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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Slc7a7
solute carrier family 7 (cationic amino acid transporter, y+ system), member 7
MGI:1337120
44 phenotypes from 3 alleles in 7 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Slc7a7em1(IMPC)Bay/Slc7a7+
C57BL/6N-Slc7a7em1(IMPC)Bay/BayMmucd 		increased lean body mass J:211773
Slc7a7em1(IMPC)Bay/Slc7a7em1(IMPC)Bay
C57BL/6N-Slc7a7em1(IMPC)Bay 		cardiac hypertrophy J:293773
cleft palate J:293773
decreased fetal size J:293773
hydrocephaly J:293773
preweaning lethality, complete penetrance J:293773
short snout J:293773
ventricular septal defect J:293773
Slc7a7em1(IMPC)Bay/Slc7a7em1(IMPC)Bay
C57BL/6N-Slc7a7em1(IMPC)Bay/BayMmucd 		abnormal embryo size J:211773
abnormal placenta size J:211773
embryonic growth retardation J:211773
preweaning lethality, complete penetrance J:211773
Slc7a7em1(IMPC)Bay/Slc7a7em1(IMPC)Bay
C57BL/6N-Slc7a7em1(IMPC)Bay/Mcmud 		abnormal embryo size J:211773
preweaning lethality, complete penetrance J:211773
Slc7a7em1Lbu/Slc7a7em1Lbu
C57BL/6-Slc7a7em1Lbu 		preweaning lethality, complete penetrance J:293773
Slc7a7em1Lbu/Slc7a7em1Lbu
involves: 129/SvEv * C57BL/6 		abnormal lung development J:293773
abnormal proximal convoluted tubule morphology J:293773
abnormal skeleton development J:293773
abnormal spleen germinal center morphology J:293773
aminoaciduria J:293773
argininuria J:293773
decreased bone mineralization J:293773
decreased lymphocyte cell number J:293773
decreased spleen weight J:293773
delayed hepatic development J:293773
delayed kidney development J:293773
dilated renal tubule J:293773
impaired lung alveolus development J:293773
increased neutrophil cell number J:293773
increased spleen red pulp amount J:293773
kidney cortex atrophy J:293773
lysinuria J:293773
preweaning lethality, incomplete penetrance J:293773
slow postnatal weight gain J:293773
Slc7a7em1Lbu/Slc7a7em1Lbu
involves: C57BL/6 * FVB/N 		preweaning lethality, complete penetrance J:293773
Slc7a7Gt(OST41878)Lex/Slc7a7Gt(OST41878)Lex
B6.129S-Slc7a7Gt(OST41878)Lex 		abnormal skeleton development J:125847
aminoaciduria J:125847
decreased birth body size J:125847
decreased embryo size J:125847
embryonic growth retardation J:125847
hypotonia J:125847
increased circulating ammonia level J:125847
increased spleen weight J:125847
neonatal lethality, incomplete penetrance J:125847
perinatal lethality, incomplete penetrance J:125847
postnatal growth retardation J:125847
premature death J:125847
pup cannibalization J:125847
reduced female fertility J:125847
tremors J:125847
unresponsive to tactile stimuli J:125847
weight loss J:125847
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