Atp1b2 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Atp1b2
ATPase, Na+/K+ transporting, beta 2 polypeptide
MGI:88109

20 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Atp1b2^tm1Msch/Atp1b2^tm1Msch involves: 129S2/SvPas * C57BL/6J	abnormal brainstem morphology	J:21121
	abnormal cerebellar granule layer morphology	J:21121
	abnormal food intake	J:21121
	abnormal retina photoreceptor morphology	J:21121
	enlarged lateral ventricles	J:21121
	enlarged third ventricle	J:21121
	eyelids fail to open	J:21121
	forelimb paralysis	J:21121
	impaired coordination	J:21121
	impaired righting response	J:21121
	normal nervous system phenotype	J:21121
	postnatal lethality, complete penetrance	J:21121
	retina degeneration	J:21121
	retina outer nuclear layer degeneration	J:21121
	retina photoreceptor degeneration	J:21121, J:74968
	short photoreceptor inner segment	J:21121
	short photoreceptor outer segment	J:21121
	thin retina outer nuclear layer	J:21121
	tremors	J:21121
	normal vision/eye phenotype	J:21121

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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