Nxnl2 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Nxnl2
nucleoredoxin-like 2
MGI:1922374

13 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Nxnl2^{em1(IMPC)Ccpcz}/Nxnl2⁺ C57BL/6NCrl-Nxnl2^{em1(IMPC)Ccpcz}/Ccpcz	abnormal coat/ hair morphology	J:211773
	abnormal spleen morphology	J:211773
	abnormal thymus morphology	J:211773
	enlarged spleen	J:211773
	enlarged thymus	J:211773
Nxnl2^{em1(IMPC)Ccpcz}/Nxnl2^{em1(IMPC)Ccpcz} C57BL/6NCrl-Nxnl2^{em1(IMPC)Ccpcz}/Ccpcz	abnormal skeletal muscle morphology	J:211773
	abnormal spleen morphology	J:211773
	abnormal thymus morphology	J:211773
	enlarged spleen	J:211773
	enlarged thymus	J:211773
	shortened QRS complex duration	J:211773
Nxnl2^tm1.2Tlev/Nxnl2^tm1.2Tlev BALB/c-Nxnl2^tm1.2Tlev	abnormal cone electrophysiology	J:183790
	abnormal olfactory sensory neuron morphology	J:183790
	abnormal rod electrophysiology	J:183790
	decreased retina cone cell number	J:183790
	impaired olfaction	J:183790
	short photoreceptor outer segment	J:183790

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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