Symbol Name ID |
Reln
reelin MGI:103022 |
! | Indicates phenotype varies with strain background. |
Darker colors indicate more annotations |
Human Phenotypes | Intrauterine growth retardation |
Disease(s) Associated with RELN | |
Norman-Roberts syndrome |
Mouse Phenotypes | decreased body weight |
slow postnatal weight gain |
decreased body size |
postnatal growth retardation |
enlarged spleen |
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Availability | Mouse Genotype | |||||
Relnm1Anu/Relnm1Anu | ||||||
Relnrl-4J/Relnrl-4J | ||||||
Relnrl-Alb/Relnrl-Alb | ||||||
Relnrl-od/Relnrl-od | ||||||
Relnrl/Relnrl | ! | ! | ! | |||
Relnem1(IMPC)Mbp/Reln+ |
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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