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Symbol Name ID |
Meis2
Meis homeobox 2 MGI:108564 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Short 2nd finger |
Short 5th finger |
Broad thumb |
Broad hallux |
Sandal gap |
2-3 toe syndactyly |
Cutaneous syndactyly |
| Disease(s) Associated with MEIS2 | ||||||||
| cleft palate, cardiac defects, and intellectual disabillity |
| Mouse Phenotypes | absent maxillary shelf |
absent palatine bone horizontal plate |
absent palate bones |
abnormal intramembranous bone ossification |
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| Availability | Mouse Genotype | ||||
| H2az2Tg(Wnt1-cre)11Rth/H2az2+ Meis2tm1.1Zkoz/Meis2tm1.1Zkoz (conditional) |
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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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