1. Gene
  2. TET1 - tet methylcytosine dioxygenase 1 Gene

TET1 - tet methylcytosine dioxygenase 1 Gene

Homo sapiens

Also known as LCX; CXXC6; bA119F7.1

Gene ID: 80312 | Gene type: protein coding

About TET1

Cytogenetic location: 10q21.3 Genomic coordinates (GRCh38): 10:68,560,337-68,694,487 (from NCBI)

This gene has 1 transcript (splice variant), 205 orthologues, 2 paralogues and is associated with 106 phenotypes. Low expression observed in reference dataset.

Summary

DNA methylation is an epigenetic mechanism that is important for controlling gene expression. The protein encoded by this gene is a demethylase that belongs to the TET (ten-eleven translocation) family. Members of the TET Protein family play a role in the DNA methylation process and gene activation. [provided by RefSeq, Sep 2015]

TET1 Products(12)

mRNA Protein Name
NM_001406365.1 NP_001393294.1 methylcytosine dioxygenase TET1 isoform 1
NM_001406367.1 NP_001393296.1 methylcytosine dioxygenase TET1 isoform 3
NM_001406368.1 NP_001393297.1 methylcytosine dioxygenase TET1 isoform 4
NM_001406369.1 NP_001393298.1 methylcytosine dioxygenase TET1 isoform 4
NM_001406370.1 NP_001393299.1 methylcytosine dioxygenase TET1 isoform 4
NM_001406371.1 NP_001393300.1 methylcytosine dioxygenase TET1 isoform 5
NM_001406372.1 NP_001393301.1 methylcytosine dioxygenase TET1 isoform 5
NM_001406373.1 NP_001393302.1 methylcytosine dioxygenase TET1 isoform 6
NM_001406374.1 NP_001393303.1 methylcytosine dioxygenase TET1 isoform 7
NM_001406375.1 NP_001393304.1 methylcytosine dioxygenase TET1 isoform 8
NM_001406376.1 NP_001393305.1 methylcytosine dioxygenase TET1 isoform 9
NM_030625.3 NP_085128.2 methylcytosine dioxygenase TET1 isoform 2

TET1 Protein Structure

zf-CXXC

zf-CXXC: CXXC zinc finger domain (585 - 624)

Tet_JBP

Tet_JBP: Oxygenase domain of the 2OGFeDO superfamily (1580 - 2052)

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  • 2136 a.a.
Protein Preferred Names Protein Names

methylcytosine dioxygenase TET1

CXXC finger 6

Related Diseases

Diseases Alias
Glioblastoma

Glioblastoma Multiforme

Gbm

Adult Glioblastoma Multiforme

Grade Iv Adult Astrocytic Tumor

Primary Glioblastoma Multiforme

Spongioblastoma Multiforme

Adult Glioblastoma

Primary Glioblastoma

Rett Syndrome

Atypical Rett Syndrome

RTT

Rett Disorder

Rts

Autism, Dementia, Ataxia, And Loss Of Purposeful Hand Use

Rett Syndrome, Preserved Speech Variant

Rett Syndrome, Atypical

Rett'S Disorder

Rett Syndrome Variant

Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use Syndrome

Cerebroatrophic Hyperammonemia

Rett Like Syndrome

Rett'S Syndrome

Atypical Rtt

Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use

Rett Syndrome Preserved Speech Variant

Rett Syndrome Zappella Variant

Rett Syndrome, Zappella Variant

Hypoascorbemia

Scurvy

Ascorbic Acid Deficiency

Vitamin C Deficiency

Vitamin C, Inability To Synthesize

Deficiency Of Vitamin C

Scorbutus

Vitamin C

Chronic Myelomonocytic Leukemia

Leukemia, Myelomonocytic, Chronic

Cmml

Leukemia Myelomonocytic Chronic

Cmml - [Chronic Myelomonocytic Leukaemia]

Chronic Myelomonocytic Leukaemia Without Mention Of Remission

Chronic Monocytic Leukaemia

Chronic Monocytoid Leukaemia

Cartilage-Hair Hypoplasia

Metaphyseal Chondrodysplasia, Mckusick Type

CHH

Mckusick Type Metaphyseal Chondrodysplasia

Metaphyseal Dysplasia Without Hypotrichosis

Cartilage Hair Hypoplasia Like Syndrome

Metaphyseal Chondrodysplasia Mckusick Type

Chhv

Cartilage-Hair Hypoplasia Variant, Skeletal Manifestations Only

Cartilage-Hair Hypoplasia-Like Skeletal Dysplasia Without Hypotrichosis Or Immunodeficiency

Cartilage-Hair Syndrome

Mckusick'S Metaphyseal Chondrodysplasia Syndrome

Metaphyseal Chondrodysplasia, Recessive Type

Autosomal Recessive Metaphyseal Chondrodysplasia

Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome

Icf Syndrome

Immunodeficiency Syndrome, Variable

Ciid

Centromeric Instability, Immunodeficiency Syndrome

Immune Deficiency, Variable, With Centromeric Instability Of Chromosomes 1, 9, And 16

Icf

Leukemia, Acute Myeloid

Acute Myeloid Leukemia

Leukemia, Acute Myelogenous

Acute Myelogenous Leukemia

AML

Leukemia, Acute Myeloid, Susceptibility To

Acute Myeloblastic Leukemia

Leukemia, Acute Myeloid, Reduced Survival In, Somatic

Acute Myeloid Leukaemia

Leukemia, Myelocytic, Acute

Therapy Related Acute Myeloid Leukemia And Myelodysplastic Syndrome

Secondary Aml

Acute Myelocytic Leukemia

Acute Myeloid Leukemia, Somatic

Leukemia, Acute Myeloid, Somatic

Myeloid Leukemia, Acute, M4/M4eo Subtype, Somatic

Acute Myeloblastic Leukaemia

Acute Myelogenous Leukaemia

Aml - Acute Myeloid Leukemia

Acute Myeloid Leukemia With Cebpa Somatic Mutations

Aml With Cebpa Somatic Mutations

Inherited Acute Myeloid Leukemia

Familial Aml

Inherited Aml

Pure Familial Aml

Pure Familial Acute Myeloid Leukemia

Secondary Acute Myeloid Leukemia

Therapy-Related Aml And Myelodysplastic Syndrome

Acute Myeloid Leukemia, Secondary

Acute Non-Lymphoblastic Leukemia

Acute Non-Lymphocytic Leukemia

Acute Biphenotypic Leukemia

Acute Undifferentiated Leukemia

Acute Myeloblastic Leukaemia With Multilineage Dysplasia

Acute Myeloid Leukaemia With Multilineage Dysplasia Without Mention Of Remission

Acute Myeloid Leukaemia With Myelodysplasia-Related Features

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Rattus norvegicus TET1 RGD RGD:1310993
Mus musculus TET1 MGD MGI:1098693
Canis familiaris TET1 VGNC VGNC:47260
Macaca mulatta TET1 VGNC VGNC:79811
Felis catus TET1 VGNC VGNC:66092
Bos taurus TET1 VGNC VGNC:55994
Others TET1 NCBI