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Symbol
Name
ID
Cenpj
centromere protein J
MGI:2684927
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Retrognathia
Microcephaly
Steep acetabular roof
11 pairs of ribs
Abnormal cortical bone morphology
Disease(s) Associated with CENPJ
primary autosomal recessive microcephaly
primary autosomal recessive microcephaly 6
Seckel syndrome 4

Mouse Phenotypes
abnormal cranium morphology
decreased cranium length
small cranium
abnormal occipital bone morphology
abnormal parietal bone morphology
abnormal humerus morphology
abnormal deltoid tuberosity morphology
bowed humerus
abnormal ulna morphology
abnormal femur morphology
abnormal tibia morphology
abnormal caudal vertebrae morphology
caudal vertebral fusion
abnormal sternocostal joint morphology
abnormal pelvic girdle bone morphology
abnormal thoracic cage morphology
abnormal vertebrae morphology
short lumbar vertebrae
increased sacral vertebrae number
small sacral vertebrae
vertebral fusion
decreased bone mineral content
abnormal joint morphology
abnormal intramembranous bone ossification
Availability Mouse Genotype
Cenpjtm1a(EUCOMM)Wtsi/Cenpjtm1a(EUCOMM)Wtsi

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
04/16/2024
MGI 6.23
The Jackson Laboratory