KIT ligand

Summary
Gene Symbol
  • KITLG
Organism
Homo sapiens (human)
NCBI Gene
4254
PubChem
4254
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Alternative splicing
  • Cell adhesion
  • Cell membrane
  • Cell projection
  • Cytoskeleton
  • Direct protein sequencing
  • Disease variant
  • Disulfide bond
  • Glycoprotein
  • Growth factor
  • Non-syndromic deafness
  • Reference proteome
  • Secreted
  • Signal
  • Transmembrane helix
  • Waardenburg syndrome
Proteins
Displaying 1 entry
UniProt Protein Name
P21583
  • Mast cell growth factor
  • Stem cell factor
  • c-Kit ligand
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
Kit ligand
Functional Category
  • K: Transcription
  • O: Posttranslational modification, protein turnover, chaperones
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying all 4 entries
DO ID Disease Name Source
DOID:0110590 autosomal dominant nonsyndromic deafness 69
DOID:0111373 familial progressive hyperpigmentation with or without hypopigmentation
DOID:10123 pigmentation disease
DOID:9258 Waardenburg 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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Last updated: April 7, 2025