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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Slc1a4
solute carrier family 1 (glutamate/neutral amino acid transporter), member 4
MGI:2135601
10 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Slc1a4em2Tmg/Slc1a4em2Tmg
involves: C57BL/6J 		abnormal cerebral cortex morphology J:344184
abnormal corpus callosum morphology J:344184
abnormal response to novel object J:344184
normal behavior/neurological phenotype J:344184
decreased brain weight J:344184
normal growth/size/body region phenotype J:344184
microcephaly J:344184
Slc1a4tm1e(KOMP)Wtsi/Slc1a4tm1e(KOMP)Wtsi
C57BL/6N-Slc1a4tm1e(KOMP)Wtsi/Wtsi 		decreased circulating serum albumin level J:211773
improved glucose tolerance J:211773
increased red blood cell distribution width 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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Send questions and comments to User Support. 		last database update
04/16/2024
MGI 6.23 		The Jackson Laboratory