Srcin1 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Srcin1
SRC kinase signaling inhibitor 1
MGI:1933179

10 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Srcin1^{tm1.1(KOMP)Vlcg}/Srcin1⁺ C57BL/6N-Srcin1^{tm1.1(KOMP)Vlcg}/J	increased bone mineral content	J:211773
	increased heart weight	J:211773
Srcin1^tm1Fdc/Srcin1⁺ Not Specified	abnormal dendritic spine morphology	J:206962
Srcin1^tm1Fdc/Srcin1^tm1Fdc Not Specified	abnormal CNS synaptic transmission	J:206962
	abnormal dendritic spine morphology	J:206962
	abnormal excitatory postsynaptic potential	J:206962
	abnormal motor learning	J:206962
	abnormal object recognition memory	J:206962
	impaired synaptic plasticity	J:206962
	reduced long-term depression	J:206962
	reduced long-term potentiation	J:206962

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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