Genomic imprinting
Gene: SNORD115-1EnsemblGeneIds (GRCh38): ENSG00000201831
EnsemblGeneIds (GRCh37): ENSG00000201831
OMIM: 609837, Gene2Phenotype
SNORD115-1 is in 0 panels
1 review
Sarah Leigh (Genomics England Curator)
SNORD115@ was listed in Table S1 PMID 30794780. In http://igc.otago.ac.nzl as being associated with HBII-52, which is listed under the entry for SNORD115-1 in OMIM 6098376Created: 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
- 609837
- Clinvar variants
- Variants in SNORD115-1
- 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: SNORD115-1. Tag locus-type-small-nucleolar tag was added to gene: SNORD115-1.
Added Tag
Sarah Leigh (Genomics England Curator)Tag locus-type-rna-small-nuclear tag was added to gene: SNORD115-1.
Created, Added New Source, Set mode of inheritance, Set publications
Sarah Leigh (Genomics England Curator)gene: SNORD115-1 was added gene: SNORD115-1 was added to Imprinted Genes. Sources: Literature Mode of inheritance for gene: SNORD115-1 was set to MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed) Publications for gene: SNORD115-1 were set to 30794780; http://igc.otago.ac.nz/home.html