Symbol Name ID |
Lat2
linker for activation of T cells family, member 2 MGI:1926479 |
Darker colors indicate more annotations |
Human Phenotypes | Inguinal hernia |
Umbilical hernia |
Short stature |
Failure to thrive in infancy |
Obesity |
Intrauterine growth retardation |
Disease(s) Associated with LAT2 | ||||||
Williams-Beuren syndrome |
Mouse Phenotypes | enlarged spleen |
spleen hyperplasia |
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Availability | Mouse Genotype | ||
Lat2tm1Wz/Lat2tm1Wz | |||
Lat2tm3.1Wz/Lat2tm3.1Wz | |||
Lat2tm2Wz/Lat2tm2Wz Tg(Lck-cre)548Jxm/0 (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 04/30/2024 MGI 6.23 |
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