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Mendeliome

Gene: PTPRR

Red List (low evidence)

PTPRR (protein tyrosine phosphatase, receptor type R)
EnsemblGeneIds (GRCh38): ENSG00000153233
EnsemblGeneIds (GRCh37): ENSG00000153233
OMIM: 602853, Gene2Phenotype
PTPRR is in 1 panel

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Red List (low evidence)

No evidence currently for Mendelian disease association.
Created: 19 Nov 2019, 8:12 a.m. | Last Modified: 19 Nov 2019, 8:12 a.m.
Panel Version: 0.16

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
OMIM
602853
Clinvar variants
Variants in PTPRR
Penetrance
None
Panels with this gene

History Filter Activity

21 Jan 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

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

19 Nov 2019, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

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

17 Nov 2019, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: PTPRR was added gene: PTPRR was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: PTPRR was set to Unknown