Gene
acsl6
- ID
- ZDB-GENE-030131-6776
- Name
- acyl-CoA synthetase long chain family member 6
- Symbol
- acsl6 Nomenclature History
- Previous Names
-
- wu:fa04h02
- wu:fc05h07
- Type
- protein_coding_gene
- Location
- Chr: 21 Mapping Details/Browsers
- Description
- Human ortholog(s) of this gene implicated in acute myeloid leukemia and leukemia. Is expressed in brain; digestive system; eye; gill; and pleuroperitoneal region. Orthologous to human ACSL6 (acyl-CoA synthetase long chain family member 6).
- Genome Resources
-
- Alliance (1)
- Gene:566863 (1)
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Lopes-Marques et al., 2013
- 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 |
|---|---|---|---|
| Myelodysplastic syndrome | |||
| Myelogenous leukemia, acute |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | AMP-dependent synthetase/ligase domain | ANL, N-terminal domain | Long-chain fatty acid CoA synthetase, eukaryotic |
|---|---|---|---|---|
|
UniProtKB:A0A8M9P3G8
|
674 |
- Genome Browsers
Interactions and Pathways
No data available
Plasmids
No data available
- Comparative Orthology
- Alliance