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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Rtbdn
retbindin
MGI:2443686
13 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Rtbdntm1.1Itl/Rtbdn+
involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6 * C57BL/6NTac
decreased a-wave amplitude J:257162
decreased b-wave amplitude J:257162
decreased retina cone cell number J:257162
decreased retina rod cell number J:257162
Rtbdntm1.1Itl/Rtbdntm1.1Itl
involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6 * C57BL/6NTac
abnormal cone electrophysiology J:257162
abnormal photoreceptor outer segment morphology J:257162
abnormal retina neuronal layer morphology J:257162
abnormal rod electrophysiology J:257162
decreased a-wave amplitude J:257162
decreased b-wave amplitude J:257162
decreased retina cone cell number J:257162
decreased retina rod cell number J:257162
retina photoreceptor degeneration J:257162
Rtbdntm1a(EUCOMM)Wtsi/Rtbdntm1a(EUCOMM)Wtsi
C57BL/6N-Rtbdntm1a(EUCOMM)Wtsi/Wtsi
abnormal hair growth J:211773
abnormal retina morphology J:211773
improved glucose tolerance J:211773
thrombocytosis 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
04/16/2024
MGI 6.23
The Jackson Laboratory