Symbol Name ID |
Cenpj
centromere protein J MGI:2684927 |
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 |
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Availability | Mouse Genotype | ||||||||||||||||||||||||
Cenpjtm1a(EUCOMM)Wtsi/Cenpjtm1a(EUCOMM)Wtsi |
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 |
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