ENSG00000197601


Homo sapiens

Features
Gene ID: ENSG00000197601
  
Biological name :FAR1
  
Synonyms : FAR1 / fatty acyl-CoA reductase 1 / Q8WVX9
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 11
Strand: 1
Band: p15.3
Gene start: 13668670
Gene end: 13732346
  
Corresponding Affymetrix probe sets: 1558014_s_at (Human Genome U133 Plus 2.0 Array)   224865_at (Human Genome U133 Plus 2.0 Array)   224866_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000346874
Ensembl peptide - ENSP00000437111
Ensembl peptide - ENSP00000434624
NCBI entrez gene - 84188     See in Manteia.
OMIM - 616107
RefSeq - NM_032228
RefSeq - XM_011520400
RefSeq Peptide - NP_115604
swissprot - E9PPB8
swissprot - E9PNW8
swissprot - Q8WVX9
Ensembl - ENSG00000197601
  
Related genetic diseases (OMIM): 616154 - Peroxisomal fatty acyl-CoA reductase 1 disorder, 616154
See expression report in BioGPS
See gene description in Wikigenes
See gene description in GeneCards
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 far1ENSDARG00000006899Danio rerio
 FAR1ENSGALG00000005353Gallus gallus
 Far1ENSMUSG00000030759Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
FAR2 / Q96K12 / fatty acyl-CoA reductase 2ENSG0000006476359


Protein motifs (from Interpro)
Interpro ID Name
 IPR013120  Male sterility, NAD-binding
 IPR026055  Fatty acyl-CoA reductase
 IPR033640  Fatty acyl-CoA reductase, C-terminal
 IPR036291  NAD(P)-binding domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006629 lipid metabolic process IEA
 biological_processGO:0008611 ether lipid biosynthetic process IMP
 biological_processGO:0010025 wax biosynthetic process IEA
 biological_processGO:0035336 long-chain fatty-acyl-CoA metabolic process IDA
 biological_processGO:0046474 glycerophospholipid biosynthetic process IDA
 biological_processGO:0055114 oxidation-reduction process IEA
 cellular_componentGO:0005777 peroxisome IDA
 cellular_componentGO:0005778 peroxisomal membrane IEA
 cellular_componentGO:0005779 integral component of peroxisomal membrane IDA
 cellular_componentGO:0005782 peroxisomal matrix TAS
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 molecular_functionGO:0016491 oxidoreductase activity IEA
 molecular_functionGO:0080019 fatty-acyl-CoA reductase (alcohol-forming) activity IEA
 molecular_functionGO:0102965 alcohol-forming fatty acyl-CoA reductase activity IEA


Pathways (from Reactome)
Pathway description
Wax biosynthesis


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000007 Autosomal recessive inheritance "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in homozygotes. In the context of medical genetics, autosomal recessive disorders manifest in homozygotes (with two copies of the mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele)." [HPO:curators]
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 HP:0000219 Thin upper lip 
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 HP:0000252 Microcephaly "Microcephaly is a neurodevelopmental disorder in which the circumference of the head is more than two standard deviations smaller than the age- and gender-dependent norm." [HPO:curators]
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 HP:0000280 Coarse facial features 
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 HP:0000343 Long philtrum 
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 HP:0000400 Large ears 
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 HP:0000518 Cataract "A cataract is an opacity or clouding that develops in the crystalline `lens` (FMA:58241) of the eye or in its `capsule` (FMA:58881)." [HPO:probinson]
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 HP:0001249 Mental retardation 
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 HP:0001250 Seizures "Seizures are an intermittent `abnormality of the central nervous system` (FMA:HP:0002011) due to a sudden, excessive, disorderly discharge of cerebral neurons and characterized clinically by some combination of disturbance of sensation, loss of consciousness, impairment of psychic function, or convulsive movements." [HPO:probinson]
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 HP:0001257 Spasticity "A motor disorder characterized by a velocity-dependent increase in tonic stretch reflexes with increased muscle tone, exaggerated (hyperexcitable) tendon reflexes." [HPO:curators]
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 HP:0001263 Developmental retardation "A delay in the achievement of motor or mental milestones manifested prior to age 18 and generally associated with lifelong mental and/or physical impairments." [HPO:curators]
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 HP:0001272 Cerebellar atrophy 
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 HP:0001290 Generalized hypotonia "Generalized muscular hypotonia (abnormally low muscle tone)." [HPO:curators]
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 HP:0001510 Growth retardation 
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 HP:0002553 Arched eyebrows 
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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