Symbol Name ID |
Hoxb1
homeobox B1 MGI:96182 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Mouse Phenotypes | behavior/neurological phenotype |
abnormal reflex |
abnormal blinking |
abnormal vibrissae reflex |
paralysis |
facial paralysis |
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Availability | Mouse Genotype | ||||||
Hoxb1tm1(cre)Og/Hoxb1tm1(cre)Og | * | ||||||
Hoxb1tm1Mrc/Hoxb1tm1Mrc | |||||||
Hoxb1tm2Mrc/Hoxb1tm2Mrc | |||||||
Hoxb1tm5Mrc/Hoxb1tm9Mrc | |||||||
Hoxb1tm5Mrc/Hoxb1tm7Mrc H2az2Tg(Wnt1-cre)11Rth/H2az2+ (conditional) |
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Hoxb1tm5Mrc/Hoxb1tm7Mrc Tfap2atm1(cre)Moon/Tfap2a+ (conditional) |
* |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 08/02/2024 MGI 6.24 |
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