FAR1
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 11[13]
- Cytogenetic location
- 11p15.3[16]
- Encodes
- Fatty acyl-CoA reductase 1, Fatty acyl-CoA reductase 1[11]
- Expressed in
- corpus callosum, jejunal mucosa, oral cavity, monocyte, spinal cord, C1 segment, rectum, bone marrow cell, subthalamic nucleus, inferior ganglion of vagus nerve[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- severe intellectual disability-epilepsy-cataract syndrome due to fatty acyl-CoA reductase 1 deficiency[14]
- HomoloGene ID
- 41718[3]
- Strand orientation
- forward strand[15]
🏷️ Also known as
en CSPSD
en FAR1
en fatty acyl-CoA reductase 1
en MLSTD2
en PFCRD
en SDR10E1
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000197601
- Ensembl transcript ID
- ENST00000532769, ENST00000354817, ENST00000524933, ENST00000527202, ENST00000532502, ENST00000532701
- Entrez Gene ID
- 84188
- Exact match
- identifiers.org
- Freebase ID
- /m/0408nh1
- HGNC ID
- 26222
- HGNC gene symbol
- FAR1
- OMIM ID
- 616107
- RefSeq RNA ID
- NM_032228, XM_011520400, XM_047427690
- UMLS CUI
- C1428564
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