Symbol Name ID |
Nme5
NME/NM23 family member 5 MGI:1922783 |
Darker colors indicate more annotations |
Human Phenotypes | Morphological central nervous system abnormality |
Hydrocephalus |
Ventriculomegaly |
Delayed speech and language development |
Disease(s) Associated with NME5 | ||||
primary ciliary dyskinesia |
Mouse Phenotypes | intraventricular hemorrhage |
hydrocephaly |
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Availability | Mouse Genotype | ||
Nme5tm1Lex/Nme5tm1Lex |
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 08/02/2024 MGI 6.24 |
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