Nxnl1 Phenotype Annotations

About Help FAQ

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Nxnl1
nucleoredoxin-like 1
MGI:1924446

8 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Nxnl1^tm1.2Tlev/Nxnl1^tm1.2Tlev involves: BALB/c * BALB/cJ * C57BL/6	abnormal cone electrophysiology	J:186370
	abnormal eye physiology	J:186370
	abnormal lipid homeostasis	J:186370
	abnormal rod electrophysiology	J:186370
	abnormal vision	J:186370
	decreased retina cone cell number	J:186370
	microgliosis	J:186370
	thin retina outer nuclear layer	J:186370

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 12/17/2024 MGI 6.24