Genomic imprinting
Gene: SNORD116-1EnsemblGeneIds (GRCh38): ENSG00000207063
EnsemblGeneIds (GRCh37): ENSG00000207063
OMIM: 605436, Gene2Phenotype
SNORD116-1 is in 0 panels
1 review
Sarah Leigh (Genomics England Curator)
SNORD116@ was listed in Table S1 PMID 30794780. In http://igc.otago.ac.nzl as being associated with PWCR1; HBII-85, which are listed under the entry for SNORD116-1 in OMIM 605436Created: 22 Dec 2020, 6:10 p.m. | Last Modified: 22 Dec 2020, 6:10 p.m.
Panel Version: 0.26
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)
- Sources
-
- Literature
- Tags
- OMIM
- 605436
- Clinvar variants
- Variants in SNORD116-1
- Penetrance
- None
- Publications
-
- 30794780
- http://igc.otago.ac.nz/home.html
- Panels with this gene
-
History Filter Activity
Removed Tag, Added Tag
Sarah Leigh (Genomics England Curator)Tag locus-type-rna-small-nuclear was removed from gene: SNORD116-1. Tag locus-type-small-nucleolar tag was added to gene: SNORD116-1.
Added Tag
Sarah Leigh (Genomics England Curator)Tag locus-type-rna-small-nuclear tag was added to gene: SNORD116-1.
Created, Added New Source, Set mode of inheritance, Set publications
Sarah Leigh (Genomics England Curator)gene: SNORD116-1 was added gene: SNORD116-1 was added to Imprinted Genes. Sources: Literature Mode of inheritance for gene: SNORD116-1 was set to MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed) Publications for gene: SNORD116-1 were set to 30794780; http://igc.otago.ac.nz/home.html