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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Slc38a3
solute carrier family 38, member 3
MGI:1923507
32 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Slc38a3em1(IMPC)Bay/Slc38a3+
C57BL/6N-Slc38a3em1(IMPC)Bay/BayMmucd 		abnormal bone structure J:211773
decreased body length J:211773
increased bone mineral content J:211773
Slc38a3em1(IMPC)Bay/Slc38a3em1(IMPC)Bay
C57BL/6N-Slc38a3em1(IMPC)Bay/BayMmucd 		preweaning lethality, complete penetrance J:211773
preweaning lethality, incomplete penetrance J:211773
Slc38a3m1Ingm/Slc38a3m1Ingm
B6.C3Fe-Slc38a3m1Ingm 		abnormal amino acid level J:234835
abnormal circulating amino acid level J:234835
abnormal insulin-like growth factor I level J:234835
ataxia J:234835
decreased body size J:234835
decreased body weight J:234835
decreased circulating alanine level J:234835
decreased circulating glucose level J:234835
decreased circulating insulin level J:234835
decreased circulating tyrosine level J:234835
decreased gamma-aminobutyric acid level J:234835
decreased glutamic acid level J:234835
decreased glutamine level J:234835
decreased leucine level J:234835
decreased phenylalanine level J:234835
decreased urine ammonia level J:234835
decreased urine urea nitrogen level J:234835
normal homeostasis/metabolism phenotype J:234835
increased blood urea nitrogen level J:234835
increased circulating cysteine level J:234835
increased circulating histidine level J:234835
increased circulating homocysteine level J:234835
increased circulating leucine level J:234835
increased circulating threonine level J:234835
increased glutamine level J:234835
lethargy J:234835
postnatal lethality, complete penetrance J:234835
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04/16/2024
MGI 6.23 		The Jackson Laboratory