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Genomic imprinting

Gene: ARVCF

Red List (low evidence)
ARVCF (ARVCF, delta catenin family member)
EnsemblGeneIds (GRCh38): ENSG00000099889
EnsemblGeneIds (GRCh37): ENSG00000099889
OMIM: 602269, Gene2Phenotype
ARVCF is in 1 panel

1 review

Sarah Leigh (Genomics England Curator)

I don't know

Imprinted, not known which allele is expressed. 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, imprinted status unknown
Sources
  • Literature
OMIM
602269
Clinvar variants
Variants in ARVCF
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: ARVCF was added gene: ARVCF was added to Imprinted Genes. Sources: Literature Mode of inheritance for gene: ARVCF was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: ARVCF were set to 30794780; 26769960