|
Symbol Name ID |
Orc1
origin recognition complex, subunit 1 MGI:1328337 |
| Darker colors indicate more annotations |
| Human Phenotypes | Frontal bossing |
Small anterior fontanelle |
Micrognathia |
Hypoplasia of the maxilla |
Microcephaly |
Genu valgum |
Genu varum |
Clinodactyly of the 5th finger |
Cutaneous finger syndactyly |
Coxa valga |
Aplasia/Hypoplasia of the patella |
Patellar aplasia |
Short palm |
Small hand |
Genu recurvatum |
Joint contracture of the hand |
Elbow dislocation |
Flexion contracture |
Camptodactyly |
Osteochondritis dissecans |
Slender long bone |
Abnormal pelvic girdle bone morphology |
Absent glenoid fossa |
Flat glenoid fossa |
Lateral clavicle hook |
Abnormal rib cage morphology |
Short ribs |
Thin ribs |
Absent sternal ossification |
Pectus carinatum |
Hemivertebrae |
| Disease(s) Associated with ORC1 | |||||||||||||||||||||||||||||||
| Meier-Gorlin syndrome 1 |
| Mouse Phenotypes | abnormal bone structure |
increased bone mineral content |
increased bone mineral density |
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| Availability | Mouse Genotype | |||
| Orc1tm1a(KOMP)Wtsi/Orc1+ | ||||
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 06/09/2026 MGI 6.24 |
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