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  3. CALHM1
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Incidentalome

Gene: CALHM1

Red List (low evidence)
CALHM1 (calcium homeostasis modulator 1)
EnsemblGeneIds (GRCh38): ENSG00000185933
EnsemblGeneIds (GRCh37): ENSG00000185933
OMIM: 612234, Gene2Phenotype
CALHM1 is in 1 panel

1 review

Sangavi Sivagnanasundram (Melbourne Health)

Red List (low evidence)

PMID:19472444 – Study to identify whether mutations in CALHM1 had any correlation to Alzheimers Disease. Study showed no association between CALHM1 and Alzheimers Disease (AD)

No evidence showing correlation between CALHM1 mutations and AD
Created: 29 Mar 2023, 1:48 a.m. | Last Modified: 29 Mar 2023, 1:48 a.m.
Panel Version: 0.223

Mode of inheritance
Unknown

Publications

Mode of pathogenicity
Other

Created: 29 Mar 2023, 1:48 a.m.
Last Modified: 29 Mar 2023, 1:48 a.m.
Panel version: 0.223

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
OMIM
612234
Clinvar variants
Variants in CALHM1
Penetrance
None
Panels with this gene

History Filter Activity

21 Aug 2023, Gel status: 1

Entity classified by Genomics England curator

Bryony Thompson (Royal Melbourne Hospital)

Gene: calhm1 has been classified as Red List (Low Evidence).

21 Aug 2023, Gel status: 1

Entity classified by Genomics England curator

Bryony Thompson (Royal Melbourne Hospital)

Gene: calhm1 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: CALHM1 was added gene: CALHM1 was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: CALHM1 was set to Unknown