Slc18a1 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc18a1
solute carrier family 18 (vesicular monoamine), member 1
MGI:106684

5 phenotypes from 1 allele in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc18a1^tm1Dgen/Slc18a1^tm1Dgen B6.129P2-Slc18a1^tm1Dgen/J	abnormal neuron proliferation	J:194189
	abnormal object recognition memory	J:194189
	normal behavior/neurological phenotype	J:194189
	increased neuron apoptosis	J:194189
Slc18a1^tm1Dgen/Slc18a1^tm1Dgen involves: 129P2/OlaHsd * C57BL/6	normal no abnormal phenotype detected	J:101679

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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