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Symbol
Name
ID
Slc35d1
solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1
MGI:2140361
Phenotype annotations related to embryo
Darker colors indicate more annotations
Human Phenotypes
Nonimmune hydrops fetalis
Polyhydramnios
Disease(s) Associated with SLC35D1
schneckenbecken dysplasia

Mouse Phenotypes
abnormal embryo size
Availability Mouse Genotype
Slc35d1tm2b(EUCOMM)Hmgu/Slc35d1tm2b(EUCOMM)Hmgu

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
04/09/2024
MGI 6.23
The Jackson Laboratory