Alpha-sarcoglycan

Summary
UniProt ID
Q16586
Gene Symbol
  • ADL
  • DAG2
  • SGCA
Gene ID
6442
Organism
Homo sapiens (human)
PubChem
Q16586
Re-Glyco
Q16586
Annotation
Keyword
  • Alternative splicing
  • Cell membrane
  • Cytoskeleton
  • Disease variant
  • Glycoprotein
  • Limb-girdle muscular dystrophy
  • Phosphoprotein
  • Reference proteome
  • Signal
  • Transmembrane helix
Gene Ontology (GO)
Subcellular Location(GO Annotation)

Subcellular in which this glycoprotein is expressed are highlighted in blue.

Displaying 1 entry
GO Term
calcium ion binding
Sequence
MAETLFWTPLLVVLLAGLGDTEAQQTTLHPLVGRVFVHTLDHETFLSLPEHVAVPPAVHITYHAHLQGHPDLPRWLRYTQRSPHHPGFLYGSATPEDRGLQVIEVTAYNRDSFDTTRQRLVLEIGDPEGPLLPYQAEFLVRSHDAEEVLPSTPASRFLSALGGLWEPGELQLLNVTSALDRGGRVPLPIEGRKEGVYIKVGSASPFSTCLKMVASPDSHARCAQGQPPLLSCYDTLAPHFRVDWCNVTLVDKSVPEPADEVPTPGDGILEHDPFFCPPTEAPDRDFLVDALVTLLVPLLVALLLTLLLAYVMCCRREGRLKRDLATSDIQMVHHCTIHGNTEELRQMAASREVPRPLSTLPMFNVHTGERLPPRVDSAQVPLILDQH
Glycosylation Sites
Displaying all 2 entries
Position Description PubMed ID GlyTouCan ID Source
174 N-linked (GlcNAc...) asparagine
246 N-linked (GlcNAc...) asparagine
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Disease
Displaying all 2 entries
DO ID Disease Name Source
DOID:0110278 autosomal recessive limb-girdle muscular dystrophy type 2D
DOID:9884 muscular dystrophy

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: April 7, 2025