PCDH19 Chromosome X

Protocadherin 19
418 variants 418 Health Risk

Upload your DNA to see your personal genotypes for variants in PCDH19.

What This Gene Does
The protein encoded by this gene is a member of the delta-2 protocadherin subclass of the cadherin superfamily. The encoded protein is thought to be a calcium-dependent cell-adhesion protein that is primarily expressed in the brain. Mutations in this gene on human chromosome X are associated with sporadic infantile epileptic encephalopathy and to a female-restricted form of epilepsy (EFMR; also known as PCDH19RE). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2017]
Gene Info
Gene Group
Non-clustered protocadherins
Locus Type
gene with protein product
Location
Xq22.1
Ensembl
ENSG00000165194
Associated Conditions (24)
Developmental and epileptic encephalopathy
9
Inborn genetic diseases
PCDH19-related disorder
Glycine encephalopathy
Familial GGE
sporadic NAFE
Neurodevelopmental disorder with epilepsy
Bilateral tonic-clonic seizure
Refractory epilepsy with Lennox Gastaut syndrome
PCDH19-related epilespy
See cases
Intellectual disability
developmental delay with seizures
Seizure
Epileptic encephalopathy
Epilepsy
PCDH19-related epilepsy syndrome
Nonpapillary renal cell carcinoma
Complex febrile seizure
+4 more conditions
Key Variants
RS1064794763
Conflicting classifications of pathogenicity
Health Risk
RS1241637351
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
Health Risk
RS1325807867
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 9, Inborn genetic diseases
Health Risk
RS137962077
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
Health Risk
RS138771033
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 9, Inborn genetic diseases
Health Risk
RS1403828540
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
Health Risk
RS1422167083
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
Health Risk
RS1555972516
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
Health Risk
RS1555985687
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
Health Risk
RS1602600445
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
Health Risk
RS1602636688
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
Health Risk
RS189342249
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 9, PCDH19-related disorder
Health Risk
All Variants (418)
RSID Category Clinical Significance Conditions
RS2520996566 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
RS2520997876 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
RS2520997930 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
RS2520998607 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, Inborn genetic diseases
RS2520999081 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
RS2520999960 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
RS267606933 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
RS34651888 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
RS56307810 Health Risk Pathogenic
RS587784295 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
RS749662385 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
RS756414485 Health Risk Pathogenic Inborn genetic diseases, Developmental and epileptic encephalopathy, 9
RS758946412 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, 11 conditions
RS759398718 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
RS762069884 Health Risk Pathogenic Seizure, Seizure
RS764650219 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
RS769967221 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, Inborn genetic diseases
RS770935301 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
RS779665170 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
RS794726897 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
RS796052794 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
RS796052797 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
RS796052800 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
RS796052801 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
RS796052802 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, Seizure
RS796052807 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
RS796052813 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
RS796052817 Health Risk Pathogenic
RS796052819 Health Risk Pathogenic Inborn genetic diseases, Developmental and epileptic encephalopathy, 9
RS796052820 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
RS796052826 Health Risk Pathogenic
RS796052827 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
RS796052828 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
RS796052829 Health Risk Pathogenic
RS796052830 Health Risk Pathogenic
RS796052831 Health Risk Pathogenic
RS796052832 Health Risk Pathogenic
RS796052833 Health Risk Pathogenic
RS796052834 Health Risk Pathogenic
RS796052835 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
RS796052836 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
RS796052837 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
RS796052841 Health Risk Pathogenic
RS796052842 Health Risk Pathogenic
RS796052844 Health Risk Pathogenic
RS797045873 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
RS868762744 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
RS886039707 Health Risk Pathogenic
RS886039728 Health Risk Pathogenic
RS886043572 Health Risk Pathogenic Developmental and epileptic encephalopathy, 9, Developmental and epileptic encephalopathy
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