Homo sapiens Gene:
ACSF3
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InnateDB Gene
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IDBG-47147.5
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Last Modified
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2012-02-14 [Report errors or provide feedback]
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Gene Symbol
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ACSF3
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Gene Name
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acyl-CoA synthetase family member 3
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Synonyms
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Species
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Homo sapiens
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Ensembl Gene
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ENSG00000176715
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Encoded Proteins
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| Summary |
This gene encodes a member of the acyl-CoA synthetase family of enzymes that activate fatty acids by catalyzing the formation of a thioester linkage between fatty acids and coenzyme A. The encoded protein is localized to mitochondria, has high specificity for malonate and methylmalonate and possesses malonyl-CoA synthetase activity. Mutations in this gene are a cause of combined malonic and methylmalonic aciduria. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]
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| Type |
Protein coding
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Genomic Location
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Chromosome 16:
89154783-89222254
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Strand
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Forward strand
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Band
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q24.3
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Transcripts
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Number of Interactions
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This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
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| Predicted by orthology |
| Total |
1 [view]
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| Molecular Function |
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| Biological Process |
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| Cellular Component |
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| Species |
Mus musculus
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Bos taurus
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| NETPATH |
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| REACTOME |
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| KEGG |
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| INOH |
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| PID BIOCARTA |
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| PID NCI |
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SwissProt
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Q4G176
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TrEMBL
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F5GX20
F5H2G6
F5H362
F5H3B2
F5H5A1
F5H755
H0YH37
H3BTS0
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UniProt Splice Variant
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Entrez Gene
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197322
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UniGene
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Hs.670100
Hs.737565
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RefSeq
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NM_001127214
NM_001243279
NM_174917
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HUGO
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27288
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OMIM
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614245
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CCDS
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CCDS10974
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| HPRD |
14117
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IMGT
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EMBL
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AC009113
AC135782
AK075499
AK290963
BC028399
BC072391
CH471184
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GenPept
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AAH28399
AAH72391
BAC11654
BAF83652
EAW66744
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ImmGen
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ACSF3 (murine)
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RNA Seq Atlas
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197322
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