This Panel is marked as Internal
Renal and urinary tract disorders
Gene: KIT
KIT (KIT proto-oncogene receptor tyrosine kinase)
EnsemblGeneIds (GRCh38): ENSG00000157404
EnsemblGeneIds (GRCh37): ENSG00000157404
OMIM: 164920, Gene2Phenotype
KIT is in 15 panels
EnsemblGeneIds (GRCh38): ENSG00000157404
EnsemblGeneIds (GRCh37): ENSG00000157404
OMIM: 164920, Gene2Phenotype
KIT is in 15 panels
1 review
Helen Stuart (University of Manchester)
Details
- Mode of Inheritance
- Unknown
- Sources
-
- Expert Review Red
- OMIM
- 164920
- Clinvar variants
- Variants in KIT
- Penetrance
- None
- Panels with this gene
-
- CAKUT
- Monogenic hearing loss
- Sarcoma cancer susceptibility
- Inherited predisposition to GIST
- Cytopenias and congenital anaemias
- Adult solid tumours for rare disease
- Sarcoma susceptibility
- Unexplained kidney failure in young people
- Intellectual disability
- Pigmentary skin disorders
- Adult solid tumours cancer susceptibility
- Unexplained young onset end-stage renal disease - additional genes
- Fetal anomalies
- DDG2P
- Rare genetic inflammatory skin disorders
History Filter Activity
30 Jan 2019, Gel status: 1
Panel promoted to version 1.0
Eleanor Williams (Genomics England Curator)Miranda Durkie: May act as modifier. Possible
20 Dec 2018, Gel status: 1
Created, Added New Source, Set mode of inheritance
Ellen McDonagh (Genomics England Curator)gene: KIT was added gene: KIT was added to Renal and urinary tract disorders. Sources: Expert Review Red Mode of inheritance for gene: KIT was set to Unknown