Newborns additional phenotypes panel 1
Gene: KLHL3EnsemblGeneIds (GRCh38): ENSG00000146021
EnsemblGeneIds (GRCh37): ENSG00000146021
OMIM: 605775, Gene2Phenotype
KLHL3 is in 2 panels
2 reviews
Arina Puzriakova (Genomics England Curator)
Special Consideration: Multiple MOIs for the same phenotype included.
Additional Information: AD and AR forms of Pseudohypoaldosteronism are included.Created: 26 Sep 2024, 3:46 p.m. | Last Modified: 18 Nov 2025, 3:30 p.m.
Panel Version: 0.102
Mafalda Gomes (Genomics England Curator)
The mechanism of pathogenicity is loss-of-function (LOF).Created: 5 Jul 2023, 3:12 p.m. | Last Modified: 5 Jul 2023, 3:12 p.m.
Panel Version: 0.31
PMID: 34622103 - 50 KLHL3 casesCreated: 5 Jul 2023, 3:12 p.m. | Last Modified: 5 Jul 2023, 3:12 p.m.
Panel Version: 0.31
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
- Sources
-
- Expert Review Green
- Phenotypes
-
- Pseudohypoaldosteronism, type IID, autosomal dominant
- Tags
- OMIM
- 605775
- Clinvar variants
- Variants in KLHL3
- Penetrance
- None
- Panels with this gene
History Filter Activity
Added Tag
Arina Puzriakova (Genomics England Curator)Tag special_consideration tag was added to gene: KLHL3.
Set Phenotypes
Sarah Leigh (Genomics England Curator)Phenotypes for gene: KLHL3 were changed from Pseudohypoaldosteronism, type IID to Pseudohypoaldosteronism, type IID, autosomal dominant
Set Phenotypes
Mafalda Gomes (Genomics England Curator)Added phenotypes Pseudohypoaldosteronism, type IID for gene: KLHL3
Created, Added New Source, Set mode of inheritance, Set Phenotypes
Mafalda Gomes (Genomics England Curator)gene: KLHL3 was added gene: KLHL3 was added to Newborns additional phenotypes panel 1. Sources: Expert Review Green Mode of inheritance for gene: KLHL3 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Phenotypes for gene: KLHL3 were set to Pseudohypoaldosteronism, type IID