Gene
snx10a
- ID
- ZDB-GENE-050809-44
- Name
- sorting nexin 10a
- Symbol
- snx10a Nomenclature History
- Previous Names
-
- im:7153949
- Type
- protein_coding_gene
- Location
- Chr: 19 Mapping Details/Browsers
- Description
- Predicted to have phosphatidylinositol binding activity. Involved in several processes, including Kupffer's vesicle development; heart looping; and left/right axis specification. Predicted to colocalize with centrosome. 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
- 2 figures from 2 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- IMAGE:7153949 (1 image)
Wild Type Expression Summary
- All Phenotype Data
- 1 Figure from Chen et al., 2012
- 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:A0A8M9P1S3
|
229 | |||
|
UniProtKB:F1Q506
|
229 |
- Genome Browsers
Interactions and Pathways
No data available
Plasmids
No data available