Gene
rab39ba
- ID
- ZDB-GENE-070620-7
- Name
- RAB39B, member RAS oncogene family a
- Symbol
- rab39ba Nomenclature History
- Previous Names
-
- tmem230
- zgc:165464
- Type
- protein_coding_gene
- Location
- Chr: 21 Mapping Details/Browsers
- Description
- Predicted to have GTPase activity. Predicted to be involved in Rab protein signal transduction and intracellular protein transport. Predicted to localize to endomembrane system. Human ortholog(s) of this gene implicated in Waisman syndrome and non-syndromic X-linked intellectual disability. Orthologous to human RAB39B (RAB39B, member RAS oncogene family).
- 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 |
---|---|---|---|
non-syndromic X-linked intellectual disability 72 | Alliance | Intellectual developmental disorder, X-linked 72 | 300271 |
Waisman syndrome | Alliance | Waisman syndrome | 311510 |
Domain, Family, and Site Summary
Domain Details Per Protein
Protein | Length | P-loop containing nucleoside triphosphate hydrolase | Rab39 | Rab GTPases family involved in membrane trafficking | Small GTPase |
---|---|---|---|---|---|
UniProtKB:A5PLA1
|
213 |
Type | Name | Annotation Method | Length (nt) | Analysis |
---|---|---|---|---|
mRNA |
rab39ba-201
(1)
|
Havana | 1367 nt |
Interactions and Pathways
No data available
Plasmids