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Symbol Name ID |
Psph
phosphoserine phosphatase MGI:97788 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
| Disease(s) Associated with PSPH | |
| PSPH deficiency |
| Mouse Phenotypes | fragmented Meckel's cartilage |
short Meckel's cartilage |
abnormal sphenoid bone morphology |
absent maxilla |
abnormal middle ear ossicle morphology |
abnormal femur morphology |
abnormal pelvic girdle bone morphology |
increased rib number |
rib fusion |
fusion of vertebral arches |
abnormal vertebral body morphology |
fusion of vertebral bodies |
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| Availability | Mouse Genotype | ||||||||||||
| Psphtm1a(EUCOMM)Hmgu/Psphtm1a(EUCOMM)Hmgu | |||||||||||||
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 04/30/2024 MGI 6.23 |
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