Gene
cnot2
- ID
- ZDB-GENE-070410-70
- Name
- CCR4-NOT transcription complex, subunit 2
- Symbol
- cnot2 Nomenclature History
- Previous Names
-
- zgc:162316
- Type
- protein_coding_gene
- Location
- Chr: 25 Mapping Details/Browsers
- Description
- Predicted to be involved in negative regulation of translation and nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay. Predicted to localize to CCR4-NOT core complex and P-body. Orthologous to human CNOT2 (CCR4-NOT transcription complex subunit 2).
- Genome Resources
- Note
- None
- Comparative Information
- All Expression Data
- 1 figure from Diotel et al., 2015
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- No data available
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
---|---|---|---|
Intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies | 618608 |
Domain, Family, and Site Summary
Domain Details Per Protein
Protein | Length | CCR4-NOT complex subunit 2/3/5, C-terminal domain superfamily | Not2/Not3/Not5 | NOT2/NOT3/NOT5, C-terminal |
---|---|---|---|---|
UniProtKB:A4QN63
|
520 | |||
UniProtKB:A0A8M2BA34
|
530 |
Interactions and Pathways
No data available
Plasmids
No data available