Aldh1l2 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Aldh1l2
aldehyde dehydrogenase 1 family, member L2
MGI:2444680

22 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Aldh1l2^{tm2e(KOMP)Wtsi}/Aldh1l2^{tm2e(KOMP)Wtsi} involves: C57BL/6 * C57BL/6N	abnormal amino acid level	J:299012
	abnormal cell physiology	J:299012
	abnormal enzyme/coenzyme level	J:299012
	abnormal folic acid level	J:299012
	abnormal metabolism	J:299012
	abnormal vitamin C level	J:299012
	normal behavior/neurological phenotype	J:299012
	normal cardiovascular system phenotype	J:299012
	decreased cystathionine level	J:299012
	decreased cysteine level	J:299012
	decreased fatty acid beta-oxidation	J:299012
	decreased glutathione level	J:299012
	normal endocrine/exocrine gland phenotype	J:299012
	normal growth/size/body region phenotype	J:299012
	hepatic steatosis	J:299012
	normal immune system phenotype	J:299012
	normal liver/biliary system phenotype	J:299012
	normal mortality/aging	J:299012
	normal nervous system phenotype	J:299012
	normal renal/urinary system phenotype	J:299012
	normal reproductive system phenotype	J:299012
	normal respiratory system phenotype	J:299012

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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