calpain 3

Summary
Gene Symbol
  • CAPN3
Organism
Homo sapiens (human)
NCBI Gene
825
PubChem
825
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Alternative splicing
  • Calcium
  • Cytoplasm
  • Disease variant
  • Limb-girdle muscular dystrophy
  • Metal-binding
  • Nucleus
  • Reference proteome
  • Repeat
  • Thiol protease
Proteins
Displaying all 2 entries
UniProt Protein Name
A0A0S2Z3E1
P20807
  • Calcium-activated neutral proteinase 3
  • Calpain L3
  • Calpain p94
  • Muscle-specific calcium-activated neutral protease 3
  • New calpain 1
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
calpain
Functional Category
  • K: Transcription
  • O: Posttranslational modification, protein turnover, chaperones
  • Q: Secondary metabolites biosynthesis, transport and catabolism
Disease
Disease Ontology
Displaying all 9 entries
DO ID Disease Name Source
DOID:0110273 autosomal dominant limb-girdle muscular dystrophy
DOID:0110275 autosomal recessive limb-girdle muscular dystrophy type 2A
DOID:0110821 hereditary spastic paraplegia 76
DOID:1059 intellectual disability
DOID:11723 Duchenne muscular dystrophy
DOID:2476 hereditary spastic paraplegia
DOID:684 hepatocellular carcinoma
DOID:9884 muscular dystrophy
DOID:9970 obesity

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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