Symbol Name ID

Foxc1 forkhead box C1 MGI:1347466

---

5 matching Alleles (1 Gene/Marker represented)

---

                        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                                                 

Foxc1hith
forkhead box C1; hole-in-the-head
                          13   Foxc1line351, m351Asp             Chemically induced (ENU)  cellular, craniofacial, nervous system, other, skeleton, vision/eye                                                                                                                                                                                                   

Foxc1tm1.1Tsku
forkhead box C1; targeted mutation 1.1, Tsutomu Kume  13   Foxc1delta                        Targeted (knock-out)      nervous system, vision/eye                                                                                                                                                                                                                                            

Foxc1tm1Blh
forkhead box C1; targeted mutation 1, Brigid L Hogan     13   Foxc1-, Foxc1Lacz, Mf1-, Mf1lacZ  Targeted (Reporter)       cardiovascular, cellular, craniofacial, embryogenesis, endocrine/exocrine, homeostasis, limbs/digits/tail, mortality/aging, nervous system, pigmentation, renal/urinary, reproductive, skeleton, vision/eye            Glaucoma 3, Primary Congenital, A; GLC3A 231300

Foxc1tm1Tsku
forkhead box C1; targeted mutation 1, Tsutomu Kume      13   Foxc1flx                          Targeted (Floxed/Frt)     cellular