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Intellectual disability syndromic and non-syndromic

Gene: DDX59

Green List (high evidence)

DDX59 (DEAD-box helicase 59)
EnsemblGeneIds (GRCh38): ENSG00000118197
EnsemblGeneIds (GRCh37): ENSG00000118197
OMIM: 615464, Gene2Phenotype
DDX59 is in 11 panels

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Green List (high evidence)

Some affected individuals are reported as having ID.
Created: 30 Nov 2019, 3:54 a.m. | Last Modified: 30 Nov 2019, 3:54 a.m.
Panel Version: 0.89
Some affected individuals are reported as having ID.
Created: 30 Nov 2019, 3:51 a.m. | Last Modified: 30 Nov 2019, 3:51 a.m.
Panel Version: 0.89

Phenotypes
Orofaciodigital syndrome V, MIM#174300

Publications

Details

History Filter Activity

3 Jul 2021, Gel status: 3

Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Mode of inheritance for gene: DDX59 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal

30 Nov 2019, Gel status: 3

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: ddx59 has been classified as Green List (High Evidence).

30 Nov 2019, Gel status: 3

Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Phenotypes for gene: DDX59 were changed from to Orofaciodigital syndrome V, MIM#174300

30 Nov 2019, Gel status: 3

Set publications

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Publications for gene: DDX59 were set to

22 Nov 2019, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: DDX59 was added gene: DDX59 was added to Intellectual disability, syndromic and non-syndromic_GHQ. Sources: Expert Review Green,Genetic Health Queensland Mode of inheritance for gene: DDX59 was set to Unknown