Mfsd8 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Mfsd8
major facilitator superfamily domain containing 8
MGI:1919425

15 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Mfsd8^{tm1a(EUCOMM)Hmgu}/Mfsd8^{tm1a(EUCOMM)Hmgu} involves: C57BL/6N	abnormal kidney morphology	J:211608
	abnormal liver morphology	J:211608
	abnormal lysosome morphology	J:211608
	abnormal myocardial fiber morphology	J:211608
	abnormal nervous system morphology	J:211608
	abnormal spleen morphology	J:211608
	astrocytosis	J:211608
	CNS inflammation	J:211608
	microgliosis	J:211608
	retina photoreceptor degeneration	J:211608
Mfsd8^{tm1b(EUCOMM)Hmgu}/Mfsd8^{tm1b(EUCOMM)Hmgu} C57BL/6N-Mfsd8^{tm1b(EUCOMM)Hmgu}/H	abnormal coat/hair pigmentation	J:211773
	abnormal retina morphology	J:211773
	abnormal retina vasculature morphology	J:211773
	impaired pupillary reflex	J:211773
	increased circulating aspartate transaminase level	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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