Fa2h - fatty acid 2-hydroxylase Gene
Also Known as Wdr59; RGD1310347
Species: Rattus norvegicus
Gene Type: protein coding
Gene ID: 307855
Summary
Enables fatty acid alpha-hydroxylase activity. Involved in galactosylceramide biosynthetic process. Predicted to be located in membrane. Predicted to be active in endoplasmic reticulum. Human ortholog(s) of this gene implicated in hereditary spastic paraplegia 35. Orthologous to human FA2H (fatty acid 2-hydroxylase). [provided by Alliance of Genome Resources, Apr 2022]
Fa2h Products (1)
| mRNA | Protein | Name |
|---|---|---|
| NM_001135583.1 | NP_001129055.1 | fatty acid 2-hydroxylase |
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
fatty acid 2-hydroxylase |
|
Related Agents
- Pre-clinical Phase
Pre-clinical Phase
Bioactive Molecules
(1)
| Cat. No. | Product Name |
Effect
|
Purity |
Rare Diseases
|
|---|---|---|---|---|
| HY-RS04649 | FA2H Human Pre-designed siRNA Set A | Pre-designed Set | / | Unkown |
Compound Screening Libraries
Virtual Screening
Customize Your Library
Drug Screening Service