Baiap2l2 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Baiap2l2
BAI1-associated protein 2-like 2
MGI:2652819

19 phenotypes from 3 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Baiap2l2^em1Pgg/Baiap2l2^em1Pgg involves: C57BL/6	abnormal cochlear sensory epithelium morphology	J:305454
	abnormal ear morphology	J:305454
	abnormal hair cell mechanoelectric transduction	J:305454
	abnormal hearing physiology	J:305454
Baiap2l2^{tm1a(EUCOMM)Hmgu}/Baiap2l2^{tm1a(EUCOMM)Hmgu} C57BL/6N-Baiap2l2^{tm1a(EUCOMM)Hmgu}/Ics	abnormal auditory brainstem response	J:211773
	decreased grip strength	J:211773
	decreased prepulse inhibition	J:211773
	decreased startle reflex	J:211773
	increased cardiac muscle contractility	J:211773
	increased circulating bilirubin level	J:211773
Baiap2l2^{tm1b(EUCOMM)Hmgu}/Baiap2l2^{tm1b(EUCOMM)Hmgu} C57BL/6N-Baiap2l2^{tm1b(EUCOMM)Hmgu}	abnormal cochlear sensory epithelium morphology	J:305454
	abnormal hair cell mechanoelectric transduction	J:305454
	deafness	J:305454
	decreased inner hair cell stereocilia number	J:305454
	decreased outer hair cell stereocilia number	J:305454
	impaired hearing	J:305454
	increased or absent distortion product otoacoustic emission threshold	J:305454
	increased or absent threshold for auditory brainstem response	J:305454
Baiap2l2^{tm1b(EUCOMM)Hmgu}/Baiap2l2^{tm1b(EUCOMM)Hmgu} C57BL/6N-Baiap2l2^{tm1b(EUCOMM)Hmgu}/Ics	abnormal auditory brainstem response	J:211773
	abnormal gait	J:211773
	abnormal startle reflex	J:211773
	decreased hematocrit	J:211773
	decreased prepulse inhibition	J:211773
	decreased startle reflex	J:211773

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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