Genomic imprinting
Gene: RTL1EnsemblGeneIds (GRCh38): ENSG00000254656
EnsemblGeneIds (GRCh37): ENSG00000254656
OMIM: 611896, Gene2Phenotype
RTL1 is in 0 panels
1 review
Achchuthan Shanmugasundram (Genomics England Curator)
Comment on publications: PMID:35567414 provides functional evidence from mouse models and human postmortem and surgical resection brains.Created: 1 Mar 2023, 9:20 a.m. | Last Modified: 1 Mar 2023, 9:20 a.m.
Panel Version: 0.149
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)
- Sources
-
- Literature
- OMIM
- 611896
- Clinvar variants
- Variants in RTL1
- Penetrance
- None
- Publications
- Panels with this gene
-
History Filter Activity
Set publications
Achchuthan Shanmugasundram (Genomics England Curator)Publications for gene: RTL1 were set to 30794780; 35567414; http://igc.otago.ac.nz/home.html
Set publications
Achchuthan Shanmugasundram (Genomics England Curator)Publications for gene: RTL1 were set to 30794780; http://igc.otago.ac.nz/home.html
Created, Added New Source, Set mode of inheritance, Set publications
Sarah Leigh (Genomics England Curator)gene: RTL1 was added gene: RTL1 was added to Imprinted Genes. Sources: Literature Mode of inheritance for gene: RTL1 was set to MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed) Publications for gene: RTL1 were set to 30794780; http://igc.otago.ac.nz/home.html