Gene
snx10b
- ID
- ZDB-GENE-070628-1
- Name
- sorting nexin 10b
- Symbol
- snx10b Nomenclature History
- Previous Names
- None
- Type
- protein_coding_gene
- Location
- Chr: 16 Mapping Details/Browsers
- Description
- Predicted to have phosphatidylinositol binding activity. Predicted to be involved in protein transport. Predicted to localize to endosome membrane. Human ortholog(s) of this gene implicated in autosomal recessive osteopetrosis 8. Orthologous to human SNX10 (sorting nexin 10).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Chen et al., 2012
- 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 osteopetrosis 8 | Alliance | Osteopetrosis, autosomal recessive 8 | 615085 |
Domain, Family, and Site Summary
Domain Details Per Protein
Protein | Length | Phox homology | PX domain superfamily | Sorting nexin-10/11 |
---|---|---|---|---|
UniProtKB:A8WG21
|
170 |
Type | Name | Annotation Method | Length (nt) | Analysis |
---|---|---|---|---|
mRNA |
snx10b-201
(1)
|
Havana | 2241 nt |
Interactions and Pathways
No data available
Plasmids
No data available