ZFIN is now using GRCz12tu for Genomic Data
Gene
snta1
- ID
- ZDB-GENE-120919-5
- Name
- syntrophin, alpha 1
- Symbol
- snta1 Nomenclature History
- Previous Names
- None
- Type
- protein_coding_gene
- Location
- Chr: 6 Mapping Details/Browsers
- Genome Assembly
- GRCz12tu
- Annotation Status
- Current
- Description
- Predicted to enable sodium channel regulator activity. Predicted to be involved in ventricular cardiac muscle cell action potential. Predicted to be located in cytoplasm and cytoskeleton. Predicted to be part of dystrophin-associated glycoprotein complex. Predicted to be active in neuromuscular junction and sarcolemma. Human ortholog(s) of this gene implicated in long QT syndrome; long QT syndrome 12; and sudden infant death syndrome. Orthologous to human SNTA1 (syntrophin alpha 1).
- Genome Resources
-
- Alliance (1)
- Gene:100332905 (1)
- Note
- None
- Comparative Information
-
- All Expression Data
- No data available
- 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 |
|---|---|---|---|
| long QT syndrome 12 | Alliance | Long QT syndrome 12 | 612955 |
Domain, Family, and Site Summary
No data available
Domain Details Per Protein
| Protein | Additional Resources | Length |
|---|---|---|
| UniProtKB:A0A8M1RLW3 | InterPro | 479 |
| UniProtKB:A0AC58JWS6 | InterPro | 479 |
- Genome Browsers
Interactions and Pathways
No data available
Plasmids
No data available
- Genome Browsers
- Comparative Orthology
- Alliance