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Genomic imprinting

Gene: INPP5F

Red List (low evidence)
INPP5F (inositol polyphosphate-5-phosphatase F)
EnsemblGeneIds (GRCh38): ENSG00000198825
EnsemblGeneIds (GRCh37): ENSG00000198825
OMIM: 609389, Gene2Phenotype
INPP5F is in 0 panels

1 review

Sarah Leigh (Genomics England Curator)

I don't know

INPP5F_V2; inositol polyphosphate-5-phosphatase F, isoform 2 is exclusively expressed from the paternal allele in fetal brain, heart and tongue in one informative fetus, and monoallelically expressed in two additional fetuses (same tissues). Its promoter shows germline maternal methylation (PMID )
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
609389
Clinvar variants
Variants in INPP5F
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: INPP5F was added gene: INPP5F was added to Imprinted Genes. Sources: Literature Mode of inheritance for gene: INPP5F was set to MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed) Publications for gene: INPP5F were set to 17291163; 30794780; http://igc.otago.ac.nz/home.html