Symbol Name ID |
Nexmif
neurite extension and migration factor MGI:2148050 |
Darker colors indicate more annotations |
Human Phenotypes | Mandibular prognathia |
Secondary microcephaly |
Clinodactyly of the 5th finger |
Short digit |
Disease(s) Associated with NEXMIF | ||||
non-syndromic X-linked intellectual disability 98 |
Mouse Phenotypes | abnormal sternum morphology |
decreased bone mineral content |
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Availability | Mouse Genotype | ||
Nexmifem1(IMPC)Tcp/Nexmif+ | |||
Nexmifem1(IMPC)Tcp/Y |
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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