Symbol Name ID |
Cul7
cullin 7 MGI:1913765 |
Darker colors indicate more annotations |
Human Phenotypes | Frontal bossing |
Dolichocephaly |
Mandibular prognathia |
Malar flattening |
J-shaped sella turcica |
Microcephaly |
Relative macrocephaly |
Abnormal dental enamel morphology |
Short neck |
Short 5th finger |
Clinodactyly of the 5th finger |
Clinodactyly |
Rocker bottom foot |
Prominent calcaneus |
Abnormal metaphysis morphology |
Hypoplasia of the ulna |
Hip dislocation |
Congenital hip dislocation |
Scapular winging |
Abnormality of the elbow |
Micromelia |
Joint hypermobility |
Delayed skeletal maturation |
Slender long bone |
Hypoplastic ischia |
Hypoplastic pubic bone |
Hip dysplasia |
Hypoplastic pelvis |
Short ribs |
Horizontal ribs |
Thin ribs |
Enlarged thorax |
Pectus carinatum |
Pectus excavatum |
Short thorax |
Hyperlordosis |
Lumbar hyperlordosis |
Kyphosis |
Scoliosis |
Increased vertebral height |
Joint dislocation |
Disease(s) Associated with CUL7 | |||||||||||||||||||||||||||||||||||||||||
3-M syndrome |
Mouse Phenotypes | decreased bone mineral density |
abnormal bone mineralization |
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Availability | Mouse Genotype | ||
Cul7tm1a(EUCOMM)Wtsi/Cul7+ |
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 03/12/2024 MGI 6.23 |
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