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  3. PTPRZ1
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Molecular autopsy

Gene: PTPRZ1

Red List (low evidence)
PTPRZ1 (protein tyrosine phosphatase, receptor type Z1)
EnsemblGeneIds (GRCh38): ENSG00000106278
EnsemblGeneIds (GRCh37): ENSG00000106278
OMIM: 176891, Gene2Phenotype
PTPRZ1 is in 2 panels

0 reviews

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
Phenotypes
  • Hyperlysinaemia (Disorders of histidine, tryptophan or lysine metabolism)
  • {H. pylori infection, susceptibility to} 600263
OMIM
176891
Clinvar variants
Variants in PTPRZ1
Penetrance
None
Publications
Panels with this gene

History Filter Activity

20 Dec 2018, Gel status: 1

Set Phenotypes

Ellen McDonagh (Genomics England Curator)

Added phenotypes Hyperlysinaemia (Disorders of histidine, tryptophan or lysine metabolism); {H. pylori infection, susceptibility to} 600263 for gene: PTPRZ1

20 Dec 2018, Gel status: 1

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

Ellen McDonagh (Genomics England Curator)

gene: PTPRZ1 was added gene: PTPRZ1 was added to Molecular autopsy. Sources: Expert Review Red Mode of inheritance for gene: PTPRZ1 was set to Unknown Publications for gene: PTPRZ1 were set to 27604308 Phenotypes for gene: PTPRZ1 were set to Hyperlysinaemia (Disorders of histidine, tryptophan or lysine metabolism); {H. pylori infection, susceptibility to} 600263