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Symbol
Name
ID
Cul7
cullin 7
MGI:1913765
Phenotype annotations related to skeleton
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
Availability Mouse Genotype
Cul7tm1a(EUCOMM)Wtsi/Cul7+

Contributing Projects:
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
The Jackson Laboratory