Elfn1 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Elfn1
leucine rich repeat and fibronectin type III, extracellular 1
MGI:2442479

21 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Elfn1^{tm1(KOMP)Vlcg}/Elfn1^{tm1(KOMP)Vlcg} involves: C57BL/6NTac	decreased anxiety-related response	J:209758
	decreased grip strength	J:209758
	hyperactivity	J:209758
	impaired coordination	J:209758
	normal nervous system phenotype	J:209758
	seizures	J:209758
Elfn1^{tm1.1(KOMP)Vlcg}/Elfn1^{tm1.1(KOMP)Vlcg} C57BL/6N-Elfn1^{tm1.1(KOMP)Vlcg}/Ucd	abnormal behavior	J:211773
	abnormal spinal cord morphology	J:211773
	decreased thigmotaxis	J:211773
	hyperactivity	J:211773
Elfn1^tm1.1Jaru/Elfn1^tm1.1Jaru involves: C57BL/6	abnormal brain wave pattern	J:226212
	abnormal dendritic spine morphology	J:226212
	abnormal excitatory postsynaptic currents	J:226212
	abnormal impulsive behavior control	J:226212
	abnormal response to novelty	J:226212
	decreased vertical activity	J:226212
	environmentally induced seizures	J:226212
	hyperactivity	J:226212
	impaired synaptic plasticity	J:226212
	increased locomotor activity	J:226212
	increased susceptibility to pharmacologically induced seizures	J:226212
	increased synaptic depression	J:226212
	reduced long-term potentiation	J:226212

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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