Tet methylcytosine dioxygenase 3

Tet methylcytosine dioxygenase 3 is a protein that in humans is encoded by the TET3 gene. [5]

TET3
Identifiers
AliasesTET3, hCG_40738, tet methylcytosine dioxygenase 3, BEFAHRS
External IDsOMIM: 613555 MGI: 2446229 HomoloGene: 35360 GeneCards: TET3
Gene location (Human)
Chr.Chromosome 2 (human)[1]
Band2p13.1Start73,986,404 bp[1]
End74,108,176 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

200424

194388

Ensembl

ENSG00000187605

ENSMUSG00000034832

UniProt

O43151

Q8BG87

RefSeq (mRNA)

NM_001287491
NM_001366022

NM_183138
NM_001347313

RefSeq (protein)

NP_001274420
NP_001352951

NP_001334242
NP_898961

Location (UCSC)Chr 2: 73.99 – 74.11 MbChr 6: 83.36 – 83.46 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Function

Members of the ten-eleven translocation (TET) gene family, including TET3, play a role in the DNA methylation process (Langemeijer et al., 2009 [PubMed 19923888]).[supplied by OMIM, Nov 2010].


Clinical

Mutations in this gene have been associated a number of abnormal phenotypic features including intellectual disability, developmental delay, hypotonia, autistic traits, movement disorders, growth abnormalities and facial dysmorphism.[6]

References

  1. GRCh38: Ensembl release 89: ENSG00000187605 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000034832 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. "Entrez Gene: Tet methylcytosine dioxygenase 3". Retrieved 2018-08-13.
  6. Beck DB, Petracovici A, He C, Moore HW4, Louie RJ, Ansar M, Douzgou S, Sithambaram S, Cottrell T, Santos-Cortez RLP, Prijoles EJ, Bend R, Keren B, Mignot C, Nougues MC, Õunap K, Reimand T, Pajusalu S, Zahid M, Saqib MAN, Buratti J, Seaby EG, McWalter K, Telegrafi A, Baldridge D, Shinawi M, Leal SM, Schaefer GB, Stevenson RE, Banka S, Bonasio R, Fahrner JA (2020) Delineation of a Human Mendelian Disorder of the DNA Demethylation Machinery: TET3 Deficiency. Am J Hum Genet

Further reading


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