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Genetic Epilepsy v0.1842 DNAH14 Zornitza Stark Tag disputed tag was added to gene: DNAH14.
Genetic Epilepsy v0.1842 DNAH14 Elena Savva Classified gene: DNAH14 as Red List (low evidence)
Genetic Epilepsy v0.1842 DNAH14 Elena Savva Gene: dnah14 has been classified as Red List (Low Evidence).
Genetic Epilepsy v0.1842 DNAH14 Elena Savva Classified gene: DNAH14 as Red List (low evidence)
Genetic Epilepsy v0.1842 DNAH14 Elena Savva Gene: dnah14 has been classified as Red List (Low Evidence).
Genetic Epilepsy v0.1841 DNAH14 Elena Savva reviewed gene: DNAH14: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Genetic Epilepsy v0.1591 DNAH14 Zornitza Stark Marked gene: DNAH14 as ready
Genetic Epilepsy v0.1591 DNAH14 Zornitza Stark Gene: dnah14 has been classified as Green List (High Evidence).
Genetic Epilepsy v0.1591 DNAH14 Zornitza Stark Phenotypes for gene: DNAH14 were changed from Neurodevelopmental disorder, DNAH14-related (MONDO#0700092) to Neurodevelopmental disorder (MONDO#0700092), DNAH14-related
Genetic Epilepsy v0.1590 DNAH14 Zornitza Stark Classified gene: DNAH14 as Green List (high evidence)
Genetic Epilepsy v0.1590 DNAH14 Zornitza Stark Gene: dnah14 has been classified as Green List (High Evidence).
Genetic Epilepsy v0.1589 DNAH14 Chern Lim gene: DNAH14 was added
gene: DNAH14 was added to Genetic Epilepsy. Sources: Literature
Mode of inheritance for gene: DNAH14 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: DNAH14 were set to PMID: 35438214
Phenotypes for gene: DNAH14 were set to Neurodevelopmental disorder, DNAH14-related (MONDO#0700092)
Review for gene: DNAH14 was set to GREEN
gene: DNAH14 was marked as current diagnostic
Added comment: PMID: 35438214:
- Three previously unreported patients with compound heterozygous DNAH14 variants, including one nonsense, one frameshift, and four missense variants. A spectrum of neurological and developmental phenotypes was observed, including seizures, global developmental delay, microcephaly, and hypotonia.
Sources: Literature