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  3. FGF12
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Genomic imprinting

Gene: FGF12

Red List (low evidence)
FGF12 (fibroblast growth factor 12)
EnsemblGeneIds (GRCh38): ENSG00000114279
EnsemblGeneIds (GRCh37): ENSG00000114279
OMIM: 601513, Gene2Phenotype
FGF12 is in 5 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
601513
Clinvar variants
Variants in FGF12
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: FGF12 was added gene: FGF12 was added to Imprinted Genes. Sources: Literature Mode of inheritance for gene: FGF12 was set to MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed) Publications for gene: FGF12 were set to 27835649; 30794780