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Early onset familial premature ovarian failure

Gene: FOXL2

Red List (low evidence)

FOXL2 (forkhead box L2)
EnsemblGeneIds (GRCh38): ENSG00000183770
EnsemblGeneIds (GRCh37): ENSG00000183770
OMIM: 605597, Gene2Phenotype
FOXL2 is in 4 panels

0 reviews

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
Phenotypes
  • BPES (MIM 110100)
OMIM
605597
Clinvar variants
Variants in FOXL2
Penetrance
Complete
Publications
Panels with this gene

History Filter Activity

15 Aug 2017, Gel status: 0

Approved Gene

Ellen McDonagh (Genomics England Curator)

This proposed gene was validated and added to this panel

3 Feb 2016, Gel status: 0

Created

Maria Bitner-Glindzicz (UCL)

FOXL2 was created by mbitnerg

3 Feb 2016, Gel status: 0

Added New Source

Maria Bitner-Glindzicz (UCL)

FOXL2 was added to Early onset familial premature ovarian failurepanel. Sources: Expert Review