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Symbol
Name
ID
Ret
ret proto-oncogene
MGI:97902
Phenotype annotations related to muscle
Darker colors indicate more annotations
Human Phenotypes
Myopathy
Muscular hypotonia
Generalized hypotonia
Disease(s) Associated with RET
congenital central hypoventilation syndrome
multiple endocrine neoplasia type 2B

Mouse Phenotypes
abnormal intestinal peristalsis
intestinal hypoperistalsis
abnormal hypaxial muscle morphology
abnormal gastrocnemius morphology
abnormal muscle spindle morphology
muscular atrophy
Availability Mouse Genotype
Rettm1Cos/Rettm1Cos
Rettm1Heno/Rettm1Heno
Rettm2.1Heno/Rettm2.1Heno
Rettm2Cos/Rettm2Cos
Rettm3(RET)Vpa/Rettm3(RET)Vpa
Rettm12(RET)Jmi/Rettm12(RET)Jmi
Rettm1Cos/Ret+
Rettm11(RET)Jmi/Rettm12(RET)Jmi

Contributing Projects:
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
08/13/2019
MGI 6.14
The Jackson Laboratory