TET1 (tet methylcytosine dioxygenase 1) - Rat Genome Database

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Gene: TET1 (tet methylcytosine dioxygenase 1) Homo sapiens
Analyze
Symbol: TET1
Name: tet methylcytosine dioxygenase 1
RGD ID: 1322209
HGNC Page HGNC:29484
Description: Enables 5-methylcytosine dioxygenase activity; sequence-specific DNA binding activity; and transition metal ion binding activity. Involved in cellular response to reactive oxygen species; positive regulation of gene expression via chromosomal CpG island demethylation; and positive regulation of transcription by RNA polymerase II. Predicted to be located in chromosome. Predicted to be part of Sin3-type complex. Predicted to be active in nucleus. Biomarker of hepatocellular carcinoma.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: bA119F7.1; CXXC finger 6; CXXC zinc finger 6; CXXC-type zinc finger protein 6; CXXC6; FLJ10839; FLJ41442; KIAA1676; LCX; leukemia-associated protein with a CXXC domain; methylcytosine dioxygenase TET1; MLL-TET1; ten-eleven translocation 1 gene protein; ten-eleven translocation-1; tet oncogene 1; TET1 splice variant VP_DE4; TET1 splice variant VP_DE456; TET1-MLL
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Related Pseudogenes: TET1P1  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381068,560,337 - 68,694,487 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1068,560,337 - 68,694,487 (+)EnsemblGRCh38hg38GRCh38
GRCh371070,320,094 - 70,454,244 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361069,990,123 - 70,124,245 (+)NCBINCBI36Build 36hg18NCBI36
Build 341069,990,418 - 70,123,454NCBI
Celera1063,596,035 - 63,730,160 (+)NCBICelera
Cytogenetic Map10q21.3NCBI
HuRef1064,321,678 - 64,456,326 (+)NCBIHuRef
CHM1_11070,602,173 - 70,737,025 (+)NCBICHM1_1
T2T-CHM13v2.01069,429,559 - 69,563,685 (+)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
17alpha-ethynylestradiol  (ISO)
2,2',4,4'-Tetrabromodiphenyl ether  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (EXP)
3,4-methylenedioxymethamphetamine  (ISO)
4,4'-sulfonyldiphenol  (EXP,ISO)
5-(hydroxymethyl)cytosine  (ISO)
5-methylcytosine  (ISO)
6-propyl-2-thiouracil  (ISO)
acrylamide  (EXP,ISO)
aflatoxin B1  (EXP)
all-trans-retinoic acid  (ISO)
allethrin  (ISO)
alpha-Zearalanol  (ISO)
amitrole  (ISO)
amphetamine  (ISO)
antirheumatic drug  (EXP)
aristolochic acid A  (EXP)
arsenous acid  (ISO)
atrazine  (EXP)
azathioprine  (EXP)
benzo[a]pyrene  (EXP)
bilirubin IXalpha  (ISO)
bis(2-ethylhexyl) phthalate  (ISO)
bisphenol A  (ISO)
Bisphenol A diglycidyl ether  (ISO)
bisphenol AF  (ISO)
bisphenol F  (EXP)
buta-1,3-diene  (ISO)
butanal  (EXP)
cadmium atom  (ISO)
cadmium dichloride  (ISO)
carbamazepine  (EXP)
carbon nanotube  (ISO)
chloroprene  (ISO)
copper(II) sulfate  (ISO)
Cuprizon  (ISO)
cyclosporin A  (EXP)
cyhalothrin  (ISO)
cypermethrin  (ISO)
DDE  (EXP)
DDT  (ISO)
diarsenic trioxide  (ISO)
dicrotophos  (EXP)
dioxygen  (ISO)
dorsomorphin  (EXP)
doxorubicin  (EXP)
endosulfan  (ISO)
ethanol  (ISO)
fenvalerate  (ISO)
folic acid  (ISO)
Geniposide  (EXP)
gentamycin  (ISO)
glutathione  (EXP)
hydrogen peroxide  (EXP)
hydroquinone  (EXP,ISO)
ibuprofen  (EXP,ISO)
L-ascorbic acid  (EXP)
lead diacetate  (ISO)
lead(0)  (EXP)
lipopolysaccharide  (EXP)
malathion  (ISO)
melphalan  (EXP)
methimazole  (ISO)
methotrexate  (EXP)
methylmercury chloride  (EXP)
morphine  (ISO)
N-acetyl-L-cysteine  (EXP,ISO)
N-methyl-4-phenylpyridinium  (EXP)
nickel atom  (EXP)
nickel dichloride  (EXP)
ozone  (ISO)
paracetamol  (EXP,ISO)
paraquat  (ISO)
pentanal  (EXP)
perfluorooctane-1-sulfonic acid  (EXP)
perfluorooctanoic acid  (EXP,ISO)
permethrin  (ISO)
phenylmercury acetate  (EXP)
pioglitazone  (ISO)
pirinixic acid  (ISO)
pregnenolone 16alpha-carbonitrile  (ISO)
pyrethrins  (ISO)
quercetin  (EXP)
resorcinol  (EXP)
S-(1,2-dichlorovinyl)-L-cysteine  (EXP)
SB 431542  (EXP)
silver atom  (EXP)
silver(0)  (EXP)
sodium arsenite  (EXP,ISO)
sulfadimethoxine  (ISO)
tert-butyl hydroperoxide  (EXP)
tetrachloro-1,4-benzoquinone  (ISO)
tetrachlorohydroquinone  (ISO)
thimerosal  (EXP)
titanium dioxide  (ISO)
triphenyl phosphate  (EXP)
valproic acid  (EXP,ISO)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
chromosome  (IEA)
nucleus  (IBA,IC,IEA,NAS)
Sin3-type complex  (NAS)

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. Cancer epigenetics: from mechanism to therapy. Dawson MA and Kouzarides T, Cell. 2012 Jul 6;150(1):12-27. doi: 10.1016/j.cell.2012.06.013.
2. Playing TETris with DNA modifications. Delatte B, etal., EMBO J. 2014 Jun 2;33(11):1198-211. doi: 10.15252/embj.201488290. Epub 2014 May 13.
3. Decrease of 5-hydroxymethylcytosine is associated with progression of hepatocellular carcinoma through downregulation of TET1. Liu C, etal., PLoS One. 2013 May 9;8(5):e62828. doi: 10.1371/journal.pone.0062828. Print 2013.
4. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:11214970   PMID:12124344   PMID:12477932   PMID:12646957   PMID:15164054   PMID:15489334   PMID:16385451   PMID:18029348   PMID:18163421   PMID:19144982   PMID:19372391   PMID:19420352  
PMID:19923888   PMID:21251613   PMID:21311766   PMID:21496894   PMID:21873635   PMID:22196727   PMID:22320381   PMID:22688054   PMID:22865885   PMID:22948384   PMID:22984288   PMID:22999938  
PMID:23100278   PMID:23213213   PMID:23328087   PMID:23685628   PMID:23716660   PMID:23818607   PMID:23820384   PMID:23938174   PMID:24323992   PMID:24325350   PMID:24469454   PMID:24507562  
PMID:24743738   PMID:24804542   PMID:24835990   PMID:24875481   PMID:24915579   PMID:24958354   PMID:25089631   PMID:25175940   PMID:25284789   PMID:25362856   PMID:25367851   PMID:25466250  
PMID:25476119   PMID:25517638   PMID:25557551   PMID:25568311   PMID:25735355   PMID:25824049   PMID:25925565   PMID:26013976   PMID:26063725   PMID:26136340   PMID:26165803   PMID:26207381  
PMID:26294212   PMID:26356709   PMID:26376879   PMID:26524525   PMID:26546041   PMID:26631571   PMID:26684294   PMID:26703470   PMID:26711177   PMID:26776158   PMID:26791235   PMID:26917261  
PMID:26931431   PMID:27014907   PMID:27121319   PMID:27225590   PMID:27251462   PMID:27257062   PMID:27346347   PMID:27705803   PMID:27733505   PMID:27846738   PMID:27977763   PMID:28150354  
PMID:28218476   PMID:28228863   PMID:28249902   PMID:28252217   PMID:28294974   PMID:28349832   PMID:28351182   PMID:28449087   PMID:28513825   PMID:28524723   PMID:28531272   PMID:28554894  
PMID:28643947   PMID:28648900   PMID:28661477   PMID:28731456   PMID:28758831   PMID:28776568   PMID:28808304   PMID:28851501   PMID:28923852   PMID:29108636   PMID:29186571   PMID:29235481  
PMID:29276034   PMID:29277934   PMID:29395067   PMID:29402726   PMID:29449217   PMID:29484426   PMID:29512746   PMID:29531217   PMID:29549908   PMID:29659445   PMID:29715584   PMID:29891505  
PMID:29938218   PMID:30045709   PMID:30058675   PMID:30074219   PMID:30075814   PMID:30130982   PMID:30249104   PMID:30279502   PMID:30362292   PMID:30367454   PMID:30411496   PMID:30431097  
PMID:30551127   PMID:30554333   PMID:30606231   PMID:30617255   PMID:30635654   PMID:30651599   PMID:30735628   PMID:30771438   PMID:30784212   PMID:30809307   PMID:30825236   PMID:30883733  
PMID:31022963   PMID:31089182   PMID:31153371   PMID:31167695   PMID:31216336   PMID:31266538   PMID:31304631   PMID:31399111   PMID:31616436   PMID:31623662   PMID:31935962   PMID:31941838  
PMID:31994732   PMID:32003827   PMID:32024762   PMID:32295898   PMID:32342329   PMID:32374060   PMID:32385352   PMID:32483272   PMID:32542727   PMID:32574963   PMID:32587369   PMID:32730644  
PMID:32740973   PMID:32863235   PMID:32913111   PMID:32919305   PMID:33120142   PMID:33126331   PMID:33142244   PMID:33358913   PMID:33410283   PMID:33493518   PMID:33684567   PMID:33878446  
PMID:33926529   PMID:33961781   PMID:33970549   PMID:34079125   PMID:34349018   PMID:34435328   PMID:34628789   PMID:34644730   PMID:34667079   PMID:34709266   PMID:34731191   PMID:34844636  
PMID:34879277   PMID:34926132   PMID:35235761   PMID:35271311   PMID:35290126   PMID:35395805   PMID:35439318   PMID:35489280   PMID:35627266   PMID:35650007   PMID:35798741   PMID:35835915  
PMID:35942521   PMID:35998875   PMID:36056023   PMID:36195596   PMID:36413827   PMID:36682704   PMID:36692670   PMID:36931259   PMID:37020036   PMID:37121742   PMID:37347215   PMID:37430206  
PMID:37474847   PMID:37562656   PMID:37610277   PMID:37643326   PMID:37788672   PMID:37995981   PMID:38280479   PMID:38297188   PMID:38334954   PMID:38369780   PMID:38431880   PMID:39358380  


Genomics

Comparative Map Data
TET1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381068,560,337 - 68,694,487 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1068,560,337 - 68,694,487 (+)EnsemblGRCh38hg38GRCh38
GRCh371070,320,094 - 70,454,244 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361069,990,123 - 70,124,245 (+)NCBINCBI36Build 36hg18NCBI36
Build 341069,990,418 - 70,123,454NCBI
Celera1063,596,035 - 63,730,160 (+)NCBICelera
Cytogenetic Map10q21.3NCBI
HuRef1064,321,678 - 64,456,326 (+)NCBIHuRef
CHM1_11070,602,173 - 70,737,025 (+)NCBICHM1_1
T2T-CHM13v2.01069,429,559 - 69,563,685 (+)NCBIT2T-CHM13v2.0
Tet1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391062,640,349 - 62,723,242 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1062,640,349 - 62,744,775 (-)EnsemblGRCm39 Ensembl
GRCm381062,804,570 - 62,887,469 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1062,804,570 - 62,908,996 (-)EnsemblGRCm38mm10GRCm38
MGSCv371062,267,318 - 62,342,762 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361062,207,059 - 62,275,371 (-)NCBIMGSCv36mm8
Celera1063,905,755 - 63,981,217 (-)NCBICelera
Cytogenetic Map10B4NCBI
cM Map1032.48NCBI
Tet1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr82025,766,806 - 25,839,598 (+)NCBIGRCr8
mRatBN7.22025,761,042 - 25,840,926 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl2025,768,120 - 25,833,052 (+)EnsemblmRatBN7.2 Ensembl
Rnor_6.02027,359,122 - 27,438,039 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl2027,366,213 - 27,437,427 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.02029,200,519 - 29,267,971 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.42025,131,169 - 25,155,785 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.12025,145,587 - 25,220,858 (-)NCBI
Celera2027,057,215 - 27,136,909 (+)NCBICelera
Cytogenetic Map20q11NCBI
Tet1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0NW_00495542520,767,406 - 20,857,165 (+)NCBIChiLan1.0ChiLan1.0
TET1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2880,712,893 - 80,853,460 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11080,718,227 - 80,858,781 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01065,036,313 - 65,168,051 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11067,575,157 - 67,705,834 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1067,586,586 - 67,703,160 (+)Ensemblpanpan1.1panPan2
TET1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1419,759,661 - 19,898,345 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl419,768,137 - 19,889,907 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha419,891,023 - 20,029,547 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0420,031,603 - 20,170,708 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl420,040,122 - 20,165,077 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1419,932,890 - 20,071,946 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0420,135,757 - 20,275,156 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0420,478,282 - 20,617,403 (+)NCBIUU_Cfam_GSD_1.0
TET1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1471,675,671 - 71,815,618 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11471,675,671 - 71,812,732 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21477,728,167 - 77,830,058 (+)NCBISscrofa10.2Sscrofa10.2susScr3
TET1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1962,709,800 - 62,843,322 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl962,712,484 - 62,837,138 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604823,461,866 - 23,597,039 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Tet1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247542,873,456 - 2,965,097 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247542,846,479 - 2,966,845 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in TET1
183 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 10q21.2-22.2(chr10:62229688-74468143)x1 copy number loss See cases [RCV000052530] Chr10:62229688..74468143 [GRCh38]
Chr10:63989447..76227901 [GRCh37]
Chr10:63659453..75897907 [NCBI36]
Chr10:10q21.2-22.2		 pathogenic
GRCh38/hg38 10q21.1-22.2(chr10:58436466-74415216)x1 copy number loss See cases [RCV000052511] Chr10:58436466..74415216 [GRCh38]
Chr10:60196226..76174974 [GRCh37]
Chr10:59866232..75844980 [NCBI36]
Chr10:10q21.1-22.2		 pathogenic
GRCh38/hg38 10q21.3-22.1(chr10:68543815-68977524)x1 copy number loss See cases [RCV000134927] Chr10:68543815..68977524 [GRCh38]
Chr10:70303572..70737280 [GRCh37]
Chr10:69973578..70407286 [NCBI36]
Chr10:10q21.3-22.1		 likely benign|uncertain significance
GRCh38/hg38 10q11.21-22.2(chr10:42685306-73715908)x3 copy number gain See cases [RCV000134848] Chr10:42685306..73715908 [GRCh38]
Chr10:43180754..75475666 [GRCh37]
Chr10:42500760..75145672 [NCBI36]
Chr10:10q11.21-22.2		 pathogenic
GRCh38/hg38 10q21.3-22.3(chr10:67196567-79422057)x3 copy number gain See cases [RCV000135438] Chr10:67196567..79422057 [GRCh38]
Chr10:68956325..81181813 [GRCh37]
Chr10:68626331..80851819 [NCBI36]
Chr10:10q21.3-22.3		 pathogenic
GRCh38/hg38 10q21.3-22.2(chr10:63402579-75296099)x1 copy number loss See cases [RCV000136658] Chr10:63402579..75296099 [GRCh38]
Chr10:65162339..77055857 [GRCh37]
Chr10:64832345..76725863 [NCBI36]
Chr10:10q21.3-22.2		 pathogenic|likely benign
GRCh38/hg38 10q11.23-23.2(chr10:50729367-87147204)x3 copy number gain See cases [RCV000138007] Chr10:50729367..87147204 [GRCh38]
Chr10:52489127..88906961 [GRCh37]
Chr10:52159133..88896941 [NCBI36]
Chr10:10q11.23-23.2		 pathogenic
GRCh37/hg19 10q21.3(chr10:70178856-70396017)x3 copy number gain See cases [RCV000239824] Chr10:70178856..70396017 [GRCh37]
Chr10:10q21.3		 uncertain significance
GRCh37/hg19 10q21.3(chr10:70048400-70580859)x3 copy number gain See cases [RCV000448733] Chr10:70048400..70580859 [GRCh37]
Chr10:10q21.3		 likely benign
GRCh37/hg19 10p15.3-q26.3(chr10:93297-135378918)x3 copy number gain See cases [RCV000448750] Chr10:93297..135378918 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143) copy number gain See cases [RCV000511389] Chr10:100027..135427143 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic|uncertain significance
GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143)x3 copy number gain See cases [RCV000510861] Chr10:100027..135427143 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic
NM_030625.3(TET1):c.2759A>C (p.Glu920Ala) single nucleotide variant not specified [RCV004313213] Chr10:68645488 [GRCh38]
Chr10:70405245 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.2760G>T (p.Glu920Asp) single nucleotide variant not specified [RCV004313215] Chr10:68645489 [GRCh38]
Chr10:70405246 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.3062T>C (p.Ile1021Thr) single nucleotide variant not specified [RCV004288712] Chr10:68645791 [GRCh38]
Chr10:70405548 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.830T>C (p.Val277Ala) single nucleotide variant not specified [RCV004303302] Chr10:68573168 [GRCh38]
Chr10:70332925 [GRCh37]
Chr10:10q21.3		 uncertain significance
GRCh37/hg19 10q11.21-26.3(chr10:42347406-135534747)x1 copy number loss Poly (ADP-Ribose) polymerase inhibitor response [RCV000626438] Chr10:42347406..135534747 [GRCh37]
Chr10:10q11.21-26.3		 drug response
NM_030625.3(TET1):c.5173A>G (p.Met1725Val) single nucleotide variant not specified [RCV004297202] Chr10:68686476 [GRCh38]
Chr10:70446233 [GRCh37]
Chr10:10q21.3		 uncertain significance
GRCh37/hg19 10q21.3-22.1(chr10:68394411-70673475)x1 copy number loss not provided [RCV000513331] Chr10:68394411..70673475 [GRCh37]
Chr10:10q21.3-22.1		 likely pathogenic
GRCh37/hg19 10q21.3-23.32(chr10:69040366-93194993)x3 copy number gain not provided [RCV000683289] Chr10:69040366..93194993 [GRCh37]
Chr10:10q21.3-23.32		 pathogenic
GRCh37/hg19 10q21.3(chr10:70102749-70332271)x3 copy number gain not provided [RCV000737177] Chr10:70102749..70332271 [GRCh37]
Chr10:10q21.3		 benign
GRCh37/hg19 10p15.3-q26.3(chr10:98087-135477883)x3 copy number gain not provided [RCV000749465] Chr10:98087..135477883 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:73232-135524321)x3 copy number gain not provided [RCV000749464] Chr10:73232..135524321 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic
NM_030625.3(TET1):c.5235G>A (p.Thr1745=) single nucleotide variant not provided [RCV000971777] Chr10:68686538 [GRCh38]
Chr10:70446295 [GRCh37]
Chr10:10q21.3		 benign|likely benign
NM_030625.3(TET1):c.2495G>A (p.Cys832Tyr) single nucleotide variant not provided [RCV000959108] Chr10:68645224 [GRCh38]
Chr10:70404981 [GRCh37]
Chr10:10q21.3		 benign
NM_030625.3(TET1):c.4509G>C (p.Arg1503=) single nucleotide variant TET1-related disorder [RCV003936124]|not provided [RCV000971567] Chr10:68667092 [GRCh38]
Chr10:70426849 [GRCh37]
Chr10:10q21.3		 benign
NM_030625.3(TET1):c.4261A>G (p.Thr1421Ala) single nucleotide variant TET1-related disorder [RCV003926263]|not provided [RCV000965723] Chr10:68646990 [GRCh38]
Chr10:70406747 [GRCh37]
Chr10:10q21.3		 benign
NM_030625.3(TET1):c.6387G>A (p.Ala2129=) single nucleotide variant not provided [RCV000947258] Chr10:68691790 [GRCh38]
Chr10:70451547 [GRCh37]
Chr10:10q21.3		 benign
NM_030625.3(TET1):c.2953G>T (p.Ala985Ser) single nucleotide variant TET1-related disorder [RCV003926098]|not provided [RCV000959109] Chr10:68645682 [GRCh38]
Chr10:70405439 [GRCh37]
Chr10:10q21.3		 benign
NM_030625.3(TET1):c.516A>C (p.Leu172=) single nucleotide variant TET1-related disorder [RCV003942951]|not provided [RCV000938984] Chr10:68572854 [GRCh38]
Chr10:70332611 [GRCh37]
Chr10:10q21.3		 benign|likely benign
NM_030625.3(TET1):c.3840A>C (p.Lys1280Asn) single nucleotide variant not specified [RCV004318587] Chr10:68646569 [GRCh38]
Chr10:70406326 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.5060C>G (p.Thr1687Ser) single nucleotide variant not specified [RCV004300285] Chr10:68686363 [GRCh38]
Chr10:70446120 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.2102G>A (p.Ser701Asn) single nucleotide variant not provided [RCV000960268] Chr10:68644831 [GRCh38]
Chr10:70404588 [GRCh37]
Chr10:10q21.3		 benign
NM_030625.3(TET1):c.496C>T (p.Leu166Phe) single nucleotide variant TET1-related disorder [RCV003940770]|not provided [RCV000895400] Chr10:68572834 [GRCh38]
Chr10:70332591 [GRCh37]
Chr10:10q21.3		 benign
GRCh37/hg19 10q21.3(chr10:70290828-70428321)x3 copy number gain not provided [RCV000847905] Chr10:70290828..70428321 [GRCh37]
Chr10:10q21.3		 uncertain significance
GRCh37/hg19 10q21.3(chr10:70169551-70426424)x3 copy number gain not provided [RCV000849585] Chr10:70169551..70426424 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.2372A>T (p.Tyr791Phe) single nucleotide variant not specified [RCV004301631] Chr10:68645101 [GRCh38]
Chr10:70404858 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.5362A>G (p.Thr1788Ala) single nucleotide variant not specified [RCV004301632] Chr10:68686665 [GRCh38]
Chr10:70446422 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.2406C>T (p.Asn802=) single nucleotide variant TET1-related disorder [RCV003970614]|not provided [RCV000938985] Chr10:68645135 [GRCh38]
Chr10:70404892 [GRCh37]
Chr10:10q21.3		 benign|likely benign
NM_030625.3(TET1):c.1303G>A (p.Val435Ile) single nucleotide variant not provided [RCV000955416] Chr10:68573641 [GRCh38]
Chr10:70333398 [GRCh37]
Chr10:10q21.3		 benign
NM_030625.3(TET1):c.5763C>T (p.Leu1921=) single nucleotide variant not provided [RCV000955417] Chr10:68691166 [GRCh38]
Chr10:70450923 [GRCh37]
Chr10:10q21.3		 benign
NM_030625.3(TET1):c.2751G>A (p.Glu917=) single nucleotide variant not provided [RCV001665260] Chr10:68645480 [GRCh38]
Chr10:68645480..68645481 [GRCh38]
Chr10:70405237 [GRCh37]
Chr10:70405237..70405238 [GRCh37]
Chr10:10q21.3		 benign
NM_030625.3(TET1):c.5904G>A (p.Glu1968=) single nucleotide variant not provided [RCV000957624] Chr10:68691307 [GRCh38]
Chr10:70451064 [GRCh37]
Chr10:10q21.3		 benign
NM_030625.3(TET1):c.5378G>A (p.Ser1793Asn) single nucleotide variant not provided [RCV000889904] Chr10:68686681 [GRCh38]
Chr10:70446438 [GRCh37]
Chr10:10q21.3		 benign
GRCh37/hg19 10q21.3-22.3(chr10:68735254-78885714) copy number loss not specified [RCV002052875] Chr10:68735254..78885714 [GRCh37]
Chr10:10q21.3-22.3		 pathogenic
NC_000010.10:g.(?_67680088)_(71332799_?)del deletion not provided [RCV001956019] Chr10:67680088..71332799 [GRCh37]
Chr10:10q21.3-22.1		 pathogenic|uncertain significance
NM_030625.3(TET1):c.3974T>A (p.Val1325Asp) single nucleotide variant not provided [RCV003120323] Chr10:68646703 [GRCh38]
Chr10:70406460 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.664C>T (p.Arg222Cys) single nucleotide variant not specified [RCV004233720] Chr10:68573002 [GRCh38]
Chr10:70332759 [GRCh37]
Chr10:10q21.3		 likely benign
NM_030625.3(TET1):c.3473G>A (p.Arg1158Gln) single nucleotide variant not specified [RCV004333094] Chr10:68646202 [GRCh38]
Chr10:70405959 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.5687C>T (p.Ala1896Val) single nucleotide variant not specified [RCV004169157] Chr10:68691090 [GRCh38]
Chr10:70450847 [GRCh37]
Chr10:10q21.3		 likely benign
NM_030625.3(TET1):c.3877A>T (p.Asn1293Tyr) single nucleotide variant not specified [RCV004111100] Chr10:68646606 [GRCh38]
Chr10:70406363 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.5165A>G (p.Lys1722Arg) single nucleotide variant not specified [RCV004136905] Chr10:68686468 [GRCh38]
Chr10:70446225 [GRCh37]
Chr10:10q21.3		 likely benign
NM_030625.3(TET1):c.2288T>A (p.Val763Glu) single nucleotide variant not specified [RCV004100904] Chr10:68645017 [GRCh38]
Chr10:70404774 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.2464G>A (p.Val822Ile) single nucleotide variant not specified [RCV004194971] Chr10:68645193 [GRCh38]
Chr10:70404950 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.3742C>G (p.Pro1248Ala) single nucleotide variant not specified [RCV004160963] Chr10:68646471 [GRCh38]
Chr10:70406228 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.1444A>C (p.Asn482His) single nucleotide variant not specified [RCV004090123] Chr10:68573782 [GRCh38]
Chr10:70333539 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.5509G>A (p.Ala1837Thr) single nucleotide variant not specified [RCV004191256] Chr10:68690912 [GRCh38]
Chr10:70450669 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.3214C>A (p.Gln1072Lys) single nucleotide variant not specified [RCV004236185] Chr10:68645943 [GRCh38]
Chr10:70405700 [GRCh37]
Chr10:10q21.3		 likely benign
NM_030625.3(TET1):c.4040C>G (p.Pro1347Arg) single nucleotide variant not specified [RCV004189707] Chr10:68646769 [GRCh38]
Chr10:70406526 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.1897G>A (p.Val633Ile) single nucleotide variant not specified [RCV004236014] Chr10:68574235 [GRCh38]
Chr10:70333992 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.5714G>A (p.Gly1905Asp) single nucleotide variant not specified [RCV004115491] Chr10:68691117 [GRCh38]
Chr10:70450874 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.4067T>C (p.Val1356Ala) single nucleotide variant not specified [RCV004145409] Chr10:68646796 [GRCh38]
Chr10:70406553 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.5596G>C (p.Ala1866Pro) single nucleotide variant not specified [RCV004140492] Chr10:68690999 [GRCh38]
Chr10:70450756 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.2912A>G (p.Asn971Ser) single nucleotide variant not specified [RCV004141702] Chr10:68645641 [GRCh38]
Chr10:70405398 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.2164G>A (p.Val722Met) single nucleotide variant not specified [RCV004209280] Chr10:68644893 [GRCh38]
Chr10:70404650 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.5234C>T (p.Thr1745Met) single nucleotide variant not specified [RCV004243596] Chr10:68686537 [GRCh38]
Chr10:70446294 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.1277T>C (p.Val426Ala) single nucleotide variant not specified [RCV004247206] Chr10:68573615 [GRCh38]
Chr10:70333372 [GRCh37]
Chr10:10q21.3		 likely benign
NM_030625.3(TET1):c.2029T>A (p.Cys677Ser) single nucleotide variant not specified [RCV004175040] Chr10:68644758 [GRCh38]
Chr10:70404515 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.2914G>T (p.Gly972Trp) single nucleotide variant not specified [RCV004118296] Chr10:68645643 [GRCh38]
Chr10:70405400 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.788A>G (p.Gln263Arg) single nucleotide variant not specified [RCV004148237] Chr10:68573126 [GRCh38]
Chr10:70332883 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.2164G>T (p.Val722Leu) single nucleotide variant not specified [RCV004219145] Chr10:68644893 [GRCh38]
Chr10:70404650 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.3508G>C (p.Glu1170Gln) single nucleotide variant not specified [RCV004231811] Chr10:68646237 [GRCh38]
Chr10:70405994 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.695C>T (p.Thr232Ile) single nucleotide variant not specified [RCV004148270] Chr10:68573033 [GRCh38]
Chr10:70332790 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.1284C>G (p.Asp428Glu) single nucleotide variant not specified [RCV004143942] Chr10:68573622 [GRCh38]
Chr10:70333379 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.4046C>T (p.Ser1349Leu) single nucleotide variant not specified [RCV004165223] Chr10:68646775 [GRCh38]
Chr10:70406532 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.3346T>C (p.Tyr1116His) single nucleotide variant not specified [RCV004134286] Chr10:68646075 [GRCh38]
Chr10:70405832 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.3545T>G (p.Met1182Arg) single nucleotide variant not specified [RCV004202323] Chr10:68646274 [GRCh38]
Chr10:70406031 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.4910A>G (p.Asn1637Ser) single nucleotide variant not specified [RCV004129516] Chr10:68681484 [GRCh38]
Chr10:70441241 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.176A>G (p.Lys59Arg) single nucleotide variant not specified [RCV004181867] Chr10:68572514 [GRCh38]
Chr10:70332271 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.3364A>G (p.Thr1122Ala) single nucleotide variant not specified [RCV004132306] Chr10:68646093 [GRCh38]
Chr10:70405850 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.242G>C (p.Arg81Pro) single nucleotide variant not specified [RCV004106646] Chr10:68572580 [GRCh38]
Chr10:70332337 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.686C>T (p.Ser229Phe) single nucleotide variant not specified [RCV004114642] Chr10:68573024 [GRCh38]
Chr10:70332781 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.1150G>T (p.Val384Phe) single nucleotide variant not specified [RCV004175951] Chr10:68573488 [GRCh38]
Chr10:70333245 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.2198C>T (p.Ala733Val) single nucleotide variant not specified [RCV004176958] Chr10:68644927 [GRCh38]
Chr10:70404684 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.1534A>G (p.Thr512Ala) single nucleotide variant not specified [RCV004069579] Chr10:68573872 [GRCh38]
Chr10:70333629 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.3091T>C (p.Cys1031Arg) single nucleotide variant not specified [RCV004283068] Chr10:68645820 [GRCh38]
Chr10:70405577 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.419G>A (p.Cys140Tyr) single nucleotide variant not specified [RCV004270976] Chr10:68572757 [GRCh38]
Chr10:70332514 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.5891C>T (p.Ser1964Phe) single nucleotide variant not specified [RCV004287483] Chr10:68691294 [GRCh38]
Chr10:70451051 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.38T>C (p.Val13Ala) single nucleotide variant not specified [RCV004270179] Chr10:68572376 [GRCh38]
Chr10:70332133 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.4317C>G (p.His1439Gln) single nucleotide variant not specified [RCV004272247] Chr10:68651886 [GRCh38]
Chr10:70411643 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.3866C>T (p.Thr1289Met) single nucleotide variant not specified [RCV004255667] Chr10:68646595 [GRCh38]
Chr10:70406352 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.2030G>A (p.Cys677Tyr) single nucleotide variant not specified [RCV004330124] Chr10:68644759 [GRCh38]
Chr10:70404516 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.4085G>A (p.Gly1362Asp) single nucleotide variant not specified [RCV004261088] Chr10:68646814 [GRCh38]
Chr10:70406571 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.5776C>G (p.Pro1926Ala) single nucleotide variant not specified [RCV004272487] Chr10:68691179 [GRCh38]
Chr10:70450936 [GRCh37]
Chr10:10q21.3		 uncertain significance
GRCh37/hg19 10p13-q26.3(chr10:12829206-135427143) copy number loss Distal 10q deletion syndrome [RCV003319583] Chr10:12829206..135427143 [GRCh37]
Chr10:10p13-q26.3		 pathogenic
NM_030625.3(TET1):c.3826G>A (p.Ala1276Thr) single nucleotide variant not specified [RCV004290148] Chr10:68646555 [GRCh38]
Chr10:70406312 [GRCh37]
Chr10:10q21.3		 uncertain significance
GRCh37/hg19 10p14-q26.3(chr10:11138692-135427143) copy number gain Distal trisomy 10q [RCV003319593] Chr10:11138692..135427143 [GRCh37]
Chr10:10p14-q26.3		 pathogenic
NM_030625.3(TET1):c.418T>C (p.Cys140Arg) single nucleotide variant not specified [RCV004356853] Chr10:68572756 [GRCh38]
Chr10:70332513 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.2774G>A (p.Ser925Asn) single nucleotide variant not specified [RCV004354240] Chr10:68645503 [GRCh38]
Chr10:70405260 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.253G>A (p.Asp85Asn) single nucleotide variant not specified [RCV004341553] Chr10:68572591 [GRCh38]
Chr10:70332348 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.1454A>C (p.Lys485Thr) single nucleotide variant not specified [RCV004365206] Chr10:68573792 [GRCh38]
Chr10:70333549 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.5994G>C (p.Glu1998Asp) single nucleotide variant not specified [RCV004359754] Chr10:68691397 [GRCh38]
Chr10:70451154 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.5422G>A (p.Val1808Met) single nucleotide variant TET1-related disorder [RCV003939050]|not provided [RCV003456705] Chr10:68690825 [GRCh38]
Chr10:70450582 [GRCh37]
Chr10:10q21.3		 likely benign
GRCh37/hg19 10q11.21-24.2(chr10:42709645-100834951)x3 copy number gain not provided [RCV003484798] Chr10:42709645..100834951 [GRCh37]
Chr10:10q11.21-24.2		 pathogenic
GRCh37/hg19 10q11.23-22.1(chr10:51735638-70791246)x1 copy number loss not provided [RCV003483092] Chr10:51735638..70791246 [GRCh37]
Chr10:10q11.23-22.1		 pathogenic
NM_030625.3(TET1):c.775A>G (p.Lys259Glu) single nucleotide variant not provided [RCV003417446] Chr10:68573113 [GRCh38]
Chr10:70332870 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.2823C>T (p.Leu941=) single nucleotide variant not provided [RCV003417447] Chr10:68645552 [GRCh38]
Chr10:70405309 [GRCh37]
Chr10:10q21.3		 likely benign
NM_030625.3(TET1):c.5053-3C>T single nucleotide variant not provided [RCV003417448] Chr10:68686353 [GRCh38]
Chr10:70446110 [GRCh37]
Chr10:10q21.3		 likely benign
NM_030625.3(TET1):c.5716G>A (p.Glu1906Lys) single nucleotide variant not provided [RCV003491666] Chr10:68691119 [GRCh38]
Chr10:70450876 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.5916C>T (p.Asp1972=) single nucleotide variant TET1-related disorder [RCV003907385] Chr10:68691319 [GRCh38]
Chr10:70451076 [GRCh37]
Chr10:10q21.3		 likely benign
NM_030625.3(TET1):c.2298A>G (p.Leu766=) single nucleotide variant TET1-related disorder [RCV003909276] Chr10:68645027 [GRCh38]
Chr10:70404784 [GRCh37]
Chr10:10q21.3		 likely benign
NM_030625.3(TET1):c.260C>G (p.Thr87Ser) single nucleotide variant TET1-related disorder [RCV003924748] Chr10:68572598 [GRCh38]
Chr10:70332355 [GRCh37]
Chr10:10q21.3		 likely benign
NM_030625.3(TET1):c.5496G>A (p.Ser1832=) single nucleotide variant TET1-related disorder [RCV003971633] Chr10:68690899 [GRCh38]
Chr10:70450656 [GRCh37]
Chr10:10q21.3		 likely benign
NM_030625.3(TET1):c.6084C>T (p.His2028=) single nucleotide variant TET1-related disorder [RCV003943892] Chr10:68691487 [GRCh38]
Chr10:70451244 [GRCh37]
Chr10:10q21.3		 likely benign
NM_030625.3(TET1):c.1644C>T (p.Val548=) single nucleotide variant TET1-related disorder [RCV003957392] Chr10:68573982 [GRCh38]
Chr10:70333739 [GRCh37]
Chr10:10q21.3		 likely benign
NM_030625.3(TET1):c.5541C>T (p.Gly1847=) single nucleotide variant TET1-related disorder [RCV003927197] Chr10:68690944 [GRCh38]
Chr10:70450701 [GRCh37]
Chr10:10q21.3		 likely benign
NM_030625.3(TET1):c.3998G>A (p.Arg1333Lys) single nucleotide variant TET1-related disorder [RCV003969122] Chr10:68646727 [GRCh38]
Chr10:70406484 [GRCh37]
Chr10:10q21.3		 likely benign
NM_030625.3(TET1):c.2328A>G (p.Lys776=) single nucleotide variant TET1-related disorder [RCV003964177] Chr10:68645057 [GRCh38]
Chr10:70404814 [GRCh37]
Chr10:10q21.3		 benign
NM_030625.3(TET1):c.5106T>C (p.Asp1702=) single nucleotide variant TET1-related disorder [RCV003976903] Chr10:68686409 [GRCh38]
Chr10:70446166 [GRCh37]
Chr10:10q21.3		 likely benign
NM_030625.3(TET1):c.4215C>T (p.Asn1405=) single nucleotide variant TET1-related disorder [RCV003956961] Chr10:68646944 [GRCh38]
Chr10:70406701 [GRCh37]
Chr10:10q21.3		 likely benign
NM_030625.3(TET1):c.732T>C (p.Ala244=) single nucleotide variant TET1-related disorder [RCV003909701] Chr10:68573070 [GRCh38]
Chr10:70332827 [GRCh37]
Chr10:10q21.3		 likely benign
NM_030625.3(TET1):c.1022C>T (p.Ala341Val) single nucleotide variant not specified [RCV004472072] Chr10:68573360 [GRCh38]
Chr10:70333117 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.103A>G (p.Asn35Asp) single nucleotide variant not specified [RCV004472073] Chr10:68572441 [GRCh38]
Chr10:70332198 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.2554G>A (p.Glu852Lys) single nucleotide variant not specified [RCV004472079] Chr10:68645283 [GRCh38]
Chr10:70405040 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.3162C>G (p.Ser1054Arg) single nucleotide variant not specified [RCV004472087] Chr10:68645891 [GRCh38]
Chr10:70405648 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.3205A>T (p.Thr1069Ser) single nucleotide variant not specified [RCV004472088] Chr10:68645934 [GRCh38]
Chr10:70405691 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.3283C>T (p.Pro1095Ser) single nucleotide variant not specified [RCV004472089] Chr10:68646012 [GRCh38]
Chr10:70405769 [GRCh37]
Chr10:10q21.3		 likely benign
NM_030625.3(TET1):c.3454T>C (p.Ser1152Pro) single nucleotide variant not specified [RCV004472091] Chr10:68646183 [GRCh38]
Chr10:70405940 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.629C>T (p.Ala210Val) single nucleotide variant not specified [RCV004472106] Chr10:68572967 [GRCh38]
Chr10:70332724 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.1043C>G (p.Ala348Gly) single nucleotide variant not specified [RCV004472074] Chr10:68573381 [GRCh38]
Chr10:70333138 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.2746G>T (p.Asp916Tyr) single nucleotide variant not specified [RCV004472081] Chr10:68645475 [GRCh38]
Chr10:70405232 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.2851C>A (p.Pro951Thr) single nucleotide variant not specified [RCV004472083] Chr10:68645580 [GRCh38]
Chr10:70405337 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.2965G>A (p.Ala989Thr) single nucleotide variant not specified [RCV004472086] Chr10:68645694 [GRCh38]
Chr10:70405451 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.3989T>C (p.Met1330Thr) single nucleotide variant not specified [RCV004472097] Chr10:68646718 [GRCh38]
Chr10:70406475 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.5324A>G (p.Lys1775Arg) single nucleotide variant not specified [RCV004472102] Chr10:68686627 [GRCh38]
Chr10:70446384 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.2038G>T (p.Gly680Trp) single nucleotide variant not specified [RCV004472076] Chr10:68644767 [GRCh38]
Chr10:70404524 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.2586A>G (p.Ile862Met) single nucleotide variant not specified [RCV004472080] Chr10:68645315 [GRCh38]
Chr10:70405072 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.2770G>C (p.Ala924Pro) single nucleotide variant not specified [RCV004472082] Chr10:68645499 [GRCh38]
Chr10:70405256 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.2961C>A (p.Asn987Lys) single nucleotide variant not specified [RCV004472084] Chr10:68645690 [GRCh38]
Chr10:70405447 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.3518G>T (p.Arg1173Leu) single nucleotide variant not specified [RCV004472093] Chr10:68646247 [GRCh38]
Chr10:70406004 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.470C>T (p.Ser157Leu) single nucleotide variant not specified [RCV004472098] Chr10:68572808 [GRCh38]
Chr10:70332565 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.5270A>G (p.Lys1757Arg) single nucleotide variant not specified [RCV004472100] Chr10:68686573 [GRCh38]
Chr10:70446330 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.5630G>A (p.Ser1877Asn) single nucleotide variant not specified [RCV004472104] Chr10:68691033 [GRCh38]
Chr10:70450790 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.1822T>G (p.Tyr608Asp) single nucleotide variant not specified [RCV004472075] Chr10:68574160 [GRCh38]
Chr10:70333917 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.2219A>G (p.Glu740Gly) single nucleotide variant not specified [RCV004472077] Chr10:68644948 [GRCh38]
Chr10:70404705 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.2255T>G (p.Phe752Cys) single nucleotide variant not specified [RCV004472078] Chr10:68644984 [GRCh38]
Chr10:70404741 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.3448A>G (p.Thr1150Ala) single nucleotide variant not specified [RCV004472090] Chr10:68646177 [GRCh38]
Chr10:70405934 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.3502T>G (p.Tyr1168Asp) single nucleotide variant not specified [RCV004472092] Chr10:68646231 [GRCh38]
Chr10:70405988 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.364G>A (p.Val122Ile) single nucleotide variant not specified [RCV004472094] Chr10:68572702 [GRCh38]
Chr10:70332459 [GRCh37]
Chr10:10q21.3		 likely benign
NM_030625.3(TET1):c.3788T>C (p.Leu1263Pro) single nucleotide variant not specified [RCV004472095] Chr10:68646517 [GRCh38]
Chr10:70406274 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.3982C>A (p.Gln1328Lys) single nucleotide variant not specified [RCV004472096] Chr10:68646711 [GRCh38]
Chr10:70406468 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.5249C>T (p.Pro1750Leu) single nucleotide variant not specified [RCV004472099] Chr10:68686552 [GRCh38]
Chr10:70446309 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.5320G>C (p.Glu1774Gln) single nucleotide variant not specified [RCV004472101] Chr10:68686623 [GRCh38]
Chr10:70446380 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.5365A>C (p.Thr1789Pro) single nucleotide variant not specified [RCV004472103] Chr10:68686668 [GRCh38]
Chr10:70446425 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.5654C>T (p.Ser1885Leu) single nucleotide variant not specified [RCV004472105] Chr10:68691057 [GRCh38]
Chr10:70450814 [GRCh37]
Chr10:10q21.3		 likely benign
NM_030625.3(TET1):c.778G>A (p.Val260Ile) single nucleotide variant not specified [RCV004472107] Chr10:68573116 [GRCh38]
Chr10:70332873 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.3218T>C (p.Ile1073Thr) single nucleotide variant not specified [RCV004675995] Chr10:68645947 [GRCh38]
Chr10:70405704 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.5264G>T (p.Gly1755Val) single nucleotide variant not specified [RCV004676733] Chr10:68686567 [GRCh38]
Chr10:70446324 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.2003A>T (p.Lys668Met) single nucleotide variant not specified [RCV004676735] Chr10:68644732 [GRCh38]
Chr10:70404489 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.899C>A (p.Ser300Tyr) single nucleotide variant not specified [RCV004676732] Chr10:68573237 [GRCh38]
Chr10:70332994 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.5167G>C (p.Glu1723Gln) single nucleotide variant not specified [RCV004676734] Chr10:68686470 [GRCh38]
Chr10:70446227 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.5659A>G (p.Arg1887Gly) single nucleotide variant not specified [RCV004675988] Chr10:68691062 [GRCh38]
Chr10:70450819 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.3442A>C (p.Lys1148Gln) single nucleotide variant not specified [RCV004675989] Chr10:68646171 [GRCh38]
Chr10:70405928 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.4841A>G (p.Asp1614Gly) single nucleotide variant not specified [RCV004675990] Chr10:68681415 [GRCh38]
Chr10:70441172 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.4661C>A (p.Thr1554Asn) single nucleotide variant not specified [RCV004675991] Chr10:68667244 [GRCh38]
Chr10:70427001 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.6041C>G (p.Ala2014Gly) single nucleotide variant not specified [RCV004675992] Chr10:68691444 [GRCh38]
Chr10:70451201 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.1703T>C (p.Met568Thr) single nucleotide variant not specified [RCV004675993] Chr10:68574041 [GRCh38]
Chr10:70333798 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.5953G>C (p.Glu1985Gln) single nucleotide variant not specified [RCV004675994] Chr10:68691356 [GRCh38]
Chr10:70451113 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.3332_3336del (p.Asn1111fs) microsatellite not provided [RCV004811330] Chr10:68646056..68646060 [GRCh38]
Chr10:70405813..70405817 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.5822A>T (p.His1941Leu) single nucleotide variant TET1-related disorder [RCV004731358] Chr10:68691225 [GRCh38]
Chr10:70450982 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.2047C>G (p.Gln683Glu) single nucleotide variant TET1-related disorder [RCV004757761] Chr10:68644776 [GRCh38]
Chr10:70404533 [GRCh37]
Chr10:10q21.3		 likely benign
NM_030625.3(TET1):c.1702A>G (p.Met568Val) single nucleotide variant not specified [RCV004874595] Chr10:68574040 [GRCh38]
Chr10:70333797 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.199C>T (p.Pro67Ser) single nucleotide variant not specified [RCV004874596] Chr10:68572537 [GRCh38]
Chr10:70332294 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.171T>A (p.Asp57Glu) single nucleotide variant not specified [RCV004874597] Chr10:68572509 [GRCh38]
Chr10:70332266 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.2403A>C (p.Lys801Asn) single nucleotide variant not specified [RCV004874598] Chr10:68645132 [GRCh38]
Chr10:70404889 [GRCh37]
Chr10:10q21.3		 likely benign
NM_030625.3(TET1):c.5636C>A (p.Pro1879His) single nucleotide variant not specified [RCV004874599] Chr10:68691039 [GRCh38]
Chr10:70450796 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.5843C>G (p.Ser1948Cys) single nucleotide variant not specified [RCV004874600] Chr10:68691246 [GRCh38]
Chr10:70451003 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.3361G>T (p.Gly1121Cys) single nucleotide variant not specified [RCV004874601] Chr10:68646090 [GRCh38]
Chr10:70405847 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.3529G>C (p.Glu1177Gln) single nucleotide variant not specified [RCV004874602] Chr10:68646258 [GRCh38]
Chr10:70406015 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.3821G>A (p.Gly1274Glu) single nucleotide variant not specified [RCV004874604] Chr10:68646550 [GRCh38]
Chr10:70406307 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.2197G>A (p.Ala733Thr) single nucleotide variant not specified [RCV004874606] Chr10:68644926 [GRCh38]
Chr10:70404683 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.2234G>A (p.Arg745Gln) single nucleotide variant not specified [RCV004874589] Chr10:68644963 [GRCh38]
Chr10:70404720 [GRCh37]
Chr10:10q21.3		 likely benign
NM_030625.3(TET1):c.3287A>C (p.Glu1096Ala) single nucleotide variant not specified [RCV004874590] Chr10:68646016 [GRCh38]
Chr10:70405773 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.4915G>C (p.Val1639Leu) single nucleotide variant not specified [RCV004874591] Chr10:68682836 [GRCh38]
Chr10:70442593 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.6116A>G (p.Asn2039Ser) single nucleotide variant not specified [RCV004874592] Chr10:68691519 [GRCh38]
Chr10:70451276 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.2347G>A (p.Gly783Ser) single nucleotide variant not specified [RCV004874593] Chr10:68645076 [GRCh38]
Chr10:70404833 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.257G>A (p.Arg86Lys) single nucleotide variant not specified [RCV004874594] Chr10:68572595 [GRCh38]
Chr10:70332352 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.3475C>T (p.Arg1159Trp) single nucleotide variant not specified [RCV004874610] Chr10:68646204 [GRCh38]
Chr10:70405961 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.6198T>G (p.Ile2066Met) single nucleotide variant not specified [RCV004874611] Chr10:68691601 [GRCh38]
Chr10:70451358 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.6105C>A (p.His2035Gln) single nucleotide variant not specified [RCV004874603] Chr10:68691508 [GRCh38]
Chr10:70451265 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.4009T>A (p.Leu1337Met) single nucleotide variant not specified [RCV004874605] Chr10:68646738 [GRCh38]
Chr10:70406495 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.5090G>C (p.Gly1697Ala) single nucleotide variant not specified [RCV004874607] Chr10:68686393 [GRCh38]
Chr10:70446150 [GRCh37]
Chr10:10q21.3		 uncertain significance
NM_030625.3(TET1):c.944T>C (p.Leu315Ser) single nucleotide variant not specified [RCV004874608] Chr10:68573282 [GRCh38]
Chr10:70333039 [GRCh37]
Chr10:10q21.3		 uncertain significance
miRNA Target Status (No longer updated)

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
MIR29Ahsa-miR-29a-3pMirtarbaseexternal_infoqRT-PCRFunctional MTI (Weak)19850741
MIR29Ahsa-miR-29a-3pMirecordsexternal_info{changed}NA19850741

Predicted Target Of
Summary Value
Count of predictions:899
Count of miRNA genes:594
Interacting mature miRNAs:678
Transcripts:ENST00000373644
Prediction methods:Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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

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


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
597241946GWAS1338020_Haspartate aminotransferase measurement, serum alanine aminotransferase measurement, low density lipoprotein triglyceride measurement, body fat percentage, high density lipoprotein cholesterol measurement, sex hormone-binding globulin measurement QTL GWAS1338020 (human)4e-10body fat mass (VT:0010482)blood high density lipoprotein cholesterol level (CMO:0000052)106858753568587540Human
597133011GWAS1229085_Hpulse pressure measurement QTL GWAS1229085 (human)6e-10pulse pressure measurementpulse pressure (CMO:0000292)106864440268644403Human
597347167GWAS1443241_Hlean body mass QTL GWAS1443241 (human)1e-13body lean mass (VT:0010483)total body lean mass (CMO:0003950)106857113568571136Human
597087187GWAS1183261_Htype 2 diabetes mellitus QTL GWAS1183261 (human)1e-15type 2 diabetes mellitus106862242268622423Human
597159441GWAS1255515_Hopen-angle glaucoma QTL GWAS1255515 (human)5e-08open-angle glaucoma106858537068585371Human
596979986GWAS1099505_Hbody height QTL GWAS1099505 (human)4e-39body height106863285368632854Human
597338962GWAS1435036_Hdiastolic blood pressure QTL GWAS1435036 (human)6e-09diastolic blood pressurediastolic blood pressure (CMO:0000005)106857291568572916Human
597338963GWAS1435037_Hdiastolic blood pressure QTL GWAS1435037 (human)1e-08diastolic blood pressurediastolic blood pressure (CMO:0000005)106858698368586984Human
597110686GWAS1206760_Hchronotype measurement QTL GWAS1206760 (human)4e-09chronotype measurement106858698368586984Human
597427030GWAS1523104_Hgout QTL GWAS1523104 (human)3e-08gout106862916368629164Human
597322577GWAS1418651_Hcup-to-disc ratio measurement QTL GWAS1418651 (human)7e-21cup-to-disc ratio measurement106863935268639353Human
597282839GWAS1378913_HBMI-adjusted hip circumference QTL GWAS1378913 (human)5e-11BMI-adjusted hip circumferencehip circumference (CMO:0000014)106857310568573106Human
596974171GWAS1093690_Hmemory performance, cognitive function measurement, major depressive disorder QTL GWAS1093690 (human)0.0000007memory performance, cognitive function measurement, major depressive disorder106857634868576349Human
597055556GWAS1151630_Hmetabolic syndrome QTL GWAS1151630 (human)9e-09metabolic syndrome106857230968572310Human
597273931GWAS1370005_HBMI-adjusted hip circumference QTL GWAS1370005 (human)2e-09BMI-adjusted hip circumferencehip circumference (CMO:0000014)106868456268684563Human
597273930GWAS1370004_HBMI-adjusted hip circumference QTL GWAS1370004 (human)7e-09BMI-adjusted hip circumferencehip circumference (CMO:0000014)106861006568610066Human
597280717GWAS1376791_Hmemory performance, cognitive function measurement, major depressive disorder QTL GWAS1376791 (human)0.0000007memory performance, cognitive function measurement, major depressive disorder106857634868576349Human
597602954GWAS1659814_Htype 2 diabetes mellitus QTL GWAS1659814 (human)4e-18type 2 diabetes mellitus106861838268618383Human
597086400GWAS1182474_Htype 2 diabetes mellitus QTL GWAS1182474 (human)2e-11type 2 diabetes mellitus106858301868583019Human
597219983GWAS1316057_Hcorneal resistance factor QTL GWAS1316057 (human)3e-10corneal resistance factor106857815868578159Human
597290574GWAS1386648_Hage at menarche QTL GWAS1386648 (human)5e-08age at menarche106860512768605128Human
407347551GWAS996527_Hunipolar depression, memory performance, cognitive function measurement QTL GWAS996527 (human)0.0000007unipolar depression, memory performance, cognitive function measurement106857634868576349Human
597212929GWAS1309003_Htriglyceride measurement QTL GWAS1309003 (human)2e-09triglyceride measurementblood triglyceride level (CMO:0000118)106858698368586984Human
597108174GWAS1204248_Hpulse pressure measurement QTL GWAS1204248 (human)2e-09pulse pressure measurementpulse pressure (CMO:0000292)106864440268644403Human
597041036GWAS1137110_Happendicular lean mass QTL GWAS1137110 (human)3e-09appendicular lean mass106863803268638033Human
597135820GWAS1231894_Hdiastolic blood pressure QTL GWAS1231894 (human)3e-10diastolic blood pressurediastolic blood pressure (CMO:0000005)106857291568572916Human
597245570GWAS1341644_Hbody fat percentage QTL GWAS1341644 (human)8e-11body fat mass (VT:0010482)body fat percentage (CMO:0000302)106858753568587540Human
597138635GWAS1234709_Halpha fetoprotein measurement QTL GWAS1234709 (human)6e-17blood alpha-fetoprotein amount (VT:0010776)106862140068621401Human
597233529GWAS1329603_Happendicular lean mass QTL GWAS1329603 (human)8e-45appendicular lean mass106863935268639353Human
597341054GWAS1437128_Hserum gamma-glutamyl transferase measurement QTL GWAS1437128 (human)5e-10serum gamma-glutamyl transferase measurementserum gamma-glutamyltransferase activity level (CMO:0002241)106862242268622423Human
597329968GWAS1426042_Hdiastolic blood pressure QTL GWAS1426042 (human)4e-08diastolic blood pressurediastolic blood pressure (CMO:0000005)106858698368586984Human
597323383GWAS1419457_Hcup-to-disc ratio measurement QTL GWAS1419457 (human)9e-17cup-to-disc ratio measurement106858965968589660Human
597059512GWAS1155586_HBMI-adjusted waist circumference QTL GWAS1155586 (human)1e-09body size trait (VT:0100005)106857310568573106Human
597242166GWAS1338240_Hserum alanine aminotransferase measurement QTL GWAS1338240 (human)0.0000009serum alanine aminotransferase measurementserum alanine aminotransferase activity level (CMO:0000575)106858753568587540Human
597202359GWAS1298433_Halpha fetoprotein measurement QTL GWAS1298433 (human)6e-14blood alpha-fetoprotein amount (VT:0010776)106866924868669249Human
597059174GWAS1155248_Hreaction time measurement QTL GWAS1155248 (human)0.0000005reaction time measurement106856469168564692Human
596978599GWAS1098118_Hbody height QTL GWAS1098118 (human)4e-11body height106859036968590370Human
597245930GWAS1342004_HHbA1c measurement QTL GWAS1342004 (human)2e-36HbA1c measurementblood hemoglobin A1c level (CMO:0002786)106869250368692504Human
596963808GWAS1083327_Htype 2 diabetes mellitus QTL GWAS1083327 (human)0.0000001type 2 diabetes mellitus106858836168588362Human
597329967GWAS1426041_Hdiastolic blood pressure QTL GWAS1426041 (human)3e-09diastolic blood pressurediastolic blood pressure (CMO:0000005)106857291568572916Human
597297263GWAS1393337_Htype 2 diabetes mellitus QTL GWAS1393337 (human)0.0000001type 2 diabetes mellitus106858836168588362Human
596961635GWAS1081154_Hmetabolic syndrome QTL GWAS1081154 (human)9e-09metabolic syndrome106857230968572310Human
596962542GWAS1082061_Hage at menarche QTL GWAS1082061 (human)5e-08age at menarche106860512768605128Human
407056312GWAS705288_Hresponse to trauma exposure QTL GWAS705288 (human)0.000003response to trauma exposure106856047968560480Human
597255975GWAS1352049_Htotal cholesterol measurement QTL GWAS1352049 (human)4e-08total cholesterol measurementblood total cholesterol level (CMO:0000051)106864960068649601Human

Markers in Region
SHGC-3962  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371070,354,923 - 70,355,072UniSTSGRCh37
Build 361070,024,929 - 70,025,078RGDNCBI36
Celera1063,630,840 - 63,630,989RGD
Cytogenetic Map10q21UniSTS
HuRef1064,356,754 - 64,356,903UniSTS
TNG Radiation Hybrid Map1032449.0UniSTS
Stanford-G3 RH Map103076.0UniSTS
RH48131  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371070,392,332 - 70,392,454UniSTSGRCh37
GRCh371245,005,544 - 245,006,448UniSTSGRCh37
Build 361070,062,338 - 70,062,460RGDNCBI36
Celera1218,295,495 - 218,296,399UniSTS
Celera1063,668,250 - 63,668,372RGD
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map10q21UniSTS
Cytogenetic Map1q44UniSTS
HuRef1215,388,706 - 215,389,610UniSTS
HuRef1064,394,333 - 64,394,455UniSTS
GeneMap99-GB4 RH Map10366.74UniSTS
G59568  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371070,392,335 - 70,392,449UniSTSGRCh37
Build 361070,062,341 - 70,062,455RGDNCBI36
Celera1063,668,253 - 63,668,367RGD
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map10q21UniSTS
Cytogenetic Map1q44UniSTS
HuRef1064,394,336 - 64,394,450UniSTS
TNG Radiation Hybrid Map1032478.0UniSTS
SHGC-6703  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371070,418,999 - 70,419,119UniSTSGRCh37
Build 361070,089,005 - 70,089,125RGDNCBI36
Celera1063,694,924 - 63,695,042RGD
Cytogenetic Map10q21UniSTS
HuRef1064,421,095 - 64,421,215UniSTS
Stanford-G3 RH Map103063.0UniSTS
CXXC6_3680  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371070,452,910 - 70,453,624UniSTSGRCh37
Build 361070,122,916 - 70,123,630RGDNCBI36
Celera1063,728,831 - 63,729,545RGD
HuRef1064,454,997 - 64,455,711UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
renal system
reproductive system
respiratory system
sensory system
1204 2415 2788 2244 4942 1712 2328 4 611 1898 453 2268 7195 6401 52 3708 836 1725 1606 170

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001406365 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001406367 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001406368 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001406369 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001406370 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001406371 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001406372 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001406373 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001406374 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001406375 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001406376 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_030625 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011540206 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011540207 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017016686 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017016687 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017016688 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017016689 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054366805 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054366806 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054366807 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001747210 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001747211 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001747212 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008488268 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008488269 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008488270 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB051463 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF430147 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK123436 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL080082 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL360177 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL513534 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL713658 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL713888 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL832334 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL832337 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC053905 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471083 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068268 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FM165196 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FM165197 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FM165199 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX311858 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX311859 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000373644   ⟹   ENSP00000362748
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1068,560,337 - 68,694,487 (+)Ensembl
RefSeq Acc Id: NM_001406365   ⟹   NP_001393294
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381068,560,337 - 68,694,487 (+)NCBI
T2T-CHM13v2.01069,429,559 - 69,563,685 (+)NCBI
RefSeq Acc Id: NM_001406367   ⟹   NP_001393296
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381068,600,474 - 68,694,487 (+)NCBI
T2T-CHM13v2.01069,469,696 - 69,563,685 (+)NCBI
RefSeq Acc Id: NM_001406368   ⟹   NP_001393297
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381068,600,268 - 68,694,487 (+)NCBI
T2T-CHM13v2.01069,469,490 - 69,563,685 (+)NCBI
RefSeq Acc Id: NM_001406369   ⟹   NP_001393298
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381068,600,474 - 68,694,487 (+)NCBI
T2T-CHM13v2.01069,469,696 - 69,563,685 (+)NCBI
RefSeq Acc Id: NM_001406370   ⟹   NP_001393299
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381068,600,474 - 68,694,487 (+)NCBI
T2T-CHM13v2.01069,469,696 - 69,563,685 (+)NCBI
RefSeq Acc Id: NM_001406371   ⟹   NP_001393300
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381068,600,268 - 68,694,487 (+)NCBI
T2T-CHM13v2.01069,469,490 - 69,563,685 (+)NCBI
RefSeq Acc Id: NM_001406372   ⟹   NP_001393301
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381068,600,474 - 68,694,487 (+)NCBI
T2T-CHM13v2.01069,469,696 - 69,563,685 (+)NCBI
RefSeq Acc Id: NM_001406373   ⟹   NP_001393302
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381068,560,337 - 68,694,487 (+)NCBI
T2T-CHM13v2.01069,429,559 - 69,563,685 (+)NCBI
RefSeq Acc Id: NM_001406374   ⟹   NP_001393303
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381068,560,337 - 68,694,487 (+)NCBI
T2T-CHM13v2.01069,429,559 - 69,563,685 (+)NCBI
RefSeq Acc Id: NM_001406375   ⟹   NP_001393304
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381068,600,268 - 68,694,487 (+)NCBI
T2T-CHM13v2.01069,469,490 - 69,563,685 (+)NCBI
RefSeq Acc Id: NM_001406376   ⟹   NP_001393305
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381068,600,474 - 68,694,487 (+)NCBI
T2T-CHM13v2.01069,469,696 - 69,563,685 (+)NCBI
RefSeq Acc Id: NM_030625   ⟹   NP_085128
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381068,560,337 - 68,694,487 (+)NCBI
GRCh371070,320,117 - 70,454,239 (+)RGD
Build 361069,990,123 - 70,124,245 (+)NCBI Archive
Celera1063,596,035 - 63,730,160 (+)RGD
HuRef1064,321,678 - 64,456,326 (+)RGD
CHM1_11070,602,173 - 70,737,025 (+)NCBI
T2T-CHM13v2.01069,429,559 - 69,563,685 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011540206   ⟹   XP_011538508
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381068,560,337 - 68,665,897 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017016686   ⟹   XP_016872175
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381068,636,616 - 68,694,487 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017016687   ⟹   XP_016872176
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381068,600,474 - 68,694,487 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017016688   ⟹   XP_016872177
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381068,600,268 - 68,694,487 (+)NCBI
Sequence:
RefSeq Acc Id: XM_054366805   ⟹   XP_054222780
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01069,505,834 - 69,563,685 (+)NCBI
RefSeq Acc Id: XM_054366806   ⟹   XP_054222781
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01069,469,692 - 69,563,685 (+)NCBI
RefSeq Acc Id: XM_054366807   ⟹   XP_054222782
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01069,429,559 - 69,535,103 (+)NCBI
RefSeq Acc Id: XR_001747210
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381068,560,337 - 68,651,938 (+)NCBI
Sequence:
RefSeq Acc Id: XR_001747211
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381068,560,337 - 68,667,153 (+)NCBI
Sequence:
RefSeq Acc Id: XR_001747212
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381068,560,337 - 68,665,894 (+)NCBI
Sequence:
RefSeq Acc Id: XR_008488268
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01069,429,559 - 69,521,135 (+)NCBI
RefSeq Acc Id: XR_008488269
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01069,429,559 - 69,536,360 (+)NCBI
RefSeq Acc Id: XR_008488270
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01069,429,559 - 69,535,100 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001393294 (Get FASTA)   NCBI Sequence Viewer  
  NP_001393296 (Get FASTA)   NCBI Sequence Viewer  
  NP_001393297 (Get FASTA)   NCBI Sequence Viewer  
  NP_001393298 (Get FASTA)   NCBI Sequence Viewer  
  NP_001393299 (Get FASTA)   NCBI Sequence Viewer  
  NP_001393300 (Get FASTA)   NCBI Sequence Viewer  
  NP_001393301 (Get FASTA)   NCBI Sequence Viewer  
  NP_001393302 (Get FASTA)   NCBI Sequence Viewer  
  NP_001393303 (Get FASTA)   NCBI Sequence Viewer  
  NP_001393304 (Get FASTA)   NCBI Sequence Viewer  
  NP_001393305 (Get FASTA)   NCBI Sequence Viewer  
  NP_085128 (Get FASTA)   NCBI Sequence Viewer  
  XP_011538508 (Get FASTA)   NCBI Sequence Viewer  
  XP_016872175 (Get FASTA)   NCBI Sequence Viewer  
  XP_016872176 (Get FASTA)   NCBI Sequence Viewer  
  XP_016872177 (Get FASTA)   NCBI Sequence Viewer  
  XP_054222780 (Get FASTA)   NCBI Sequence Viewer  
  XP_054222781 (Get FASTA)   NCBI Sequence Viewer  
  XP_054222782 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH53905 (Get FASTA)   NCBI Sequence Viewer  
  AAM88301 (Get FASTA)   NCBI Sequence Viewer  
  AGK83641 (Get FASTA)   NCBI Sequence Viewer  
  AGK83642 (Get FASTA)   NCBI Sequence Viewer  
  BAB21767 (Get FASTA)   NCBI Sequence Viewer  
  CAD28467 (Get FASTA)   NCBI Sequence Viewer  
  CAQ60120 (Get FASTA)   NCBI Sequence Viewer  
  CAQ60121 (Get FASTA)   NCBI Sequence Viewer  
  CAQ60123 (Get FASTA)   NCBI Sequence Viewer  
  EAW54299 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000362748
  ENSP00000362748.4
GenBank Protein Q8NFU7 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_085128   ⟸   NM_030625
- Peptide Label: isoform 2
- UniProtKB: Q8TCR1 (UniProtKB/Swiss-Prot),   Q7Z6B6 (UniProtKB/Swiss-Prot),   Q5VUP7 (UniProtKB/Swiss-Prot),   A0A023HHL0 (UniProtKB/Swiss-Prot),   A0A023HHK9 (UniProtKB/Swiss-Prot),   Q9C0I7 (UniProtKB/Swiss-Prot),   Q8NFU7 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_011538508   ⟸   XM_011540206
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_016872177   ⟸   XM_017016688
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_016872176   ⟸   XM_017016687
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_016872175   ⟸   XM_017016686
- Peptide Label: isoform X1
- Sequence:
Ensembl Acc Id: ENSP00000362748   ⟸   ENST00000373644
RefSeq Acc Id: NP_001393294   ⟸   NM_001406365
- Peptide Label: isoform 1
RefSeq Acc Id: NP_001393302   ⟸   NM_001406373
- Peptide Label: isoform 6
RefSeq Acc Id: NP_001393303   ⟸   NM_001406374
- Peptide Label: isoform 7
RefSeq Acc Id: NP_001393297   ⟸   NM_001406368
- Peptide Label: isoform 4
RefSeq Acc Id: NP_001393300   ⟸   NM_001406371
- Peptide Label: isoform 5
RefSeq Acc Id: NP_001393304   ⟸   NM_001406375
- Peptide Label: isoform 8
RefSeq Acc Id: NP_001393296   ⟸   NM_001406367
- Peptide Label: isoform 3
RefSeq Acc Id: NP_001393299   ⟸   NM_001406370
- Peptide Label: isoform 4
RefSeq Acc Id: NP_001393301   ⟸   NM_001406372
- Peptide Label: isoform 5
RefSeq Acc Id: NP_001393298   ⟸   NM_001406369
- Peptide Label: isoform 4
RefSeq Acc Id: NP_001393305   ⟸   NM_001406376
- Peptide Label: isoform 9
RefSeq Acc Id: XP_054222782   ⟸   XM_054366807
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054222781   ⟸   XM_054366806
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054222780   ⟸   XM_054366805
- Peptide Label: isoform X1

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q8NFU7-F1-model_v2 AlphaFold Q8NFU7 1-2136 view protein structure

Promoters
RGD ID:7217709
Promoter ID:EPDNEW_H14600
Type:initiation region
Name:TET1_1
Description:tet methylcytosine dioxygenase 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381068,560,337 - 68,560,397EPDNEW
RGD ID:6788303
Promoter ID:HG_KWN:9824
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562,   Lymphoblastoid,   NB4
Transcripts:NM_030625
Position:
Human AssemblyChrPosition (strand)Source
Build 361069,989,861 - 69,990,361 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:29484 AgrOrtholog
COSMIC TET1 COSMIC
Ensembl Genes ENSG00000138336 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000373644 ENTREZGENE
  ENST00000373644.5 UniProtKB/Swiss-Prot
GTEx ENSG00000138336 GTEx
HGNC ID HGNC:29484 ENTREZGENE
Human Proteome Map TET1 Human Proteome Map
InterPro 2OGFeDO_noxygenase_dom UniProtKB/Swiss-Prot
  TET1/2/3 UniProtKB/Swiss-Prot
  TET_oxygenase UniProtKB/Swiss-Prot
  Znf_CXXC UniProtKB/Swiss-Prot
KEGG Report hsa:80312 UniProtKB/Swiss-Prot
NCBI Gene 80312 ENTREZGENE
OMIM 607790 OMIM
PANTHER METHYLCYTOSINE DIOXYGENASE TET1 UniProtKB/Swiss-Prot
  PTHR23358 UniProtKB/Swiss-Prot
Pfam Tet_JBP UniProtKB/Swiss-Prot
  zf-CXXC UniProtKB/Swiss-Prot
PharmGKB PA162405605 PharmGKB
PROSITE ZF_CXXC UniProtKB/Swiss-Prot
SMART Tet_JBP UniProtKB/Swiss-Prot
UniProt A0A023HHK9 ENTREZGENE
  A0A023HHL0 ENTREZGENE
  Q5VUP7 ENTREZGENE
  Q7Z6B6 ENTREZGENE
  Q8NFU7 ENTREZGENE
  Q8TCR1 ENTREZGENE
  Q9C0I7 ENTREZGENE
  TET1_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary A0A023HHK9 UniProtKB/Swiss-Prot
  A0A023HHL0 UniProtKB/Swiss-Prot
  Q5VUP7 UniProtKB/Swiss-Prot
  Q7Z6B6 UniProtKB/Swiss-Prot
  Q8TCR1 UniProtKB/Swiss-Prot
  Q9C0I7 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2011-10-04 TET1  tet methylcytosine dioxygenase 1  TET1  tet oncogene 1  Symbol and/or name change 5135510 APPROVED