Rtbdn Phenotype Annotations

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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

Allelic Composition Genetic Background	Annotated Term	Reference
Rtbdn^tm1.1Itl/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
Rtbdn^tm1.1Itl/Rtbdn^tm1.1Itl 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
Rtbdn^{tm1a(EUCOMM)Wtsi}/Rtbdn^{tm1a(EUCOMM)Wtsi} C57BL/6N-Rtbdn^{tm1a(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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