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Genetic Epilepsy v0.1833 TRPM3 Zornitza Stark Phenotypes for gene: TRPM3 were changed from Neurodevelopmental disorder, MONDO:0700092, TRPM3-related to Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures, MIM# 620224
Genetic Epilepsy v0.1832 TRPM3 Zornitza Stark edited their review of gene: TRPM3: Changed phenotypes: Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures, MIM# 620224
Genetic Epilepsy v0.1628 TRPM3 Zornitza Stark Phenotypes for gene: TRPM3 were changed from Intellectual disability; epilepsy to Neurodevelopmental disorder, MONDO:0700092, TRPM3-related
Genetic Epilepsy v0.133 TRPM3 Zornitza Stark Marked gene: TRPM3 as ready
Genetic Epilepsy v0.133 TRPM3 Zornitza Stark Gene: trpm3 has been classified as Green List (High Evidence).
Genetic Epilepsy v0.133 TRPM3 Zornitza Stark Classified gene: TRPM3 as Green List (high evidence)
Genetic Epilepsy v0.133 TRPM3 Zornitza Stark Gene: trpm3 has been classified as Green List (High Evidence).
Genetic Epilepsy v0.132 TRPM3 Zornitza Stark Classified gene: TRPM3 as Green List (high evidence)
Genetic Epilepsy v0.132 TRPM3 Zornitza Stark Gene: trpm3 has been classified as Green List (High Evidence).
Genetic Epilepsy v0.131 TRPM3 Zornitza Stark gene: TRPM3 was added
gene: TRPM3 was added to Genetic Epilepsy_AustralianGenomics_VCGS. Sources: Literature
Mode of inheritance for gene: TRPM3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: TRPM3 were set to 31278393
Phenotypes for gene: TRPM3 were set to Intellectual disability; epilepsy
Review for gene: TRPM3 was set to GREEN
Added comment: 8 unrelated individuals with de novo variants in this gene. Recurrent variant p.(Val837Met) identified in 7/8.
Sources: Literature