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Genomic imprinting

Gene: LRRTM1

Red List (low evidence)
LRRTM1 (leucine rich repeat transmembrane neuronal 1)
EnsemblGeneIds (GRCh38): ENSG00000162951
EnsemblGeneIds (GRCh37): ENSG00000162951
OMIM: 610867, Gene2Phenotype
LRRTM1 is in 0 panels

1 review

Sarah Leigh (Genomics England Curator)

I don't know

Circadian expression reported in CircaDB (http://circadb.hogeneschlab.org/human)
Created: 22 Dec 2020, 6:10 p.m. | Last Modified: 22 Dec 2020, 6:10 p.m.
Panel Version: 0.26
Created: 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
OMIM
610867
Clinvar variants
Variants in LRRTM1
Penetrance
None
Publications
  • 30794780
  • http://igc.otago.ac.nz/home.html
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: LRRTM1 was added gene: LRRTM1 was added to Imprinted Genes. Sources: Literature Mode of inheritance for gene: LRRTM1 was set to MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed) Publications for gene: LRRTM1 were set to 30794780; http://igc.otago.ac.nz/home.html