FOXC1 peptide (541-553) (ab23069)
- ARAdrosophilaFKH L7
- FKHL 7FKHL7ForkheadForkhead (Drosophila) like 7forkhead (Drosophila)-like 7forkhead box C1Forkhead box protein C1Forkhead drosophila homolog like 7Forkhead like 7Forkhead related activator 3Forkhead related protein FKHL7Forkhead related transcription factor 3forkhead-related activator 3Forkhead-related protein FKHL7Forkhead-related transcription factor 3FOX C1FOXC 1FOXC1FOXC1_HUMANFREAC 3FREAC-3FREAC3homolog-like 7IGDAIHG 1IHG1IRID 1IRID1iridogoniodysgenesis type 1Myeloid factor delta
Defects in FOXC1 are the cause of iridogoniodysgenesis anomaly (IGDA) [MIM:601631]. IGDA is an autosomal dominant phenotype characterized by iris hypoplasia, goniodysgenesis, and juvenile glaucoma.
Defects in FOXC1 are a cause of Peters anomaly (PAN) [MIM:604229]. Peters anomaly consists of a central corneal leukoma, absence of the posterior corneal stroma and Descemet membrane, and a variable degree of iris and lenticular attachments to the central aspect of the posterior cornea.
References for FOXC1 peptide (541-553) (ab23069)
ab23069 has not yet been referenced specifically in any publications.