myosin VIIA

Summary
Gene Symbol
  • MYO7A
Organism
Homo sapiens (human)
NCBI Gene
4647
PubChem
4647
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • ATP-binding
  • Actin-binding
  • Alternative splicing
  • Calmodulin-binding
  • Cytoskeleton
  • Disease variant
  • Hearing
  • Leber congenital amaurosis
  • Myosin
  • Non-syndromic deafness
  • Phosphoprotein
  • Reference proteome
  • Repeat
  • Retinitis pigmentosa
  • SH3 domain
  • Synapse
  • Usher syndrome
Proteins
Displaying 1 entry
UniProt Protein Name
Q13402
Gene Ontology (GO)
GO Hierarchy
Displaying entries 1 - 5 of 17 in total
GO Term Evidence Code PMID
membrane
cell cortex
microvillus
apical plasma membrane
myosin VII complex
GO Hierarchy
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
myosin
Functional Category
  • G: Carbohydrate transport and metabolism
  • K: Transcription
  • O: Posttranslational modification, protein turnover, chaperones
Disease
Disease Ontology
Displaying all 8 entries
DO ID Disease Name Source
DOID:0050439 Usher syndrome
DOID:0110477 autosomal recessive nonsyndromic deafness 2
DOID:0110543 autosomal dominant nonsyndromic deafness 11
DOID:0110826 Usher syndrome type 1
DOID:10003 sensorineural hearing loss
DOID:14791 Leber congenital amaurosis
DOID:2742 auditory system disease
DOID:9649 congenital nystagmus

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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