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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Ss18l1
SS18, nBAF chromatin remodeling complex subunit like 1
MGI:2444061
12 phenotypes from 3 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Ss18l1em1Zqi/Ss18l1+
involves: C57BL/6
impaired coordination J:278840
increased microglial cell activation J:278840
Ss18l1em1Zqi/Ss18l1em1Zqi
involves: C57BL/6
abnormal innervation pattern to muscle J:278840
abnormal locomotor behavior J:278840
decreased body size J:278840
increased microglial cell activation J:278840
premature death J:278840
Ss18l1em2Zqi/Ss18l1em2Zqi
involves: C57BL/6
impaired coordination J:278840
increased microglial cell activation J:278840
Ss18l1tm1Ghsh/Ss18l1tm1Ghsh
Not Specified
abnormal cerebral cortex morphology J:87443
abnormal forebrain morphology J:87443
abnormal hindbrain morphology J:87443
abnormal hippocampus CA3 region morphology J:87443
decreased body size J:87443
impaired coordination J:87443
infertility J:87443
premature death J:87443
small cerebellum J:87443

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
04/09/2024
MGI 6.23
The Jackson Laboratory