This Panel is marked as Deleted
Kidneyome_SuperPanel_KidGen_VCGS
Gene: KCNJ10
KCNJ10 (potassium voltage-gated channel subfamily J member 10)
EnsemblGeneIds (GRCh38): ENSG00000177807
EnsemblGeneIds (GRCh37): ENSG00000177807
OMIM: 602208, Gene2Phenotype
KCNJ10 is in 12 panels
EnsemblGeneIds (GRCh38): ENSG00000177807
EnsemblGeneIds (GRCh37): ENSG00000177807
OMIM: 602208, Gene2Phenotype
KCNJ10 is in 12 panels
0 reviews
Details
- Mode of Inheritance
- Unknown
- Sources
-
- KidGen_Magnesium v38.1.0
- KidGen_Tubulopathies v38.1.0
- Expert Review Green
- OMIM
- 602208
- Clinvar variants
- Variants in KCNJ10
- Penetrance
- None
- Panels with this gene
-
- Hereditary ataxia
- Ataxia and cerebellar anomalies - narrow panel
- Hereditary ataxia with onset in adulthood
- Intellectual disability
- Early onset or syndromic epilepsy
- Monogenic hearing loss
- Fetal anomalies
- Familial Neural Tube Defects
- Adult onset neurodegenerative disorder
- Childhood onset dystonia, chorea or related movement disorder
- DDG2P
- Renal tubulopathies
History Filter Activity
23 Dec 2019, Gel status: 3
Added New Source
Ivone Leong (Genomics England Curator)Source KidGen_Magnesium v38.1.0 was added to KCNJ10.
23 Dec 2019, Gel status: 3
Created, Added New Source, Set mode of inheritance
Ivone Leong (Genomics England Curator)gene: KCNJ10 was added gene: KCNJ10 was added to Kidneyome_SuperPanel_KidGen_VCGS. Sources: Expert Review Green,KidGen_Tubulopathies v38.1.0 Mode of inheritance for gene: KCNJ10 was set to Unknown