Gene
zgc:154077
- ID
- ZDB-GENE-061110-34
- Name
- zgc:154077
- Symbol
- zgc:154077 Nomenclature History
- Previous Names
- None
- Type
- protein_coding_gene
- Location
- Chr: 25 Mapping Details/Browsers
- Description
- Human ortholog(s) of this gene implicated in autosomal recessive non-syndromic intellectual disability. Orthologous to human C12orf4 (chromosome 12 open reading frame 4).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- No data available
- 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 |
|---|---|---|---|
| autosomal recessive intellectual developmental disorder 66 | Alliance | Intellectual developmental disorder, autosomal recessive 66 | 618221 |
Domain, Family, and Site Summary
| Type | InterPro ID | Name |
|---|---|---|
| Family | IPR019311 | Ferry endosomal RAB5 effector complex subunit 3 |
Domain Details Per Protein
| Protein | Length | Ferry endosomal RAB5 effector complex subunit 3 |
|---|---|---|
|
UniProtKB:A0JMN9
|
551 |
| Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
|---|---|---|---|---|---|
| mRNA |
zgc:154077-201
(1)
|
Ensembl | 2,541 nt |
Interactions and Pathways
No data available
Plasmids
No data available