Symbol Name ID |
Slc35d1
solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1 MGI:2140361 |
Darker colors indicate more annotations |
Human Phenotypes | Malar flattening |
Macrocephaly |
Midface retrusion |
Cleft palate |
Short nose |
Disease(s) Associated with SLC35D1 | |||||
schneckenbecken dysplasia |
Mouse Phenotypes | abnormal craniofacial bone morphology |
abnormal facial morphology |
cleft palate |
protruding tongue |
short snout |
abnormal head shape |
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Availability | Mouse Genotype | ||||||
Slc35d1tm1Hko/Slc35d1tm1Hko | |||||||
Slc35d1tm2b(EUCOMM)Hmgu/Slc35d1tm2b(EUCOMM)Hmgu |
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 05/07/2024 MGI 6.23 |
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