Symbol Name ID |
Lbx1
ladybird homeobox 1 MGI:104867 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Hypotonia |
Disease(s) Associated with LBX1 | |
congenital central hypoventilation syndrome |
Mouse Phenotypes | muscle phenotype |
abnormal muscle precursor cell migration |
abnormal limb muscle morphology |
abnormal myogenesis |
abnormal skeletal muscle morphology |
absent hypaxial muscle |
decreased skeletal muscle mass |
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Availability | Mouse Genotype | |||||||
Lbx1tm1Gld/Lbx1tm1Gld | * | |||||||
Lbx1tm1Thbr/Lbx1tm1Thbr | * | |||||||
Lbx1tm1.1Khan/Lbx1tm1.1Khan Tg(CAG-cre/Esr1*)5Amc/0 (conditional) |
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Lbx1tm1.1Khan/Lbx1tm1.1Khan Myf5tm3(cre)Sor/Myf5+ (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 07/05/2024 MGI 6.24 |
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