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Mendeliome

Gene: KEL

Red List (low evidence)

KEL (Kell blood group, metallo-endopeptidase)
EnsemblGeneIds (GRCh38): ENSG00000197993
EnsemblGeneIds (GRCh37): ENSG00000197993
OMIM: 613883, Gene2Phenotype
KEL is in 1 panel

1 review

Ain Roesley (Victorian Clinical Genetics Services)

Red List (low evidence)

there is currently no mendelian disease association.
This gene is known for it's involvement in the Kell anigen system
Created: 31 Dec 2021, 1:14 a.m. | Last Modified: 31 Dec 2021, 1:14 a.m.
Panel Version: 0.10426

Variants in this GENE are reported as part of current diagnostic practice

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • [Blood group, Kell] 110900
OMIM
613883
Clinvar variants
Variants in KEL
Penetrance
None
Panels with this gene

History Filter Activity

31 Dec 2021, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: kel has been classified as Red List (Low Evidence).

31 Dec 2021, Gel status: 1

Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Phenotypes for gene: KEL were changed from to [Blood group, Kell] 110900

31 Dec 2021, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: kel has been classified as Red List (Low Evidence).

17 Nov 2019, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: KEL was added gene: KEL was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: KEL was set to Unknown