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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Cib2
calcium and integrin binding family member 2
MGI:1929293
17 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Cib2tm1.1Aela/Cib2tm1.1Aela
involves: BALB/c * C57BL/6 * C57BL/6N
abnormal cochlear hair cell morphology J:262464
abnormal hair cell mechanoelectric transduction J:262464
abnormal hearing physiology J:262464
absent cochlear microphonics J:262464
absent distortion product otoacoustic emissions J:262464
cochlear hair cell degeneration J:262464
deafness J:262464
increased or absent threshold for auditory brainstem response J:262464
normal vision/eye phenotype J:262464
Cib2tm1b(EUCOMM)Wtsi/Cib2tm1b(EUCOMM)Wtsi
C57BL/6N-Cib2tm1b(EUCOMM)Wtsi/H
abnormal ear morphology J:211773
absent startle reflex J:211773
decreased prepulse inhibition J:211773
decreased startle reflex J:211773
increased circulating cholesterol level J:211773
increased circulating HDL cholesterol level J:211773
limb grasping J:211773
tremors 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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last database update
11/05/2019
MGI 6.14
The Jackson Laboratory