HDAC7 (histone deacetylase 7) - Rat Genome Database

Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models   new Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Gene: HDAC7 (histone deacetylase 7) Homo sapiens
Analyze
Symbol: HDAC7
Name: histone deacetylase 7
RGD ID: 1349346
HGNC Page HGNC:14067
Description: Enables several functions, including 14-3-3 protein binding activity; protein kinase C binding activity; and protein lysine deacetylase activity. Involved in several processes, including negative regulation of interleukin-2 production; negative regulation of non-canonical NF-kappaB signal transduction; and negative regulation of osteoblast differentiation. Located in cytosol and nucleus. Biomarker of alopecia areata and colorectal cancer.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: DKFZp586J0917; FLJ99588; HD7; HD7A; HDAC7A; histone deacetylase 7A
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381247,782,722 - 47,821,344 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1247,782,722 - 47,833,132 (-)EnsemblGRCh38hg38GRCh38
GRCh371248,176,505 - 48,213,686 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361246,462,772 - 46,499,924 (-)NCBINCBI36Build 36hg18NCBI36
Build 341246,462,775 - 46,479,190NCBI
Celera1246,974,055 - 47,011,314 (-)NCBICelera
Cytogenetic Map12q13.11NCBI
HuRef1245,207,665 - 45,244,811 (-)NCBIHuRef
CHM1_11248,142,408 - 48,179,666 (-)NCBICHM1_1
T2T-CHM13v2.01247,744,115 - 47,782,739 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(S)-nicotine  (EXP)
1,2-dimethylhydrazine  (ISO)
17beta-estradiol  (EXP)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
3,5-diethoxycarbonyl-1,4-dihydrocollidine  (ISO)
3-isobutyl-1-methyl-7H-xanthine  (EXP)
4,4'-sulfonyldiphenol  (EXP)
5-aza-2'-deoxycytidine  (ISO)
5-fluorouracil  (ISO)
acrolein  (EXP)
acrylamide  (ISO)
alpha-pinene  (EXP)
amphetamine  (ISO)
antirheumatic drug  (EXP)
arsenite(3-)  (EXP)
benzo[a]pyrene  (EXP)
benzylpenicillin  (ISO)
bisphenol A  (EXP,ISO)
buta-1,3-diene  (ISO)
butanal  (EXP)
C60 fullerene  (ISO)
cadmium atom  (ISO)
cadmium dichloride  (ISO)
caffeine  (EXP,ISO)
carbamazepine  (EXP)
carbon nanotube  (ISO)
chlorpyrifos  (ISO)
copper(II) sulfate  (EXP)
corticosterone  (ISO)
coumarin  (EXP)
Cuprizon  (ISO)
curcumin  (ISO)
dexamethasone  (EXP,ISO)
dibutyl phthalate  (ISO)
dicrotophos  (EXP)
diethylstilbestrol  (EXP)
disodium selenite  (EXP)
doxorubicin  (ISO)
ethanol  (ISO)
folic acid  (ISO)
FR900359  (EXP)
indometacin  (EXP)
ivermectin  (EXP)
lead diacetate  (ISO)
lead(0)  (ISO)
lithium chloride  (ISO)
methamphetamine  (ISO)
mifepristone  (ISO)
Muraglitazar  (ISO)
nickel dichloride  (ISO)
nicotine  (EXP)
ozone  (EXP)
paraquat  (ISO)
pelargonidin  (ISO)
perfluorohexanesulfonic acid  (EXP)
perfluorononanoic acid  (EXP)
perfluorooctane-1-sulfonic acid  (EXP)
perfluorooctanoic acid  (EXP)
phenytoin  (ISO)
propanal  (EXP)
quercetin  (EXP)
resveratrol  (EXP)
saccharin  (ISO)
sodium arsenite  (EXP)
sunitinib  (EXP)
tauroursodeoxycholic acid  (ISO)
tert-butyl hydroperoxide  (ISO)
triptonide  (ISO)
tungsten  (ISO)
valproic acid  (EXP,ISO)
vorinostat  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
cytoplasm  (IDA,IEA)
cytosol  (IDA)
intracellular organelle  (IEA)
nucleoplasm  (TAS)
nucleus  (IDA,IEA,ISO)

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. Isolation of a novel histone deacetylase reveals that class I and class II deacetylases promote SMRT-mediated repression. Kao HY, etal., Genes Dev 2000 Jan 1;14(1):55-66.
3. Neuroprotection by histone deacetylase-7 (HDAC7) occurs by inhibition of c-jun expression through a deacetylase-independent mechanism. Ma C and D'Mello SR, J Biol Chem. 2011 Feb 11;286(6):4819-28. doi: 10.1074/jbc.M110.146860. Epub 2010 Nov 30.
4. Physical and functional HAT/HDAC interplay regulates protein acetylation balance. Peserico A and Simone C, J Biomed Biotechnol. 2011;2011:371832. doi: 10.1155/2011/371832. Epub 2010 Dec 5.
5. PID Annotation Import Pipeline Pipeline to import Pathway Interaction Database annotations from NCI into RGD
6. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
7. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
8. HDAC up-regulation in early colon field carcinogenesis is involved in cell tumorigenicity through regulation of chromatin structure. Stypula-Cyrus Y, etal., PLoS One. 2013 May 28;8(5):e64600. doi: 10.1371/journal.pone.0064600. Print 2013.
9. Abnormal epigenetic modifications in peripheral blood mononuclear cells from patients with alopecia areata. Zhao M, etal., Br J Dermatol. 2012 Feb;166(2):226-73. doi: 10.1111/j.1365-2133.2011.10646.x. Epub 2012 Jan 9.
Additional References at PubMed
PMID:8125298   PMID:10922406   PMID:11262386   PMID:11279209   PMID:11466315   PMID:11929873   PMID:12015313   PMID:12239305   PMID:12477932   PMID:12551922   PMID:12711221   PMID:12753745  
PMID:12970571   PMID:14702039   PMID:15161933   PMID:15166223   PMID:15194749   PMID:15280364   PMID:15302935   PMID:15324660   PMID:15364908   PMID:15489334   PMID:15623513   PMID:15738054  
PMID:15778465   PMID:16541075   PMID:16860317   PMID:16956611   PMID:16980305   PMID:16980613   PMID:17353931   PMID:17360565   PMID:17369396   PMID:17373667   PMID:17379597   PMID:17827213  
PMID:17873065   PMID:17947801   PMID:17962809   PMID:17979178   PMID:17997710   PMID:18029348   PMID:18285338   PMID:18339811   PMID:18458084   PMID:18463162   PMID:18506539   PMID:18509061  
PMID:18617643   PMID:18625722   PMID:19029091   PMID:19240061   PMID:19351956   PMID:19355988   PMID:19738286   PMID:19784544   PMID:19913121   PMID:19917725   PMID:19966789   PMID:20188095  
PMID:20224040   PMID:20590529   PMID:20628086   PMID:20693714   PMID:21048031   PMID:21120446   PMID:21148070   PMID:21324898   PMID:21516116   PMID:21836063   PMID:21873635   PMID:22155184  
PMID:22172637   PMID:22308472   PMID:22584896   PMID:22658674   PMID:23128233   PMID:23251661   PMID:23263486   PMID:23401860   PMID:23565059   PMID:23696748   PMID:23752268   PMID:23853092  
PMID:23880157   PMID:23891737   PMID:24189120   PMID:24239178   PMID:24255178   PMID:24658140   PMID:25173798   PMID:25402006   PMID:25411248   PMID:25416956   PMID:25511694   PMID:26186194  
PMID:26272600   PMID:26469385   PMID:26496610   PMID:26853466   PMID:27173435   PMID:27684187   PMID:27796421   PMID:28178760   PMID:28299580   PMID:28514442   PMID:28538176   PMID:29071516  
PMID:29126425   PMID:29490434   PMID:29664401   PMID:30538141   PMID:30572598   PMID:30628670   PMID:30691485   PMID:30737378   PMID:30854734   PMID:31081251   PMID:31375747   PMID:31527052  
PMID:31930344   PMID:31980649   PMID:32152128   PMID:32152265   PMID:32284070   PMID:32296183   PMID:32376822   PMID:32709923   PMID:33262526   PMID:33734898   PMID:33878891   PMID:33961781  
PMID:34011384   PMID:34288252   PMID:34373451   PMID:34581821   PMID:35013556   PMID:35256949   PMID:35303381   PMID:35595735   PMID:35748872   PMID:36163081   PMID:36215168   PMID:36931259  
PMID:37369679   PMID:37507770   PMID:37960766  


Genomics

Comparative Map Data
HDAC7
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381247,782,722 - 47,821,344 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1247,782,722 - 47,833,132 (-)EnsemblGRCh38hg38GRCh38
GRCh371248,176,505 - 48,213,686 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361246,462,772 - 46,499,924 (-)NCBINCBI36Build 36hg18NCBI36
Build 341246,462,775 - 46,479,190NCBI
Celera1246,974,055 - 47,011,314 (-)NCBICelera
Cytogenetic Map12q13.11NCBI
HuRef1245,207,665 - 45,244,811 (-)NCBIHuRef
CHM1_11248,142,408 - 48,179,666 (-)NCBICHM1_1
T2T-CHM13v2.01247,744,115 - 47,782,739 (-)NCBIT2T-CHM13v2.0
Hdac7
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391597,690,542 - 97,742,383 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1597,690,545 - 97,742,383 (-)EnsemblGRCm39 Ensembl
GRCm381597,792,661 - 97,844,502 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1597,792,664 - 97,844,502 (-)EnsemblGRCm38mm10GRCm38
MGSCv371597,623,112 - 97,662,102 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361597,620,715 - 97,659,705 (-)NCBIMGSCv36mm8
Celera1599,920,309 - 99,939,192 (-)NCBICelera
Cytogenetic Map15F1NCBI
cM Map1553.79NCBI
Hdac7
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr87130,803,013 - 130,841,181 (-)NCBIGRCr8
mRatBN7.27128,923,918 - 128,961,926 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl7128,923,920 - 128,962,072 (-)EnsemblmRatBN7.2 Ensembl
Rnor_6.07139,280,396 - 139,319,108 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl7139,281,187 - 139,318,455 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.07139,471,977 - 139,510,581 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.47136,501,738 - 136,523,073 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.17136,593,467 - 136,597,288 (-)NCBI
Celera7125,415,230 - 125,435,773 (-)NCBICelera
Cytogenetic Map7q36NCBI
Hdac7
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049555006,693,668 - 6,709,864 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049555006,692,656 - 6,707,453 (-)NCBIChiLan1.0ChiLan1.0
HDAC7
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21046,347,359 - 46,384,891 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11246,344,312 - 46,381,649 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01240,913,301 - 40,950,542 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11241,788,202 - 41,825,123 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1241,789,367 - 41,825,123 (+)Ensemblpanpan1.1panPan2
HDAC7
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1276,941,287 - 6,968,370 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl276,929,829 - 6,979,317 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2739,338,114 - 39,375,845 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0276,998,714 - 7,036,476 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl276,997,822 - 7,036,540 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1276,935,774 - 6,973,459 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0276,971,287 - 7,008,847 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02739,626,577 - 39,664,313 (-)NCBIUU_Cfam_GSD_1.0
Hdac7
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494567,447,349 - 67,482,511 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365125,682,490 - 5,697,869 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365125,680,564 - 5,701,182 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
HDAC7
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl578,150,561 - 78,186,072 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1578,150,554 - 78,186,051 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2581,388,011 - 81,393,534 (-)NCBISscrofa10.2Sscrofa10.2susScr3
HDAC7
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11144,002,616 - 44,040,766 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1144,003,736 - 44,039,902 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_023666037202,340,868 - 202,378,940 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Hdac7
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248164,441,849 - 4,475,437 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248164,441,543 - 4,476,520 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in HDAC7
74 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_001098416.2(HDAC7):c.2453C>T (p.Ser818Phe) single nucleotide variant Malignant melanoma [RCV000070007] Chr12:47786593 [GRCh38]
Chr12:48180376 [GRCh37]
Chr12:46466643 [NCBI36]
Chr12:12q13.11		 not provided
GRCh38/hg38 12p13.33-q24.33(chr12:121271-133196807)x3 copy number gain See cases [RCV000139555] Chr12:121271..133196807 [GRCh38]
Chr12:282465..133773393 [GRCh37]
Chr12:100698..132283466 [NCBI36]
Chr12:12p13.33-q24.33		 pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:1-133851895)x3 copy number gain See cases [RCV000258805] Chr12:1..133851895 [GRCh37]
Chr12:12p13.33-q24.33		 pathogenic|likely pathogenic
GRCh37/hg19 12p11.21-q13.12(chr12:31886971-50360461)x3 copy number gain See cases [RCV000207454] Chr12:31886971..50360461 [GRCh37]
Chr12:12p11.21-q13.12		 pathogenic
GRCh37/hg19 12q11-13.12(chr12:37857750-49791459)x3 copy number gain See cases [RCV000448835] Chr12:37857750..49791459 [GRCh37]
Chr12:12q11-13.12		 pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)x3 copy number gain See cases [RCV000510482] Chr12:173787..133777902 [GRCh37]
Chr12:12p13.33-q24.33		 pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902) copy number gain See cases [RCV000511643] Chr12:173787..133777902 [GRCh37]
Chr12:12p13.33-q24.33		 pathogenic
NM_015401.5(HDAC7):c.1319G>A (p.Arg440Gln) single nucleotide variant Inborn genetic diseases [RCV003270498] Chr12:47794899 [GRCh38]
Chr12:48188682 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.584A>C (p.Glu195Ala) single nucleotide variant Inborn genetic diseases [RCV003299849] Chr12:47797136 [GRCh38]
Chr12:48190919 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.932C>G (p.Pro311Arg) single nucleotide variant Inborn genetic diseases [RCV003240786] Chr12:47795742 [GRCh38]
Chr12:48189525 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.1040C>A (p.Pro347His) single nucleotide variant Inborn genetic diseases [RCV003285386] Chr12:47795634 [GRCh38]
Chr12:48189417 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.1019C>T (p.Thr340Ile) single nucleotide variant Inborn genetic diseases [RCV003269602] Chr12:47795655 [GRCh38]
Chr12:48189438 [GRCh37]
Chr12:12q13.11		 uncertain significance
NC_000012.11:g.26370251_54361538inv inversion not specified [RCV000714265] Chr12:26370251..54361538 [GRCh37]
Chr12:12p12.1-q13.13		 uncertain significance
GRCh37/hg19 12p13.33-q24.33(chr12:621220-133779118)x3 copy number gain not provided [RCV000750253] Chr12:621220..133779118 [GRCh37]
Chr12:12p13.33-q24.33		 pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:191619-133777645)x3 copy number gain not provided [RCV000750246] Chr12:191619..133777645 [GRCh37]
Chr12:12p13.33-q24.33		 pathogenic
NM_015401.5(HDAC7):c.729G>A (p.Thr243=) single nucleotide variant not provided [RCV000965957] Chr12:47796273 [GRCh38]
Chr12:48190056 [GRCh37]
Chr12:12q13.11		 benign
NM_015401.5(HDAC7):c.482C>T (p.Thr161Met) single nucleotide variant not provided [RCV000971931] Chr12:47797479 [GRCh38]
Chr12:48191262 [GRCh37]
Chr12:12q13.11		 likely benign
NM_015401.5(HDAC7):c.1934-5C>T single nucleotide variant not provided [RCV000902237] Chr12:47791313 [GRCh38]
Chr12:48185096 [GRCh37]
Chr12:12q13.11		 benign
NM_015401.5(HDAC7):c.1538C>G (p.Ala513Gly) single nucleotide variant not provided [RCV000972164] Chr12:47793509 [GRCh38]
Chr12:48187292 [GRCh37]
Chr12:12q13.11		 likely benign
NM_015401.5(HDAC7):c.1135A>G (p.Thr379Ala) single nucleotide variant Inborn genetic diseases [RCV003291620] Chr12:47795333 [GRCh38]
Chr12:48189116 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.699C>T (p.Leu233=) single nucleotide variant not provided [RCV000953312] Chr12:47797021 [GRCh38]
Chr12:48190804 [GRCh37]
Chr12:12q13.11		 benign|likely benign
NM_015401.5(HDAC7):c.603C>T (p.Arg201=) single nucleotide variant not provided [RCV000953313] Chr12:47797117 [GRCh38]
Chr12:48190900 [GRCh37]
Chr12:12q13.11		 benign|likely benign
GRCh37/hg19 12q11-13.12(chr12:37873948-49578619)x3 copy number gain See cases [RCV001353185] Chr12:37873948..49578619 [GRCh37]
Chr12:12q11-13.12		 likely pathogenic
GRCh37/hg19 12q11-13.12(chr12:37857750-49791459) copy number gain not specified [RCV002052988] Chr12:37857750..49791459 [GRCh37]
Chr12:12q11-13.12		 pathogenic
NM_015401.5(HDAC7):c.316C>G (p.Arg106Gly) single nucleotide variant Inborn genetic diseases [RCV003293844] Chr12:47798595 [GRCh38]
Chr12:48192378 [GRCh37]
Chr12:12q13.11		 uncertain significance
GRCh37/hg19 12q12-13.11(chr12:44661149-48921204)x1 copy number loss not provided [RCV002291537] Chr12:44661149..48921204 [GRCh37]
Chr12:12q12-13.11		 pathogenic
NM_015401.5(HDAC7):c.1006G>A (p.Glu336Lys) single nucleotide variant Inborn genetic diseases [RCV003260266] Chr12:47795668 [GRCh38]
Chr12:48189451 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.2440C>G (p.Leu814Val) single nucleotide variant Inborn genetic diseases [RCV003305154] Chr12:47787725 [GRCh38]
Chr12:48181508 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.1492C>T (p.Arg498Trp) single nucleotide variant Inborn genetic diseases [RCV002752954] Chr12:47793555 [GRCh38]
Chr12:48187338 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.919C>T (p.Arg307Cys) single nucleotide variant Inborn genetic diseases [RCV002689963] Chr12:47795755 [GRCh38]
Chr12:48189538 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.1093G>A (p.Gly365Arg) single nucleotide variant Inborn genetic diseases [RCV002839584] Chr12:47795375 [GRCh38]
Chr12:48189158 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.2007T>A (p.Asn669Lys) single nucleotide variant Inborn genetic diseases [RCV002836995] Chr12:47789897 [GRCh38]
Chr12:48183680 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.1510A>G (p.Thr504Ala) single nucleotide variant Inborn genetic diseases [RCV002728685] Chr12:47793537 [GRCh38]
Chr12:48187320 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.2727A>C (p.Glu909Asp) single nucleotide variant Inborn genetic diseases [RCV002841405] Chr12:47785451 [GRCh38]
Chr12:48179234 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.502A>G (p.Met168Val) single nucleotide variant Inborn genetic diseases [RCV002691858] Chr12:47797459 [GRCh38]
Chr12:48191242 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.768C>A (p.His256Gln) single nucleotide variant Inborn genetic diseases [RCV002912010] Chr12:47796234 [GRCh38]
Chr12:48190017 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.797C>T (p.Ala266Val) single nucleotide variant Inborn genetic diseases [RCV002761737] Chr12:47796015 [GRCh38]
Chr12:48189798 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.151G>C (p.Glu51Gln) single nucleotide variant Inborn genetic diseases [RCV002782772] Chr12:47798892 [GRCh38]
Chr12:48192675 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.974C>G (p.Thr325Ser) single nucleotide variant Inborn genetic diseases [RCV002844399] Chr12:47795700 [GRCh38]
Chr12:48189483 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.2420C>G (p.Pro807Arg) single nucleotide variant Inborn genetic diseases [RCV002978297] Chr12:47787745 [GRCh38]
Chr12:48181528 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.196C>T (p.Arg66Cys) single nucleotide variant Inborn genetic diseases [RCV002952246] Chr12:47798847 [GRCh38]
Chr12:48192630 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.1873G>A (p.Val625Met) single nucleotide variant Inborn genetic diseases [RCV002886902] Chr12:47791646 [GRCh38]
Chr12:48185429 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.1694C>G (p.Ser565Trp) single nucleotide variant Inborn genetic diseases [RCV002916294] Chr12:47791989 [GRCh38]
Chr12:48185772 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.251C>A (p.Pro84His) single nucleotide variant Inborn genetic diseases [RCV002787650] Chr12:47798792 [GRCh38]
Chr12:48192575 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.110C>T (p.Pro37Leu) single nucleotide variant Inborn genetic diseases [RCV002664623] Chr12:47798933 [GRCh38]
Chr12:48192716 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.2879A>T (p.Glu960Val) single nucleotide variant Inborn genetic diseases [RCV002743224] Chr12:47784130 [GRCh38]
Chr12:48177913 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.755A>G (p.Asn252Ser) single nucleotide variant Inborn genetic diseases [RCV002983411] Chr12:47796247 [GRCh38]
Chr12:48190030 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.2713C>T (p.Pro905Ser) single nucleotide variant Inborn genetic diseases [RCV002787189] Chr12:47785465 [GRCh38]
Chr12:48179248 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.548C>T (p.Pro183Leu) single nucleotide variant Inborn genetic diseases [RCV002699032] Chr12:47797413 [GRCh38]
Chr12:48191196 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.2024A>G (p.Asn675Ser) single nucleotide variant Inborn genetic diseases [RCV002743824] Chr12:47789880 [GRCh38]
Chr12:48183663 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.13G>C (p.Gly5Arg) single nucleotide variant Inborn genetic diseases [RCV002921004] Chr12:47819773 [GRCh38]
Chr12:48213556 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.161C>T (p.Pro54Leu) single nucleotide variant Inborn genetic diseases [RCV002807609] Chr12:47798882 [GRCh38]
Chr12:48192665 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.759C>G (p.Asp253Glu) single nucleotide variant Inborn genetic diseases [RCV002896244] Chr12:47796243 [GRCh38]
Chr12:48190026 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.266T>C (p.Met89Thr) single nucleotide variant Inborn genetic diseases [RCV003008702] Chr12:47798645 [GRCh38]
Chr12:48192428 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.1298C>G (p.Pro433Arg) single nucleotide variant Inborn genetic diseases [RCV002835935] Chr12:47794920 [GRCh38]
Chr12:48188703 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.2420C>A (p.Pro807His) single nucleotide variant Inborn genetic diseases [RCV002677713] Chr12:47787745 [GRCh38]
Chr12:48181528 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.253A>C (p.Met85Leu) single nucleotide variant Inborn genetic diseases [RCV002723243] Chr12:47798790 [GRCh38]
Chr12:48192573 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.1927C>G (p.Leu643Val) single nucleotide variant Inborn genetic diseases [RCV003193497] Chr12:47791592 [GRCh38]
Chr12:48185375 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.1921G>A (p.Gly641Arg) single nucleotide variant Inborn genetic diseases [RCV003208515] Chr12:47791598 [GRCh38]
Chr12:48185381 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.188G>A (p.Arg63His) single nucleotide variant Inborn genetic diseases [RCV003185872] Chr12:47798855 [GRCh38]
Chr12:48192638 [GRCh37]
Chr12:12q13.11		 likely benign
NM_015401.5(HDAC7):c.682C>T (p.Arg228Trp) single nucleotide variant Inborn genetic diseases [RCV003188749] Chr12:47797038 [GRCh38]
Chr12:48190821 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.1298C>T (p.Pro433Leu) single nucleotide variant Inborn genetic diseases [RCV003214830] Chr12:47794920 [GRCh38]
Chr12:48188703 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.636G>C (p.Lys212Asn) single nucleotide variant Inborn genetic diseases [RCV003212728] Chr12:47797084 [GRCh38]
Chr12:48190867 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.697C>T (p.Leu233Phe) single nucleotide variant Inborn genetic diseases [RCV003359895] Chr12:47797023 [GRCh38]
Chr12:48190806 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.1619G>A (p.Ser540Asn) single nucleotide variant Inborn genetic diseases [RCV003347304] Chr12:47793428 [GRCh38]
Chr12:48187211 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.2816G>A (p.Arg939His) single nucleotide variant Inborn genetic diseases [RCV003352004] Chr12:47784193 [GRCh38]
Chr12:48177976 [GRCh37]
Chr12:12q13.11		 uncertain significance
NM_015401.5(HDAC7):c.2319C>T (p.Asp773=) single nucleotide variant not provided [RCV003391767] Chr12:47788081 [GRCh38]
Chr12:48181864 [GRCh37]
Chr12:12q13.11		 likely benign
GRCh37/hg19 12q12-13.11(chr12:38258635-48235837)x3 copy number gain not specified [RCV003987001] Chr12:38258635..48235837 [GRCh37]
Chr12:12q12-13.11		 pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:12691
Count of miRNA genes:1274
Interacting mature miRNAs:1688
Transcripts:ENST00000080059, ENST00000354334, ENST00000380610, ENST00000417107, ENST00000417902, ENST00000421231, ENST00000422254, ENST00000425451, ENST00000427332, ENST00000430670, ENST00000433685, ENST00000434070, ENST00000440293, ENST00000445237, ENST00000447463, ENST00000450805, ENST00000459625, ENST00000463732, ENST00000470668, ENST00000471235, ENST00000477203, ENST00000477937, ENST00000485796, ENST00000488927, ENST00000491464, ENST00000547259, ENST00000548080, ENST00000548938, ENST00000549883, ENST00000552960
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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

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

Markers in Region
RH93449  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371248,176,231 - 48,176,373UniSTSGRCh37
Build 361246,462,498 - 46,462,640RGDNCBI36
Celera1246,973,781 - 46,973,923RGD
Cytogenetic Map12q13.1UniSTS
Cytogenetic Map12q13.11UniSTS
HuRef1245,207,391 - 45,207,533UniSTS
GeneMap99-GB4 RH Map12211.47UniSTS
WI-18194  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371248,177,346 - 48,177,470UniSTSGRCh37
Build 361246,463,613 - 46,463,737RGDNCBI36
Celera1246,974,896 - 46,975,020RGD
Cytogenetic Map12q13.1UniSTS
HuRef1245,208,506 - 45,208,630UniSTS
GeneMap99-GB4 RH Map12215.84UniSTS
Whitehead-RH Map12295.9UniSTS
NCBI RH Map12367.2UniSTS
G65674  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37202,962,407 - 2,962,602UniSTSGRCh37
Build 36202,910,407 - 2,910,602RGDNCBI36
Celera203,024,373 - 3,024,568RGD
Cytogenetic Map12q13.1UniSTS
Cytogenetic Map20p13UniSTS
SHGC-63529  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371248,198,081 - 48,198,267UniSTSGRCh37
Build 361246,484,348 - 46,484,534RGDNCBI36
Celera1246,995,631 - 46,995,817RGD
Cytogenetic Map12q13.1UniSTS
HuRef1245,229,270 - 45,229,456UniSTS
TNG Radiation Hybrid Map1221587.0UniSTS
SHGC-30216  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371248,186,819 - 48,186,943UniSTSGRCh37
Build 361246,473,086 - 46,473,210RGDNCBI36
Celera1246,984,369 - 46,984,493RGD
Cytogenetic Map12q13.1UniSTS
HuRef1245,218,008 - 45,218,132UniSTS
Stanford-G3 RH Map121867.0UniSTS
GeneMap99-GB4 RH Map12202.82UniSTS
Whitehead-RH Map12295.8UniSTS
NCBI RH Map12362.9UniSTS
GeneMap99-G3 RH Map121813.0UniSTS
STS-R00262  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371248,204,409 - 48,204,530UniSTSGRCh37
Build 361246,490,676 - 46,490,797RGDNCBI36
Celera1247,001,959 - 47,002,080RGD
Cytogenetic Map12q13.1UniSTS
HuRef1245,235,642 - 45,235,763UniSTS
GeneMap99-GB4 RH Map12210.76UniSTS
NCBI RH Map12394.0UniSTS
WI-14839  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371248,179,638 - 48,179,767UniSTSGRCh37
Build 361246,465,905 - 46,466,034RGDNCBI36
Celera1246,977,188 - 46,977,317RGD
Cytogenetic Map12q13.1UniSTS
HuRef1245,210,798 - 45,210,927UniSTS
GeneMap99-GB4 RH Map12211.9UniSTS
Whitehead-RH Map12294.0UniSTS
NCBI RH Map12360.9UniSTS
MARC_4297-4298:996679522:1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371248,179,577 - 48,180,398UniSTSGRCh37
Build 361246,465,844 - 46,466,665RGDNCBI36
Celera1246,977,127 - 46,977,948RGD
HuRef1245,210,737 - 45,211,558UniSTS
L30021  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map12q13.1UniSTS
Cytogenetic Map2q31.2UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map6q21UniSTS
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 2403 2930 1370 270 1675 111 4064 1906 2882 365 1444 1568 175 1 1204 2521 3 2
Low 35 61 356 354 274 354 293 291 852 54 16 42 267 3
Below cutoff 1 1 3

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001098416 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001308090 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001368046 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_015401 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_160435 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_160436 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011538478 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011538480 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011538481 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011538482 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011538483 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019455 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019456 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024449018 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428978 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428979 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428980 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428981 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428982 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428983 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428984 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054372244 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054372245 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054372246 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054372247 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054372248 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054372249 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054372250 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054372251 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054372252 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054372253 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054372254 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001748761 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC004466 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF239243 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK001032 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK001190 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK024387 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK024469 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK026767 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK027781 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK122588 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK128383 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK225910 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK299292 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK301545 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK303481 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK309547 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL117455 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY302468 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY321367 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC006453 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC020505 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC064840 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM144303 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BT009771 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471111 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068266 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC376749 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KT584462 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000080059   ⟹   ENSP00000080059
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1247,782,722 - 47,819,903 (-)Ensembl
RefSeq Acc Id: ENST00000354334   ⟹   ENSP00000351326
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1247,782,722 - 47,819,866 (-)Ensembl
RefSeq Acc Id: ENST00000380610   ⟹   ENSP00000369984
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1247,783,721 - 47,802,512 (-)Ensembl
RefSeq Acc Id: ENST00000417107   ⟹   ENSP00000387792
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1247,798,560 - 47,819,980 (-)Ensembl
RefSeq Acc Id: ENST00000417902   ⟹   ENSP00000400811
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1247,798,118 - 47,819,961 (-)Ensembl
RefSeq Acc Id: ENST00000421231   ⟹   ENSP00000412155
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1247,797,430 - 47,813,051 (-)Ensembl
RefSeq Acc Id: ENST00000422254   ⟹   ENSP00000410068
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1247,797,107 - 47,813,051 (-)Ensembl
RefSeq Acc Id: ENST00000425451   ⟹   ENSP00000401872
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1247,795,377 - 47,819,883 (-)Ensembl
RefSeq Acc Id: ENST00000427332   ⟹   ENSP00000404394
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1247,783,841 - 47,820,612 (-)Ensembl
RefSeq Acc Id: ENST00000430670   ⟹   ENSP00000396159
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1247,795,667 - 47,819,875 (-)Ensembl
RefSeq Acc Id: ENST00000433685   ⟹   ENSP00000403149
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1247,798,188 - 47,820,573 (-)Ensembl
RefSeq Acc Id: ENST00000434070   ⟹   ENSP00000388561
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1247,797,384 - 47,833,132 (-)Ensembl
RefSeq Acc Id: ENST00000440293   ⟹   ENSP00000411058
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1247,797,118 - 47,819,886 (-)Ensembl
RefSeq Acc Id: ENST00000445237   ⟹   ENSP00000390415
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1247,798,640 - 47,813,484 (-)Ensembl
RefSeq Acc Id: ENST00000447463   ⟹   ENSP00000389501
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1247,797,384 - 47,820,601 (-)Ensembl
RefSeq Acc Id: ENST00000450805   ⟹   ENSP00000397236
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1247,798,114 - 47,819,262 (-)Ensembl
RefSeq Acc Id: ENST00000459625
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1247,782,726 - 47,793,498 (-)Ensembl
RefSeq Acc Id: ENST00000463732
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1247,794,836 - 47,795,850 (-)Ensembl
RefSeq Acc Id: ENST00000470668
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1247,782,726 - 47,798,189 (-)Ensembl
RefSeq Acc Id: ENST00000471235
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1247,785,451 - 47,788,169 (-)Ensembl
RefSeq Acc Id: ENST00000477203   ⟹   ENSP00000449171
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1247,783,674 - 47,799,140 (-)Ensembl
RefSeq Acc Id: ENST00000477937
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1247,790,377 - 47,793,386 (-)Ensembl
RefSeq Acc Id: ENST00000485796   ⟹   ENSP00000448448
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1247,794,869 - 47,797,492 (-)Ensembl
RefSeq Acc Id: ENST00000488927   ⟹   ENSP00000482003
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1247,788,096 - 47,792,000 (-)Ensembl
RefSeq Acc Id: ENST00000491464
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1247,794,807 - 47,795,604 (-)Ensembl
RefSeq Acc Id: ENST00000547259   ⟹   ENSP00000447191
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1247,783,800 - 47,786,667 (-)Ensembl
RefSeq Acc Id: ENST00000548080   ⟹   ENSP00000446538
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1247,783,516 - 47,792,004 (-)Ensembl
RefSeq Acc Id: ENST00000548938   ⟹   ENSP00000448305
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1247,782,726 - 47,793,542 (-)Ensembl
RefSeq Acc Id: ENST00000549883
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1247,783,638 - 47,785,381 (-)Ensembl
RefSeq Acc Id: ENST00000552960   ⟹   ENSP00000448532
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1247,783,651 - 47,819,886 (-)Ensembl
RefSeq Acc Id: NM_001098416   ⟹   NP_001091886
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381247,782,722 - 47,819,903 (-)NCBI
GRCh371248,176,505 - 48,213,763 (-)ENTREZGENE
Build 361246,462,772 - 46,499,924 (-)NCBI Archive
HuRef1245,207,665 - 45,244,811 (-)ENTREZGENE
CHM1_11248,142,396 - 48,179,666 (-)NCBI
T2T-CHM13v2.01247,744,115 - 47,781,298 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001308090   ⟹   NP_001295019
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381247,782,722 - 47,819,903 (-)NCBI
CHM1_11248,142,396 - 48,179,666 (-)NCBI
T2T-CHM13v2.01247,744,115 - 47,781,298 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001368046   ⟹   NP_001354975
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381247,782,722 - 47,819,903 (-)NCBI
T2T-CHM13v2.01247,744,115 - 47,781,298 (-)NCBI
Sequence:
RefSeq Acc Id: NM_015401   ⟹   NP_056216
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381247,782,722 - 47,819,903 (-)NCBI
GRCh371248,176,505 - 48,213,763 (-)ENTREZGENE
Build 361246,462,772 - 46,479,190 (-)NCBI Archive
HuRef1245,207,665 - 45,244,811 (-)ENTREZGENE
CHM1_11248,142,396 - 48,179,666 (-)NCBI
T2T-CHM13v2.01247,744,115 - 47,781,298 (-)NCBI
Sequence:
RefSeq Acc Id: NR_160435
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381247,782,722 - 47,819,903 (-)NCBI
T2T-CHM13v2.01247,744,115 - 47,781,298 (-)NCBI
Sequence:
RefSeq Acc Id: NR_160436
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381247,782,722 - 47,819,903 (-)NCBI
T2T-CHM13v2.01247,744,115 - 47,781,298 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011538480   ⟹   XP_011536782
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381247,782,722 - 47,813,095 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011538481   ⟹   XP_011536783
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381247,782,722 - 47,820,719 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011538483   ⟹   XP_011536785
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381247,792,373 - 47,813,095 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024449018   ⟹   XP_024304786
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381247,782,722 - 47,815,653 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047428978   ⟹   XP_047284934
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381247,782,722 - 47,819,903 (-)NCBI
RefSeq Acc Id: XM_047428979   ⟹   XP_047284935
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381247,782,722 - 47,820,719 (-)NCBI
RefSeq Acc Id: XM_047428980   ⟹   XP_047284936
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381247,782,722 - 47,821,344 (-)NCBI
RefSeq Acc Id: XM_047428981   ⟹   XP_047284937
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381247,782,722 - 47,815,652 (-)NCBI
RefSeq Acc Id: XM_047428982   ⟹   XP_047284938
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381247,782,722 - 47,810,953 (-)NCBI
RefSeq Acc Id: XM_047428983   ⟹   XP_047284939
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381247,782,722 - 47,819,903 (-)NCBI
RefSeq Acc Id: XM_047428984   ⟹   XP_047284940
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381247,782,722 - 47,803,885 (-)NCBI
RefSeq Acc Id: XM_054372244   ⟹   XP_054228219
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01247,744,115 - 47,782,114 (-)NCBI
RefSeq Acc Id: XM_054372245   ⟹   XP_054228220
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01247,744,115 - 47,781,298 (-)NCBI
RefSeq Acc Id: XM_054372246   ⟹   XP_054228221
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01247,744,115 - 47,777,048 (-)NCBI
RefSeq Acc Id: XM_054372247   ⟹   XP_054228222
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01247,744,115 - 47,774,490 (-)NCBI
RefSeq Acc Id: XM_054372248   ⟹   XP_054228223
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01247,744,115 - 47,782,114 (-)NCBI
RefSeq Acc Id: XM_054372249   ⟹   XP_054228224
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01247,744,115 - 47,782,739 (-)NCBI
RefSeq Acc Id: XM_054372250   ⟹   XP_054228225
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01247,744,115 - 47,777,047 (-)NCBI
RefSeq Acc Id: XM_054372251   ⟹   XP_054228226
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01247,744,115 - 47,772,348 (-)NCBI
RefSeq Acc Id: XM_054372252   ⟹   XP_054228227
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01247,744,115 - 47,781,298 (-)NCBI
RefSeq Acc Id: XM_054372253   ⟹   XP_054228228
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01247,744,115 - 47,765,278 (-)NCBI
RefSeq Acc Id: XM_054372254   ⟹   XP_054228229
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01247,753,766 - 47,774,490 (-)NCBI
Protein Sequences
Protein RefSeqs NP_001091886 (Get FASTA)   NCBI Sequence Viewer  
  NP_001295019 (Get FASTA)   NCBI Sequence Viewer  
  NP_001354975 (Get FASTA)   NCBI Sequence Viewer  
  NP_056216 (Get FASTA)   NCBI Sequence Viewer  
  XP_011536782 (Get FASTA)   NCBI Sequence Viewer  
  XP_011536783 (Get FASTA)   NCBI Sequence Viewer  
  XP_011536785 (Get FASTA)   NCBI Sequence Viewer  
  XP_024304786 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284934 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284935 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284936 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284937 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284938 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284939 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284940 (Get FASTA)   NCBI Sequence Viewer  
  XP_054228219 (Get FASTA)   NCBI Sequence Viewer  
  XP_054228220 (Get FASTA)   NCBI Sequence Viewer  
  XP_054228221 (Get FASTA)   NCBI Sequence Viewer  
  XP_054228222 (Get FASTA)   NCBI Sequence Viewer  
  XP_054228223 (Get FASTA)   NCBI Sequence Viewer  
  XP_054228224 (Get FASTA)   NCBI Sequence Viewer  
  XP_054228225 (Get FASTA)   NCBI Sequence Viewer  
  XP_054228226 (Get FASTA)   NCBI Sequence Viewer  
  XP_054228227 (Get FASTA)   NCBI Sequence Viewer  
  XP_054228228 (Get FASTA)   NCBI Sequence Viewer  
  XP_054228229 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAF63491 (Get FASTA)   NCBI Sequence Viewer  
  AAH06453 (Get FASTA)   NCBI Sequence Viewer  
  AAH20505 (Get FASTA)   NCBI Sequence Viewer  
  AAH64840 (Get FASTA)   NCBI Sequence Viewer  
  AAP84704 (Get FASTA)   NCBI Sequence Viewer  
  AAP88773 (Get FASTA)   NCBI Sequence Viewer  
  AAQ18232 (Get FASTA)   NCBI Sequence Viewer  
  BAA91474 (Get FASTA)   NCBI Sequence Viewer  
  BAA91545 (Get FASTA)   NCBI Sequence Viewer  
  BAB15546 (Get FASTA)   NCBI Sequence Viewer  
  BAB15759 (Get FASTA)   NCBI Sequence Viewer  
  BAB55363 (Get FASTA)   NCBI Sequence Viewer  
  BAC56929 (Get FASTA)   NCBI Sequence Viewer  
  BAG54670 (Get FASTA)   NCBI Sequence Viewer  
  BAG61307 (Get FASTA)   NCBI Sequence Viewer  
  BAG63042 (Get FASTA)   NCBI Sequence Viewer  
  BAG64517 (Get FASTA)   NCBI Sequence Viewer  
  CAB55935 (Get FASTA)   NCBI Sequence Viewer  
  EAW57952 (Get FASTA)   NCBI Sequence Viewer  
  EAW57953 (Get FASTA)   NCBI Sequence Viewer  
  EAW57954 (Get FASTA)   NCBI Sequence Viewer  
  EAW57955 (Get FASTA)   NCBI Sequence Viewer  
  EAW57956 (Get FASTA)   NCBI Sequence Viewer  
  EAW57957 (Get FASTA)   NCBI Sequence Viewer  
  EAW57958 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000080059
  ENSP00000080059.7
  ENSP00000351326
  ENSP00000351326.3
  ENSP00000369984.4
  ENSP00000387792.1
  ENSP00000388561.1
  ENSP00000389501.2
  ENSP00000390415.2
  ENSP00000396159.1
  ENSP00000397236.1
  ENSP00000400811.1
  ENSP00000401872.2
  ENSP00000403149.1
  ENSP00000404394
  ENSP00000404394.2
  ENSP00000410068.1
  ENSP00000411058.1
  ENSP00000412155.1
  ENSP00000446538.1
  ENSP00000447191.1
  ENSP00000448305.1
  ENSP00000448448.1
  ENSP00000448532
  ENSP00000448532.1
  ENSP00000449171.1
  ENSP00000482003.1
GenBank Protein Q8WUI4 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_001091886   ⟸   NM_001098416
- Peptide Label: isoform d
- UniProtKB: J3KPH8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_056216   ⟸   NM_015401
- Peptide Label: isoform a
- UniProtKB: J3KPH8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011536783   ⟸   XM_011538481
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_011536782   ⟸   XM_011538480
- Peptide Label: isoform X4
- UniProtKB: J3KPH8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011536785   ⟸   XM_011538483
- Peptide Label: isoform X10
- Sequence:
RefSeq Acc Id: NP_001295019   ⟸   NM_001308090
- Peptide Label: isoform e
- UniProtKB: J3KPH8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_024304786   ⟸   XM_024449018
- Peptide Label: isoform X3
- UniProtKB: J3KPH8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001354975   ⟸   NM_001368046
- Peptide Label: isoform f
- UniProtKB: J3KPH8 (UniProtKB/TrEMBL)
RefSeq Acc Id: ENSP00000449171   ⟸   ENST00000477203
RefSeq Acc Id: ENSP00000401872   ⟸   ENST00000425451
RefSeq Acc Id: ENSP00000397236   ⟸   ENST00000450805
RefSeq Acc Id: ENSP00000404394   ⟸   ENST00000427332
RefSeq Acc Id: ENSP00000447191   ⟸   ENST00000547259
RefSeq Acc Id: ENSP00000411058   ⟸   ENST00000440293
RefSeq Acc Id: ENSP00000448305   ⟸   ENST00000548938
RefSeq Acc Id: ENSP00000446538   ⟸   ENST00000548080
RefSeq Acc Id: ENSP00000387792   ⟸   ENST00000417107
RefSeq Acc Id: ENSP00000400811   ⟸   ENST00000417902
RefSeq Acc Id: ENSP00000396159   ⟸   ENST00000430670
RefSeq Acc Id: ENSP00000390415   ⟸   ENST00000445237
RefSeq Acc Id: ENSP00000448448   ⟸   ENST00000485796
RefSeq Acc Id: ENSP00000351326   ⟸   ENST00000354334
RefSeq Acc Id: ENSP00000403149   ⟸   ENST00000433685
RefSeq Acc Id: ENSP00000389501   ⟸   ENST00000447463
RefSeq Acc Id: ENSP00000369984   ⟸   ENST00000380610
RefSeq Acc Id: ENSP00000388561   ⟸   ENST00000434070
RefSeq Acc Id: ENSP00000482003   ⟸   ENST00000488927
RefSeq Acc Id: ENSP00000448532   ⟸   ENST00000552960
RefSeq Acc Id: ENSP00000412155   ⟸   ENST00000421231
RefSeq Acc Id: ENSP00000410068   ⟸   ENST00000422254
RefSeq Acc Id: ENSP00000080059   ⟸   ENST00000080059
RefSeq Acc Id: XP_047284936   ⟸   XM_047428980
- Peptide Label: isoform X6
RefSeq Acc Id: XP_047284935   ⟸   XM_047428979
- Peptide Label: isoform X5
RefSeq Acc Id: XP_047284939   ⟸   XM_047428983
- Peptide Label: isoform X9
RefSeq Acc Id: XP_047284934   ⟸   XM_047428978
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047284937   ⟸   XM_047428981
- Peptide Label: isoform X7
RefSeq Acc Id: XP_047284938   ⟸   XM_047428982
- Peptide Label: isoform X8
- UniProtKB: Q9NYK9 (UniProtKB/Swiss-Prot),   Q9NWA9 (UniProtKB/Swiss-Prot),   Q9NW41 (UniProtKB/Swiss-Prot),   Q9H7L0 (UniProtKB/Swiss-Prot),   Q9BR73 (UniProtKB/Swiss-Prot),   Q96K01 (UniProtKB/Swiss-Prot),   Q8WUI4 (UniProtKB/Swiss-Prot),   Q7Z5I1 (UniProtKB/Swiss-Prot),   Q7Z4K2 (UniProtKB/Swiss-Prot),   Q6W9G7 (UniProtKB/Swiss-Prot),   Q6P1W9 (UniProtKB/Swiss-Prot),   B4E0Q5 (UniProtKB/Swiss-Prot),   B4DWI0 (UniProtKB/Swiss-Prot),   B3KY08 (UniProtKB/Swiss-Prot),   Q9UFU7 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_047284940   ⟸   XM_047428984
- Peptide Label: isoform X8
- UniProtKB: Q9NYK9 (UniProtKB/Swiss-Prot),   Q9NWA9 (UniProtKB/Swiss-Prot),   Q9NW41 (UniProtKB/Swiss-Prot),   Q9H7L0 (UniProtKB/Swiss-Prot),   Q9BR73 (UniProtKB/Swiss-Prot),   Q96K01 (UniProtKB/Swiss-Prot),   Q8WUI4 (UniProtKB/Swiss-Prot),   Q7Z5I1 (UniProtKB/Swiss-Prot),   Q7Z4K2 (UniProtKB/Swiss-Prot),   Q6W9G7 (UniProtKB/Swiss-Prot),   Q6P1W9 (UniProtKB/Swiss-Prot),   B4E0Q5 (UniProtKB/Swiss-Prot),   B4DWI0 (UniProtKB/Swiss-Prot),   B3KY08 (UniProtKB/Swiss-Prot),   Q9UFU7 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054228224   ⟸   XM_054372249
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054228223   ⟸   XM_054372248
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054228219   ⟸   XM_054372244
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054228227   ⟸   XM_054372252
- Peptide Label: isoform X9
RefSeq Acc Id: XP_054228220   ⟸   XM_054372245
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054228221   ⟸   XM_054372246
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054228225   ⟸   XM_054372250
- Peptide Label: isoform X7
RefSeq Acc Id: XP_054228222   ⟸   XM_054372247
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054228226   ⟸   XM_054372251
- Peptide Label: isoform X8
- UniProtKB: Q9NYK9 (UniProtKB/Swiss-Prot),   Q9NWA9 (UniProtKB/Swiss-Prot),   Q9NW41 (UniProtKB/Swiss-Prot),   Q9H7L0 (UniProtKB/Swiss-Prot),   Q9BR73 (UniProtKB/Swiss-Prot),   Q96K01 (UniProtKB/Swiss-Prot),   Q8WUI4 (UniProtKB/Swiss-Prot),   Q7Z5I1 (UniProtKB/Swiss-Prot),   Q7Z4K2 (UniProtKB/Swiss-Prot),   Q6W9G7 (UniProtKB/Swiss-Prot),   Q6P1W9 (UniProtKB/Swiss-Prot),   B4E0Q5 (UniProtKB/Swiss-Prot),   B4DWI0 (UniProtKB/Swiss-Prot),   B3KY08 (UniProtKB/Swiss-Prot),   Q9UFU7 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054228228   ⟸   XM_054372253
- Peptide Label: isoform X8
- UniProtKB: Q9NYK9 (UniProtKB/Swiss-Prot),   Q9NWA9 (UniProtKB/Swiss-Prot),   Q9NW41 (UniProtKB/Swiss-Prot),   Q9H7L0 (UniProtKB/Swiss-Prot),   Q9BR73 (UniProtKB/Swiss-Prot),   Q96K01 (UniProtKB/Swiss-Prot),   Q8WUI4 (UniProtKB/Swiss-Prot),   Q7Z5I1 (UniProtKB/Swiss-Prot),   Q7Z4K2 (UniProtKB/Swiss-Prot),   Q6W9G7 (UniProtKB/Swiss-Prot),   Q6P1W9 (UniProtKB/Swiss-Prot),   B4E0Q5 (UniProtKB/Swiss-Prot),   B4DWI0 (UniProtKB/Swiss-Prot),   B3KY08 (UniProtKB/Swiss-Prot),   Q9UFU7 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054228229   ⟸   XM_054372254
- Peptide Label: isoform X10
Protein Domains
Histone deacetylase

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q8WUI4-F1-model_v2 AlphaFold Q8WUI4 1-952 view protein structure

Promoters
RGD ID:6790097
Promoter ID:HG_KWN:15473
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   K562
Transcripts:OTTHUMT00000328799
Position:
Human AssemblyChrPosition (strand)Source
Build 361246,468,161 - 46,468,812 (-)MPROMDB
RGD ID:6790105
Promoter ID:HG_KWN:15474
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3,   K562
Transcripts:OTTHUMT00000328798,   OTTHUMT00000328816,   OTTHUMT00000328817,   OTTHUMT00000328818,   UC001RQE.1,   UC009ZKU.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361246,472,161 - 46,474,632 (-)MPROMDB
RGD ID:6790104
Promoter ID:HG_KWN:15475
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562,   NB4
Transcripts:OTTHUMT00000328814,   OTTHUMT00000328815
Position:
Human AssemblyChrPosition (strand)Source
Build 361246,475,701 - 46,476,201 (-)MPROMDB
RGD ID:6790103
Promoter ID:HG_KWN:15476
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell
Transcripts:OTTHUMT00000328813
Position:
Human AssemblyChrPosition (strand)Source
Build 361246,477,391 - 46,477,891 (-)MPROMDB
RGD ID:6790095
Promoter ID:HG_KWN:15478
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   NB4
Transcripts:ENST00000380610,   OTTHUMT00000328794,   UC009ZKV.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361246,479,391 - 46,479,891 (-)MPROMDB
RGD ID:6790099
Promoter ID:HG_KWN:15479
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   NB4
Transcripts:OTTHUMT00000328808
Position:
Human AssemblyChrPosition (strand)Source
Build 361246,483,066 - 46,483,566 (-)MPROMDB
RGD ID:6790100
Promoter ID:HG_KWN:15480
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:OTTHUMT00000328806,   OTTHUMT00000328807,   OTTHUMT00000328812
Position:
Human AssemblyChrPosition (strand)Source
Build 361246,492,986 - 46,494,242 (-)MPROMDB
RGD ID:6790098
Promoter ID:HG_KWN:15481
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:OTTHUMT00000328801
Position:
Human AssemblyChrPosition (strand)Source
Build 361246,498,961 - 46,500,287 (-)MPROMDB
RGD ID:6790096
Promoter ID:HG_KWN:15482
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   HeLa_S3,   NB4
Transcripts:OTTHUMT00000328792,   OTTHUMT00000328793,   OTTHUMT00000328800,   OTTHUMT00000328809,   OTTHUMT00000328810,   OTTHUMT00000328811,   UC001RQK.2
Position:
Human AssemblyChrPosition (strand)Source
Build 361246,500,666 - 46,501,166 (-)MPROMDB
RGD ID:7223721
Promoter ID:EPDNEW_H17606
Type:initiation region
Name:HDAC7_1
Description:histone deacetylase 7
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381247,819,903 - 47,819,963EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:14067 AgrOrtholog
COSMIC HDAC7 COSMIC
Ensembl Genes ENSG00000061273 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000080059 ENTREZGENE
  ENST00000080059.12 UniProtKB/Swiss-Prot
  ENST00000354334 ENTREZGENE
  ENST00000354334.7 UniProtKB/Swiss-Prot
  ENST00000380610.8 UniProtKB/TrEMBL
  ENST00000417107.5 UniProtKB/TrEMBL
  ENST00000417902.5 UniProtKB/TrEMBL
  ENST00000421231.5 UniProtKB/TrEMBL
  ENST00000422254.5 UniProtKB/TrEMBL
  ENST00000425451.2 UniProtKB/TrEMBL
  ENST00000427332 ENTREZGENE
  ENST00000427332.6 UniProtKB/Swiss-Prot
  ENST00000430670.5 UniProtKB/TrEMBL
  ENST00000433685.5 UniProtKB/TrEMBL
  ENST00000434070.5 UniProtKB/TrEMBL
  ENST00000440293.5 UniProtKB/TrEMBL
  ENST00000445237.2 UniProtKB/TrEMBL
  ENST00000447463.5 UniProtKB/TrEMBL
  ENST00000450805.5 UniProtKB/TrEMBL
  ENST00000470668 ENTREZGENE
  ENST00000477203.6 UniProtKB/TrEMBL
  ENST00000485796.5 UniProtKB/TrEMBL
  ENST00000488927.2 UniProtKB/TrEMBL
  ENST00000547259.1 UniProtKB/TrEMBL
  ENST00000548080.5 UniProtKB/TrEMBL
  ENST00000548938.5 UniProtKB/TrEMBL
  ENST00000552960 ENTREZGENE
  ENST00000552960.5 UniProtKB/Swiss-Prot
Gene3D-CATH 3.40.800.20 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000061273 GTEx
HGNC ID HGNC:14067 ENTREZGENE
Human Proteome Map HDAC7 Human Proteome Map
InterPro HDAC4/5/7/9 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  His_deacetylse UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  His_deacetylse_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  His_deacetylse_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ureohydrolase_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:51564 UniProtKB/Swiss-Prot
NCBI Gene 51564 ENTREZGENE
OMIM 606542 OMIM
PANTHER HISTONE DEACETYLASE UniProtKB/TrEMBL
  HISTONE DEACETYLASE 7 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  HISTONE DEACETYLASE 9 UniProtKB/TrEMBL
  HISTONE DEACETYLASE HDAC1-RELATED UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR45364 UniProtKB/TrEMBL
Pfam Hist_deacetyl UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA162390579 PharmGKB
PIRSF HDAC_II_euk UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PRINTS HDASUPER UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF52768 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A087WYQ4_HUMAN UniProtKB/TrEMBL
  B3KY08 ENTREZGENE
  B4DWI0 ENTREZGENE
  B4E0Q5 ENTREZGENE
  C9J102_HUMAN UniProtKB/TrEMBL
  C9JAH2_HUMAN UniProtKB/TrEMBL
  C9JBC2_HUMAN UniProtKB/TrEMBL
  C9JEB6_HUMAN UniProtKB/TrEMBL
  C9JF80_HUMAN UniProtKB/TrEMBL
  C9JGF5_HUMAN UniProtKB/TrEMBL
  C9JH46_HUMAN UniProtKB/TrEMBL
  C9JKN3_HUMAN UniProtKB/TrEMBL
  C9JNI4_HUMAN UniProtKB/TrEMBL
  C9JVZ1_HUMAN UniProtKB/TrEMBL
  C9JZ79_HUMAN UniProtKB/TrEMBL
  F8VWY3_HUMAN UniProtKB/TrEMBL
  H0YH91_HUMAN UniProtKB/TrEMBL
  H0YHJ5_HUMAN UniProtKB/TrEMBL
  H0YI15_HUMAN UniProtKB/TrEMBL
  H0YI41_HUMAN UniProtKB/TrEMBL
  HDAC7_HUMAN UniProtKB/Swiss-Prot
  J3KPH8 ENTREZGENE, UniProtKB/TrEMBL
  Q6P1W9 ENTREZGENE
  Q6W9G7 ENTREZGENE
  Q7Z4K2 ENTREZGENE
  Q7Z5I1 ENTREZGENE
  Q8WUI4 ENTREZGENE
  Q96K01 ENTREZGENE
  Q9BR73 ENTREZGENE
  Q9H7L0 ENTREZGENE
  Q9NW41 ENTREZGENE
  Q9NWA9 ENTREZGENE
  Q9NYK9 ENTREZGENE
  Q9UFU7 ENTREZGENE
UniProt Secondary B3KY08 UniProtKB/Swiss-Prot
  B4DWI0 UniProtKB/Swiss-Prot
  B4E0Q5 UniProtKB/Swiss-Prot
  C9JS90 UniProtKB/TrEMBL
  Q6P1W9 UniProtKB/Swiss-Prot
  Q6W9G7 UniProtKB/Swiss-Prot
  Q7Z4K2 UniProtKB/Swiss-Prot
  Q7Z5I1 UniProtKB/Swiss-Prot
  Q96K01 UniProtKB/Swiss-Prot
  Q9BR73 UniProtKB/Swiss-Prot
  Q9H7L0 UniProtKB/Swiss-Prot
  Q9NW41 UniProtKB/Swiss-Prot
  Q9NWA9 UniProtKB/Swiss-Prot
  Q9NYK9 UniProtKB/Swiss-Prot
  Q9UFU7 UniProtKB/Swiss-Prot