SLC25A20

GENERAL INFORMATION

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Gene name

SLC25A20

Gene description

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

Protein class

Disease related genes
Mitochondrial proteins
Potential drug targets
Predicted intracellular proteins
Predicted membrane proteins
Transporters

Predicted localization

Intracellular,Membrane

Number of transcripts

2
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Expressed in all
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

Cytoplasmic expression in several different cell types.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Uncertain based on 2 antibodies.
HPA016862 , HPA029863
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Expressed in all

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



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 BROWSER

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ENST00000319017
 
ENST00000430379
 
 
 
 


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