Symbol Name ID |
Cog4
component of oligomeric golgi complex 4 MGI:2142808 |
Darker colors indicate more annotations |
Human Phenotypes | Frontal bossing |
Micrognathia |
Malar flattening |
Microcephaly |
Wide anterior fontanel |
Short distal phalanx of finger |
Cone-shaped epiphyses of the phalanges of the hand |
Pseudoepiphyses of the metacarpals |
Coxa valga |
Hypoplasia of proximal fibula |
Short metatarsal |
Flared metaphysis |
Short metacarpal |
Short palm |
Small hand |
Madelung deformity |
Enlarged epiphyses |
Overtubulated long bones |
Pectus carinatum |
Pectus excavatum |
Hypoplasia of the odontoid process |
Irregular vertebral endplates |
Irregularity of vertebral bodies |
Platyspondyly |
Disease(s) Associated with COG4 | ||||||||||||||||||||||||
congenital disorder of glycosylation type IIj | ||||||||||||||||||||||||
Saul-Wilson syndrome |
Mouse Phenotypes | increased bone mineral content |
decreased bone mineral density |
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Availability | Mouse Genotype | ||
Cog4em1(IMPC)Bay/Cog4+ |
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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