Snph Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Snph
syntaphilin
MGI:2139270

11 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Snph^{tm1.1(KOMP)Vlcg}/Snph^{tm1.1(KOMP)Vlcg} C57BL/6N-Snph^{tm1.1(KOMP)Vlcg}/Ucd	decreased body length	J:211773
	decreased bone mineral content	J:211773
	decreased brain weight	J:211773
	hyperactivity	J:211773
Snph^tm1Zhs/Snph^tm1Zhs involves: 129S6/SvEvTac	abnormal mitochondrial morphology	J:145318
	abnormal mitochondrial physiology	J:145318
	abnormal neuron physiology	J:145318
	abnormal synaptic bouton morphology	J:145318
	enhanced paired-pulse facilitation	J:145318
	impaired coordination	J:145318
	normal nervous system phenotype	J:145318

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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