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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Acss2
acyl-CoA synthetase short-chain family member 2
MGI:1890410
12 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Acss2em1Slbr/Acss2em1Slbr
C57BL/6J-Acss2em1Slbr 		abnormal epigenetic regulation of gene expression J:346349
abnormal long-term spatial reference memory J:346349
normal behavior/neurological phenotype J:346349
impaired contextual conditioning behavior J:346349
impaired cued conditioning behavior J:346349
normal nervous system phenotype J:346349
Acss2em22Gpt/Acss2em22Gpt
C57BL/6JGpt-Acss2em22Gpt/Gpt 		abnormal kidney cortex morphology J:346990
decreased blood urea nitrogen level J:346990
decreased circulating creatinine level J:346990
decreased interleukin-1 beta secretion J:346990
decreased pyroptosis J:346990
decreased susceptibility to endotoxin shock J:346990
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
06/09/2026
MGI 6.24 		The Jackson Laboratory