Symbol Name ID |
Cenpj
centromere protein J MGI:2684927 |
Darker colors indicate more annotations |
Human Phenotypes | Short stature |
Severe short stature |
Decreased body weight |
Severe failure to thrive |
Growth delay |
Intrauterine growth retardation |
Disease(s) Associated with CENPJ | ||||||
primary autosomal recessive microcephaly | ||||||
Seckel syndrome 4 |
Mouse Phenotypes | sloping forehead |
decreased lean body mass |
decreased body weight |
abnormal head morphology |
decreased body length |
decreased body size |
postnatal growth retardation |
decreased fetal size |
decreased fetal weight |
prenatal growth retardation |
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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 04/23/2024 MGI 6.23 |
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