Slc44a1 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc44a1
solute carrier family 44, member 1
MGI:2140592

13 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Slc44a1^{tm1b(EUCOMM)Hmgu}/Slc44a1^{tm1b(EUCOMM)Hmgu} C57BL/6N-Slc44a1^{tm1b(EUCOMM)Hmgu}/Bay	abnormal bone structure	J:211773
	abnormal coat appearance	J:211773
	abnormal eye anterior chamber depth	J:211773
	abnormal eye posterior chamber depth	J:211773
	abnormal retina blood vessel morphology	J:211773
	abnormal retina outer nuclear layer morphology	J:211773
	decreased prepulse inhibition	J:211773
	decreased total retina thickness	J:211773
	hyperactivity	J:211773
	increased bone mineral content	J:211773
	increased heart rate	J:211773
	increased vertical activity	J:211773
	irregularly shaped pupil	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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