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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Slc38a8
solute carrier family 38, member 8
MGI:2685433
14 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Slc38a8em1(IMPC)Bay/Slc38a8em1(IMPC)Bay
C57BL/6N-Slc38a8em1(IMPC)Bay/BayMmucd 		hyperactivity J:211773
Slc38a8em1Cya/Slc38a8em1Cya
C57BL/6J-Slc38a8em1Cya 		decreased aspartic acid level J:336781
decreased circulating aspartate transaminase level J:336781
decreased susceptibility to viral infection J:336781
decreased susceptibility to viral infection induced morbidity/mortality J:336781
Slc38a8em1Lmon/Slc38a8+
B6.Cg-Slc38a8em1Lmon 		abnormal choroid pigmentation J:343795
abnormal iris pigmentation J:343795
abnormal retina pigment epithelium morphology J:343795
decreased visual acuity J:343795
Slc38a8em1Lmon/Slc38a8em1Lmon
B6.Cg-Slc38a8em1Lmon 		abnormal choroid pigmentation J:343795
abnormal innervation J:343795
abnormal lateral geniculate nucleus morphology J:343795
abnormal retina pigment epithelium morphology J:343795
decreased a-wave amplitude J:343795
decreased b-wave amplitude J:343795
decreased visual acuity J:343795
normal pigmentation phenotype J:343795
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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Send questions and comments to User Support. 		last database update
04/23/2024
MGI 6.23 		The Jackson Laboratory