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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Slc35c2
solute carrier family 35, member C2
MGI:2385166
7 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background		 Annotated Term Reference
Slc35c1tm1Cknr/Slc35c1tm1Cknr
Slc35c2tm1.1Pst/Slc35c2tm1.1Pst
129X1.Cg-Slc35c1tm1Cknr Slc35c2tm1.1Pst 		abnormal skeleton morphology J:354047
embryonic growth retardation J:354047
preweaning lethality, complete penetrance J:354047
Slc35c1tm1Cknr/Slc35c1tm1Cknr
Slc35c2tm1.1Pst/Slc35c2tm1.1Pst
B6.Cg-Slc35c1tm1Cknr Slc35c2tm1.1Pst 		abnormal skeleton morphology J:354047
abnormal sternum morphology J:354047
decreased lumbar vertebrae number J:354047
decreased rib number J:354047
decreased thoracic vertebrae number J:354047
embryonic growth retardation J:354047
preweaning lethality, complete penetrance J:354047
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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Send questions and comments to User Support. 		last database update
11/19/2024
MGI 6.24 		The Jackson Laboratory