|
Symbol Name ID |
Tmco1
transmembrane and coiled-coil domains 1 MGI:1921173 |
| Darker colors indicate more annotations |
| Human Phenotypes | Decreased fetal movement |
Feeding difficulties |
Attention deficit hyperactivity disorder |
Self-mutilation |
| Disease(s) Associated with TMCO1 | ||||
| craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 1 |
| Mouse Phenotypes | impaired spatial learning |
ataxia |
impaired coordination |
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| Availability | Mouse Genotype | |||
| Tmco1em1Smoc/Tmco1em1Smoc | ||||
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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