vacuolar protein sorting 4 homolog A

Summary
Gene Symbol
  • VPS4A
Aliases
  • FLJ22197
  • SKD1
  • SKD1A
  • SKD2
  • VPS4
  • VPS4-1
Organism
Homo sapiens (human)
NCBI Gene
27183
HGNC
13488
KEGG Gene ID
PubChem
27183
Alliance of Genome Resources
Gene Ontology (GO)
GO Hierarchy
Displaying entries 21 - 25 of 33 in total
GO Term Evidence Code PMID
endosome membrane
midbody
midbody
midbody
midbody
GO Hierarchy
Displaying entries 1 - 5 of 11 in total
GO Term Evidence Code PMID
protein binding
ATP binding
ATP binding
ATP hydrolysis activity
ATP hydrolysis activity
GO Hierarchy
Disease
The Human Phenotype Ontology
Displaying entries 1 - 10 of 32 in total
HPO ID HPO Term
HP:0000006 Autosomal dominant inheritance
HP:0000135 Hypogonadism
HP:0000252 Microcephaly
HP:0000407 Sensorineural hearing impairment
HP:0000505 Visual impairment
HP:0000519 Developmental cataract
HP:0000556 Retinal dystrophy
HP:0000750 Delayed speech and language development
HP:0001081 Cholelithiasis
HP:0001250 Seizure
Displaying 1 entry
Disease ID Disease Name
OMIM:619273
  • cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome

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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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