integrin subunit alpha 7

Summary
Gene Symbol
  • ITGA7
Organism
Homo sapiens (human)
NCBI Gene
3679
PubChem
3679
Alliance of Genome Resources
Annotation
Keyword
  • ADP-ribosylation
  • Alternative splicing
  • Calcium
  • Cell adhesion
  • Cell shape
  • Cleavage on pair of basic residues
  • Congenital muscular dystrophy
  • Direct protein sequencing
  • Disulfide bond
  • Glycoprotein
  • Integrin
  • Metal-binding
  • Receptor
  • Reference proteome
  • Repeat
  • Signal
  • Transmembrane helix
Proteins
Displaying all 2 entries
UniProt Protein Name
Q4LE35
Q13683
Gene Ontology (GO)
OrthoDB (Group)
Group level
Eukaryota
Group Name
integrin
Functional Category
  • E: Amino acid transport and metabolism
  • O: Posttranslational modification, protein turnover, chaperones
  • Q: Secondary metabolites biosynthesis, transport and catabolism
Disease
Disease Ontology
Displaying all 7 entries
DO ID Disease Name Source
DOID:0050700 cardiomyopathy
DOID:0080000 muscular disease
DOID:0110639 congenital muscular dystrophy due to integrin alpha-7 deficiency
DOID:11723 Duchenne muscular dystrophy
DOID:162 cancer
DOID:1826 epilepsy
DOID:2349 arteriosclerosis

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: December 9, 2024