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Symbol
Name
ID
Scube3
signal peptide, CUB domain, EGF-like 3
MGI:3045253
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Bicoronal synostosis
Microcephaly
Enamel hypoplasia
Brachydactyly
Short palm
Joint hypermobility
Joint stiffness
Short long bone
11 pairs of ribs
Scoliosis
Disease(s) Associated with SCUBE3
short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies

Mouse Phenotypes
abnormal temporal bone morphology
abnormal middle ear ossicle morphology
small incus
abnormal malleus morphology
abnormal malleus head morphology
small middle ear ossicles
fused phalanges
abnormal tarsal bone morphology
short femur
abnormal metacarpal bone morphology
abnormal metatarsal bone morphology
abnormal pectoral girdle bone morphology
rib fusion
abnormal thoracic vertebrae morphology
abnormal vertebral column morphology
kyphosis
abnormal lumbar vertebrae morphology
abnormal vertebral pedicle morphology
decreased bone mineral content
decreased bone mineral density
abnormal bone ossification
increased bone resorption
Availability Mouse Genotype
Scube3m1Btlr/Scube3m1Btlr
Scube3m1Mhda/Scube3m1Mhda

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
04/09/2024
MGI 6.23
The Jackson Laboratory