Vascular Malformations_Somatic

Gene: KDR

Red List (low evidence)

KDR (kinase insert domain receptor)
EnsemblGeneIds (GRCh38): ENSG00000128052
EnsemblGeneIds (GRCh37): ENSG00000128052
OMIM: 191306, Gene2Phenotype
KDR is in 6 panels

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Red List (low evidence)

Limited reports, may be susceptibility factor.
Sources: Expert list
Created: 1 Jul 2020, 11:13 p.m.

Mode of inheritance
Other

Phenotypes
Hemangioma, capillary infantile, somatic, MIM# 602089

Publications

Details

Mode of Inheritance
Other
Sources
  • Expert list
Phenotypes
  • Hemangioma, capillary infantile, somatic, MIM# 602089
OMIM
191306
Clinvar variants
Variants in KDR
Penetrance
None
Publications
Panels with this gene

History Filter Activity

1 Jul 2020, Gel status: 1

Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: KDR was added gene: KDR was added to Vascular Malformations_Somatic. Sources: Expert list Mode of inheritance for gene: KDR was set to Other Publications for gene: KDR were set to 11807987; 18931684 Phenotypes for gene: KDR were set to Hemangioma, capillary infantile, somatic, MIM# 602089 Review for gene: KDR was set to RED