OCLN (occludin) - Rat Genome Database

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Gene: OCLN (occludin) Homo sapiens
Analyze
Symbol: OCLN
Name: occludin
RGD ID: 732985
HGNC Page HGNC:8104
Description: Enables protein domain specific binding activity. Involved in several processes, including bicellular tight junction assembly; positive regulation of blood-brain barrier permeability; and regulation of gene expression. Acts upstream of or within cell-cell junction organization. Located in several cellular components, including bicellular tight junction; cytoplasmic vesicle; and lysosomal membrane. Part of protein-containing complex. Implicated in Crohn's disease and pseudo-TORCH syndrome 1.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: BLCPMG; FLJ08163; FLJ18079; FLJ77961; FLJ94056; MGC34277; phosphatase 1, regulatory subunit 115; PPP1R115; PTORCH1; tight junction protein occludin; tight junction protein occludin TM4 minus
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Related Pseudogenes: OCLNP1  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38569,492,547 - 69,558,104 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl569,492,292 - 69,558,104 (+)EnsemblGRCh38hg38GRCh38
GRCh37568,788,374 - 68,853,931 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36568,823,875 - 68,885,889 (+)NCBINCBI36Build 36hg18NCBI36
Build 34568,823,874 - 68,885,887NCBI
Cytogenetic Map5q13.2NCBI
HuRef565,744,381 - 65,800,380 (+)NCBIHuRef
HuRef565,800,577 - 65,803,347 (+)NCBIHuRef
CHM1_1568,787,783 - 68,853,763 (+)NCBICHM1_1
T2T-CHM13v2.0570,316,240 - 70,383,882 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(R)-carnitine  (ISO)
(S)-amphetamine  (ISO)
(S)-colchicine  (ISO)
1,10-phenanthroline  (EXP)
1,2-dichloroethane  (ISO)
1,2-dimethylhydrazine  (ISO)
1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine  (ISO)
1-naphthyl isothiocyanate  (ISO)
17beta-estradiol  (EXP,ISO)
17beta-estradiol 17-glucosiduronic acid  (ISO)
17beta-estradiol 3-benzoate  (EXP,ISO)
2,2',4,4',5,5'-hexachlorobiphenyl  (EXP,ISO)
2,3',4,4',5-Pentachlorobiphenyl  (EXP,ISO)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
2,3-bis(4-hydroxyphenyl)propionitrile  (EXP)
2,4,6-trinitrobenzenesulfonic acid  (ISO)
2,4-D  (ISO)
2-amino-2-deoxy-D-galactopyranose  (ISO)
2-palmitoylglycerol  (EXP)
3,3',4,4',5-pentachlorobiphenyl  (EXP,ISO)
3,3',5-triiodo-L-thyronine  (ISO)
3-\{1-[3-(dimethylamino)propyl]-1H-indol-3-yl\}-4-(1H-indol-3-yl)-1H-pyrrole-2,5-dione  (EXP)
4,4'-sulfonyldiphenol  (ISO)
4-(N-nitrosomethylamino)-1-(3-pyridyl)butan-1-one  (EXP)
4-\{[(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl)carbonyl]amino\}benzoic acid  (EXP)
4-hydroxyphenyl retinamide  (ISO)
4-phenylbutyric acid  (ISO)
4-tert-Octylphenol  (ISO)
5-azacytidine  (EXP)
6-chloro-2,3,4,9-tetrahydro-1H-carbazole-1-carboxamide  (EXP)
6-propyl-2-thiouracil  (ISO)
7,8-dihydroxycoumarin  (ISO)
acadesine  (ISO)
acetaldehyde  (EXP)
acetic acid [2-[[(5-nitro-2-thiazolyl)amino]-oxomethyl]phenyl] ester  (ISO)
acrylonitrile  (EXP)
actinidine  (EXP)
aflatoxin B1  (EXP,ISO)
aldehydo-D-glucose  (EXP,ISO)
all-trans-retinoic acid  (EXP,ISO)
alpha,alpha-trehalose  (ISO)
alpha-D-galactose  (ISO)
Alpinetin  (EXP)
ammonium chloride  (ISO)
Ammothamnine  (ISO)
ampicillin  (ISO)
arsane  (EXP,ISO)
arsenic atom  (EXP,ISO)
arsenite(3-)  (ISO)
arsenous acid  (EXP,ISO)
benzalkonium chloride  (ISO)
benzo[a]pyrene  (EXP,ISO)
beta-naphthoflavone  (EXP)
biochanin A  (ISO)
bis(2-chloroethyl) sulfide  (ISO)
bis(2-ethylhexyl) phthalate  (ISO)
bisphenol A  (EXP,ISO)
bisphenol F  (ISO)
busulfan  (ISO)
Butylbenzyl phthalate  (ISO)
butyric acid  (EXP,ISO)
cadmium atom  (ISO)
cadmium dichloride  (EXP,ISO)
caffeine  (EXP)
calcitriol  (EXP)
calcium atom  (EXP)
calcium(0)  (EXP)
carbendazim  (ISO)
carbon nanotube  (ISO)
chlorogenic acid  (ISO)
chloroquine  (EXP)
chlorothalonil  (EXP)
chlorpyrifos  (EXP,ISO)
choline  (ISO)
chromium(6+)  (ISO)
cisplatin  (EXP)
clopidogrel  (EXP)
cobalt dichloride  (EXP,ISO)
copper atom  (EXP)
copper(0)  (EXP)
cordycepin  (ISO)
corticosterone  (ISO)
cortisol  (EXP)
curcumin  (ISO)
cyclophosphamide  (ISO)
D-glucose  (EXP,ISO)
DDE  (EXP)
decabromodiphenyl ether  (EXP)
deoxynivalenol  (EXP,ISO)
Deoxyschizandrin  (EXP)
dexamethasone  (ISO)
dextran sulfate  (ISO)
Di-n-octyl phthalate  (ISO)
diarsenic trioxide  (EXP,ISO)
dibutyl phthalate  (ISO)
diclofenac  (EXP,ISO)
Dictamnine  (EXP)
diethyl phthalate  (ISO)
diiodine  (EXP)
Diisodecyl phthalate  (ISO)
diisononyl phthalate  (ISO)
dimethyl sulfoxide  (EXP)
dioxygen  (EXP,ISO)
dizocilpine maleate  (ISO)
dodecanoic acid  (ISO)
dorsomorphin  (EXP,ISO)
elemental selenium  (EXP)
endosulfan  (ISO)
epoxiconazole  (ISO)
ethanol  (EXP,ISO)
ethylene glycol  (ISO)
excitatory amino acid agonist  (ISO)
flutamide  (ISO)
folic acid  (ISO)
FR900359  (EXP)
fulvestrant  (EXP,ISO)
fumonisin B1  (EXP)
furan  (ISO)
galactose  (ISO)
gamma-linolenic acid  (EXP)
genistein  (EXP)
gentamycin  (ISO)
Ginkgolide A  (ISO)
ginsenoside Re  (ISO)
glabridin  (ISO)
glucose  (EXP,ISO)
glycine  (EXP)
glyphosate  (EXP,ISO)
hydrogen peroxide  (EXP,ISO)
hydrogen sulfide  (ISO)
hydroquinone  (ISO)
hydroxychloroquine  (EXP)
hydroxysafflor yellow A  (ISO)
indometacin  (EXP,ISO)
irinotecan  (ISO)
iron atom  (ISO)
iron(0)  (ISO)
isoprene  (EXP)
isovitexin  (ISO)
kaempferol  (ISO)
ketamine  (ISO)
kynurenic acid  (ISO)
L-ascorbic acid  (ISO)
L-methionine  (ISO)
lactulose  (ISO)
lead diacetate  (EXP)
lead(0)  (ISO)
lipopolysaccharide  (EXP,ISO)
lithium chloride  (ISO)
lithocholic acid  (EXP)
loliolide  (EXP)
luteolin  (EXP)
LY294002  (EXP,ISO)
malaoxon  (ISO)
malathion  (ISO)
melatonin  (ISO)
mercury atom  (ISO)
mercury(0)  (ISO)
methamphetamine  (ISO)
methotrexate  (EXP,ISO)
methylmercury chloride  (ISO)
metronidazole  (ISO)
microcystin-LR  (ISO)
minocycline  (ISO)
mono(2-ethylhexyl) phthalate  (ISO)
Monobutylphthalate  (EXP,ISO)
mycophenolic acid  (EXP)
myricetin  (ISO)
N(6),N(6)-dimethyladenine  (ISO)
N-acetyl-L-cysteine  (EXP,ISO)
N-acetylsphingosine  (ISO)
neomycin  (ISO)
nickel atom  (EXP)
nitric oxide  (ISO)
nitrofen  (ISO)
Nor-9-carboxy-delta9-THC  (EXP)
obeticholic acid  (ISO)
ochratoxin A  (EXP)
okadaic acid  (EXP)
p-tert-Amylphenol  (ISO)
paclitaxel  (ISO)
papaverine  (ISO)
paracetamol  (ISO)
paraquat  (EXP)
patulin  (EXP)
perfluorooctane-1-sulfonic acid  (EXP,ISO)
perfluorooctanoic acid  (EXP,ISO)
permethrin  (ISO)
phenethyl isothiocyanate  (ISO)
phenobarbital  (EXP,ISO)
phoxim  (ISO)
pirinixic acid  (ISO)
poly(vinylpyrrolidone)  (EXP)
potassium dichromate  (EXP,ISO)
potassium iodide  (ISO)
pregnenolone 16alpha-carbonitrile  (ISO)
PRIM-O-GLUCOSYLCIMIFUGIN  (EXP)
probenecid  (ISO)
progesterone  (ISO)
propiconazole  (ISO)
puerarin  (EXP)
Pyridostigmine bromide  (ISO)
quercetin  (EXP,ISO)
quercitrin  (EXP)
raloxifene  (EXP)
resveratrol  (EXP,ISO)
rifampicin  (ISO)
rotenone  (EXP)
rottlerin  (EXP)
Salidroside  (ISO)
SB 203580  (EXP,ISO)
SB 431542  (EXP)
selenium atom  (EXP)
serpentine asbestos  (EXP)
simvastatin  (ISO)
sodium arsenite  (EXP,ISO)
sodium chloride  (EXP)
sodium fluoride  (ISO)
sodium propionate  (ISO)
sodium sulfide (anhydrous)  (ISO)
Soman  (ISO)
streptozocin  (ISO)
sulfasalazine  (ISO)
sunitinib  (EXP)
T-2 toxin  (EXP)
tamibarotene  (EXP)
tamoxifen  (EXP)
tectorigenin  (ISO)
telmisartan  (EXP,ISO)
tert-butyl hydroperoxide  (ISO)
testosterone  (EXP)
tetrachloroethene  (ISO)
tetrachloromethane  (ISO)
thalidomide  (ISO)
thioacetamide  (ISO)
tioguanine  (EXP)
titanium dioxide  (ISO)
toluene  (ISO)
trichloroethene  (ISO)
trichostatin A  (EXP)
triclosan  (EXP)
triphenyl phosphate  (ISO)
Triptolide  (ISO)
troglitazone  (ISO)
uranium atom  (ISO)
valproic acid  (EXP)
vancomycin  (ISO)
vinclozolin  (ISO)
vitamin E  (ISO)
zafirlukast  (EXP,ISO)
zileuton  (ISO)
zinc sulfate  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. S-methylation of 2-mercaptopyrazine in rat liver microsomes and cytosol. Lee DH and Kim DH, Xenobiotica 1999 Sep;29(9):909-16.
3. Alteration in intestine tight junction protein phosphorylation and apoptosis is associated with increase in IL-18 levels following alcohol intoxication and burn injury. Li X, etal., Biochim Biophys Acta. 2012 Feb;1822(2):196-203. doi: 10.1016/j.bbadis.2011.09.019. Epub 2011 Oct 7.
4. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
5. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
6. PID Annotation Import Pipeline Pipeline to import Pathway Interaction Database annotations from NCI into RGD
7. Increase in the tight junction protein claudin-1 in intestinal inflammation. Poritz LS, etal., Dig Dis Sci. 2011 Oct;56(10):2802-9. doi: 10.1007/s10620-011-1688-9. Epub 2011 Jul 12.
8. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
9. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
10. RGD HPO Phenotype Annotation Pipeline RGD automated import pipeline for human HPO-to-gene-to-disease annotations
11. Vascular tight junction disruption and angiogenesis in spontaneously hypertensive rat with neuroinflammatory white matter injury. Yang Y, etal., Neurobiol Dis. 2018 Jun;114:95-110. doi: 10.1016/j.nbd.2018.02.012. Epub 2018 Feb 24.
12. Dendrobium chrysotoxum Lindl. alleviates diabetic retinopathy by preventing retinal inflammation and tight junction protein decrease. Yu Z, etal., J Diabetes Res. 2015;2015:518317. doi: 10.1155/2015/518317. Epub 2015 Jan 1.
Additional References at PubMed
PMID:7798316   PMID:8601611   PMID:9175707   PMID:9212730   PMID:9243183   PMID:9531559   PMID:9792688   PMID:10026224   PMID:10497311   PMID:10575001   PMID:10581193   PMID:10591624  
PMID:10601346   PMID:10749869   PMID:11090614   PMID:11181995   PMID:11228248   PMID:11502742   PMID:11679090   PMID:11700038   PMID:11710912   PMID:11782481   PMID:11878825   PMID:11950934  
PMID:12071155   PMID:12118072   PMID:12169098   PMID:12184633   PMID:12419305   PMID:12477932   PMID:12639940   PMID:12667324   PMID:12668723   PMID:12728017   PMID:12804768   PMID:12932229  
PMID:14512431   PMID:14991532   PMID:15054114   PMID:15069537   PMID:15252450   PMID:15372022   PMID:15472219   PMID:15489334   PMID:15500294   PMID:15622522   PMID:15659655   PMID:15761153  
PMID:15806147   PMID:15977641   PMID:16081103   PMID:16134968   PMID:16207910   PMID:16344560   PMID:16616143   PMID:16924233   PMID:16959951   PMID:17038551   PMID:17243118   PMID:17283368  
PMID:17359339   PMID:17525332   PMID:17553883   PMID:17635647   PMID:17855770   PMID:17962811   PMID:18005733   PMID:18029348   PMID:18276783   PMID:18318008   PMID:18329007   PMID:18386163  
PMID:18397460   PMID:18474622   PMID:18489585   PMID:18550469   PMID:18560860   PMID:18574677   PMID:18662404   PMID:18667611   PMID:18782596   PMID:18802961   PMID:19017651   PMID:19052094  
PMID:19054851   PMID:19073886   PMID:19114660   PMID:19125584   PMID:19174516   PMID:19182773   PMID:19184677   PMID:19332538   PMID:19437620   PMID:19438816   PMID:19478092   PMID:19515778  
PMID:19538290   PMID:19661441   PMID:19756380   PMID:20003786   PMID:20028514   PMID:20152177   PMID:20164257   PMID:20375010   PMID:20463075   PMID:20504882   PMID:20663912   PMID:20727516  
PMID:20822789   PMID:20844048   PMID:20878095   PMID:20937238   PMID:21415414   PMID:21516116   PMID:21536752   PMID:21551950   PMID:21632765   PMID:21641584   PMID:21806988   PMID:21821450  
PMID:21857898   PMID:21858117   PMID:21873635   PMID:21956164   PMID:22031828   PMID:22134947   PMID:22135309   PMID:22197032   PMID:22448134   PMID:22591361   PMID:22711802   PMID:22761434  
PMID:22927233   PMID:23155001   PMID:23220562   PMID:23288152   PMID:23390516   PMID:23428392   PMID:23503679   PMID:23554480   PMID:23555257   PMID:23758859   PMID:23792687   PMID:23793442  
PMID:23924897   PMID:24081143   PMID:24318462   PMID:24567356   PMID:24660027   PMID:24739782   PMID:24840331   PMID:24854121   PMID:24862212   PMID:25201524   PMID:25241761   PMID:25248927  
PMID:25302477   PMID:25416956   PMID:25437307   PMID:25452107   PMID:25468996   PMID:25665057   PMID:25972430   PMID:26080028   PMID:26090670   PMID:26186194   PMID:26272951   PMID:26561856  
PMID:26571379   PMID:26607202   PMID:26638075   PMID:26662145   PMID:26689621   PMID:26731262   PMID:26731658   PMID:26863122   PMID:26887345   PMID:26977027   PMID:27151944   PMID:27185880  
PMID:27563375   PMID:27580405   PMID:27605665   PMID:27616439   PMID:27790907   PMID:28153728   PMID:28179633   PMID:28184927   PMID:28332063   PMID:28386946   PMID:28514442   PMID:28534944  
PMID:28642978   PMID:28681912   PMID:28718701   PMID:29136627   PMID:29180619   PMID:29252987   PMID:29509190   PMID:29516973   PMID:29568061   PMID:29750300   PMID:30021884   PMID:30194290  
PMID:30280653   PMID:30639242   PMID:30734065   PMID:30851935   PMID:30868853   PMID:31073040   PMID:31091453   PMID:31177093   PMID:31182728   PMID:31257482   PMID:31328852   PMID:31375213  
PMID:31678930   PMID:31794381   PMID:31871319   PMID:31995728   PMID:32031713   PMID:32240828   PMID:32296183   PMID:32788342   PMID:32814053   PMID:32884584   PMID:32994395   PMID:33001231  
PMID:33058236   PMID:33100129   PMID:33277362   PMID:33441633   PMID:33957083   PMID:33961781   PMID:34079125   PMID:34369648   PMID:34400226   PMID:34432599   PMID:34515239   PMID:34702444  
PMID:34704946   PMID:34709727   PMID:35022314   PMID:35222802   PMID:35224833   PMID:35241646   PMID:35384245   PMID:35388524   PMID:35605301   PMID:35831314   PMID:35844135   PMID:35944360  
PMID:36114006   PMID:36237976   PMID:36536183   PMID:36610398   PMID:36662163   PMID:36768287   PMID:36946050   PMID:37068248   PMID:37272842   PMID:37381005   PMID:37499664   PMID:37616343  
PMID:37721332   PMID:37931956   PMID:38141113   PMID:38157366  


Genomics

Comparative Map Data
OCLN
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38569,492,547 - 69,558,104 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl569,492,292 - 69,558,104 (+)EnsemblGRCh38hg38GRCh38
GRCh37568,788,374 - 68,853,931 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36568,823,875 - 68,885,889 (+)NCBINCBI36Build 36hg18NCBI36
Build 34568,823,874 - 68,885,887NCBI
Cytogenetic Map5q13.2NCBI
HuRef565,744,381 - 65,800,380 (+)NCBIHuRef
HuRef565,800,577 - 65,803,347 (+)NCBIHuRef
CHM1_1568,787,783 - 68,853,763 (+)NCBICHM1_1
T2T-CHM13v2.0570,316,240 - 70,383,882 (+)NCBIT2T-CHM13v2.0
Ocln
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm3913100,633,012 - 100,689,226 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl13100,633,015 - 100,689,226 (-)EnsemblGRCm39 Ensembl
GRCm3813100,496,504 - 100,552,718 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl13100,496,507 - 100,552,718 (-)EnsemblGRCm38mm10GRCm38
MGSCv3713101,267,322 - 101,322,453 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv3613101,597,624 - 101,652,755 (-)NCBIMGSCv36mm8
Celera13104,112,684 - 104,167,697 (-)NCBICelera
Cytogenetic Map13D1NCBI
cM Map1353.23NCBI
Ocln
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8233,391,303 - 33,442,207 (-)NCBIGRCr8
mRatBN7.2231,657,217 - 31,707,466 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl231,657,220 - 31,764,150 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx238,791,782 - 38,841,944 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0236,819,361 - 36,869,279 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0231,690,347 - 31,739,905 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0230,527,327 - 30,577,218 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl230,527,715 - 30,577,218 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0249,686,707 - 49,737,380 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4231,317,090 - 31,367,485 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1231,237,461 - 31,287,854 (-)NCBI
Celera227,670,881 - 27,719,967 (-)NCBICelera
Cytogenetic Map2q12NCBI
Ocln
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0NW_004955575163,646 - 210,379 (+)NCBIChiLan1.0ChiLan1.0
OCLN
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2444,366,263 - 44,428,662 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1542,519,888 - 42,582,278 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0544,447,230 - 44,509,637 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1546,022,538 - 46,080,549 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl546,023,437 - 46,069,342 (-)Ensemblpanpan1.1panPan2
OCLN
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1254,500,299 - 54,545,430 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl254,500,299 - 54,545,430 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha251,466,637 - 51,511,781 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0255,004,936 - 55,058,838 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl255,005,004 - 55,058,769 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1252,076,201 - 52,121,488 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0252,843,313 - 52,888,432 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0253,733,721 - 53,779,092 (+)NCBIUU_Cfam_GSD_1.0
Ocln
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024407213191,162,311 - 191,216,242 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493648098,371 - 152,413 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493648099,516 - 152,834 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
OCLN
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1647,600,212 - 47,654,033 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11647,600,175 - 47,652,435 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21651,547,473 - 51,598,116 (+)NCBISscrofa10.2Sscrofa10.2susScr3
OCLN
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1465,581,943 - 65,641,516 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl465,582,460 - 65,644,787 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604914,326,566 - 14,386,556 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Ocln
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_004624905333,864 - 388,880 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_004624905333,853 - 388,990 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in OCLN
100 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_001205254.2(OCLN):c.724C>T (p.Gln242Ter) single nucleotide variant not provided [RCV000522136] Chr5:69509814 [GRCh38]
Chr5:68805641 [GRCh37]
Chr5:5q13.2
likely pathogenic
NM_001205254.2(OCLN):c.1000A>G (p.Lys334Glu) single nucleotide variant not provided [RCV000522545] Chr5:69534802 [GRCh38]
Chr5:68830629 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.171_193del (p.Lys57fs) deletion Pseudo-TORCH syndrome 1 [RCV000007142] Chr5:69509260..69509282 [GRCh38]
Chr5:68805087..68805109 [GRCh37]
Chr5:5q13.2
pathogenic
NM_001205254.2(OCLN):c.512dup (p.Tyr171Ter) duplication Pseudo-TORCH syndrome 1 [RCV000007143] Chr5:69509601..69509602 [GRCh38]
Chr5:68805428..68805429 [GRCh37]
Chr5:5q13.2
pathogenic
NM_001205254.2(OCLN):c.656T>C (p.Phe219Ser) single nucleotide variant Pseudo-TORCH syndrome 1 [RCV000007144] Chr5:69509746 [GRCh38]
Chr5:68805573 [GRCh37]
Chr5:5q13.2
pathogenic
OCLN, IVS5DS, G-A, +5 single nucleotide variant Band-like calcification with simplified gyration and polymicrogyria [RCV000007145] Chr5:5q13.1 pathogenic
NM_001205254.2(OCLN):c.1014_1023del (p.Glu339fs) deletion not provided [RCV000723062] Chr5:69534813..69534822 [GRCh38]
Chr5:68830640..68830649 [GRCh37]
Chr5:5q13.2
uncertain significance
GRCh38/hg38 5q12.3-13.2(chr5:64932763-69495504)x1 copy number loss See cases [RCV000051223] Chr5:64932763..69495504 [GRCh38]
Chr5:64228590..68791331 [GRCh37]
Chr5:64264346..68827087 [NCBI36]
Chr5:5q12.3-13.2
pathogenic
NM_001205254.2(OCLN):c.469G>T (p.Val157Phe) single nucleotide variant not provided [RCV000657871] Chr5:69509559 [GRCh38]
Chr5:68805386 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.699G>A (p.Leu233=) single nucleotide variant not provided [RCV002055720]|not specified [RCV000146973] Chr5:69509789 [GRCh38]
Chr5:68805616 [GRCh37]
Chr5:5q13.2
benign
NM_001205254.2(OCLN):c.1276_1283del (p.Asp426fs) deletion not provided [RCV000722185] Chr5:69547950..69547957 [GRCh38]
Chr5:68843777..68843784 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.384C>T (p.Tyr128=) single nucleotide variant Pseudo-TORCH syndrome 1 [RCV000146970]|not provided [RCV002515969] Chr5:69509474 [GRCh38]
Chr5:68805301 [GRCh37]
Chr5:5q13.2
likely benign|uncertain significance
NM_001205254.2(OCLN):c.452C>T (p.Ala151Val) single nucleotide variant OCLN-related disorder [RCV003905271]|Pseudo-TORCH syndrome 1 [RCV000146971]|not provided [RCV002055909]|not specified [RCV000425727] Chr5:69509542 [GRCh38]
Chr5:68805369 [GRCh37]
Chr5:5q13.2
benign|uncertain significance
NM_001205254.2(OCLN):c.4T>C (p.Ser2Pro) single nucleotide variant Pseudo-TORCH syndrome 1 [RCV000146972] Chr5:69504248 [GRCh38]
Chr5:68800075 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.70C>G (p.Pro24Ala) single nucleotide variant Pseudo-TORCH syndrome 1 [RCV002478408]|not provided [RCV002055910]|not specified [RCV000146974] Chr5:69509160 [GRCh38]
Chr5:68804987 [GRCh37]
Chr5:5q13.2
benign|likely benign|conflicting interpretations of pathogenicity
GRCh38/hg38 5q12.1-13.2(chr5:63207112-71291191)x3 copy number gain See cases [RCV000135640] Chr5:63207112..71291191 [GRCh38]
Chr5:62502939..70587018 [GRCh37]
Chr5:62538695..70622774 [NCBI36]
Chr5:5q12.1-13.2
likely pathogenic
GRCh38/hg38 5p15.33-q13.3(chr5:22149-74412725)x3 copy number gain See cases [RCV000138780] Chr5:22149..74412725 [GRCh38]
Chr5:22149..73708550 [GRCh37]
Chr5:75149..73744306 [NCBI36]
Chr5:5p15.33-q13.3
pathogenic
GRCh38/hg38 5q13.2(chr5:69528381-69607014)x3 copy number gain See cases [RCV000138806] Chr5:69528381..69607014 [GRCh38]
Chr5:68824208..68902841 [GRCh37]
Chr5:68859964..68938597 [NCBI36]
Chr5:5q13.2
likely benign
GRCh38/hg38 5q13.2(chr5:69553776-71317498)x1 copy number loss See cases [RCV000139478] Chr5:69553776..71317498 [GRCh38]
Chr5:68849603..70613325 [GRCh37]
Chr5:68885359..70649081 [NCBI36]
Chr5:5q13.2
benign
GRCh38/hg38 5q13.2(chr5:69495443-71032915)x1 copy number loss See cases [RCV000139586] Chr5:69495443..71032915 [GRCh38]
Chr5:68791270..70328742 [GRCh37]
Chr5:68827026..70364498 [NCBI36]
Chr5:5q13.2
benign
GRCh38/hg38 5q12.3-13.2(chr5:65976124-71317474)x3 copy number gain See cases [RCV000142796] Chr5:65976124..71317474 [GRCh38]
Chr5:65271952..70613301 [GRCh37]
Chr5:65307708..70649057 [NCBI36]
Chr5:5q12.3-13.2
uncertain significance
CM000667.1:g.68757774_68828296dup duplication Gestational diabetes mellitus uncontrolled [RCV000161400] Chr5:69461947..69532469 [GRCh38]
Chr5:68757774..68828296 [GRCh37]
Chr5:5q13.2
not provided
NM_001205254.2(OCLN):c.514dup (p.Tyr172fs) duplication Global developmental delay [RCV000162145]|Pseudo-TORCH syndrome 1 [RCV003989338] Chr5:69509603..69509604 [GRCh38]
Chr5:68805430..68805431 [GRCh37]
Chr5:5q13.2
likely pathogenic|uncertain significance
NM_001205254.2(OCLN):c.1004G>A (p.Arg335Gln) single nucleotide variant not specified [RCV000193804] Chr5:69534806 [GRCh38]
Chr5:68830633 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.173_194del (p.Trp58fs) deletion Pseudo-TORCH syndrome 1 [RCV000192882]|not provided [RCV001268371] Chr5:69509261..69509282 [GRCh38]
Chr5:68805088..68805109 [GRCh37]
Chr5:5q13.2
pathogenic|conflicting interpretations of pathogenicity
NM_001205254.2(OCLN):c.197G>T (p.Arg66Leu) single nucleotide variant not provided [RCV001563429]|not specified [RCV000194097] Chr5:69509287 [GRCh38]
Chr5:68805114 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.1037+5G>A single nucleotide variant Pseudo-TORCH syndrome 1 [RCV000194654] Chr5:69534844 [GRCh38]
Chr5:68830671 [GRCh37]
Chr5:5q13.2
pathogenic
NM_001205254.2(OCLN):c.252del (p.Ser85fs) deletion Pseudo-TORCH syndrome 1 [RCV000201608] Chr5:69509341 [GRCh38]
Chr5:68805168 [GRCh37]
Chr5:5q13.2
pathogenic|likely pathogenic
GRCh38/hg38 5q13.2(chr5:69424592-69579800)x1 copy number loss Premature ovarian failure [RCV000225286] Chr5:69424592..69579800 [GRCh38]
Chr5:68720419..68875627 [GRCh37]
Chr5:5q13.2
benign
NM_001205254.2(OCLN):c.-68-2A>G single nucleotide variant not provided [RCV000722739] Chr5:69504175 [GRCh38]
Chr5:68800002 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.351CTATGG[2] (p.118YG[5]) microsatellite not provided [RCV000598863] Chr5:69509438..69509443 [GRCh38]
Chr5:68805265..68805270 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.1016_1017del (p.Glu339fs) microsatellite not provided [RCV000598779] Chr5:69534816..69534817 [GRCh38]
Chr5:68830643..68830644 [GRCh37]
Chr5:5q13.2
pathogenic
GRCh37/hg19 5q13.2(chr5:68728731-68849653)x3 copy number gain not specified [RCV000453642] Chr5:68728731..68849653 [GRCh37]
Chr5:5q13.2
likely benign
GRCh37/hg19 5q12.1-13.2(chr5:60722469-70792199)x1 copy number loss See cases [RCV000447549] Chr5:60722469..70792199 [GRCh37]
Chr5:5q12.1-13.2
pathogenic
NM_002538.4(OCLN):c.-86C>T single nucleotide variant not provided [RCV001703480] Chr5:69492642 [GRCh38]
Chr5:68788469 [GRCh37]
Chr5:5q13.2
benign|likely benign
NM_002538.4(OCLN):c.-75G>A single nucleotide variant not specified [RCV000431807] Chr5:69492653 [GRCh38]
Chr5:68788480 [GRCh37]
Chr5:5q13.2
likely benign
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789) copy number gain See cases [RCV000510723] Chr5:113577..180719789 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
NM_001205254.2(OCLN):c.922G>A (p.Val308Met) single nucleotide variant not provided [RCV000418997]|not specified [RCV000483988] Chr5:69534724 [GRCh38]
Chr5:68830551 [GRCh37]
Chr5:5q13.2
benign|likely benign
NM_001205254.2(OCLN):c.730-7T>C single nucleotide variant not specified [RCV000426231] Chr5:69513941 [GRCh38]
Chr5:68809768 [GRCh37]
Chr5:5q13.2
likely benign
NM_001205254.2(OCLN):c.237C>T (p.Ile79=) single nucleotide variant not specified [RCV000434014] Chr5:69509327 [GRCh38]
Chr5:68805154 [GRCh37]
Chr5:5q13.2
likely benign
NM_001205254.2(OCLN):c.754A>G (p.Met252Val) single nucleotide variant not provided [RCV001703826] Chr5:69513972 [GRCh38]
Chr5:68809799 [GRCh37]
Chr5:5q13.2
benign|likely benign
NM_001205254.2(OCLN):c.1037+1G>A single nucleotide variant Pseudo-TORCH syndrome 1 [RCV000500514] Chr5:69534840 [GRCh38]
Chr5:68830667 [GRCh37]
Chr5:5q13.2
pathogenic
NM_001205254.2(OCLN):c.455C>T (p.Ala152Val) single nucleotide variant not provided [RCV000998392] Chr5:69509545 [GRCh38]
Chr5:68805372 [GRCh37]
Chr5:5q13.2
benign|likely benign
GRCh37/hg19 5p15.1-q35.2(chr5:17628741-176575720)x1 copy number loss See cases [RCV000511978] Chr5:17628741..176575720 [GRCh37]
Chr5:5p15.1-q35.2
pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789)x3 copy number gain See cases [RCV000512039] Chr5:113577..180719789 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
GRCh37/hg19 5q12.1-13.2(chr5:58966132-68847066)x4 copy number gain See cases [RCV000510792] Chr5:58966132..68847066 [GRCh37]
Chr5:5q12.1-13.2
likely pathogenic
NM_001205254.2(OCLN):c.606G>C (p.Gln202His) single nucleotide variant Inborn genetic diseases [RCV003262289] Chr5:69509696 [GRCh38]
Chr5:68805523 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.1512G>C (p.Lys504Asn) single nucleotide variant not provided [RCV001562216] Chr5:69553614 [GRCh38]
Chr5:68849441 [GRCh37]
Chr5:5q13.2
benign|likely benign|conflicting interpretations of pathogenicity
NM_001205254.2(OCLN):c.544C>T (p.Leu182=) single nucleotide variant not specified [RCV000613578] Chr5:69509634 [GRCh38]
Chr5:68805461 [GRCh37]
Chr5:5q13.2
likely benign
NM_002538.4(OCLN):c.-69+16C>G single nucleotide variant not specified [RCV000614449] Chr5:69492675 [GRCh38]
Chr5:68788502 [GRCh37]
Chr5:5q13.2
likely benign
GRCh37/hg19 5q13.1-13.2(chr5:68313021-68847066)x4 copy number gain See cases [RCV000512580] Chr5:68313021..68847066 [GRCh37]
Chr5:5q13.1-13.2
uncertain significance
GRCh37/hg19 5p15.33-q35.3(chr5:25328-180693344)x3 copy number gain not provided [RCV000744323] Chr5:25328..180693344 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:13648-180905029)x3 copy number gain not provided [RCV000744317] Chr5:13648..180905029 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
NC_000005.10:g.69553767_71361920dup duplication Primary amenorrhea [RCV000754422] Chr5:69553767..71361920 [GRCh38]
Chr5:68849594..70657747 [GRCh37]
Chr5:5q13.2
benign
NC_000005.9:g.68818173_70657747del1839575 deletion Primary amenorrhea [RCV000754421] Chr5:69522346..71361920 [GRCh38]
Chr5:68818173..70657747 [GRCh37]
Chr5:5q13.2
benign
GRCh37/hg19 5q13.1-13.2(chr5:68278453-70369959)x3 copy number gain not provided [RCV000754758] Chr5:68278453..70369959 [GRCh37]
Chr5:5q13.1-13.2
uncertain significance
GRCh37/hg19 5q13.2(chr5:68850595-70636542)x1 copy number loss not provided [RCV000744785] Chr5:68850595..70636542 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.412A>C (p.Lys138Gln) single nucleotide variant not provided [RCV001573068] Chr5:69509502 [GRCh38]
Chr5:68805329 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.730-323C>T single nucleotide variant not provided [RCV001582031] Chr5:69513625 [GRCh38]
Chr5:68809452 [GRCh37]
Chr5:5q13.2
likely benign
Single allele deletion Neurodevelopmental disorder [RCV000787436] Chr5:14685137..149511942 [GRCh37]
Chr5:5p15.2-q32
uncertain significance
GRCh37/hg19 5q13.2(chr5:68753608-68831651)x3 copy number gain not provided [RCV000849794] Chr5:68753608..68831651 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.546G>C (p.Leu182=) single nucleotide variant Pseudo-TORCH syndrome 1 [RCV000985182] Chr5:69509636 [GRCh38]
Chr5:68805463 [GRCh37]
Chr5:5q13.2
likely pathogenic
NM_001205254.2(OCLN):c.322G>A (p.Gly108Arg) single nucleotide variant Inborn genetic diseases [RCV003290906] Chr5:69509412 [GRCh38]
Chr5:68805239 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.1400A>G (p.Tyr467Cys) single nucleotide variant not provided [RCV001577132] Chr5:69548076 [GRCh38]
Chr5:68843903 [GRCh37]
Chr5:5q13.2
likely benign
NM_001205254.2(OCLN):c.*308C>T single nucleotide variant not provided [RCV001552988] Chr5:69553979 [GRCh38]
Chr5:68849806 [GRCh37]
Chr5:5q13.2
likely benign
NM_001205254.2(OCLN):c.729+288C>T single nucleotide variant not provided [RCV001559973] Chr5:69510107 [GRCh38]
Chr5:68805934 [GRCh37]
Chr5:5q13.2
likely benign
NM_001205254.2(OCLN):c.51-224T>C single nucleotide variant not provided [RCV001640867] Chr5:69508917 [GRCh38]
Chr5:68804744 [GRCh37]
Chr5:5q13.2
benign
NM_001205254.2(OCLN):c.922G>C (p.Val308Leu) single nucleotide variant not provided [RCV001696436] Chr5:69534724 [GRCh38]
Chr5:68830551 [GRCh37]
Chr5:5q13.2
benign
NM_001205254.2(OCLN):c.1254-142C>A single nucleotide variant not provided [RCV001585174] Chr5:69547788 [GRCh38]
Chr5:68843615 [GRCh37]
Chr5:5q13.2
likely benign
NM_001205254.2(OCLN):c.51-143T>C single nucleotide variant not provided [RCV001675005] Chr5:69508998 [GRCh38]
Chr5:68804825 [GRCh37]
Chr5:5q13.2
benign
GRCh38/hg38 5q11.2-13.2(chr5:58785203-73519962)x1 copy number loss Intellectual disability [RCV000984869] Chr5:58785203..73519962 [GRCh38]
Chr5:5q11.2-13.2
likely pathogenic
NM_001205254.2(OCLN):c.1299G>A (p.Lys433=) single nucleotide variant not provided [RCV001575548] Chr5:69547975 [GRCh38]
Chr5:68843802 [GRCh37]
Chr5:5q13.2
likely benign
NM_001205254.2(OCLN):c.23del (p.Ser8fs) deletion not provided [RCV001008859] Chr5:69504267 [GRCh38]
Chr5:68800094 [GRCh37]
Chr5:5q13.2
likely pathogenic
NM_001205254.2(OCLN):c.-69+86C>T single nucleotide variant not provided [RCV001656404] Chr5:69492986 [GRCh38]
Chr5:68788813 [GRCh37]
Chr5:5q13.2
benign
NC_000005.10:g.69492434G>A single nucleotide variant not provided [RCV001694447] Chr5:69492434 [GRCh38]
Chr5:68788261 [GRCh37]
Chr5:5q13.2
benign
NM_001205254.2(OCLN):c.473C>T (p.Thr158Ile) single nucleotide variant Inborn genetic diseases [RCV002568233]|not provided [RCV001536650] Chr5:69509563 [GRCh38]
Chr5:68805390 [GRCh37]
Chr5:5q13.2
uncertain significance
GRCh37/hg19 5q13.2(chr5:68831650-70663428)x1 copy number loss not provided [RCV001258858] Chr5:68831650..70663428 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.1054C>T (p.Gln352Ter) single nucleotide variant not provided [RCV001268433] Chr5:69544920 [GRCh38]
Chr5:68840747 [GRCh37]
Chr5:5q13.2
likely pathogenic
NM_001205254.2(OCLN):c.106C>T (p.Arg36Ter) single nucleotide variant Pseudo-TORCH syndrome 1 [RCV001330739] Chr5:69509196 [GRCh38]
Chr5:68805023 [GRCh37]
Chr5:5q13.2
pathogenic
NM_001205254.2(OCLN):c.52_891del (p.Lys18_Trp297del) deletion Pseudo-TORCH syndrome 1 [RCV001376164] Chr5:69509142..69514109 [GRCh38]
Chr5:68804969..68809936 [GRCh37]
Chr5:5q13.2
pathogenic
NM_001205254.2(OCLN):c.50+2T>C single nucleotide variant Pseudo-TORCH syndrome 1 [RCV001330740] Chr5:69504296 [GRCh38]
Chr5:68800123 [GRCh37]
Chr5:5q13.2
likely pathogenic
NM_001205254.2(OCLN):c.233C>T (p.Ala78Val) single nucleotide variant not provided [RCV001507646] Chr5:69509323 [GRCh38]
Chr5:68805150 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.456G>A (p.Ala152=) single nucleotide variant not provided [RCV001531425] Chr5:69509546 [GRCh38]
Chr5:68805373 [GRCh37]
Chr5:5q13.2
likely benign
NM_001205254.2(OCLN):c.891+248dup duplication not provided [RCV001652987] Chr5:69514350..69514351 [GRCh38]
Chr5:68810177..68810178 [GRCh37]
Chr5:5q13.2
likely benign
NM_001205254.2(OCLN):c.-69+232C>T single nucleotide variant not provided [RCV001528053] Chr5:69493132 [GRCh38]
Chr5:68788959 [GRCh37]
Chr5:5q13.2
benign
NM_001205254.2(OCLN):c.513C>A (p.Tyr171Ter) single nucleotide variant Pseudo-TORCH syndrome 1 [RCV001784766] Chr5:69509603 [GRCh38]
Chr5:68805430 [GRCh37]
Chr5:5q13.2
pathogenic
NM_001205254.2(OCLN):c.469G>A (p.Val157Ile) single nucleotide variant Inborn genetic diseases [RCV003375353]|not provided [RCV001772502] Chr5:69509559 [GRCh38]
Chr5:68805386 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.842G>T (p.Trp281Leu) single nucleotide variant not provided [RCV001763899] Chr5:69514060 [GRCh38]
Chr5:68809887 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.121C>G (p.Gln41Glu) single nucleotide variant Inborn genetic diseases [RCV002540376]|not provided [RCV001765625] Chr5:69509211 [GRCh38]
Chr5:68805038 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.712G>A (p.Val238Ile) single nucleotide variant not provided [RCV001765375] Chr5:69509802 [GRCh38]
Chr5:68805629 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.891+3_891+6del deletion not provided [RCV001794718] Chr5:69514110..69514113 [GRCh38]
Chr5:68809937..68809940 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.733A>G (p.Ile245Val) single nucleotide variant not provided [RCV001806282] Chr5:69513951 [GRCh38]
Chr5:68809778 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.358T>C (p.Tyr120His) single nucleotide variant not specified [RCV001819629] Chr5:69509448 [GRCh38]
Chr5:68805275 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.659A>G (p.Tyr220Cys) single nucleotide variant Inborn genetic diseases [RCV004040978]|not specified [RCV001819630] Chr5:69509749 [GRCh38]
Chr5:68805576 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.527T>C (p.Ile176Thr) single nucleotide variant not provided [RCV001928946] Chr5:69509617 [GRCh38]
Chr5:68805444 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.199A>T (p.Ile67Phe) single nucleotide variant not provided [RCV002025790] Chr5:69509289 [GRCh38]
Chr5:68805116 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.1324G>T (p.Glu442Ter) single nucleotide variant Pseudo-TORCH syndrome 1 [RCV002052138] Chr5:69548000 [GRCh38]
Chr5:68843827 [GRCh37]
Chr5:5q13.2
pathogenic
GRCh37/hg19 5q12.3-13.2(chr5:64049692-70306646) copy number loss not specified [RCV002053499] Chr5:64049692..70306646 [GRCh37]
Chr5:5q12.3-13.2
pathogenic
NM_001205254.2(OCLN):c.208A>G (p.Met70Val) single nucleotide variant not provided [RCV002049580] Chr5:69509298 [GRCh38]
Chr5:68805125 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.871C>T (p.Pro291Ser) single nucleotide variant Inborn genetic diseases [RCV002555605]|not provided [RCV001917644] Chr5:69514089 [GRCh38]
Chr5:68809916 [GRCh37]
Chr5:5q13.2
likely benign|uncertain significance
NM_001205254.2(OCLN):c.454G>A (p.Ala152Thr) single nucleotide variant Inborn genetic diseases [RCV002573506]|not provided [RCV001990902] Chr5:69509544 [GRCh38]
Chr5:68805371 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.51-8C>A single nucleotide variant not provided [RCV002206400] Chr5:69509133 [GRCh38]
Chr5:68804960 [GRCh37]
Chr5:5q13.2
likely benign
NM_001205254.2(OCLN):c.50+18T>C single nucleotide variant not provided [RCV002166327] Chr5:69504312 [GRCh38]
Chr5:68800139 [GRCh37]
Chr5:5q13.2
likely benign
NM_001205254.2(OCLN):c.360T>C (p.Tyr120=) single nucleotide variant not provided [RCV002121468] Chr5:69509450 [GRCh38]
Chr5:68805277 [GRCh37]
Chr5:5q13.2
likely benign
NM_001205254.2(OCLN):c.51-12T>C single nucleotide variant not provided [RCV002123821] Chr5:69509129 [GRCh38]
Chr5:68804956 [GRCh37]
Chr5:5q13.2
likely benign
NM_001205254.2(OCLN):c.1542del (p.Gly515fs) deletion Pseudo-TORCH syndrome 1 [RCV003156199] Chr5:69553643 [GRCh38]
Chr5:68849470 [GRCh37]
Chr5:5q13.2
likely pathogenic
NM_001205254.2(OCLN):c.482T>C (p.Ile161Thr) single nucleotide variant not provided [RCV002261766] Chr5:69509572 [GRCh38]
Chr5:68805399 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.835A>G (p.Ile279Val) single nucleotide variant not provided [RCV003234310] Chr5:69514053 [GRCh38]
Chr5:68809880 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.631C>A (p.Gln211Lys) single nucleotide variant not provided [RCV002903739] Chr5:69509721 [GRCh38]
Chr5:68805548 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.571A>G (p.Ile191Val) single nucleotide variant not provided [RCV002731622] Chr5:69509661 [GRCh38]
Chr5:68805488 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.1218C>T (p.Gly406=) single nucleotide variant Inborn genetic diseases [RCV003103134]|not provided [RCV002462555] Chr5:69545084 [GRCh38]
Chr5:68840911 [GRCh37]
Chr5:5q13.2
likely pathogenic|uncertain significance
NM_001205254.2(OCLN):c.853C>A (p.His285Asn) single nucleotide variant Inborn genetic diseases [RCV002902746] Chr5:69514071 [GRCh38]
Chr5:68809898 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.1111G>T (p.Gly371Cys) single nucleotide variant Inborn genetic diseases [RCV002841607] Chr5:69544977 [GRCh38]
Chr5:68840804 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.860A>G (p.Tyr287Cys) single nucleotide variant Inborn genetic diseases [RCV002688305] Chr5:69514078 [GRCh38]
Chr5:68809905 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.637T>C (p.Tyr213His) single nucleotide variant Inborn genetic diseases [RCV002732774] Chr5:69509727 [GRCh38]
Chr5:68805554 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.731C>T (p.Ala244Val) single nucleotide variant Inborn genetic diseases [RCV002737354] Chr5:69513949 [GRCh38]
Chr5:68809776 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.627T>C (p.Gly209=) single nucleotide variant not provided [RCV002640501] Chr5:69509717 [GRCh38]
Chr5:68805544 [GRCh37]
Chr5:5q13.2
likely benign
NM_001205254.2(OCLN):c.161A>C (p.His54Pro) single nucleotide variant Inborn genetic diseases [RCV002822411] Chr5:69509251 [GRCh38]
Chr5:68805078 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.316T>G (p.Tyr106Asp) single nucleotide variant Inborn genetic diseases [RCV002759740] Chr5:69509406 [GRCh38]
Chr5:68805233 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.394A>G (p.Thr132Ala) single nucleotide variant not provided [RCV002912752] Chr5:69509484 [GRCh38]
Chr5:68805311 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.1515C>G (p.Ser505Arg) single nucleotide variant Inborn genetic diseases [RCV002783830] Chr5:69553617 [GRCh38]
Chr5:68849444 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.803GAA[1] (p.Arg269del) microsatellite Inborn genetic diseases [RCV002888943] Chr5:69514021..69514023 [GRCh38]
Chr5:68809848..68809850 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.1530C>G (p.Ile510Met) single nucleotide variant Inborn genetic diseases [RCV002804977] Chr5:69553632 [GRCh38]
Chr5:68849459 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.458T>C (p.Leu153Ser) single nucleotide variant not provided [RCV002800838] Chr5:69509548 [GRCh38]
Chr5:68805375 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.12G>C (p.Arg4Ser) single nucleotide variant Inborn genetic diseases [RCV002954578] Chr5:69504256 [GRCh38]
Chr5:68800083 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.634A>G (p.Ile212Val) single nucleotide variant not provided [RCV002594721] Chr5:69509724 [GRCh38]
Chr5:68805551 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.316T>C (p.Tyr106His) single nucleotide variant Inborn genetic diseases [RCV002941375] Chr5:69509406 [GRCh38]
Chr5:68805233 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.138_139del (p.Phe46fs) deletion not provided [RCV003043709] Chr5:69509225..69509226 [GRCh38]
Chr5:68805052..68805053 [GRCh37]
Chr5:5q13.2
pathogenic
NM_001205254.2(OCLN):c.1099C>T (p.Arg367Cys) single nucleotide variant Inborn genetic diseases [RCV003191124] Chr5:69544965 [GRCh38]
Chr5:68840792 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.380G>A (p.Gly127Asp) single nucleotide variant Inborn genetic diseases [RCV003173679] Chr5:69509470 [GRCh38]
Chr5:68805297 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.472A>G (p.Thr158Ala) single nucleotide variant Pseudo-TORCH syndrome 1 [RCV003133100] Chr5:69509562 [GRCh38]
Chr5:68805389 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.215T>G (p.Ile72Ser) single nucleotide variant Pseudo-TORCH syndrome 1 [RCV003131849] Chr5:69509305 [GRCh38]
Chr5:68805132 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.811A>G (p.Met271Val) single nucleotide variant Pseudo-TORCH syndrome 1 [RCV003131850] Chr5:69514029 [GRCh38]
Chr5:68809856 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.944A>T (p.Tyr315Phe) single nucleotide variant Pseudo-TORCH syndrome 1 [RCV003133101] Chr5:69534746 [GRCh38]
Chr5:68830573 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.176C>T (p.Thr59Ile) single nucleotide variant Inborn genetic diseases [RCV003214820] Chr5:69509266 [GRCh38]
Chr5:68805093 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.1216G>A (p.Gly406Ser) single nucleotide variant Pseudo-TORCH syndrome 1 [RCV003338912] Chr5:69545082 [GRCh38]
Chr5:68840909 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.175A>C (p.Thr59Pro) single nucleotide variant Pseudo-TORCH syndrome 1 [RCV003338913] Chr5:69509265 [GRCh38]
Chr5:68805092 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.1550A>G (p.Tyr517Cys) single nucleotide variant Inborn genetic diseases [RCV003376240] Chr5:69553652 [GRCh38]
Chr5:68849479 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.1254-1G>A single nucleotide variant Pseudo-TORCH syndrome 1 [RCV003447895] Chr5:69547929 [GRCh38]
Chr5:68843756 [GRCh37]
Chr5:5q13.2
likely pathogenic
NM_001205254.2(OCLN):c.513C>T (p.Tyr171=) single nucleotide variant not provided [RCV003848902] Chr5:69509603 [GRCh38]
Chr5:68805430 [GRCh37]
Chr5:5q13.2
likely benign
NM_001205254.2(OCLN):c.35dup (p.Tyr12Ter) duplication not provided [RCV003545487] Chr5:69504278..69504279 [GRCh38]
Chr5:68800105..68800106 [GRCh37]
Chr5:5q13.2
pathogenic
NM_001205254.2(OCLN):c.630_645del (p.Gln211fs) deletion Pseudo-TORCH syndrome 1 [RCV003486333] Chr5:69509718..69509733 [GRCh38]
Chr5:68805545..68805560 [GRCh37]
Chr5:5q13.2
likely pathogenic
NM_001205254.2(OCLN):c.810G>A (p.Lys270=) single nucleotide variant not provided [RCV003659161] Chr5:69514028 [GRCh38]
Chr5:68809855 [GRCh37]
Chr5:5q13.2
likely benign
NM_001205254.2(OCLN):c.57G>A (p.Pro19=) single nucleotide variant not provided [RCV003707859] Chr5:69509147 [GRCh38]
Chr5:68804974 [GRCh37]
Chr5:5q13.2
likely benign
NM_001205254.2(OCLN):c.204G>C (p.Leu68=) single nucleotide variant not provided [RCV003674890] Chr5:69509294 [GRCh38]
Chr5:68805121 [GRCh37]
Chr5:5q13.2
likely benign
GRCh37/hg19 5q13.2(chr5:68751939-68847066)x1 copy number loss not specified [RCV003986587] Chr5:68751939..68847066 [GRCh37]
Chr5:5q13.2
uncertain significance
GRCh37/hg19 5q12.3-13.2(chr5:64364710-72835471)x1 copy number loss See cases [RCV004442777] Chr5:64364710..72835471 [GRCh37]
Chr5:5q12.3-13.2
pathogenic
NM_001205254.2(OCLN):c.1106G>C (p.Ser369Thr) single nucleotide variant Inborn genetic diseases [RCV004496754] Chr5:69544972 [GRCh38]
Chr5:68840799 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.707A>G (p.Tyr236Cys) single nucleotide variant Inborn genetic diseases [RCV004496760] Chr5:69509797 [GRCh38]
Chr5:68805624 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.602C>T (p.Ala201Val) single nucleotide variant Inborn genetic diseases [RCV004496759] Chr5:69509692 [GRCh38]
Chr5:68805519 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.371A>G (p.Tyr124Cys) single nucleotide variant Inborn genetic diseases [RCV004496757] Chr5:69509461 [GRCh38]
Chr5:68805288 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.347G>A (p.Ser116Asn) single nucleotide variant Inborn genetic diseases [RCV004496756] Chr5:69509437 [GRCh38]
Chr5:68805264 [GRCh37]
Chr5:5q13.2
uncertain significance
NC_000005.9:g.(?_68800072)_(68809956_?)del deletion not provided [RCV004580608] Chr5:68800072..68809956 [GRCh37] pathogenic
NM_001205254.2(OCLN):c.493A>C (p.Met165Leu) single nucleotide variant Inborn genetic diseases [RCV003357940] Chr5:69509583 [GRCh38]
Chr5:68805410 [GRCh37]
Chr5:5q13.2
uncertain significance
NM_001205254.2(OCLN):c.430A>T (p.Met144Leu) single nucleotide variant Inborn genetic diseases [RCV003379296] Chr5:69509520 [GRCh38]
Chr5:68805347 [GRCh37]
Chr5:5q13.2
uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2249
Count of miRNA genes:917
Interacting mature miRNAs:1048
Transcripts:ENST00000355237, ENST00000380766, ENST00000396442, ENST00000510666, ENST00000514370, ENST00000538151, ENST00000542132
Prediction methods: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.

Markers in Region
STS-U19251  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37570,369,598 - 70,369,759UniSTSGRCh37
GRCh37568,849,793 - 68,849,954UniSTSGRCh37
Build 36568,885,549 - 68,885,710RGDNCBI36
Celera566,194,581 - 66,194,742RGD
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map5q13.2UniSTS
GeneMap99-GB4 RH Map5344.77UniSTS
PMC310929P1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37568,804,979 - 68,805,147UniSTSGRCh37
Build 36568,840,735 - 68,840,903RGDNCBI36
Celera565,807,296 - 65,807,464RGD
HuRef565,761,239 - 65,761,407UniSTS
STS-H94471  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37570,369,489 - 70,369,635UniSTSGRCh37
GRCh37568,849,917 - 68,850,063UniSTSGRCh37
Build 36568,885,673 - 68,885,819RGDNCBI36
Celera566,194,705 - 66,194,851RGD
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map5q13.2UniSTS
GeneMap99-GB4 RH Map5344.88UniSTS
GDB:434012  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map19q13.13UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map2q31.2-q33.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map5q21UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map17q25.2UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map1p21.3-p13.1UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map1q24-q25.3UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map1pter-q31.3UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map16p13UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16p12.1UniSTS
Cytogenetic Map10p11.1UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map2q11.2-q12UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic Map1p36-p35UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map4q13UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic MapXq21.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map6p12.3-p11.2UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map4p16UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map12q13.1-q13.2UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map6pter-p12.1UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map14q31UniSTS
RH80030  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic MapXq26.1UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map9p13UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map12q15-q21UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map2p22.2UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map11q22.2-q22.3UniSTS
Cytogenetic Map1p36-p35UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map10q26.13-q26.3UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map12q14.2UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map2q32.2UniSTS
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


Expression


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

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 228 595 170 37 176 251 18 12 147 239 746 5 51 2
Low 970 282 876 453 842 288 2120 178 2697 256 920 861 170 1 247 1299 4 2
Below cutoff 1228 2582 244 1 954 1 1923 1934 1025 16 300 6 954 1379

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_028291 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001205254 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001205255 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001410743 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_002538 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017008913 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047416593 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047416594 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054329487 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054329488 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054333009 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054333010 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054333011 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054351380 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054351381 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054351382 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB451306 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB451437 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC142525 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC145146 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC147575 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC255386 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC270584 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF246304 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AH011257 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI093221 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK290697 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK311037 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK313501 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC029886 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BK001650 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471137 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068273 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB226845 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ264390 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ786240 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ786083 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ786084 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GQ225096 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GQ225097 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GQ225098 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GQ402517 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U49184 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U53823 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000355237   ⟹   ENSP00000347379
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl569,492,292 - 69,558,104 (+)Ensembl
Ensembl Acc Id: ENST00000396442   ⟹   ENSP00000379719
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl569,492,790 - 69,558,104 (+)Ensembl
Ensembl Acc Id: ENST00000510666
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl569,544,744 - 69,553,711 (+)Ensembl
Ensembl Acc Id: ENST00000514370
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl569,544,692 - 69,553,999 (+)Ensembl
Ensembl Acc Id: ENST00000538151   ⟹   ENSP00000445940
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl569,504,177 - 69,558,104 (+)Ensembl
Ensembl Acc Id: ENST00000680027   ⟹   ENSP00000506162
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl569,493,673 - 69,555,275 (+)Ensembl
Ensembl Acc Id: ENST00000680098   ⟹   ENSP00000506561
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl569,492,790 - 69,521,815 (+)Ensembl
Ensembl Acc Id: ENST00000680496   ⟹   ENSP00000504966
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl569,493,694 - 69,555,253 (+)Ensembl
Ensembl Acc Id: ENST00000680784   ⟹   ENSP00000506305
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl569,492,790 - 69,555,253 (+)Ensembl
Ensembl Acc Id: ENST00000681041   ⟹   ENSP00000505426
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl569,492,773 - 69,555,275 (+)Ensembl
Ensembl Acc Id: ENST00000681586   ⟹   ENSP00000505541
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl569,493,552 - 69,555,275 (+)Ensembl
Ensembl Acc Id: ENST00000681588   ⟹   ENSP00000506017
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl569,492,877 - 69,555,269 (+)Ensembl
Ensembl Acc Id: ENST00000681889
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl569,549,380 - 69,554,281 (+)Ensembl
Ensembl Acc Id: ENST00000681895   ⟹   ENSP00000505831
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl569,492,801 - 69,555,253 (+)Ensembl
RefSeq Acc Id: NM_001205254   ⟹   NP_001192183
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38569,492,790 - 69,558,104 (+)NCBI
GRCh37568,788,119 - 68,853,931 (+)ENTREZGENE
HuRef565,744,381 - 65,800,380 (+)ENTREZGENE
HuRef565,800,577 - 65,803,347 (+)NCBI
CHM1_1568,788,254 - 68,853,763 (+)NCBI
T2T-CHM13v2.0570,318,430 - 70,383,882 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001205255   ⟹   NP_001192184
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38569,504,177 - 69,558,104 (+)NCBI
GRCh37568,788,119 - 68,853,931 (+)ENTREZGENE
HuRef565,744,381 - 65,800,380 (+)ENTREZGENE
HuRef565,800,577 - 65,803,347 (+)NCBI
CHM1_1568,799,665 - 68,853,763 (+)NCBI
T2T-CHM13v2.0570,329,815 - 70,383,882 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001410743   ⟹   NP_001397672
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38569,492,547 - 69,558,104 (+)NCBI
T2T-CHM13v2.0570,318,187 - 70,383,882 (+)NCBI
RefSeq Acc Id: NM_002538   ⟹   NP_002529
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38569,492,547 - 69,558,104 (+)NCBI
GRCh37568,788,119 - 68,853,931 (+)ENTREZGENE
HuRef565,744,381 - 65,800,380 (+)ENTREZGENE
HuRef565,800,577 - 65,803,347 (+)NCBI
CHM1_1568,787,783 - 68,853,763 (+)NCBI
T2T-CHM13v2.0570,318,187 - 70,383,882 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017008913   ⟹   XP_016864402
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38569,492,790 - 69,558,104 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047416593   ⟹   XP_047272549
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38569,492,547 - 69,558,104 (+)NCBI
RefSeq Acc Id: XM_047416594   ⟹   XP_047272550
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38569,495,026 - 69,558,104 (+)NCBI
RefSeq Acc Id: XM_054351380   ⟹   XP_054207355
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0570,316,240 - 70,383,882 (+)NCBI
RefSeq Acc Id: XM_054351381   ⟹   XP_054207356
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0570,319,344 - 70,383,882 (+)NCBI
RefSeq Acc Id: XM_054351382   ⟹   XP_054207357
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0570,318,430 - 70,383,882 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001192183 (Get FASTA)   NCBI Sequence Viewer  
  NP_001192184 (Get FASTA)   NCBI Sequence Viewer  
  NP_001397672 (Get FASTA)   NCBI Sequence Viewer  
  NP_002529 (Get FASTA)   NCBI Sequence Viewer  
  XP_016864402 (Get FASTA)   NCBI Sequence Viewer  
  XP_047272549 (Get FASTA)   NCBI Sequence Viewer  
  XP_047272550 (Get FASTA)   NCBI Sequence Viewer  
  XP_054185462 (Get FASTA)   NCBI Sequence Viewer  
  XP_054185463 (Get FASTA)   NCBI Sequence Viewer  
  XP_054188984 (Get FASTA)   NCBI Sequence Viewer  
  XP_054188985 (Get FASTA)   NCBI Sequence Viewer  
  XP_054188986 (Get FASTA)   NCBI Sequence Viewer  
  XP_054207355 (Get FASTA)   NCBI Sequence Viewer  
  XP_054207356 (Get FASTA)   NCBI Sequence Viewer  
  XP_054207357 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAB00195 (Get FASTA)   NCBI Sequence Viewer  
  AAC50451 (Get FASTA)   NCBI Sequence Viewer  
  AAH29886 (Get FASTA)   NCBI Sequence Viewer  
  ACT53743 (Get FASTA)   NCBI Sequence Viewer  
  ACT53744 (Get FASTA)   NCBI Sequence Viewer  
  ACT83431 (Get FASTA)   NCBI Sequence Viewer  
  ACT83432 (Get FASTA)   NCBI Sequence Viewer  
  ACT83433 (Get FASTA)   NCBI Sequence Viewer  
  ACZ80515 (Get FASTA)   NCBI Sequence Viewer  
  BAF83386 (Get FASTA)   NCBI Sequence Viewer  
  BAG70120 (Get FASTA)   NCBI Sequence Viewer  
  BAG70251 (Get FASTA)   NCBI Sequence Viewer  
  DAA01837 (Get FASTA)   NCBI Sequence Viewer  
  EAW51275 (Get FASTA)   NCBI Sequence Viewer  
  EAW51276 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000347379
  ENSP00000347379.2
  ENSP00000379719
  ENSP00000379719.2
  ENSP00000445940
  ENSP00000445940.1
  ENSP00000480303.1
  ENSP00000480674.1
  ENSP00000481921.1
  ENSP00000483480.1
  ENSP00000504966.1
  ENSP00000505426.1
  ENSP00000505541.1
  ENSP00000505831.1
  ENSP00000506017.1
  ENSP00000506162.1
  ENSP00000506305
  ENSP00000506305.1
  ENSP00000506561.1
GenBank Protein Q16625 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_002529   ⟸   NM_002538
- Peptide Label: isoform a
- UniProtKB: Q5U1V4 (UniProtKB/Swiss-Prot),   E2CYV9 (UniProtKB/Swiss-Prot),   D2IGC1 (UniProtKB/Swiss-Prot),   D2IGC0 (UniProtKB/Swiss-Prot),   D2DU65 (UniProtKB/Swiss-Prot),   D2DU64 (UniProtKB/Swiss-Prot),   B5BU70 (UniProtKB/Swiss-Prot),   Q8N6K1 (UniProtKB/Swiss-Prot),   Q16625 (UniProtKB/Swiss-Prot),   A8K3T2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001192183   ⟸   NM_001205254
- Peptide Label: isoform a
- UniProtKB: Q5U1V4 (UniProtKB/Swiss-Prot),   E2CYV9 (UniProtKB/Swiss-Prot),   D2IGC1 (UniProtKB/Swiss-Prot),   D2IGC0 (UniProtKB/Swiss-Prot),   D2DU65 (UniProtKB/Swiss-Prot),   D2DU64 (UniProtKB/Swiss-Prot),   B5BU70 (UniProtKB/Swiss-Prot),   Q8N6K1 (UniProtKB/Swiss-Prot),   Q16625 (UniProtKB/Swiss-Prot),   A8K3T2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001192184   ⟸   NM_001205255
- Peptide Label: isoform b precursor
- UniProtKB: Q16625 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016864402   ⟸   XM_017008913
- Peptide Label: isoform X2
- UniProtKB: A8K3T2 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSP00000445940   ⟸   ENST00000538151
Ensembl Acc Id: ENSP00000347379   ⟸   ENST00000355237
Ensembl Acc Id: ENSP00000379719   ⟸   ENST00000396442
Ensembl Acc Id: ENSP00000506017   ⟸   ENST00000681588
Ensembl Acc Id: ENSP00000505426   ⟸   ENST00000681041
Ensembl Acc Id: ENSP00000505541   ⟸   ENST00000681586
Ensembl Acc Id: ENSP00000504966   ⟸   ENST00000680496
Ensembl Acc Id: ENSP00000505831   ⟸   ENST00000681895
Ensembl Acc Id: ENSP00000506305   ⟸   ENST00000680784
Ensembl Acc Id: ENSP00000506162   ⟸   ENST00000680027
Ensembl Acc Id: ENSP00000506561   ⟸   ENST00000680098
RefSeq Acc Id: XP_047272549   ⟸   XM_047416593
- Peptide Label: isoform X1
- UniProtKB: Q5U1V4 (UniProtKB/Swiss-Prot),   Q16625 (UniProtKB/Swiss-Prot),   E2CYV9 (UniProtKB/Swiss-Prot),   D2IGC1 (UniProtKB/Swiss-Prot),   D2IGC0 (UniProtKB/Swiss-Prot),   D2DU65 (UniProtKB/Swiss-Prot),   D2DU64 (UniProtKB/Swiss-Prot),   B5BU70 (UniProtKB/Swiss-Prot),   Q8N6K1 (UniProtKB/Swiss-Prot),   A8K3T2 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047272550   ⟸   XM_047416594
- Peptide Label: isoform X1
- UniProtKB: Q5U1V4 (UniProtKB/Swiss-Prot),   Q16625 (UniProtKB/Swiss-Prot),   E2CYV9 (UniProtKB/Swiss-Prot),   D2IGC1 (UniProtKB/Swiss-Prot),   D2IGC0 (UniProtKB/Swiss-Prot),   D2DU65 (UniProtKB/Swiss-Prot),   D2DU64 (UniProtKB/Swiss-Prot),   B5BU70 (UniProtKB/Swiss-Prot),   Q8N6K1 (UniProtKB/Swiss-Prot),   A8K3T2 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001397672   ⟸   NM_001410743
- Peptide Label: isoform c
- UniProtKB: A8K3T2 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054207355   ⟸   XM_054351380
- Peptide Label: isoform X1
- UniProtKB: Q5U1V4 (UniProtKB/Swiss-Prot),   Q16625 (UniProtKB/Swiss-Prot),   E2CYV9 (UniProtKB/Swiss-Prot),   D2IGC1 (UniProtKB/Swiss-Prot),   D2IGC0 (UniProtKB/Swiss-Prot),   D2DU65 (UniProtKB/Swiss-Prot),   D2DU64 (UniProtKB/Swiss-Prot),   B5BU70 (UniProtKB/Swiss-Prot),   Q8N6K1 (UniProtKB/Swiss-Prot),   A8K3T2 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054207357   ⟸   XM_054351382
- Peptide Label: isoform X2
- UniProtKB: A8K3T2 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054207356   ⟸   XM_054351381
- Peptide Label: isoform X1
- UniProtKB: Q5U1V4 (UniProtKB/Swiss-Prot),   Q16625 (UniProtKB/Swiss-Prot),   E2CYV9 (UniProtKB/Swiss-Prot),   D2IGC1 (UniProtKB/Swiss-Prot),   D2IGC0 (UniProtKB/Swiss-Prot),   D2DU65 (UniProtKB/Swiss-Prot),   D2DU64 (UniProtKB/Swiss-Prot),   B5BU70 (UniProtKB/Swiss-Prot),   Q8N6K1 (UniProtKB/Swiss-Prot),   A8K3T2 (UniProtKB/TrEMBL)
Protein Domains
MARVEL   OCEL

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q16625-F1-model_v2 AlphaFold Q16625 1-522 view protein structure

Promoters
RGD ID:6803107
Promoter ID:HG_KWN:50322
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562,   Lymphoblastoid
Transcripts:ENST00000380766,   OTTHUMT00000216794,   UC003JWV.2
Position:
Human AssemblyChrPosition (strand)Source
Build 36568,824,146 - 68,824,646 (+)MPROMDB
RGD ID:6869884
Promoter ID:EPDNEW_H8072
Type:initiation region
Name:OCLN_2
Description:occludin
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H8073  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38569,492,547 - 69,492,607EPDNEW
RGD ID:6869816
Promoter ID:EPDNEW_H8073
Type:initiation region
Name:OCLN_1
Description:occludin
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H8072  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38569,492,790 - 69,492,850EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:8104 AgrOrtholog
COSMIC OCLN COSMIC
Ensembl Genes ENSG00000197822 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ENSG00000273814 UniProtKB/TrEMBL
Ensembl Transcript ENST00000355237 ENTREZGENE
  ENST00000355237.6 UniProtKB/Swiss-Prot
  ENST00000396442 ENTREZGENE
  ENST00000396442.7 UniProtKB/Swiss-Prot
  ENST00000538151 ENTREZGENE
  ENST00000538151.2 UniProtKB/Swiss-Prot
  ENST00000613193.4 UniProtKB/TrEMBL
  ENST00000615870.4 UniProtKB/TrEMBL
  ENST00000617110.4 UniProtKB/TrEMBL
  ENST00000620655.1 UniProtKB/TrEMBL
  ENST00000680027.1 UniProtKB/Swiss-Prot
  ENST00000680098.1 UniProtKB/TrEMBL
  ENST00000680496.1 UniProtKB/Swiss-Prot
  ENST00000680784 ENTREZGENE
  ENST00000680784.1 UniProtKB/Swiss-Prot
  ENST00000681041.1 UniProtKB/Swiss-Prot
  ENST00000681586.1 UniProtKB/Swiss-Prot
  ENST00000681588.1 UniProtKB/TrEMBL
  ENST00000681895.1 UniProtKB/TrEMBL
Gene3D-CATH 6.10.140.340 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000197822 GTEx
  ENSG00000273814 GTEx
HGNC ID HGNC:8104 ENTREZGENE
Human Proteome Map OCLN Human Proteome Map
InterPro ELL/occludin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Marvel UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MFS_trans_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Occludin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Occludin_ELL UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:100506658 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 100506658 ENTREZGENE
OMIM 602876 OMIM
PANTHER PTHR23288 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR23288:SF4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam MARVEL UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Occludin_ELL UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA31893 PharmGKB
PIRSF Occludin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PRINTS OCCLUDIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE MARVEL UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  OCEL UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP occludin/ELL-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF103473 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A0G2JMZ8 ENTREZGENE, UniProtKB/TrEMBL
  A0A0G2JPF2_HUMAN UniProtKB/TrEMBL
  A0A7P0T9T6_HUMAN UniProtKB/TrEMBL
  A0A7P0TB95_HUMAN UniProtKB/TrEMBL
  A8K3T2 ENTREZGENE, UniProtKB/TrEMBL
  B5BU70 ENTREZGENE
  D2DU64 ENTREZGENE
  D2DU65 ENTREZGENE
  D2IGC0 ENTREZGENE
  D2IGC1 ENTREZGENE
  E2CYV9 ENTREZGENE
  OCLN_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  Q5U1V4 ENTREZGENE
  Q8N6K1 ENTREZGENE
UniProt Secondary B5BU70 UniProtKB/Swiss-Prot
  D2DU64 UniProtKB/Swiss-Prot
  D2DU65 UniProtKB/Swiss-Prot
  D2IGC0 UniProtKB/Swiss-Prot
  D2IGC1 UniProtKB/Swiss-Prot
  E2CYV9 UniProtKB/Swiss-Prot
  Q5U1V4 UniProtKB/Swiss-Prot
  Q8N6K1 UniProtKB/Swiss-Prot