Wnt family member 10A

Summary
Gene Symbol
  • WNT10A
Organism
Homo sapiens (human)
NCBI Gene
80326
PubChem
80326
Alliance of Genome Resources
Annotation
Keyword
  • Developmental protein
  • Disease variant
  • Disulfide bond
  • Ectodermal dysplasia
  • Extracellular matrix
  • Glycoprotein
  • Hypotrichosis
  • Lipoprotein
  • Palmoplantar keratoderma
  • Phosphoprotein
  • Reference proteome
  • Signal
  • Wnt signaling pathway
Proteins
Displaying all 2 entries
UniProt Protein Name
A0A2K8FR47
Q9GZT5
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
Wnt
Functional Category
  • J: Translation, ribosomal structure and biogenesis
  • K: Transcription
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying all 3 entries
DO ID Disease Name Source
DOID:0050591 tooth agenesis
DOID:0111647 Schopf-Schulz-Passarge syndrome
DOID:2121 ectodermal dysplasia

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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