Gene
samd7
- ID
- ZDB-GENE-070912-549
- Name
- sterile alpha motif domain containing 7
- Symbol
- samd7 Nomenclature History
- Previous Names
-
- si:dkey-52k20.12
- Type
- protein_coding_gene
- Location
- Chr: 2 Mapping Details/Browsers
- Description
- Predicted to enable chromatin binding activity and histone binding activity. Predicted to be involved in negative regulation of DNA-templated transcription. Predicted to be active in nucleus. Is expressed in photoreceptor cell. Human ortholog(s) of this gene implicated in macular degeneration. Orthologous to human SAMD7 (sterile alpha motif domain containing 7).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 3 figures from Volkov et al., 2024
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- 1 Figure from Volkov et al., 2024
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| Macular dystrophy with or without cone dysfunction | 620762 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Additional Resources | Length | Polycomb group and chromatin remodeling factors | Sterile alpha motif domain | Sterile alpha motif/pointed domain superfamily |
|---|---|---|---|---|---|
| UniProtKB:F1R0H6 | InterPro | 526 | |||
| UniProtKB:B3DJI7 | InterPro | 526 | |||
| UniProtKB:A0A8M3B7T1 | InterPro | 527 |
- Genome Browsers
Interactions and Pathways
No data available
Plasmids
No data available