Symbol Name ID |
Mid1
midline 1 MGI:1100537 |
Darker colors indicate more annotations |
Human Phenotypes | Hoarse voice |
Disease(s) Associated with MID1 | |
Opitz GBBB syndrome |
Mouse Phenotypes | abnormal learning/memory/conditioning |
abnormal motor learning |
increased freezing behavior |
increased startle reflex |
impaired coordination |
impaired limb coordination |
hyperactivity |
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Availability | Mouse Genotype | |||||||
Mid1em1(IMPC)Mbp/Mid1+ | ||||||||
Mid1tm1Mero/Y |
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 04/09/2024 MGI 6.23 |
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