Symbol Name ID |
Lmx1b
LIM homeobox transcription factor 1 beta MGI:1100513 |
Darker colors indicate more annotations |
Human Phenotypes | Internal carotid artery hypoplasia |
Coronary artery dissection |
Abnormality of the vasculature |
Disease(s) Associated with LMX1B | |||
nail-patella syndrome |
Mouse Phenotypes | abnormal glomerular capillary endothelium morphology |
absent glomerular endothelium fenestra |
abnormal glomerular capillary morphology |
corneal vascularization |
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Availability | Mouse Genotype | ||||
Lmx1btm1Rjo/Lmx1btm1Rjo | |||||
Lmx1bIcst/Lmx1b+ | |||||
Lmx1btm1Rjo/Lmx1btm4.1Rjo H2az2Tg(Wnt1-cre)11Rth/H2az2+ (conditional) |
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Lmx1btm1Rjo/Lmx1btm4.1Rjo Tg(CAG-cre/Esr1*)5Amc/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 04/23/2024 MGI 6.23 |
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