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Symbol Name ID |
Foxc1 forkhead box C1 MGI:1347466 |
Allele Symbol
Name Chr Synonyms Category Phenotypic Classes Human Diseases
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
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/22/2013 MGI 5.13 |
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