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MIRAGE
Delta-sarcoglycan

Summary
UniProt ID
Q92629
Gene Symbol
  • SGCD
Gene ID
6444
Organism
Homo sapiens (human)
GlyGen
Q92629
PubChem
Q92629
RaftProt
Q92629
Re-Glyco
Q92629
Annotation
Keyword
  • Alternative splicing
  • Cardiomyopathy
  • Cell membrane
  • Cytoskeleton
  • Disease variant
  • Disulfide bond
  • Glycoprotein
  • Limb-girdle muscular dystrophy
  • Reference proteome
  • Signal-anchor
  • Transmembrane helix
Gene Ontology (GO)
Displaying all 6 entries
GO Term
sarcoglycan complex
dystrophin-associated glycoprotein complex
sarcolemma
sarcoplasmic reticulum
cytoskeleton
plasma membrane
Subcellular Location(GO Annotation)

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

Annotation information from UniProt.
Sequence
MPQEQYTHHRSTMPGSVGPQVYKVGIYGWRKRCLYFFVLLLMILILVNLAMTIWILKVMNFTIDGMGNLRITEKGLKLEGDSEFLQPLYAKEIQSRPGNALYFKSARNVTVNILNDQTKVLTQLITGPKAVEAYGKKFEVKTVSGKLLFSADNNEVVVGAERLRVLGAEGTVFPKSIETPNVRADPFKELRLESPTRSLVMEAPKGVEINAEAGNMEATCRTELRLESKDGEIKLDAAKIRLPRLPHGSYTPTGTRQKVFEICVCANGRLFLSQAGAGSTCQINTSVCL
  • N : N-glycosylation Site
  • ___ : Potential Sequon
Glycosylation Sites
Displaying all 3 entries
Position Description PubMed ID GlyTouCan ID Source
60 N-linked (GlcNAc...) asparagine
108 N-linked (GlcNAc...) asparagine
284 N-linked (GlcNAc...) asparagine
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Disease
Displaying all 3 entries
DO ID Disease Name Source
DOID:0110280 autosomal recessive limb-girdle muscular dystrophy type 2F
DOID:0110436 dilated cardiomyopathy 1L
DOID:9884 muscular dystrophy
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International Collaboration

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: December 8, 2025