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Newborns main panel

Gene: CA12

Amber List (moderate evidence)
CA12 (carbonic anhydrase 12)
EnsemblGeneIds (GRCh38): ENSG00000074410
EnsemblGeneIds (GRCh37): ENSG00000074410
OMIM: 603263, Gene2Phenotype
CA12 is in 0 panels

1 review

Mafalda Gomes (Genomics England Curator)

The mechanism of pathogenicity is loss-of-function (LOF).
Created: 1 Jun 2023, 2:40 p.m. | Last Modified: 1 Jun 2023, 2:40 p.m.
Panel Version: 0.137
PMID: 35359895 - 1 case and review of 3 other families,
Created: 1 Jun 2023, 12:22 p.m. | Last Modified: 1 Jun 2023, 12:22 p.m.
Panel Version: 0.134
Created: 1 Jun 2023, 12:22 p.m.
Last Modified: 1 Jun 2023, 12:22 p.m.
Panel version: 0.137

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
Phenotypes
  • Isolated hyperchlorhidrosis
OMIM
603263
Clinvar variants
Variants in CA12
Penetrance
None
Panels with this gene

History Filter Activity

14 Sep 2023, Gel status: 2

Added New Source, Set Phenotypes, Status Update

Mafalda Gomes (Genomics England Curator)

Source Expert Review Amber was added to CA12. Added phenotypes Isolated hyperchlorhidrosis for gene: CA12 Rating Changed from Green List (high evidence) to Amber List (moderate evidence)

5 Jul 2023, Gel status: 3

Added New Source, Set Phenotypes, Status Update

Mafalda Gomes (Genomics England Curator)

Source Expert Review Green was added to CA12. Added phenotypes Isolated hyperchlorhidrosis for gene: CA12 Rating Changed from Amber List (moderate evidence) to Green List (high evidence)

31 May 2023, Gel status: 2

Added New Source, Set Phenotypes, Status Update

Mafalda Gomes (Genomics England Curator)

Source Expert Review Amber was added to CA12. Added phenotypes Isolated hyperchlorhidrosis for gene: CA12 Rating Changed from No List (delete) to Amber List (moderate evidence)

27 Mar 2023, Gel status: 0

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

Mafalda Gomes (Genomics England Curator)

gene: CA12 was added gene: CA12 was added to Newborns main panel. Sources: Expert Review Removed Mode of inheritance for gene: CA12 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: CA12 were set to Isolated hyperchlorhidrosis