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Cerebral Palsy v0.156 | KDM7A | Zornitza Stark Marked gene: KDM7A as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Cerebral Palsy v0.156 | KDM7A | Zornitza Stark Gene: kdm7a has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Cerebral Palsy v0.156 | KDM7A | Zornitza Stark Phenotypes for gene: KDM7A were changed from to Cerebral palsy | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Cerebral Palsy v0.155 | KDM7A | Zornitza Stark Classified gene: KDM7A as Red List (low evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Cerebral Palsy v0.155 | KDM7A | Zornitza Stark Gene: kdm7a has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Cerebral Palsy v0.152 | KDM7A |
Krithika Murali changed review comment from: Synonyms: JHDMID, KDM7, KIAA1718 De novo missense VUS identified in a WES CP cohort study in a gene not known to be associated with disease. Sources: Expert list, Literature; to: Synonyms: JHDMID, KDM7, KIAA1718 De novo missense VUS identified in a WES CP cohort study in a gene not known to be associated with disease. Sources: Literature |
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Cerebral Palsy v0.152 | KDM7A |
Krithika Murali gene: KDM7A was added gene: KDM7A was added to Cerebral Palsy. Sources: Expert list,Literature Mode of inheritance for gene: KDM7A was set to Unknown Publications for gene: KDM7A were set to 25666757 Review for gene: KDM7A was set to RED Added comment: Synonyms: JHDMID, KDM7, KIAA1718 De novo missense VUS identified in a WES CP cohort study in a gene not known to be associated with disease. Sources: Expert list, Literature |