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Mendeliome

Gene: GGN

Amber List (moderate evidence)

GGN (gametogenetin)
EnsemblGeneIds (GRCh38): ENSG00000179168
EnsemblGeneIds (GRCh37): ENSG00000179168
OMIM: 609966, Gene2Phenotype
GGN is in 1 panel

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

I don't know

Three individuals from two unrelated families reported.
Sources: Literature
Created: 6 Apr 2022, 11:58 p.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Spermatogenic failure 69, MIM# 619826

Publications

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Spermatogenic failure 69, MIM# 619826
OMIM
609966
Clinvar variants
Variants in GGN
Penetrance
None
Publications
Panels with this gene

History Filter Activity

7 Apr 2022, Gel status: 2

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: ggn has been classified as Amber List (Moderate Evidence).

7 Apr 2022, Gel status: 2

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: ggn has been classified as Amber List (Moderate Evidence).

6 Apr 2022, Gel status: 1

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

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: GGN was added gene: GGN was added to Mendeliome. Sources: Literature Mode of inheritance for gene: GGN was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: GGN were set to 31985809; 33108537 Phenotypes for gene: GGN were set to Spermatogenic failure 69, MIM# 619826 Review for gene: GGN was set to AMBER