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  3. KDM7A
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Cerebral Palsy

Gene: KDM7A

Red List (low evidence)
KDM7A (lysine demethylase 7A)
EnsemblGeneIds (GRCh38): ENSG00000006459
EnsemblGeneIds (GRCh37): ENSG00000006459
KDM7A is in 2 panels

1 review

Krithika Murali (Victorian Clinical Genetics Services)

Red List (low evidence)

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
Created: 27 Sep 2021, 3:25 a.m. | Last Modified: 27 Sep 2021, 3:26 a.m.
Panel Version: 0.152

Mode of inheritance
Unknown

Publications

Created: 27 Sep 2021, 3:25 a.m.
Last Modified: 27 Sep 2021, 3:26 a.m.
Panel version: 0.152

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Literature
  • Expert list
Phenotypes
  • Cerebral palsy
Clinvar variants
Variants in KDM7A
Penetrance
None
Publications
Panels with this gene

History Filter Activity

27 Sep 2021, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: kdm7a has been classified as Red List (Low Evidence).

27 Sep 2021, Gel status: 1

Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Phenotypes for gene: KDM7A were changed from to Cerebral palsy

27 Sep 2021, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: kdm7a has been classified as Red List (Low Evidence).

27 Sep 2021, Gel status: 0

Created, Added New Source, Set mode of inheritance, Set publications

Krithika Murali (Victorian Clinical Genetics Services)

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