Unc13b Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Unc13b
unc-13 homolog B
MGI:1342278

10 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Unc13b^{tm1b(KOMP)Wtsi}/Unc13b⁺ C57BL/6N-Unc13b^{tm1b(KOMP)Wtsi}/Ucd	abnormal testis morphology	J:211773
	small testis	J:211773
Unc13b^{tm1b(KOMP)Wtsi}/Unc13b^{tm1b(KOMP)Wtsi} C57BL/6N-Unc13b^{tm1b(KOMP)Wtsi}/Ucd	preweaning lethality, incomplete penetrance	J:211773
Unc13b^tm2Bros/Unc13b^tm2Bros Not Specified	abnormal cone electrophysiology	J:185276
	abnormal eye electrophysiology	J:185276
	abnormal rod electrophysiology	J:185276
	abnormal synapse morphology	J:185276
	normal nervous system phenotype	J:77339
	sporadic seizures	J:77339
	normal vision/eye phenotype	J:185276

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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