Cytopenias and congenital anaemias
Gene: GNRHR2EnsemblGeneIds (GRCh38): ENSG00000211451
EnsemblGeneIds (GRCh37): ENSG00000211451
OMIM: 612875, Gene2Phenotype
GNRHR2 is in 1 panel
2 reviews
Olivia Niblock (Genomics England Curator)
Within the area associated with the 1q21.1 deletion, which is thought to cause TAR syndrome. No phenotypes associated with it on OMIM or Gene2Phenotype. No results on pubmed for literature linking gene or variants to Anaemia, cytopenia or TAR syndrome.Created: 9 Mar 2017, 4:32 p.m.
Phenotypes
Thrombocytopenia Absent-Radius Syndrome
Ellen McDonagh (Genomics England Curator)
Added tag to explain why there is no Ensembl gene ID for this entity.Created: 6 Jan 2017, 3:20 p.m.
The UKGTN gene dossier explains that a 200kb deletion at 1q21.1 encompassing the genes; HFE2, TXNIP, PLOR3GL, ANKRD34A, LIX1L, RBM8A, GNRHR2, PEX11B, ITGA10, ANKRD35, PIAS3, NUDT1, is tested for diagnosis of Thrombocytopenia Absent-Radius Syndrome. "PLOR3GL" is likely to be POLR3GL, the correct spelling for this gene in this region.Created: 25 Jun 2015, 10:58 a.m.
Details
- Sources
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- Expert Review Red
- UKGTN
- Phenotypes
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- Thrombocytopenia Absent-Radius Syndrome
- Tags
- OMIM
- 612875
- Clinvar variants
- Variants in GNRHR2
- Penetrance
- Complete
- Panels with this gene
History Filter Activity
panel promoted to version 1
Arianna Tucci (Genomics England Curator)Promoted to V1 on 11 March 2017, after internal review and discussion with the clinical team.
Added New Source
Sarah Leigh (Genomics England Curator)GNRHR2 was added to Cytopaenias and congenital anaemiaspanel. Source: Expert Review Red
Added New Source
Louise Daugherty (Genomics England Curator)GNRHR2 was added to Cytopaenias and congenital anaemiaspanel. Sources: UKGTN
Created
Louise Daugherty (Genomics England Curator)GNRHR2 was created by LouiseD