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Symbol Name ID |
Foxg1 forkhead box G1 MGI:1347464 |
Allele Symbol
Name Chr Synonyms Category Phenotypic Classes Human Diseases
Foxg1tm1(cre)Skm
forkhead box G1; targeted mutation 1, Susan K McConnell 12 BF1-cre, Foxg1-, Foxg1Cre, Foxg1-Cre, Foxg1:Cre, FoxG1Cre, Foxg1KiCre, TgH(Foxg1-Cre)1Skm Targeted (knock-in) behavior, cardiovascular, cellular, craniofacial, digestive/alimentary, embryogenesis, endocrine/exocrine, growth/size, hearing/vestibular/ear, hematopoietic, homeostasis, immune, integument, mortality/aging, muscle, nervous system, respiratory, skeleton, taste/olfaction, vision/eye Alpha-Thalassemia/Mental Retardation Syndrome, X-Linked; ATRX 301040; DiGeorge Syndrome; DGS 188400; Holoprosencephaly 2; HPE2 157170
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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