SCARB2

GENERAL INFORMATION

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Gene name

SCARB2

Gene description

Scavenger receptor class B, member 2

Protein class

Disease related genes
Predicted membrane proteins

Predicted localization

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

Ubiquitous cytoplasmic expression, often with a granular pattern.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Supportive based on 2 antibodies.
HPA018014 , CAB015415
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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

SCARB2 (HGNC Symbol)

Synonyms

CD36L2, HLGP85, LIMP-2, LIMPII, SR-BII

Description

Scavenger receptor class B, member 2 (HGNC Symbol)

Entrez gene summary

The protein encoded by this gene is a type III glycoprotein that is located primarily in limiting membranes of lysosomes and endosomes. Earlier studies in mice and rat suggested that this protein may participate in membrane transportation and the reorganization of endosomal/lysosomal compartment. The protein deficiency in mice was reported to impair cell membrane transport processes and cause pelvic junction obstruction, deafness, and peripheral neuropathy. Further studies in human showed that this protein is a ubiquitously expressed protein and that it is involved in the pathogenesis of HFMD (hand, foot, and mouth disease) caused by enterovirus-71 and possibly by coxsackievirus A16. Mutations in this gene caused an autosomal recessive progressive myoclonic epilepsy-4 (EPM4), also known as action myoclonus-renal failure syndrome (AMRF). Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Feb 2011]

Chromosome

4

Cytoband

q21.1

Chromosome location (bp)

76158737 - 76213893

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000138760 (version 78.38)

Entrez gene

950

UniProt

Q14108 (UniProt - Evidence at protein level)

neXtProt

NX_Q14108

Antibodypedia

SCARB2 antibodies


PROTEIN BROWSER

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ENST00000264896
 
ENST00000452464
 
 
 
 


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)

SCARB2-001 ENSP00000264896
ENST00000264896
Q14108
Show all »
Show » Show » 478 54.3 Yes 1
SCARB2-002 ENSP00000399154
ENST00000452464
Q14108
Show all »
Show » Show » 335 37.8 Yes 1