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Phenotypic Alleles
Query Results -- Summary
 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
images 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
images 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
images 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
images 13 Foxc1flx Targeted (Floxed/Frt) cellular

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
04/08/2014
MGI 5.17
The Jackson Laboratory