Genes in panel
Regions in panel
Prev Next

Mendeliome

Gene: DPY19L2

Green List (high evidence)

DPY19L2 (dpy-19 like 2)
EnsemblGeneIds (GRCh38): ENSG00000177990
EnsemblGeneIds (GRCh37): ENSG00000177990
OMIM: 613893, Gene2Phenotype
DPY19L2 is in 1 panel

1 review

Krithika Murali (Victorian Clinical Genetics Services)

Green List (high evidence)

Multiple unrelated families reported.
Created: 14 May 2022, 12:26 p.m. | Last Modified: 14 May 2022, 12:26 p.m.
Panel Version: 0.14291

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Spermatogenic failure 9 - MIM#613958

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Spermatogenic failure 9 - MIM#613958
OMIM
613893
Clinvar variants
Variants in DPY19L2
Penetrance
None
Publications
Panels with this gene

History Filter Activity

28 Feb 2025, Gel status: 3

Set publications

Bryony Thompson (Royal Melbourne Hospital)

Publications for gene: DPY19L2 were set to

20 May 2022, Gel status: 3

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: dpy19l2 has been classified as Green List (High Evidence).

20 May 2022, Gel status: 3

Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Phenotypes for gene: DPY19L2 were changed from to Spermatogenic failure 9 - MIM#613958

20 May 2022, Gel status: 3

Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Mode of inheritance for gene: DPY19L2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal

17 Nov 2019, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: DPY19L2 was added gene: DPY19L2 was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: DPY19L2 was set to Unknown