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Mendeliome

Gene: KCNMB1

Red List (low evidence)

KCNMB1 (potassium calcium-activated channel subfamily M regulatory beta subunit 1)
EnsemblGeneIds (GRCh38): ENSG00000145936
EnsemblGeneIds (GRCh37): ENSG00000145936
OMIM: 603951, Gene2Phenotype
KCNMB1 is in 1 panel

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Red List (low evidence)

Not associated with Mendelian disease.
Created: 14 Mar 2022, 5:47 a.m. | Last Modified: 14 Mar 2022, 5:47 a.m.
Panel Version: 0.11318

Phenotypes
{Hypertension, diastolic, resistance to} 608622

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • {Hypertension, diastolic, resistance to} 608622
OMIM
603951
Clinvar variants
Variants in KCNMB1
Penetrance
None
Panels with this gene

History Filter Activity

14 Mar 2022, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: kcnmb1 has been classified as Red List (Low Evidence).

14 Mar 2022, Gel status: 1

Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Phenotypes for gene: KCNMB1 were changed from to {Hypertension, diastolic, resistance to} 608622

14 Mar 2022, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: kcnmb1 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: KCNMB1 was added gene: KCNMB1 was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: KCNMB1 was set to Unknown