Bex2 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Bex2
brain expressed X-linked 2
MGI:1338017

9 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Bex2^{tm1b(EUCOMM)Hmgu}/Y C57BL/6N-Bex2^{tm1b(EUCOMM)Hmgu}/Ieg	abnormal lens morphology	J:211773
	abnormal retina morphology	J:211773
	decreased locomotor activity	J:211773
	increased startle reflex	J:211773
Bex2^{tm1b(EUCOMM)Hmgu}/Bex2^{tm1b(EUCOMM)Hmgu} C57BL/6N-Bex2^{tm1b(EUCOMM)Hmgu}/Ieg	abnormal coat/hair pigmentation	J:211773
	decreased locomotor activity	J:211773
	decreased prepulse inhibition	J:211773
	decreased red blood cell distribution width	J:211773
	increased leukocyte cell number	J:211773
	increased startle reflex	J:211773
Bex2^tm1Kami/Bex2⁺ C57BL/6NSlc-Bex2^tm1Kami	no abnormal phenotype detected	J:274541
Bex2^tm1Kami/Y C57BL/6NSlc-Bex2^tm1Kami	no abnormal phenotype detected	J:274541

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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