Gene
scd
- ID
- ZDB-GENE-031106-3
- Name
- stearoyl-CoA desaturase (delta-9-desaturase)
- Symbol
- scd Nomenclature History
- Previous Names
-
- SCD1 (1)
- Type
- protein_coding_gene
- Location
- Chr: 12 Mapping Details/Browsers
- Description
- Predicted to enable iron ion binding activity; palmitoyl-CoA 9-desaturase activity; and stearoyl-CoA 9-desaturase activity. Acts upstream of or within swimming behavior. Predicted to be located in membrane. Predicted to be active in endoplasmic reticulum membrane. Is expressed in brain; female organism; heart; liver; and muscle. Human ortholog(s) of this gene implicated in autosomal dominant nonsyndromic deafness 79. Orthologous to human SCD (stearoyl-CoA desaturase) and SCD5 (stearoyl-CoA desaturase 5).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 22 figures from 18 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- 3 figures from Zhang et al., 2022
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Acyl-CoA desaturase | Fatty acid desaturase domain | Fatty acid desaturase type 1, conserved site |
|---|---|---|---|---|
|
UniProtKB:F1QG70
|
326 |
Interactions and Pathways
No data available
Plasmids
No data available