Gene
slc10a7
- ID
- ZDB-GENE-040801-5
- Name
- solute carrier family 10 member 7
- Symbol
- slc10a7 Nomenclature History
- Previous Names
-
- zgc:92251 (1)
- Type
- protein_coding_gene
- Location
- Chr: 23 Mapping Details/Browsers
- Description
- Predicted to have symporter activity. Involved in bone mineralization and cartilage development. Predicted to localize to plasma membrane. Orthologous to human SLC10A7 (solute carrier family 10 member 7).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Thisse et al., 2004
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- IMAGE:6892499 (1 image)
Wild Type Expression Summary
- All Phenotype Data
- 2 figures from Ashikov et al., 2018
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis | 618363 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Putative sodium bile acid cotransporter | Sodium/solute symporter superfamily |
|---|---|---|---|
|
UniProtKB:Q6DHK8
|
336 |
- Genome Browsers
Interactions and Pathways
No data available
Plasmids
No data available