Slc7a10 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc7a10
solute carrier family 7 (cationic amino acid transporter, y+ system), member 10
MGI:1858261

16 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Slc7a10^tm1Dgen/Slc7a10^tm1Dgen involves: 129P2/OlaHsd * C57BL/6	abnormal amino acid level	J:122880
	abnormal CNS synaptic transmission	J:100127
	abnormal excitatory postsynaptic potential	J:100127
	abnormal nervous system physiology	J:122880
	abnormal synaptic physiology	J:122880
	ataxia	J:100127
	decreased body size	J:100127, J:122880
	decreased body weight	J:100127
	decreased locomotor activity	J:100127
	hunched posture	J:100127
	myoclonus	J:100127
	postnatal lethality, incomplete penetrance	J:100127
	premature death	J:122880
	seizures	J:100127
	tonic-clonic seizures	J:100127
	tremors	J:100127, J:122880

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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