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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Aspn
asporin
MGI:1913945
13 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Aspntm1.2Mmac/Aspntm1.2Mmac
B6.129(Cg)-Aspntm1.2Mmac
abnormal cutaneous collagen fibril morphology J:341806
abnormal glycosaminoglycan level J:341806
abnormal skin morphology J:341806
abnormal skin tensile strength J:341806
normal behavior/neurological phenotype J:341806
Aspntm1b(EUCOMM)Hmgu/Aspntm1b(EUCOMM)Hmgu
C57BL/6N-Aspntm1b(EUCOMM)Hmgu/Ieg
abnormal auditory brainstem response J:211773
abnormal lens morphology J:211773
abnormal retina morphology J:211773
abnormal vitreous body morphology J:211773
decreased circulating phosphate level J:211773
decreased mean corpuscular volume J:211773
increased circulating cholesterol level J:211773
increased circulating HDL cholesterol level J:211773

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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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory