chr11:11q23.3-24.2
pathogenic
GRCh38/hg38 11q23.3-25(chr11:119424297-135075271)x1 copy number loss See cases [RCV000138947] Chr11:119424297..135075271 [GRCh38]
Chr11:119295007..134945165 [GRCh37]
Chr11:118800217..134450377 [NCBI36]
Chr11:11q23.3-25
pathogenic|likely benign
GRCh38/hg38 11q23.3-24.2(chr11:120080142-125829106)x1 copy number loss See cases [RCV000140070] Chr11:120080142..125829106 [GRCh38]
Chr11:119950851..125699001 [GRCh37]
Chr11:119456061..125204211 [NCBI36]
Chr11:11q23.3-24.2
pathogenic
GRCh38/hg38 11q24.2-25(chr11:124315025-134818116)x1 copy number loss See cases [RCV000139907] Chr11:124315025..134818116 [GRCh38]
Chr11:124184921..134688010 [GRCh37]
Chr11:123690131..134193220 [NCBI36]
Chr11:11q24.2-25
pathogenic
GRCh38/hg38 11q24.1-25(chr11:121689052-135075271)x1 copy number loss See cases [RCV000139622] Chr11:121689052..135075271 [GRCh38]
Chr11:121559760..134945165 [GRCh37]
Chr11:121064970..134450377 [NCBI36]
Chr11:11q24.1-25
pathogenic|likely benign
GRCh38/hg38 11q24.1-25(chr11:121806547-135068576)x1 copy number loss See cases [RCV000142210] Chr11:121806547..135068576 [GRCh38]
Chr11:121677255..134938470 [GRCh37]
Chr11:121182465..134443680 [NCBI36]
Chr11:11q24.1-25
pathogenic
GRCh38/hg38 11q24.1-25(chr11:121611476-135068576)x1 copy number loss See cases [RCV000142185] Chr11:121611476..135068576 [GRCh38]
Chr11:121482185..134938470 [GRCh37]
Chr11:120987395..134443680 [NCBI36]
Chr11:11q24.1-25
pathogenic
GRCh38/hg38 11q23.3-25(chr11:116851395-134998513)x3 copy number gain See cases [RCV000148276] Chr11:116851395..134998513 [GRCh38]
Chr11:116722111..134868407 [GRCh37]
Chr11:116227321..134373617 [NCBI36]
Chr11:11q23.3-25
pathogenic
GRCh37/hg19 11q23.3-25(chr11:120615374-134868407)x1 copy number loss See cases [RCV000239781] Chr11:120615374..134868407 [GRCh37]
Chr11:11q23.3-25
pathogenic
GRCh37/hg19 11q23.3-25(chr11:119807473-134868407)x1 copy number loss See cases [RCV000240237] Chr11:119807473..134868407 [GRCh37]
Chr11:11q23.3-25
pathogenic
NM_001114122.3(CHEK1):c.1234-26G>A single nucleotide variant Hereditary cancer-predisposing syndrome [RCV000209268] Chr11:125653720 [GRCh38]
Chr11:125523615 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.290-173C>T single nucleotide variant Hereditary cancer-predisposing syndrome [RCV000209096] Chr11:125629059 [GRCh38]
Chr11:125498954 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.289+83T>G single nucleotide variant Hereditary cancer-predisposing syndrome [RCV000209301] Chr11:125627913 [GRCh38]
Chr11:125497808 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.1336-481T>C single nucleotide variant Hereditary cancer-predisposing syndrome [RCV000209594] Chr11:125654744 [GRCh38]
Chr11:125524639 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.1135C>T (p.Arg379Ter) single nucleotide variant Hereditary cancer-predisposing syndrome [RCV000210167] Chr11:125644545 [GRCh38]
Chr11:125514440 [GRCh37]
Chr11:11q24.2
uncertain significance
GRCh37/hg19 11q24.1-25(chr11:121416261-134938470)x1 copy number loss See cases [RCV000511335] Chr11:121416261..134938470 [GRCh37]
Chr11:11q24.1-25
pathogenic
NM_001612.6(ACRV1):c.794T>C (p.Ile265Thr) single nucleotide variant not specified [RCV004284708] Chr11:125672597 [GRCh38]
Chr11:125542492 [GRCh37]
Chr11:11q24.2
uncertain significance
NM_001114122.3(CHEK1):c.1260A>G (p.Arg420=) single nucleotide variant CHEK1-related disorder [RCV003962656]|not provided [RCV000587573] Chr11:125653772 [GRCh38]
Chr11:125523667 [GRCh37]
Chr11:11q24.2
benign
NM_001114122.3(CHEK1):c.1411A>G (p.Ile471Val) single nucleotide variant CHEK1-related disorder [RCV003983134]|not provided [RCV000589283] Chr11:125655300 [GRCh38]
Chr11:125525195 [GRCh37]
Chr11:11q24.2
benign
GRCh37/hg19 11q23.3-25(chr11:116700253-134904063) copy number gain not provided [RCV000767816] Chr11:116700253..134904063 [GRCh37]
Chr11:11q23.3-25
pathogenic
GRCh37/hg19 11q23.3-25(chr11:116681007-134938470)x3 copy number gain See cases [RCV000449449] Chr11:116681007..134938470 [GRCh37]
Chr11:11q23.3-25
pathogenic
GRCh37/hg19 11q23.3-25(chr11:119513909-134938470)x1 copy number loss See cases [RCV000447077] Chr11:119513909..134938470 [GRCh37]
Chr11:11q23.3-25
pathogenic
GRCh37/hg19 11q24.1-25(chr11:121501072-134868348)x1 copy number loss See cases [RCV000445814] Chr11:121501072..134868348 [GRCh37]
Chr11:11q24.1-25
pathogenic
GRCh37/hg19 11q23.3-25(chr11:116684163-134938470)x3 copy number gain See cases [RCV000447848] Chr11:116684163..134938470 [GRCh37]
Chr11:11q23.3-25
pathogenic
GRCh37/hg19 11q24.1-25(chr11:121559102-134938470)x1 copy number loss See cases [RCV000449003] Chr11:121559102..134938470 [GRCh37]
Chr11:11q24.1-25
pathogenic
GRCh37/hg19 11q24.1-25(chr11:122403610-134938470)x1 copy number loss See cases [RCV000448215] Chr11:122403610..134938470 [GRCh37]
Chr11:11q24.1-25
pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470) copy number gain See cases [RCV000511729] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25
pathogenic
GRCh37/hg19 11q24.1-25(chr11:122884694-134938470)x3 copy number gain See cases [RCV000511146] Chr11:122884694..134938470 [GRCh37]
Chr11:11q24.1-25
pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)x3 copy number gain See cases [RCV000510881] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25
pathogenic
GRCh37/hg19 11q23.3-25(chr11:120527021-134938470)x1 copy number loss See cases [RCV000511283] Chr11:120527021..134938470 [GRCh37]
Chr11:11q23.3-25
pathogenic
GRCh37/hg19 11q23.3-25(chr11:121136603-134938470)x1 copy number loss See cases [RCV000510856] Chr11:121136603..134938470 [GRCh37]
Chr11:11q23.3-25
pathogenic
GRCh37/hg19 11q24.2-25(chr11:125446101-134904063) copy number loss 11q partial monosomy syndrome [RCV000767602] Chr11:125446101..134904063 [GRCh37]
Chr11:11q24.2-25
pathogenic
NM_001114122.3(CHEK1):c.85A>G (p.Arg29Gly) single nucleotide variant not provided [RCV000586016] Chr11:125627626 [GRCh38]
Chr11:125497521 [GRCh37]
Chr11:11q24.2
uncertain significance
GRCh37/hg19 11q23.3-25(chr11:116681007-134938470)x3 copy number gain See cases [RCV000512291] Chr11:116681007..134938470 [GRCh37]
Chr11:11q23.3-25
pathogenic
GRCh37/hg19 11q23.3-25(chr11:119538664-134938470)x1 copy number loss not provided [RCV000683371] Chr11:119538664..134938470 [GRCh37]
Chr11:11q23.3-25
pathogenic
GRCh37/hg19 11q23.3-25(chr11:116681007-134938470)x3 copy number gain not provided [RCV000683373] Chr11:116681007..134938470 [GRCh37]
Chr11:11q23.3-25
pathogenic
NM_001114122.3(CHEK1):c.478C>T (p.Arg160Cys) single nucleotide variant Hereditary cancer-predisposing syndrome [RCV000708693] Chr11:125633216 [GRCh38]
Chr11:125503111 [GRCh37]
Chr11:11q24.2
uncertain significance
GRCh37/hg19 11p15.5-q25(chr11:198510-134934063)x3 copy number gain not provided [RCV000737348] Chr11:198510..134934063 [GRCh37]
Chr11:11p15.5-q25
pathogenic
Single allele duplication Schizophrenia [RCV000754124] Chr11:118989374..135076622 [GRCh38]
Chr11:11q23.3-25
likely pathogenic
GRCh37/hg19 11p15.5-q25(chr11:70864-134938470)x3 copy number gain not provided [RCV000749874] Chr11:70864..134938470 [GRCh37]
Chr11:11p15.5-q25
pathogenic
GRCh37/hg19 11q23.3-25(chr11:116697066-134934063)x3 copy number gain not provided [RCV000737686] Chr11:116697066..134934063 [GRCh37]
Chr11:11q23.3-25
pathogenic
GRCh37/hg19 11q24.2-25(chr11:125366454-134938470)x1 copy number loss not provided [RCV000750223] Chr11:125366454..134938470 [GRCh37]
Chr11:11q24.2-25
pathogenic
NM_001114122.3(CHEK1):c.1102-9G>A single nucleotide variant CHEK1-related disorder [RCV003903008]|not provided [RCV000922444] Chr11:125644503 [GRCh38]
Chr11:125514398 [GRCh37]
Chr11:11q24.2
benign
NM_001114122.3(CHEK1):c.163G>A (p.Glu55Lys) single nucleotide variant not specified [RCV004291373] Chr11:125627704 [GRCh38]
Chr11:125497599 [GRCh37]
Chr11:11q24.2
uncertain significance
GRCh37/hg19 11q23.3-25(chr11:116691675-134889485) copy number gain not provided [RCV000767667] Chr11:116691675..134889485 [GRCh37]
Chr11:11q23.3-25
pathogenic
GRCh37/hg19 11q23.3-25(chr11:117830263-134938470)x3 copy number gain not provided [RCV000848151] Chr11:117830263..134938470 [GRCh37]
Chr11:11q23.3-25
pathogenic
NM_001114121.2(CHEK1):c.66-2A>T single nucleotide variant Neoplasm of ovary [RCV000785582] Chr11:125627605 [GRCh38]
Chr11:125497500 [GRCh37]
Chr11:11q24.2
likely pathogenic
NM_001114121.2(CHEK1):c.887_888del (p.Gln295_Ser296insTer) deletion Neoplasm of ovary [RCV000785427] Chr11:125643864..125643865 [GRCh38]
Chr11:125513759..125513760 [GRCh37]
Chr11:11q24.2
pathogenic
NM_001114121.2(CHEK1):c.829C>T (p.Arg277Ter) single nucleotide variant Neoplasm of ovary [RCV000785569] Chr11:125643806 [GRCh38]
Chr11:125513701 [GRCh37]
Chr11:11q24.2
pathogenic
GRCh37/hg19 11q23.3-25(chr11:120576984-134934063)x1 copy number loss See cases [RCV000790567] Chr11:120576984..134934063 [GRCh37]
Chr11:11q23.3-25
pathogenic
GRCh37/hg19 11q23.3-25(chr11:120742540-134938470)x1 copy number loss not provided [RCV001006452] Chr11:120742540..134938470 [GRCh37]
Chr11:11q23.3-25
pathogenic
GRCh37/hg19 11q24.2(chr11:125481301-125547902)x1 copy number loss not provided [RCV001006456] Chr11:125481301..125547902 [GRCh37]
Chr11:11q24.2
uncertain significance
GRCh37/hg19 11q24.2-25(chr11:124232608-134938470)x1 copy number loss not provided [RCV001006454] Chr11:124232608..134938470 [GRCh37]
Chr11:11q24.2-25
pathogenic
GRCh37/hg19 11q23.3-25(chr11:120531028-134257553) copy number loss 11q partial monosomy syndrome [RCV003236728] Chr11:120531028..134257553 [GRCh37]
Chr11:11q23.3-25
pathogenic
GRCh37/hg19 11q24.2(chr11:125202487-125610231)x1 copy number loss not provided [RCV001006455] Chr11:125202487..125610231 [GRCh37]
Chr11:11q24.2
uncertain significance
Single allele deletion Paris-Trousseau thrombocytopenia [RCV001003843] Chr11:124226940..134944477 [GRCh37]
Chr11:11q24.2-25
pathogenic
Single allele deletion Short stature [RCV001003892] Chr11:114433313..131230466 [GRCh37]
Chr11:11q23.2-25
likely pathogenic
NM_001114122.3(CHEK1):c.1066A>C (p.Asn356His) single nucleotide variant not specified [RCV004607822] Chr11:125644233 [GRCh38]
Chr11:125514128 [GRCh37]
Chr11:11q24.2
uncertain significance
NM_001114122.3(CHEK1):c.415G>T (p.Asp139Tyr) single nucleotide variant not specified [RCV004607823] Chr11:125629451 [GRCh38]
Chr11:125499346 [GRCh37]
Chr11:11q24.2
uncertain significance
NM_001114122.3(CHEK1):c.66-160A>G single nucleotide variant not provided [RCV001645790] Chr11:125627447 [GRCh38]
Chr11:125497342 [GRCh37]
Chr11:11q24.2
benign
NC_000011.9:g.104288964_134937416dup duplication Distal trisomy 11q [RCV001250234] Chr11:104288964..134937416 [GRCh37]
Chr11:11q22.3-25
pathogenic
NC_000011.9:g.(?_123504851)_(126163012_?)dup duplication Holoprosencephaly 11 [RCV001871151] Chr11:123504851..126163012 [GRCh37]
Chr11:11q24.1-24.2
uncertain significance
GRCh37/hg19 11q23.1-24.3(chr11:112375478-128785742)x3 copy number gain not provided [RCV001829187] Chr11:112375478..128785742 [GRCh37]
Chr11:11q23.1-24.3
pathogenic
NM_001612.6(ACRV1):c.623C>T (p.Thr208Ile) single nucleotide variant Malignant tumor of prostate [RCV000149265] Chr11:125676409 [GRCh38]
Chr11:125546304 [GRCh37]
Chr11:11q24.2
uncertain significance
NC_000011.9:g.(?_123504851)_(126163012_?)del deletion Holoprosencephaly 11 [RCV003119757]|not provided [RCV003119756] Chr11:123504851..126163012 [GRCh37]
Chr11:11q24.1-24.2
uncertain significance|no classifications from unflagged records
GRCh37/hg19 11p13-q25(chr11:32799481-134938470)x3 copy number gain MISSED ABORTION [RCV002282973] Chr11:32799481..134938470 [GRCh37]
Chr11:11p13-q25
pathogenic
NM_001114122.3(CHEK1):c.1117T>C (p.Leu373=) single nucleotide variant not specified [RCV004062374] Chr11:125644527 [GRCh38]
Chr11:125514422 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.987T>C (p.Asp329=) single nucleotide variant not specified [RCV004057676] Chr11:125644154 [GRCh38]
Chr11:125514049 [GRCh37]
Chr11:11q24.2
likely benign
GRCh37/hg19 11q24.1-25(chr11:122975824-134938470)x1 copy number loss not provided [RCV002474497] Chr11:122975824..134938470 [GRCh37]
Chr11:11q24.1-25
pathogenic
NM_001114122.3(CHEK1):c.1263C>T (p.Asn421=) single nucleotide variant not specified [RCV004056189] Chr11:125653775 [GRCh38]
Chr11:125523670 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.105C>T (p.Val35=) single nucleotide variant not specified [RCV004061410] Chr11:125627646 [GRCh38]
Chr11:125497541 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.525T>C (p.Ala175=) single nucleotide variant not specified [RCV004052297] Chr11:125633263 [GRCh38]
Chr11:125503158 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.645T>C (p.Cys215=) single nucleotide variant not specified [RCV004054015] Chr11:125635460 [GRCh38]
Chr11:125505355 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.411G>A (p.Leu137=) single nucleotide variant not specified [RCV004051720] Chr11:125629447 [GRCh38]
Chr11:125499342 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.951T>C (p.Ser317=) single nucleotide variant not specified [RCV004056880] Chr11:125644118 [GRCh38]
Chr11:125514013 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.900C>T (p.Phe300=) single nucleotide variant not specified [RCV004054927] Chr11:125643877 [GRCh38]
Chr11:125513772 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.93T>C (p.Thr31=) single nucleotide variant not specified [RCV004056777] Chr11:125627634 [GRCh38]
Chr11:125497529 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.1177C>T (p.Leu393=) single nucleotide variant not specified [RCV004050811] Chr11:125644587 [GRCh38]
Chr11:125514482 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.636T>C (p.Ser212=) single nucleotide variant not specified [RCV004053897] Chr11:125635451 [GRCh38]
Chr11:125505346 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.43C>T (p.Leu15=) single nucleotide variant not specified [RCV004050634] Chr11:125626811 [GRCh38]
Chr11:125496706 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.1266T>C (p.Asn422=) single nucleotide variant not specified [RCV004056640] Chr11:125653778 [GRCh38]
Chr11:125523673 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.1002C>T (p.Tyr334=) single nucleotide variant not specified [RCV004057221] Chr11:125644169 [GRCh38]
Chr11:125514064 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.384C>T (p.His128=) single nucleotide variant not specified [RCV004048210] Chr11:125629420 [GRCh38]
Chr11:125499315 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.1407G>A (p.Gln469=) single nucleotide variant not specified [RCV004057163] Chr11:125655296 [GRCh38]
Chr11:125525191 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.783A>G (p.Lys261=) single nucleotide variant not specified [RCV004054720] Chr11:125637513 [GRCh38]
Chr11:125507408 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.690T>C (p.Pro230=) single nucleotide variant not specified [RCV004052953] Chr11:125635505 [GRCh38]
Chr11:125505400 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.1017A>G (p.Val339=) single nucleotide variant not specified [RCV004052444] Chr11:125644184 [GRCh38]
Chr11:125514079 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.762T>A (p.Ile254=) single nucleotide variant not specified [RCV004056478] Chr11:125637492 [GRCh38]
Chr11:125507387 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.459A>C (p.Thr153=) single nucleotide variant not specified [RCV004051486] Chr11:125633197 [GRCh38]
Chr11:125503092 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.723G>A (p.Leu241=) single nucleotide variant not specified [RCV004055800] Chr11:125637453 [GRCh38]
Chr11:125507348 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.476A>T (p.Asn159Ile) single nucleotide variant not specified [RCV004231298] Chr11:125633214 [GRCh38]
Chr11:125503109 [GRCh37]
Chr11:11q24.2
uncertain significance
NM_001612.6(ACRV1):c.229A>C (p.Lys77Gln) single nucleotide variant not specified [RCV004123260] Chr11:125678121 [GRCh38]
Chr11:125548016 [GRCh37]
Chr11:11q24.2
uncertain significance
NM_001114122.3(CHEK1):c.965G>A (p.Arg322His) single nucleotide variant not specified [RCV004233393] Chr11:125644132 [GRCh38]
Chr11:125514027 [GRCh37]
Chr11:11q24.2
uncertain significance
NM_001612.6(ACRV1):c.370C>T (p.Leu124Phe) single nucleotide variant not specified [RCV004170601] Chr11:125677980 [GRCh38]
Chr11:125547875 [GRCh37]
Chr11:11q24.2
uncertain significance
NM_001114122.3(CHEK1):c.860C>T (p.Pro287Leu) single nucleotide variant not specified [RCV004287204] Chr11:125643837 [GRCh38]
Chr11:125513732 [GRCh37]
Chr11:11q24.2
uncertain significance
NM_001114122.3(CHEK1):c.1036C>T (p.Gln346Ter) single nucleotide variant Male infertility due to gonadal dysgenesis or sperm disorder [RCV003991594]|not provided [RCV003322472] Chr11:125644203 [GRCh38]
Chr11:125514098 [GRCh37]
Chr11:11q24.2
likely pathogenic
NM_001612.6(ACRV1):c.611G>A (p.Arg204His) single nucleotide variant not specified [RCV004329290] Chr11:125676421 [GRCh38]
Chr11:125546316 [GRCh37]
Chr11:11q24.2
uncertain significance
NM_001114122.3(CHEK1):c.1324del (p.Arg442fs) deletion Oocyte/zygote/embryo maturation arrest 21 [RCV003444094] Chr11:125653835 [GRCh38]
Chr11:125523730 [GRCh37]
Chr11:11q24.2
pathogenic
NM_001114122.3(CHEK1):c.-83T>C single nucleotide variant CHEK1-related disorder [RCV003397289] Chr11:125625950 [GRCh38]
Chr11:125495845 [GRCh37]
Chr11:11q24.2
uncertain significance
NM_001612.6(ACRV1):c.76C>A (p.Leu26Ile) single nucleotide variant not specified [RCV004344876] Chr11:125678274 [GRCh38]
Chr11:125548169 [GRCh37]
Chr11:11q24.2
uncertain significance
NM_001114122.3(CHEK1):c.946A>G (p.Ser316Gly) single nucleotide variant not specified [RCV004365044] Chr11:125644113 [GRCh38]
Chr11:125514008 [GRCh37]
Chr11:11q24.2
uncertain significance
NM_001114122.3(CHEK1):c.466C>T (p.Arg156Trp) single nucleotide variant not specified [RCV004336306] Chr11:125633204 [GRCh38]
Chr11:125503099 [GRCh37]
Chr11:11q24.2
uncertain significance
Single allele duplication not provided [RCV003448710] Chr11:102134973..134945611 [GRCh37]
Chr11:11q22.2-25
pathogenic
NM_001114122.3(CHEK1):c.1114C>T (p.Arg372Trp) single nucleotide variant CHEK1-related disorder [RCV003399730] Chr11:125644524 [GRCh38]
Chr11:125514419 [GRCh37]
Chr11:11q24.2
uncertain significance
GRCh37/hg19 11q24.2(chr11:125208533-125519800)x1 copy number loss not provided [RCV003483143] Chr11:125208533..125519800 [GRCh37]
Chr11:11q24.2
uncertain significance
NM_001114122.3(CHEK1):c.1136G>A (p.Arg379Gln) single nucleotide variant Oocyte/zygote/embryo maturation arrest 21 [RCV003444093] Chr11:125644546 [GRCh38]
Chr11:125514441 [GRCh37]
Chr11:11q24.2
pathogenic
NM_001114122.3(CHEK1):c.1259G>A (p.Arg420Lys) single nucleotide variant Oocyte/zygote/embryo maturation arrest 21 [RCV003444096] Chr11:125653771 [GRCh38]
Chr11:125523666 [GRCh37]
Chr11:11q24.2
pathogenic
NM_001114122.3(CHEK1):c.586A>C (p.Ile196Leu) single nucleotide variant CHEK1-related disorder [RCV003394472] Chr11:125633324 [GRCh38]
Chr11:125503219 [GRCh37]
Chr11:11q24.2
uncertain significance
NM_001114122.3(CHEK1):c.1325G>A (p.Arg442Gln) single nucleotide variant Oocyte/zygote/embryo maturation arrest 21 [RCV003444095] Chr11:125653837 [GRCh38]
Chr11:125523732 [GRCh37]
Chr11:11q24.2
pathogenic
NM_001114122.3(CHEK1):c.-160C>T single nucleotide variant CHEK1-related disorder [RCV003391664] Chr11:125625873 [GRCh38]
Chr11:125495768 [GRCh37]
Chr11:11q24.2
uncertain significance
NM_001114122.3(CHEK1):c.830G>A (p.Arg277Gln) single nucleotide variant CHEK1-related disorder [RCV003392754]|not specified [RCV004362855] Chr11:125643807 [GRCh38]
Chr11:125513702 [GRCh37]
Chr11:11q24.2
uncertain significance
NM_001114122.3(CHEK1):c.467G>A (p.Arg156Gln) single nucleotide variant CHEK1-related disorder [RCV003417065] Chr11:125633205 [GRCh38]
Chr11:125503100 [GRCh37]
Chr11:11q24.2
uncertain significance
NM_001114122.3(CHEK1):c.-253A>T single nucleotide variant CHEK1-related disorder [RCV003939523] Chr11:125625780 [GRCh38]
Chr11:125495675 [GRCh37]
Chr11:11q24.2
benign
GRCh37/hg19 11q23.3-24.2(chr11:121183636-127620828)x1 copy number loss not specified [RCV003986915] Chr11:121183636..127620828 [GRCh37]
Chr11:11q23.3-24.2
pathogenic
GRCh37/hg19 11q24.1-25(chr11:123523103-134938470)x1 copy number loss not specified [RCV003986947] Chr11:123523103..134938470 [GRCh37]
Chr11:11q24.1-25
pathogenic
GRCh37/hg19 11q24.2-25(chr11:125511834-134938470)x1 copy number loss not specified [RCV003986921] Chr11:125511834..134938470 [GRCh37]
Chr11:11q24.2-25
pathogenic
GRCh37/hg19 11q24.1-25(chr11:121423232-134938470)x1 copy number loss not specified [RCV003986923] Chr11:121423232..134938470 [GRCh37]
Chr11:11q24.1-25
pathogenic
NM_001114122.3(CHEK1):c.563C>G (p.Pro188Arg) single nucleotide variant Oocyte/zygote/embryo maturation arrest 21 [RCV003988740] Chr11:125633301 [GRCh38]
Chr11:125503196 [GRCh37]
Chr11:11q24.2
uncertain significance
NM_001114122.3(CHEK1):c.499A>T (p.Met167Leu) single nucleotide variant not specified [RCV004439160] Chr11:125633237 [GRCh38]
Chr11:125503132 [GRCh37]
Chr11:11q24.2
uncertain significance
NM_001114122.3(CHEK1):c.844G>C (p.Gly282Arg) single nucleotide variant not specified [RCV004439162] Chr11:125643821 [GRCh38]
Chr11:125513716 [GRCh37]
Chr11:11q24.2
uncertain significance
NM_001114122.3(CHEK1):c.1225A>G (p.Met409Val) single nucleotide variant not specified [RCV004439157] Chr11:125644635 [GRCh38]
Chr11:125514530 [GRCh37]
Chr11:11q24.2
uncertain significance
NM_001114122.3(CHEK1):c.1389T>G (p.Ile463Met) single nucleotide variant not specified [RCV004439158] Chr11:125655278 [GRCh38]
Chr11:125525173 [GRCh37]
Chr11:11q24.2
uncertain significance
NM_001114122.3(CHEK1):c.230G>T (p.Gly77Val) single nucleotide variant not specified [RCV004439159] Chr11:125627771 [GRCh38]
Chr11:125497666 [GRCh37]
Chr11:11q24.2
uncertain significance
GRCh37/hg19 11q23.3-25(chr11:116683755-134937416)x3 copy number gain not provided [RCV004442759] Chr11:116683755..134937416 [GRCh37]
Chr11:11q23.3-25
pathogenic
NM_001114122.3(CHEK1):c.-182C>G single nucleotide variant CHEK1-related disorder [RCV003972134] Chr11:125625851 [GRCh38]
Chr11:125495746 [GRCh37]
Chr11:11q24.2
benign
NM_001114122.3(CHEK1):c.-209G>A single nucleotide variant CHEK1-related disorder [RCV003961920] Chr11:125625824 [GRCh38]
Chr11:125495719 [GRCh37]
Chr11:11q24.2
benign
NM_001114122.3(CHEK1):c.-188A>G single nucleotide variant CHEK1-related disorder [RCV003979042] Chr11:125625845 [GRCh38]
Chr11:125495740 [GRCh37]
Chr11:11q24.2
benign
NM_001114122.3(CHEK1):c.-196A>G single nucleotide variant CHEK1-related disorder [RCV003937075] Chr11:125625837 [GRCh38]
Chr11:125495732 [GRCh37]
Chr11:11q24.2
benign
NM_001114122.3(CHEK1):c.676dup (p.Thr226fs) duplication CHEK1-related disorder [RCV003979767] Chr11:125635482..125635483 [GRCh38]
Chr11:125505377..125505378 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.814+7del deletion CHEK1-related disorder [RCV003962311] Chr11:125637551 [GRCh38]
Chr11:125507446 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.1200G>A (p.Leu400=) single nucleotide variant not provided [RCV003886176] Chr11:125644610 [GRCh38]
Chr11:125514505 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.-170C>T single nucleotide variant CHEK1-related disorder [RCV003954475] Chr11:125625863 [GRCh38]
Chr11:125495758 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.-89A>T single nucleotide variant CHEK1-related disorder [RCV003969677] Chr11:125625944 [GRCh38]
Chr11:125495839 [GRCh37]
Chr11:11q24.2
uncertain significance
NM_001114122.3(CHEK1):c.-37G>A single nucleotide variant CHEK1-related disorder [RCV003909585] Chr11:125625996 [GRCh38]
Chr11:125495891 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.580T>C (p.Cys194Arg) single nucleotide variant not specified [RCV004439161] Chr11:125633318 [GRCh38]
Chr11:125503213 [GRCh37]
Chr11:11q24.2
uncertain significance
NM_001114122.3(CHEK1):c.-191T>C single nucleotide variant CHEK1-related disorder [RCV003982031] Chr11:125625842 [GRCh38]
Chr11:125495737 [GRCh37]
Chr11:11q24.2
benign
NM_001114122.3(CHEK1):c.*10C>T single nucleotide variant CHEK1-related disorder [RCV003894297] Chr11:125655330 [GRCh38]
Chr11:125525225 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.-195C>T single nucleotide variant CHEK1-related disorder [RCV003917278] Chr11:125625838 [GRCh38]
Chr11:125495733 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.-114G>T single nucleotide variant CHEK1-related disorder [RCV003904303] Chr11:125625919 [GRCh38]
Chr11:125495814 [GRCh37]
Chr11:11q24.2
likely benign
NM_001114122.3(CHEK1):c.614-8G>A single nucleotide variant CHEK1-related disorder [RCV003897427] Chr11:125635421 [GRCh38]
Chr11:125505316 [GRCh37]
Chr11:11q24.2
likely benign
NM_001612.6(ACRV1):c.176C>G (p.Ser59Cys) single nucleotide variant not specified [RCV004427622] Chr11:125678174 [GRCh38]
Chr11:125548069 [GRCh37]
Chr11:11q24.2
uncertain significance
NM_001114122.3(CHEK1):c.-266T>A single nucleotide variant CHEK1-related disorder [RCV003911466] Chr11:125625767 [GRCh38]
Chr11:125495662 [GRCh37]
Chr11:11q24.2
uncertain significance
NM_001612.6(ACRV1):c.668T>C (p.Phe223Ser) single nucleotide variant not specified [RCV004427633] Chr11:125676364 [GRCh38]
Chr11:125546259 [GRCh37]
Chr11:11q24.2
uncertain significance
miRNA Target Status

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
MIR424hsa-miR-424-5pOncomiRDBexternal_infoNANA22469983
MIR24-2hsa-miR-24-3pMirtarbaseexternal_infoReporter assay;Western blot;qRT-PCR;OtherFunctional MTI19748357
MIR24-1hsa-miR-24-3pMirtarbaseexternal_infoReporter assay;Western blot;qRT-PCR;OtherFunctional MTI19748357

Predicted Target Of
Summary Value
Count of predictions:2587
Count of miRNA genes:1012
Interacting mature miRNAs:1185
Transcripts:ENST00000278916, ENST00000427383, ENST00000428830, ENST00000438015, ENST00000498122, ENST00000524737, ENST00000525396, ENST00000526937, ENST00000527013, ENST00000528276, ENST00000528761, ENST00000531062, ENST00000531607, ENST00000532449, ENST00000532669, ENST00000533778, ENST00000534070, ENST00000534685, ENST00000544373
Prediction methods:Microtar, Miranda, Rnahybrid
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.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
406902315GWAS551291_Hsquamous cell lung carcinoma QTL GWAS551291 (human)0.000007squamous cell lung carcinoma11125640362125640363Human
1559115SCL20_HSerum cholesterol level QTL 20 (human)3.220.001213Lipid levelLDL cholesterol11100442501126442501Human

Markers in Region
RH17743  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711125,542,453 - 125,542,573UniSTSGRCh37
Build 3611125,047,663 - 125,047,783RGDNCBI36
Celera11122,702,703 - 122,702,823RGD
Cytogenetic Map11q24.2UniSTS
HuRef11121,483,831 - 121,483,951UniSTS
GeneMap99-GB4 RH Map11415.6UniSTS
D11S2092  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711125,529,411 - 125,529,570UniSTSGRCh37
Build 3611125,034,621 - 125,034,780RGDNCBI36
Celera11122,689,659 - 122,689,818RGD
Cytogenetic Map11q24.2UniSTS
HuRef11121,470,789 - 121,470,948UniSTS
RH92593  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711125,495,159 - 125,495,288UniSTSGRCh37
Build 3611125,000,369 - 125,000,498RGDNCBI36
Celera11122,655,469 - 122,655,598RGD
Cytogenetic Map11q24.2UniSTS
HuRef11121,436,525 - 121,436,654UniSTS
GeneMap99-GB4 RH Map11415.6UniSTS
RH122396  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711125,500,977 - 125,501,251UniSTSGRCh37
Build 3611125,006,187 - 125,006,461RGDNCBI36
Celera11122,661,287 - 122,661,561RGD
Cytogenetic Map11q24.2UniSTS
HuRef11121,442,344 - 121,442,618UniSTS
TNG Radiation Hybrid Map1158915.0UniSTS
A006U05  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711125,526,799 - 125,526,905UniSTSGRCh37
Build 3611125,032,009 - 125,032,115RGDNCBI36
Celera11122,687,112 - 122,687,218RGD
Cytogenetic Map11q24.2UniSTS
HuRef11121,468,177 - 121,468,283UniSTS
GeneMap99-GB4 RH Map11415.6UniSTS
ACRV1_8189  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711125,542,043 - 125,542,567UniSTSGRCh37
Build 3611125,047,253 - 125,047,777RGDNCBI36
Celera11122,702,293 - 122,702,817RGD
HuRef11121,483,421 - 121,483,945UniSTS
RH36540  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711125,526,813 - 125,526,936UniSTSGRCh37
Build 3611125,032,023 - 125,032,146RGDNCBI36
Celera11122,687,126 - 122,687,249RGD
Cytogenetic Map11q24.2UniSTS
HuRef11121,468,191 - 121,468,314UniSTS
GeneMap99-GB4 RH Map11415.6UniSTS
RH66419  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711125,530,388 - 125,530,467UniSTSGRCh37
Build 3611125,035,598 - 125,035,677RGDNCBI36
Celera11122,690,636 - 122,690,715RGD
Cytogenetic Map11q24.2UniSTS
HuRef11121,471,766 - 121,471,845UniSTS
GeneMap99-GB4 RH Map11415.6UniSTS
WI-7841  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711125,542,275 - 125,542,476UniSTSGRCh37
Build 3611125,047,485 - 125,047,686RGDNCBI36
Celera11122,702,525 - 122,702,726RGD
Cytogenetic Map11q24.2UniSTS
HuRef11121,483,653 - 121,483,854UniSTS
GeneMap99-GB4 RH Map11416.22UniSTS
Whitehead-RH Map11582.5UniSTS
Whitehead-YAC Contig Map11 UniSTS
NCBI RH Map111060.4UniSTS
ACRV1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711125,542,275 - 125,542,477UniSTSGRCh37
Build 3611125,047,485 - 125,047,687RGDNCBI36
Celera11122,702,525 - 122,702,727RGD
Cytogenetic Map11q24.2UniSTS
HuRef11121,483,653 - 121,483,855UniSTS
GeneMap99-GB4 RH Map11415.6UniSTS
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
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5q14.2UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map5q32-q34UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map8p22-p21UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map14q31-q32.1UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map20p11.23-p11.21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map12q24.11UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map7q34-q35UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map6p25.1-p23UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map13q12.1UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map12p13.1-p12.3UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map3p21.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic MapXp21.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map9q21.12UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map7q33UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map12p13-p12UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic MapXp11.2UniSTS
Cytogenetic Map19pUniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map11p15.3-p15.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8q22UniSTS
Cytogenetic Map4p15.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map2p16.3UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map6q24.3UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map10q23.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map6q22.1UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map15q22.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map3p21-p12UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3p22-p21.33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map9q22UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map2q31.3UniSTS
Cytogenetic Map1q31UniSTS
Cytogenetic Map7q32-q33UniSTS
Cytogenetic Map7q21.1UniSTS
Cytogenetic Map14q23-q24.2UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map2p24-p21UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map12p11UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map17q25.2UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic MapXq25-q26UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map15q25UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map3q26.31UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q26.2-q27UniSTS
Cytogenetic Map1q25.1-q25.2UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map5q21.3UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map14q12-q13UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic MapXq23UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map4q32-q34UniSTS
Cytogenetic MapXq25-q26.1UniSTS
Cytogenetic Map2p25-p24UniSTS
Cytogenetic Map2p25UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic MapXp22.2-p22.1UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map20q11.22-q12UniSTS
Cytogenetic Map4q34.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map12q13-q14UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map9q31.2UniSTS
Cytogenetic Map11q13.1-q13.2UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map21q21.2UniSTS
Cytogenetic Map10q24.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map8q21.1UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1q32.2UniSTS
Cytogenetic Map4q21.3UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map2q36.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map4p15.32UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map1p35UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map20p12UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map9p22UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2p22.3UniSTS
Cytogenetic MapXq26.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map22q13.3UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map11p14UniSTS
Cytogenetic Map1p32.1UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map4q34.3UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map11q23.2UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map3p13UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map15q22-q24UniSTS
Cytogenetic Map8q23UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map4q31.3UniSTS
Cytogenetic Map15q21-q22UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map15q22.1-q22.31UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic MapXq13UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map14q32.1UniSTS
Cytogenetic Map16q12-q13UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map12q11-q12UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map8q24.21UniSTS
Cytogenetic Map12q13.1UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map5q31.2-q34UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map6q24.2UniSTS
Cytogenetic Map22qUniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic MapXp22.12-p22.11UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map8p22-p21.3UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map1p36.12UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map7p14-p13UniSTS
Cytogenetic Map12q24.2UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map7q22-qterUniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map1q32.2-q41UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map5p15.1-p14.3UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map3p12.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map3q28UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic MapXq22.2UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map7p15.1UniSTS
Cytogenetic Map2q37.2UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map14q32.13UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map16p13.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map20q13.2-q13.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map13q13.3UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q33.2UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map18p11.2UniSTS
Cytogenetic Map7p11.1UniSTS
Cytogenetic Map1q31-q32UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map2p24.2UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map6q24.1UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic MapXq25UniSTS
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


Sequence

Nucleotide Sequences
RefSeq Transcripts NG_030049 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001114121 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001114122 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001244846 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001274 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001330427 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001330428 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_045204 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_045205 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011542560 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017017146 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448337 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047426311 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047426312 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047426313 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367536 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367537 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367538 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367539 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_007062447 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008488333 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA224205 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB032387 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB451222 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB451345 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF016582 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF032874 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF527555 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI750792 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK292549 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK293143 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK299783 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK300082 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP001132 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AW149126 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY304548 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC004202 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC017575 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BG191840 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BG216281 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BG218896 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BG468734 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM455102 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BP203333 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BP207812 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX114781 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX419129 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX506561 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CA441277 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CA868104 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471065 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068267 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA567616 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JF289264 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF455559 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000278916   ⟹   ENSP00000278916
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11125,625,977 - 125,655,506 (+)Ensembl
Ensembl Acc Id: ENST00000427383   ⟹   ENSP00000391090
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11125,625,726 - 125,655,476 (+)Ensembl
Ensembl Acc Id: ENST00000428830   ⟹   ENSP00000412504
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11125,625,974 - 125,676,255 (+)Ensembl
Ensembl Acc Id: ENST00000438015   ⟹   ENSP00000388648
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11125,625,163 - 125,657,147 (+)Ensembl
Ensembl Acc Id: ENST00000524737   ⟹   ENSP00000432890
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11125,626,558 - 125,676,041 (+)Ensembl
Ensembl Acc Id: ENST00000525396   ⟹   ENSP00000434141
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11125,625,665 - 125,629,437 (+)Ensembl
Ensembl Acc Id: ENST00000526937   ⟹   ENSP00000431815
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11125,626,005 - 125,633,250 (+)Ensembl
Ensembl Acc Id: ENST00000527013   ⟹   ENSP00000431525
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11125,626,002 - 125,635,435 (+)Ensembl
Ensembl Acc Id: ENST00000531062
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11125,626,316 - 125,636,135 (+)Ensembl
Ensembl Acc Id: ENST00000531607   ⟹   ENSP00000477588
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11125,626,749 - 125,633,193 (+)Ensembl
Ensembl Acc Id: ENST00000532449   ⟹   ENSP00000481616
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11125,626,229 - 125,656,845 (+)Ensembl
Ensembl Acc Id: ENST00000532669   ⟹   ENSP00000434646
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11125,625,993 - 125,637,544 (+)Ensembl
Ensembl Acc Id: ENST00000534070   ⟹   ENSP00000435371
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11125,626,341 - 125,657,147 (+)Ensembl
Ensembl Acc Id: ENST00000534685   ⟹   ENSP00000432470
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11125,626,007 - 125,629,417 (+)Ensembl
Ensembl Acc Id: ENST00000544373   ⟹   ENSP00000442317
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11125,625,977 - 125,655,710 (+)Ensembl
Ensembl Acc Id: ENST00000711049   ⟹   ENSP00000518558
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11125,625,683 - 125,676,255 (+)Ensembl
RefSeq Acc Id: NM_001114121   ⟹   NP_001107593
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811125,625,136 - 125,676,255 (+)NCBI
GRCh3711125,495,031 - 125,546,150 (+)NCBI
HuRef11121,436,397 - 121,487,529 (+)NCBI
CHM1_111125,381,155 - 125,432,283 (+)NCBI
T2T-CHM13v2.011125,653,757 - 125,704,891 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001114122   ⟹   NP_001107594
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811125,625,163 - 125,657,147 (+)NCBI
GRCh3711125,495,031 - 125,546,150 (+)NCBI
HuRef11121,436,397 - 121,487,529 (+)NCBI
CHM1_111125,381,155 - 125,413,176 (+)NCBI
T2T-CHM13v2.011125,653,784 - 125,685,781 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001244846   ⟹   NP_001231775
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811125,625,136 - 125,657,147 (+)NCBI
HuRef11121,436,397 - 121,487,529 (+)NCBI
CHM1_111125,381,155 - 125,413,176 (+)NCBI
T2T-CHM13v2.011125,653,757 - 125,685,781 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001274   ⟹   NP_001265
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811125,626,356 - 125,657,147 (+)NCBI
GRCh3711125,495,031 - 125,546,150 (+)NCBI
Build 3611125,001,547 - 125,030,847 (+)NCBI Archive
HuRef11121,436,397 - 121,487,529 (+)NCBI
CHM1_111125,382,376 - 125,413,176 (+)NCBI
T2T-CHM13v2.011125,654,978 - 125,685,781 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001330427   ⟹   NP_001317356
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811125,625,163 - 125,676,255 (+)NCBI
T2T-CHM13v2.011125,653,784 - 125,704,891 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001330428   ⟹   NP_001317357
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811125,626,224 - 125,657,154 (+)NCBI
T2T-CHM13v2.011125,654,846 - 125,685,788 (+)NCBI
Sequence:
RefSeq Acc Id: NR_045204
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811125,625,136 - 125,657,147 (+)NCBI
GRCh3711125,495,031 - 125,546,150 (+)NCBI
HuRef11121,436,397 - 121,487,529 (+)NCBI
CHM1_111125,381,155 - 125,413,176 (+)NCBI
T2T-CHM13v2.011125,653,757 - 125,685,781 (+)NCBI
Sequence:
RefSeq Acc Id: NR_045205
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811125,626,229 - 125,657,147 (+)NCBI
GRCh3711125,495,031 - 125,546,150 (+)NCBI
HuRef11121,436,397 - 121,487,529 (+)NCBI
CHM1_111125,382,249 - 125,413,176 (+)NCBI
T2T-CHM13v2.011125,654,851 - 125,685,781 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011542560   ⟹   XP_011540862
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811125,625,136 - 125,657,147 (+)NCBI
Sequence:
RefSeq Acc Id: XM_024448337   ⟹   XP_024304105
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811125,625,976 - 125,657,154 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047426311   ⟹   XP_047282267
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811125,626,224 - 125,676,255 (+)NCBI
RefSeq Acc Id: XM_047426312   ⟹   XP_047282268
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811125,626,356 - 125,657,154 (+)NCBI
RefSeq Acc Id: XM_047426313   ⟹   XP_047282269
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811125,625,976 - 125,657,154 (+)NCBI
RefSeq Acc Id: XM_054367536   ⟹   XP_054223511
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.011125,653,757 - 125,685,772 (+)NCBI
RefSeq Acc Id: XM_054367537   ⟹   XP_054223512
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.011125,654,846 - 125,704,891 (+)NCBI
RefSeq Acc Id: XM_054367538   ⟹   XP_054223513
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.011125,654,847 - 125,685,788 (+)NCBI
RefSeq Acc Id: XM_054367539   ⟹   XP_054223514
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.011125,654,978 - 125,685,788 (+)NCBI
RefSeq Acc Id: XR_007062447
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811125,625,136 - 125,681,124 (+)NCBI
RefSeq Acc Id: XR_008488333
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.011125,653,757 - 125,709,785 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001107593 (Get FASTA)   NCBI Sequence Viewer  
  NP_001107594 (Get FASTA)   NCBI Sequence Viewer  
  NP_001231775 (Get FASTA)   NCBI Sequence Viewer  
  NP_001265 (Get FASTA)   NCBI Sequence Viewer  
  NP_001317356 (Get FASTA)   NCBI Sequence Viewer  
  NP_001317357 (Get FASTA)   NCBI Sequence Viewer  
  XP_011540862 (Get FASTA)   NCBI Sequence Viewer  
  XP_024304105 (Get FASTA)   NCBI Sequence Viewer  
  XP_047282267 (Get FASTA)   NCBI Sequence Viewer  
  XP_047282268 (Get FASTA)   NCBI Sequence Viewer  
  XP_047282269 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223511 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223512 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223513 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223514 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAB88852 (Get FASTA)   NCBI Sequence Viewer  
  AAC51736 (Get FASTA)   NCBI Sequence Viewer  
  AAH04202 (Get FASTA)   NCBI Sequence Viewer  
  AAH17575 (Get FASTA)   NCBI Sequence Viewer  
  AAM78553 (Get FASTA)   NCBI Sequence Viewer  
  AAQ76038 (Get FASTA)   NCBI Sequence Viewer  
  AEB71796 (Get FASTA)   NCBI Sequence Viewer  
  BAA84577 (Get FASTA)   NCBI Sequence Viewer  
  BAF85238 (Get FASTA)   NCBI Sequence Viewer  
  BAG56691 (Get FASTA)   NCBI Sequence Viewer  
  BAG61665 (Get FASTA)   NCBI Sequence Viewer  
  BAG61885 (Get FASTA)   NCBI Sequence Viewer  
  BAG70036 (Get FASTA)   NCBI Sequence Viewer  
  BAG70159 (Get FASTA)   NCBI Sequence Viewer  
  EAW67644 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000278916
  ENSP00000278916.4
  ENSP00000388648
  ENSP00000388648.1
  ENSP00000391090
  ENSP00000391090.2
  ENSP00000412504
  ENSP00000412504.2
  ENSP00000431525.2
  ENSP00000431815.1
  ENSP00000432470.1
  ENSP00000432890
  ENSP00000432890.1
  ENSP00000434141.2
  ENSP00000434646.2
  ENSP00000435371
  ENSP00000435371.1
  ENSP00000442317
  ENSP00000442317.2
  ENSP00000477588.1
  ENSP00000481616.2
  ENSP00000518558.1
GenBank Protein O14757 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_001107593   ⟸   NM_001114121
- Peptide Label: isoform 1
- UniProtKB: F5H7S4 (UniProtKB/Swiss-Prot),   B5BTY6 (UniProtKB/Swiss-Prot),   B4DSK3 (UniProtKB/Swiss-Prot),   B4DDD0 (UniProtKB/Swiss-Prot),   A8K934 (UniProtKB/Swiss-Prot),   H2BI51 (UniProtKB/Swiss-Prot),   O14757 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001107594   ⟸   NM_001114122
- Peptide Label: isoform 1
- UniProtKB: F5H7S4 (UniProtKB/Swiss-Prot),   B5BTY6 (UniProtKB/Swiss-Prot),   B4DSK3 (UniProtKB/Swiss-Prot),   B4DDD0 (UniProtKB/Swiss-Prot),   A8K934 (UniProtKB/Swiss-Prot),   H2BI51 (UniProtKB/Swiss-Prot),   O14757 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001265   ⟸   NM_001274
- Peptide Label: isoform 1
- UniProtKB: F5H7S4 (UniProtKB/Swiss-Prot),   B5BTY6 (UniProtKB/Swiss-Prot),   B4DSK3 (UniProtKB/Swiss-Prot),   B4DDD0 (UniProtKB/Swiss-Prot),   A8K934 (UniProtKB/Swiss-Prot),   H2BI51 (UniProtKB/Swiss-Prot),   O14757 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001231775   ⟸   NM_001244846
- Peptide Label: isoform 2
- UniProtKB: O14757 (UniProtKB/Swiss-Prot),   B4DT73 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011540862   ⟸   XM_011542560
- Peptide Label: isoform X1
- UniProtKB: E7EPP6 (UniProtKB/TrEMBL),   B4DT73 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001317356   ⟸   NM_001330427
- Peptide Label: isoform 3
- Sequence:
RefSeq Acc Id: NP_001317357   ⟸   NM_001330428
- Peptide Label: isoform 4
- UniProtKB: O14757 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_024304105   ⟸   XM_024448337
- Peptide Label: isoform X2
- UniProtKB: O14757 (UniProtKB/Swiss-Prot),   F5H7S4 (UniProtKB/Swiss-Prot),   B5BTY6 (UniProtKB/Swiss-Prot),   B4DSK3 (UniProtKB/Swiss-Prot),   B4DDD0 (UniProtKB/Swiss-Prot),   A8K934 (UniProtKB/Swiss-Prot),   H2BI51 (UniProtKB/Swiss-Prot)
- Sequence:
Ensembl Acc Id: ENSP00000388648   ⟸   ENST00000438015
Ensembl Acc Id: ENSP00000442317   ⟸   ENST00000544373
Ensembl Acc Id: ENSP00000391090   ⟸   ENST00000427383
Ensembl Acc Id: ENSP00000477588   ⟸   ENST00000531607
Ensembl Acc Id: ENSP00000412504   ⟸   ENST00000428830
Ensembl Acc Id: ENSP00000481616   ⟸   ENST00000532449
Ensembl Acc Id: ENSP00000434646   ⟸   ENST00000532669
Ensembl Acc Id: ENSP00000435371   ⟸   ENST00000534070
Ensembl Acc Id: ENSP00000432470   ⟸   ENST00000534685
Ensembl Acc Id: ENSP00000432890   ⟸   ENST00000524737
Ensembl Acc Id: ENSP00000434141   ⟸   ENST00000525396
Ensembl Acc Id: ENSP00000431815   ⟸   ENST00000526937
Ensembl Acc Id: ENSP00000431525   ⟸   ENST00000527013
Ensembl Acc Id: ENSP00000278916   ⟸   ENST00000278916
RefSeq Acc Id: XP_047282269   ⟸   XM_047426313
- Peptide Label: isoform X4
RefSeq Acc Id: XP_047282267   ⟸   XM_047426311
- Peptide Label: isoform X2
- UniProtKB: O14757 (UniProtKB/Swiss-Prot),   F5H7S4 (UniProtKB/Swiss-Prot),   B5BTY6 (UniProtKB/Swiss-Prot),   B4DSK3 (UniProtKB/Swiss-Prot),   B4DDD0 (UniProtKB/Swiss-Prot),   A8K934 (UniProtKB/Swiss-Prot),   H2BI51 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_047282268   ⟸   XM_047426312
- Peptide Label: isoform X3
- UniProtKB: B4DT73 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054223511   ⟸   XM_054367536
- Peptide Label: isoform X1
- UniProtKB: B4DT73 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054223512   ⟸   XM_054367537
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054223513   ⟸   XM_054367538
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054223514   ⟸   XM_054367539
- Peptide Label: isoform X3
- UniProtKB: B4DT73 (UniProtKB/TrEMBL)
Ensembl Acc Id: ENSP00000518558   ⟸   ENST00000711049
Protein Domains
Protein kinase

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-O14757-F1-model_v2 AlphaFold O14757 1-476 view protein structure

Promoters