SLC25A20

GENE INFORMATION

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Gene name

SLC25A20 (HGNC Symbol)

Synonyms

CAC, CACT

Description

Solute carrier family 25 (carnitine/acylcarnitine translocase), member 20 (HGNC Symbol)

Entrez gene summary

This gene product is one of several closely related mitochondrial-membrane carrier proteins that shuttle substrates between cytosol and the intramitochondrial matrix space. This protein mediates the transport of acylcarnitines into mitochondrial matrix for their oxidation by the mitochondrial fatty acid-oxidation pathway. Mutations in this gene are associated with carnitine-acylcarnitine translocase deficiency, which can cause a variety of pathological conditions such as hypoglycemia, cardiac arrest, hepatomegaly, hepatic dysfunction and muscle weakness, and is usually lethal in new born and infants. [provided by RefSeq, Jul 2008]

Chromosome

3

Cytoband

p21.31

Chromosome location (bp)

48856931 - 48898993

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000178537 (version 78.38)

Entrez gene

788

UniProt

O43772 (UniProt - Evidence at protein level)

neXtProt

NX_O43772

Antibodypedia

SLC25A20 antibodies
 

PROTEIN VIEW

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SLC25A20-001
 
SLC25A20-002
 
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

SLC25A20-001 ENSP00000326305
ENST00000319017
O43772
Show all »
Show » Show » 301 32.9 No 5
SLC25A20-002 ENSP00000388986
ENST00000430379
C9JPE1
Show all »
Show » Show » 228 25.1 No 0