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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Slc2a10
solute carrier family 2 (facilitated glucose transporter), member 10
MGI:2156687
13 phenotypes from 2 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Slc2a10G128E/Slc2a10G128E
C3HeB/FeJ-Slc2a10G128E 		abnormal aorta elastic fiber morphology J:161835
abnormal aorta wall morphology J:161835
abnormal artery morphology J:161835
abnormal blood vessel elastic tissue morphology J:161835
abnormal blood vessel morphology J:161835
abnormal descending aorta morphology J:161835
abnormal kidney arterial blood vessel morphology J:161835
abnormal lung vasculature morphology J:161835
abnormal pulmonary alveolus wall morphology J:161835
abnormal pulmonary elastic fiber morphology J:161835
abnormal spleen morphology J:161835
aortic elastic tissue lesions J:161835
Slc2a10G128E/Slc2a10G128E
involves: C3HeB/FeJ 		normal cardiovascular system phenotype J:140316
Slc2a10S150F/Slc2a10S150F
C3HeB/FeJ-Slc2a10S150F 		abnormal blood vessel morphology J:161835
Slc2a10S150F/Slc2a10S150F
involves: C3HeB/FeJ 		normal cardiovascular system phenotype J:140316
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