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Mackenzie's Mission_Reproductive Carrier Screening

Gene: HPGD

Green List (high evidence)

HPGD (15-hydroxyprostaglandin dehydrogenase)
EnsemblGeneIds (GRCh38): ENSG00000164120
EnsemblGeneIds (GRCh37): ENSG00000164120
OMIM: 601688, Gene2Phenotype
HPGD is in 5 panels

0 reviews

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Mackenzie's Mission
Phenotypes
  • Cranioosteoarthropathy, 259100 (3)
OMIM
601688
Clinvar variants
Variants in HPGD
Penetrance
None
Panels with this gene

History Filter Activity

19 Apr 2020, Gel status: 3

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

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: HPGD was added gene: HPGD was added to Mackenzie's Mission_Reproductive Carrier Screening. Sources: Mackenzie's Mission,Expert Review Green Mode of inheritance for gene: HPGD was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: HPGD were set to Cranioosteoarthropathy, 259100 (3)