SGCA

GENERAL INFORMATION

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Gene name

SGCA

Gene description

Sarcoglycan, alpha (50kDa dystrophin-associated glycoprotein)

Protein class

Cytoskeleton related proteins
Disease related genes
Predicted intracellular proteins
Predicted membrane proteins
Predicted secreted proteins

Predicted localization

Intracellular,Membrane,Secreted

Number of transcripts

4
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Group enriched (heart muscle, skeletal muscle)
GTEx:Tissue enhanced (skeletal muscle)

Protein evidence

Evidence at protein level

Protein localization

Cytoplasmic expression in several tissues, most prominent in sarcolemma.

ANTIBODY RELIABILITY

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Data reliability
description

Antibody staining mainly not consistent with RNA expression data.

Data reliability

Uncertain based on 1 antibody.
HPA007537
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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

Skeletal muscle

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:  Group enriched (heart muscle, skeletal muscle)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enhanced (skeletal muscle)

Organ

Expression



GENE INFORMATION

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Gene name

SGCA (HGNC Symbol)

Synonyms

A2, adhalin, ADL, DMDA2, LGMD2D, SCARMD1

Description

Sarcoglycan, alpha (50kDa dystrophin-associated glycoprotein) (HGNC Symbol)

Entrez gene summary

This gene encodes a component of the dystrophin-glycoprotein complex (DGC), which is critical to the stability of muscle fiber membranes and to the linking of the actin cytoskeleton to the extracellular matrix. Its expression is thought to be restricted to striated muscle. Mutations in this gene result in type 2D autosomal recessive limb-girdle muscular dystrophy. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]

Chromosome

17

Cytoband

q21.33

Chromosome location (bp)

50164214 - 50175931

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000108823 (version 78.38)

Entrez gene

6442

UniProt

Q16586 (UniProt - Evidence at protein level)

neXtProt

NX_Q16586

Antibodypedia

SGCA antibodies


PROTEIN BROWSER

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ENST00000262018
 
ENST00000344627
 
ENST00000504073
 
ENST00000511303
 
 
 
 


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)

SGCA-001 ENSP00000262018
ENST00000262018
Q16586
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Show » Show » 387 42.9 Yes 1
SGCA-002 ENSP00000345522
ENST00000344627
Q16586
Show all »
Show » Show » 263 29.4 Yes 0
SGCA-008 ENSP00000426104
ENST00000511303
H7C5V0
Show all »
Show » Show » 196 21.4 No 0
SGCA-011 ENSP00000422030
ENST00000504073
Show » Show » 160 17.7 No 1