2310039L15Rik Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

2310039L15Rik
RIKEN cDNA 2310039L15 gene
MGI:1916879

19 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
2310039L15Rik^{Tg(Prnp-SNCAA53T)23Mkle}/2310039L15Rik⁺ involves: C3H/HeJ C57BL/6J	abnormal motor capabilities/coordination/movement	J:77344
	abnormal nervous system morphology	J:77344
	abnormal neuron morphology	J:77344
	abnormal spinal cord morphology	J:77344
	astrocytosis	J:77344, J:327648
	ataxia	J:77344
	bradykinesia	J:77344
	dystonia	J:77344
	impaired righting response	J:77344
	increased locomotor activity	J:327648
	increased vertical activity	J:327648
	loss of dopaminergic neurons	J:327648
	neurodegeneration	J:77344
	neuronal intranuclear inclusions	J:77344
	paralysis	J:77344
	premature death	J:77344, J:327648
2310039L15Rik^{Tg(Prnp-SNCAA53T)23Mkle}/2310039L15Rik⁺ Zfp746^tm1.1Tmd/Zfp746^tm1.1Tmd involves: 129S4/SvJae C3H/HeJ * C57BL/6J	decreased locomotor activity	J:327648
	decreased vertical activity	J:327648
	extended life span	J:327648

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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