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Symbol Name ID |
Tmco1
transmembrane and coiled-coil domains 1 MGI:1921173 |
| Darker colors indicate more annotations |
| Human Phenotypes | Brachycephaly |
Craniosynostosis |
Micrognathia |
Hypoplasia of the maxilla |
Recurrent sinusitis |
Microcephaly |
Macrocephaly |
Short neck |
Postaxial hand polydactyly |
Hyperextensibility of the finger joints |
Long fingers |
Overlapping toe |
Sacral dimple |
Joint hypermobility |
Vertebral fusion |
Bifid ribs |
Rib fusion |
Sprengel anomaly |
Pectus excavatum |
Narrow chest |
Scoliosis |
Beaking of vertebral bodies |
Hemivertebrae |
| Disease(s) Associated with TMCO1 | |||||||||||||||||||||||
| craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 1 |
| Mouse Phenotypes | abnormal osteoblast physiology |
wide cranial sutures |
abnormal cranium morphology |
short frontal bone |
short nasal bone |
delayed bone ossification |
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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 05/21/2024 MGI 6.23 |
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