CLCNKB

chloride voltage-gated channel Kb
OMIM: 602023, Gene2Phenotype

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Red CLCNKB in Hydrops fetalis Level 2: Dysmorphic and congenital abnormality syndromes Version 0.328	1 review	Other	Sources Expert Review Red Expert list Phenotypes Bartter syndrome, type 4b, digenic, MIM#613090
Green CLCNKB in Mendeliome Version 1.3499	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Bartter syndrome, type 3, MIM# 607364 Bartter syndrome, type 4b, digenic, MIM# 613090 Tags SV/CNV
Green CLCNKB in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.398	1 review	Other	Sources Expert Review Green Genetic Health Queensland Phenotypes Bartter syndrome, type 3, MIM#607364 Bartter syndrome, type 4b, digenic, MIM#613090
Green CLCNKB in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 0.110	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Bartter syndrome, type 4b, digenic, 613090 (3)
Green CLCNKB in Fetal anomalies Version 1.465	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Genetic Health Queensland Phenotypes Bartter syndrome, type 3, MIM#607364 Bartter syndrome, type 4b, digenic, MIM#613090
Green CLCNKB in Prepair 1000+ Level 2: Screening Version 2.14	3 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Bartter syndrome, type 3 MIM#607364
Green CLCNKB in Renal Tubulopathies and related disorders Level 2: Renal and urinary tract disorders Version 1.22 Component of the following Super Panels: Kidneyome_SuperPanel	4 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Expert Review Green Expert Review Literature Victorian Clinical Genetics Services Phenotypes Bartter syndrome, type 3, MIM# 607364 Bartter syndrome, type 4b, digenic, MIM# 613090