SLC27A4

GENERAL INFORMATION

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Gene name

SLC27A4

Gene description

Solute carrier family 27 (fatty acid transporter), member 4

Protein class

Disease related genes
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

General cytoplasmic expression with high levels in selected tissues including thyroid gland and the gastrointestinal tract.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Supportive based on 2 antibodies.
HPA007293 , CAB009771
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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

SLC27A4 (HGNC Symbol)

Synonyms

ACSVL4, FATP4

Description

Solute carrier family 27 (fatty acid transporter), member 4 (HGNC Symbol)

Entrez gene summary

This gene encodes a member of a family of fatty acid transport proteins, which are involved in translocation of long-chain fatty acids cross the plasma membrane. This protein is expressed at high levels on the apical side of mature enterocytes in the small intestine, and appears to be the principal fatty acid transporter in enterocytes. Clinical studies suggest this gene as a candidate gene for the insulin resistance syndrome. Mutations in this gene have been associated with ichthyosis prematurity syndrome. [provided by RefSeq, Apr 2010]

Chromosome

9

Cytoband

q34.11

Chromosome location (bp)

128340646 - 128361470

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000167114 (version 78.38)

Entrez gene

10999

UniProt

Q6P1M0 (UniProt - Evidence at protein level)

neXtProt

NX_Q6P1M0

Antibodypedia

SLC27A4 antibodies


PROTEIN BROWSER

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ENST00000300456
 
ENST00000372870
 
 
 
 


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)

SLC27A4-001 ENSP00000300456
ENST00000300456
Q6P1M0
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Show » Show » 643 72.1 Yes 2
SLC27A4-002 ENSP00000361961
ENST00000372870
Q6P1M0
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Show » Show » 237 26 No 0