White matter disorders and cerebral calcification - narrow panel
Gene: GJC2
GJC2 (gap junction protein gamma 2)
EnsemblGeneIds (GRCh38): ENSG00000198835
EnsemblGeneIds (GRCh37): ENSG00000198835
OMIM: 608803, Gene2Phenotype
GJC2 is in 17 panels
EnsemblGeneIds (GRCh38): ENSG00000198835
EnsemblGeneIds (GRCh37): ENSG00000198835
OMIM: 608803, Gene2Phenotype
GJC2 is in 17 panels
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Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Phenotypes
-
- Spastic paraplegia 44, autosomal recessive, 613206
- Leukodystrophy, hypomyelinating, 2, 608804
- Lymphedema, hereditary, IC, 613480
- OMIM
- 608803
- Clinvar variants
- Variants in GJC2
- Penetrance
- None
- Publications
- Panels with this gene
-
- White matter disorders and cerebral calcification - narrow panel
- Hereditary ataxia with onset in adulthood
- Adult onset leukodystrophy
- Intellectual disability
- DDG2P
- Ataxia and cerebellar anomalies - narrow panel
- Childhood onset dystonia, chorea or related movement disorder
- Inherited white matter disorders
- Hereditary ataxia
- Childhood onset hereditary spastic paraplegia
- Adult onset neurodegenerative disorder
- Hereditary neuropathy or pain disorder
- Hereditary spastic paraplegia
- Hereditary neuropathy
- Fetal anomalies
- Primary lymphoedema
- Adult onset hereditary spastic paraplegia
History Filter Activity
8 Jan 2019, Gel status: 4
Panel promoted to version 1.0
Louise Daugherty (Genomics England Curator)Checked against super panel made up of the panel constituents. Ready to promote to version 1
19 Dec 2018, Gel status: 4
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Ellen McDonagh (Genomics England Curator)gene: GJC2 was added gene: GJC2 was added to White matter disorders and cerebral calcification - narrow panel. Sources: Expert Review Green Mode of inheritance for gene: GJC2 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: GJC2 were set to 25655951 Phenotypes for gene: GJC2 were set to Spastic paraplegia 44, autosomal recessive, 613206; Leukodystrophy, hypomyelinating, 2, 608804; Lymphedema, hereditary, IC, 613480