Symbol Name ID |
Slc52a3
solute carrier protein family 52, member 3 MGI:1916948 |
Darker colors indicate more annotations |
Human Phenotypes | Death in childhood |
Disease(s) Associated with SLC52A3 | |
Brown-Vialetto-Van Laere syndrome 1 |
Mouse Phenotypes | premature death |
neonatal lethality, incomplete penetrance |
postnatal lethality, incomplete penetrance |
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Availability | Mouse Genotype | |||
Slc52a3tm2a(KOMP)Wtsi/Slc52a3tm2a(KOMP)Wtsi | ||||
Slc52a3tm1.1Said/Slc52a3tm1.1Said Tg(Vil1-cre)997Gum/0 (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 04/09/2024 MGI 6.23 |
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