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 enable symporter activity. Acts upstream of or within bone mineralization and cartilage development. Predicted to be located in Golgi membrane and endoplasmic reticulum membrane. Predicted to be active in 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
| Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
|---|---|---|---|---|---|
| mRNA |
slc10a7-201
(1)
|
Ensembl | 1,469 nt |
Interactions and Pathways
No data available
Plasmids
No data available