Entity Details

Primary name SGCB_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ16585
EntryNameSGCB_HUMAN
FullNameBeta-sarcoglycan
TaxID9606
Evidenceevidence at protein level
Length318
SequenceStatuscomplete
DateCreated2001-04-27
DateModified2021-06-02

Ontological Relatives

GenesSGCB

GO terms

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GOName
GO:0005737 cytoplasm
GO:0005856 cytoskeleton
GO:0005887 integral component of plasma membrane
GO:0007517 muscle organ development
GO:0016010 dystrophin-associated glycoprotein complex
GO:0016012 sarcoglycan complex
GO:0042383 sarcolemma
GO:0055013 cardiac muscle cell development
GO:0097084 vascular associated smooth muscle cell development

Subcellular Location

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Subcellular Location
Cell membrane
Cytoplasm

Domains

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DomainNameCategoryType
IPR006875 Sarcoglycan complex subunit proteinFamilyFamily
IPR027659 Beta-sarcoglycanFamilyFamily

Diseases

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Disease IDSourceNameDescription
604286 OMIMMuscular dystrophy, limb-girdle, autosomal recessive 4 (LGMDR4)An autosomal recessive degenerative myopathy characterized by pelvic and shoulder muscle wasting, onset usually in childhood and variable progression rate. The disease is caused by variants affecting the gene represented in this entry.