1. Gene
  2. CNOT3 - CCR4-NOT transcription complex subunit 3 Gene

CNOT3 - CCR4-NOT transcription complex subunit 3 Gene

Homo sapiens

Also known as NOT3; LENG2; NOT3H; IDDSADF

Gene ID: 4849 | Gene type: protein coding

About CNOT3

Cytogenetic location: 19q13.42 Genomic coordinates (GRCh38): 19:54,137,762-54,155,681 (from NCBI)

This gene has 14 transcripts (splice variants), 1 gene allele, 270 orthologues, 1 paralogue and is associated with 74 phenotypes. Ubiquitous expression in testis (RPKM 13.9), spleen (RPKM 9.7) and 25 other tissues.

Summary

Involved in regulation of stem cell population maintenance. Part of CCR4-NOT complex. [provided by Alliance of Genome Resources, Apr 2022]

CNOT3 Products(1)

mRNA Protein Name
NM_014516.4 NP_055331.1 CCR4-NOT transcription complex subunit 3

CNOT3 Protein Structure

Not3

Not3: Not1 N-terminal domain, CCR4-Not complex component (3 - 233)

NOT2_3_5

NOT2_3_5: NOT2 / NOT3 / NOT5 family (619 - 748)

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  • 753 a.a.
Protein Preferred Names Protein Names

CCR4-NOT transcription complex subunit 3

CCR4-associated factor 3

Related Diseases

Diseases Alias
Intellectual Developmental Disorder With Speech Delay, Autism, And Dysmorphic Facies

IDDSADF

Intellectual Developmental Disorder With Speech Delay, Autism And Dysmorphic Facies

Precursor T-Cell Acute Lymphoblastic Leukemia

T-All

Precursor T-Cell Acute Lymphoblastic Leukemia/Lymphoma

Precursor T-Cell Acute Lymphocytic Leukemia

Precursor T-Cell Acute Lymphocytic Leukemia/Lymphoma

Precursor T-Cell Lymphoblastic Leukemia-Lymphoma

Adult T-Cell Lymphoma/Leukemia

Non-Specific Syndromic Intellectual Disability

Complex Neurodevelopmental Disorder

Autism

Autistic Disorder

Autism Susceptibility 1

Childhood Autism

Autistic Disorder Of Childhood Onset

Infantile Autism

Kanner'S Syndrome

Autistic

Retinitis Pigmentosa

RP

Rod-Cone Dystrophy

Autosomal Recessive Retinitis Pigmentosa

Non-Syndromic Retinitis Pigmentosa

Pericentral Pigmentary Retinopathy

Pigmentary Retinopathy

Tapetoretinal Degeneration

Rcd

Retinitis Pigmentosa Autosomal Recessive

ARRP

Retinitis Pigmentosa, Autosomal Recessive

Retinitis Pigmentosa 1

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
Bos taurus CNOT3 VGNC VGNC:27518
Rattus norvegicus CNOT3 RGD RGD:1304771
Mus musculus CNOT3 MGD MGI:2385261
Macaca mulatta CNOT3 VGNC VGNC:71388
Canis familiaris CNOT3 VGNC VGNC:39414