myosin heavy chain 9

Summary
Gene Symbol
  • MYH9
Organism
Homo sapiens (human)
NCBI Gene
4627
PubChem
4627
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • ATP-binding
  • Acetylation
  • Actin-binding
  • Alport syndrome
  • Alternative splicing
  • Calmodulin-binding
  • Cataract
  • Cell adhesion
  • Cell shape
  • Coiled coil
  • Cytoplasmic vesicle
  • Cytoskeleton
  • Direct protein sequencing
  • Disease variant
  • Methylation
  • Myosin
  • Non-syndromic deafness
  • Phosphoprotein
  • Reference proteome
  • Ubl conjugation
Proteins
Displaying 1 entry
UniProt Protein Name
P35579
  • Cellular myosin heavy chain, type A
  • Myosin heavy chain 9
  • Myosin heavy chain, non-muscle IIa
  • Non-muscle myosin heavy chain A
  • Non-muscle myosin heavy chain IIa
Gene Ontology (GO)
GO Hierarchy
Displaying entries 1 - 5 of 28 in total
GO Term Evidence Code PMID
membrane
spindle
focal adhesion
myosin filament
myosin II complex
GO Hierarchy
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
myosin
Functional Category
  • G: Carbohydrate transport and metabolism
  • K: Transcription
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying entries 1 - 10 of 11 in total
DO ID Disease Name Source
DOID:0050567 orofacial cleft
DOID:0050758 metabolic acidosis
DOID:0060651 MYH-9 related disease
DOID:0110032 autosomal dominant Alport syndrome
DOID:0110548 autosomal dominant nonsyndromic deafness 17
DOID:10003 sensorineural hearing loss
DOID:1588 thrombocytopenia
DOID:557 kidney disease
DOID:576 proteinuria
DOID:783 end stage renal disease

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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