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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Med31
mediator complex subunit 31
MGI:1914529
19 phenotypes from 1 allele in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Med31l11Jus15/Med31l11Jus15
involves: 129S5/SvEvBrd * C57BL/6J
abnormal cartilage development J:161417
abnormal limb development J:161417
abnormal skeleton morphology J:161417
normal cardiovascular system phenotype J:161417
decreased bone ossification J:161417
decreased cell proliferation J:161417
decreased embryo size J:161417
decreased fetal size J:161417
decreased fibroblast proliferation J:161417
edema J:161417
embryonic growth retardation J:161417
normal hearing/vestibular/ear phenotype J:161417
lethality throughout fetal growth and development, complete penetrance J:161417
pallor J:161417
small cranium J:161417
small thoracic cage J:161417
spina bifida J:161417
Med31l11Jus15/Med31l11Jus15
involves: C57BL/6J
abnormal embryonic growth/weight/body size J:85113
edema J:85113
embryonic growth retardation J:85113
lethality throughout fetal growth and development, complete penetrance J:85113
open neural tube J:85113

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
04/23/2024
MGI 6.23
The Jackson Laboratory