About Help FAQ

Symbol
Name
ID

Slc35d1
solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1
MGI:2140361

Phenotype annotations related to craniofacial

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
Availability	Mouse Genotype	abnormal craniofacial bone morphology	abnormal facial morphology	cleft palate	protruding tongue	short snout	abnormal head shape
	Slc35d1^tm1Hko/Slc35d1^tm1Hko
	Slc35d1^{tm2b(EUCOMM)Hmgu}/Slc35d1^{tm2b(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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/16/2024 MGI 6.23