Activity

Filter

Cancel
Date Panel Item Activity
13 actions
Genetic Epilepsy v2.0 DNAH14 Gene migrated from ENSG00000185842 to ENSG00000185842 (gene set migration)
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