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Fetal anomalies

Gene: TNFRSF11B

Red List (low evidence)

TNFRSF11B (TNF receptor superfamily member 11b)
EnsemblGeneIds (GRCh38): ENSG00000164761
EnsemblGeneIds (GRCh37): ENSG00000164761
OMIM: 602643, Gene2Phenotype
TNFRSF11B is in 4 panels

1 review

Rebecca Foulger (Genomics England curator)

I don't know

DDG2P rating in original PAGE list: Possible.
Created: 11 Dec 2018, 9:05 a.m.

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • PAGE Additional Gene List
Phenotypes
  • Paget disease 239000
OMIM
602643
Clinvar variants
Variants in TNFRSF11B
Penetrance
None
Panels with this gene

History Filter Activity

8 Nov 2018, Gel status: 1

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

Rebecca Foulger (Genomics England curator)

gene: TNFRSF11B was added gene: TNFRSF11B was added to Fetal anomalies. Sources: PAGE Additional Gene List,Expert Review Red Mode of inheritance for gene: TNFRSF11B was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: TNFRSF11B were set to Paget disease 239000