Symbol Name ID |
Ret
ret proto-oncogene MGI:97902 |
Darker colors indicate more annotations |
Human Phenotypes | Hypotonia |
Generalized hypotonia |
Myopathy |
Disease(s) Associated with RET | |||
multiple endocrine neoplasia type 2B |
Mouse Phenotypes | abnormal intestinal peristalsis |
intestinal hypoperistalsis |
abnormal gastrocnemius morphology |
abnormal hypaxial muscle morphology |
abnormal muscle spindle morphology |
muscular atrophy |
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Availability | Mouse Genotype | ||||||
Rettm1Cos/Rettm1Cos | |||||||
Rettm1Heno/Rettm1Heno | |||||||
Rettm2.1Heno/Rettm2.1Heno | |||||||
Rettm2Cos/Rettm2Cos | |||||||
Rettm12(RET)Jmi/Rettm12(RET)Jmi | |||||||
Rettm1Cos/Ret+ | |||||||
Rettm11(RET)Jmi/Rettm12(RET)Jmi |
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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