|
Symbol Name ID |
Mid1
midline 1 MGI:1100537 |
| Darker colors indicate more annotations |
| Human Phenotypes | Inguinal hernia |
Umbilical hernia |
Growth delay |
| Disease(s) Associated with MID1 | |||
| Opitz GBBB syndrome |
| Mouse Phenotypes | increased heart weight |
embryonic growth retardation |
increased lean body mass |
enlarged spleen |
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| Availability | Mouse Genotype | ||||
| Mid1em1(IMPC)Mbp/Mid1em1(IMPC)Mbp | |||||
| Mid1em1(IMPC)Mbp/Mid1+ | |||||
| Arhgap6/Hccs/Mid1tm1Hzo/Arhgap6/Hccs/Mid1tm1Hzo Tg(EIIa-cre)C5379Lmgd/? (conditional) |
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| Arhgap6/Hccs/Mid1tm1Hzo/Y Tg(EIIa-cre)C5379Lmgd/? (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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