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Genomic imprinting

Gene: PWRN1

Red List (low evidence)
PWRN1 (Prader-Willi region non-protein coding RNA 1)
EnsemblGeneIds (GRCh38): ENSG00000259905
EnsemblGeneIds (GRCh37): ENSG00000259905
OMIM: 611215, Gene2Phenotype
PWRN1 is in 0 panels

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Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)
Sources
  • Literature
OMIM
611215
Clinvar variants
Variants in PWRN1
Penetrance
None
Publications
Panels with this gene

History Filter Activity

22 Dec 2020, Gel status: 1

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

Sarah Leigh (Genomics England Curator)

gene: PWRN1 was added gene: PWRN1 was added to Imprinted Genes. Sources: Literature Mode of inheritance for gene: PWRN1 was set to MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed) Publications for gene: PWRN1 were set to http://igc.otago.ac.nz/home.html; 30794780; 25953952