Symbol Name ID |
Setd5
SET domain containing 5 MGI:1920145 |
Darker colors indicate more annotations |
Human Phenotypes | Lower limb asymmetry |
Disease(s) Associated with SETD5 | |
autosomal dominant intellectual developmental disorder 23 |
Mouse Phenotypes | enlarged heart |
abnormal tooth morphology |
abnormal incisor morphology |
abnormal snout morphology |
embryonic growth retardation |
decreased embryo size |
fetal growth retardation |
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Availability | Mouse Genotype | |||||||
Setd5tm1.1Mgn/Setd5tm1.1Mgn | ||||||||
Setd5tm1a(EUCOMM)Wtsi/Setd5+ | ||||||||
Setd5tm1c(EUCOMM)Wtsi/Setd5tm1c(EUCOMM)Wtsi Mesp1tm2(cre)Ysa/Mesp1+ (conditional) |
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 04/30/2024 MGI 6.23 |
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