Symbol Name ID

Foxc1 forkhead box C1 MGI:1347466

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1 matching Allele (1 Gene/Marker represented)

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               Allele Symbol
Name                  Chr   Synonyms    Category                                                                                                     Phenotypic Classes                                                                                                   Human Diseases

Foxc1ch
forkhead box C1; congenital hydrocephalus
  13   ch, mf1ch  Spontaneous  cardiovascular, craniofacial, digestive/alimentary, embryogenesis, endocrine/exocrine, integument, limbs/digits/tail, mortality/aging, nervous system, renal/urinary, reproductive, respiratory, skeleton, vision/eye