Kit ligand - CISMeF

Preferred Label : Kit ligand;

Symbol : KITLG;

CISMeF acronym : KITLG;

Type : Gene;

Alternative titles and symbols : Kl; Mast cell growth factor; Mgf stem cell factor; Steel, mouse, homolog of; Steel factor; KITL; MGF; SCF; SF;

Ensembl ID : ENSG00000049130;

Prefixed ID : *184745;

Details

Origin ID

184745;

UMLS CUI

C1366480;

Automatic exact mappings (from CISMeF team)
- GDC Smoking Frequency Terminology [NCIt concept]
- HGF wt Allele [NCIt concept]
- Insulin-Like Growth Factor I [NCIt concept]
- Interleukin-3 [NCIt concept]
- Interleukin-3 (substance) [SNOMED CT concept]
- KIT ligand [ORDO Gene]
- KIT ligand [HGNC gene]
- KITLG Gene [NCIt concept]
- KITLG wt Allele [NCIt concept]
- KL Gene [NCIt concept]
- Kit Ligand [NCIt concept]
- Recombinant Human Stem Cell Factor [NCIt concept]
- SCF [EDAM format]
- STAT5A wt Allele [NCIt concept]
- STAT5B wt Allele [NCIt concept]
- Signal Transducer and Activator of Transcription 5A [NCIt concept]
- Standard Cubic Foot [NCIt concept]
- Stem Cell Factor Measurement [NCIt concept]
- hepatocyte growth factor [ORDO Gene]
- stem cell factor [MeSH Descriptor]
- stem cell factor [Blood Transfusion thesaurus concept]
- stem cell factor receptor binding [GO term]
- subfascicular nucleus [UBERON concept]
HGNC gene
- KIT ligand [HGNC gene]
NCIt concept(s)
- KITLG Gene [NCIt concept]
- KITLG wt Allele [NCIt concept]
- Kit Ligand [NCIt concept]
ORDO concept(s)
- KIT ligand [ORDO Gene]
Phenotypes related
- Deafness, autosomal dominant 69 [OMIM Phenotype]
- Hyperpigmentation with or without hypopigmentation, familial progressive [OMIM Phenotype]
- Skin/hair/eye pigmentation, variation in, 7 [OMIM Phenotype]
- Waardenburg syndrome, type 2f [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- KIT ligand [HGNC gene]
- KITLG Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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