SCP2

GENERAL INFORMATION

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Gene name

SCP2

Gene description

Sterol carrier protein 2

Protein class

Disease related genes
Enzymes
Mitochondrial proteins
Plasma proteins
Potential drug targets
Predicted intracellular proteins

Predicted localization

Intracellular

Number of transcripts

12
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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 in essentially all cells except in lymphoid tissues and CNS.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Supportive based on 3 antibodies.
HPA027101 , HPA027135 , HPA027317
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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

SCP2

Synonyms

Description

Sterol carrier protein 2 (HGNC Symbol)

Entrez gene summary

This gene encodes two proteins: sterol carrier protein X (SCPx) and sterol carrier protein 2 (SCP2), as a result of transcription initiation from 2 independently regulated promoters. The transcript initiated from the proximal promoter encodes the longer SCPx protein, and the transcript initiated from the distal promoter encodes the shorter SCP2 protein, with the 2 proteins sharing a common C-terminus. Evidence suggests that the SCPx protein is a peroxisome-associated thiolase that is involved in the oxidation of branched chain fatty acids, while the SCP2 protein is thought to be an intracellular lipid transfer protein. This gene is highly expressed in organs involved in lipid metabolism, and may play a role in Zellweger syndrome, in which cells are deficient in peroxisomes and have impaired bile acid synthesis. Alternative splicing of this gene produces multiple transcript variants, some encoding different isoforms.[provided by RefSeq, Aug 2010]

Chromosome

1

Cytoband

p32.3

Chromosome location (bp)

52927229 - 53051703

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000116171 (version 78.38)

Entrez gene

6342

UniProt

P22307 (UniProt - Evidence at protein level)

neXtProt

NX_P22307

Antibodypedia

SCP2 antibodies


PROTEIN BROWSER

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ENST00000371509
 
ENST00000371513
 
ENST00000371514
 
ENST00000407246
 
ENST00000408941
 
ENST00000430330
 
ENST00000435345
 
ENST00000478274
 
ENST00000484100
 
ENST00000488965
 
ENST00000528311
 
ENST00000529363
 
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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)

SCP2-001 ENSP00000360569
ENST00000371514
P22307
Show all »
Show » Show » 547 59 No 0
SCP2-002 ENSP00000435783
ENST00000488965
P22307
Show all »
Show » Show » 59 6.7 No 0
SCP2-004 ENSP00000360568
ENST00000371513
P22307
Show all »
Show » Show » 322 35 No 0
SCP2-005 ENSP00000432645
ENST00000484100
Show » 78 8.5 No 0
SCP2-006 ENSP00000437317
ENST00000478274
B4E0J3
Show all »
Show » 140 14.9 No 0
SCP2-007 ENSP00000360564
ENST00000371509
P22307
Show all »
Show » Show » 503 54.4 No 0
SCP2-008 ENSP00000406636
ENST00000430330
P22307
Show all »
Show » Show » 140 15.1 No 0
SCP2-010 ENSP00000434132
ENST00000528311
P22307
Show all »
Show » Show » 466 50.3 No 0
SCP2-011 ENSP00000384569
ENST00000407246
P22307
Show all »
Show » Show » 523 56.5 No 0
SCP2-013 ENSP00000431279
ENST00000529363
Show » Show » 240 25.8 No 0
SCP2-015 ENSP00000396413
ENST00000435345
P22307
Show all »
Show » Show » 143 15.4 No 0
SCP2-201 ENSP00000386214
ENST00000408941
P22307
Show all »
Show » Show » 59 6.7 No 0