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Intellectual disability syndromic and non-syndromic

Gene: GRPR

Red List (low evidence)

GRPR (gastrin releasing peptide receptor)
EnsemblGeneIds (GRCh38): ENSG00000126010
EnsemblGeneIds (GRCh37): ENSG00000126010
OMIM: 305670, Gene2Phenotype
GRPR is in 1 panel

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Red List (low evidence)

No evidence of Mendelian gene-disease association.
Created: 4 Dec 2019, 7:40 p.m. | Last Modified: 4 Dec 2019, 7:40 p.m.
Panel Version: 0.326

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Genetic Health Queensland
OMIM
305670
Clinvar variants
Variants in GRPR
Penetrance
None
Panels with this gene

History Filter Activity

4 Dec 2019, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

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

4 Dec 2019, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

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

22 Nov 2019, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

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