Slc17a8 Phenotype Annotations - Multigenic Genotypes

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc17a8
solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8
MGI:3039629

5 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Runx1^tm3Spe/Runx1^tm3Spe Slc17a8^tm1(cre)Lowl/Slc17a8⁺ involves: 129S4/SvJae	normal behavior/neurological phenotype	J:193903
	hypoalgesia	J:193903
Slc17a8^tm1(cre)Lowl/Slc17a8⁺ Runx1^tm3Spe/Runx1^tm3Spe involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6NCr	abnormal sensory neuron innervation pattern	J:193903
	abnormal sympathetic neuron physiology	J:193903
	decreased sensory neuron number	J:193903

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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