Snord118 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Snord118
small nucleolar RNA, C/D box 118
MGI:3819519

13 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Emx1^tm1(cre)Krj/Emx1⁺ Snord118^em1Jfch/Snord118⁺ B6.Cg-Emx1^tm1(cre)Krj Snord118^em1Jfch	abnormal cell physiology	J:344970
	decreased body weight	J:344970
	decreased brain weight	J:344970
	decreased fetal weight	J:344970
	decreased neuronal precursor cell number	J:344970
	decreased neuronal precursor proliferation	J:344970
	thin cerebral cortex	J:344970
Emx1^tm1(cre)Krj/Emx1⁺ Snord118^em1Jfch/Snord118^em1Jfch B6.Cg-Emx1^tm1(cre)Krj Snord118^em1Jfch	abnormal brain development	J:344970
	abnormal cell physiology	J:344970
	abnormal neocortex morphology	J:344970
	absent corpus callosum	J:344970
	absent hippocampus	J:344970
	decreased body weight	J:344970
	decreased brain weight	J:344970
	decreased fetal weight	J:344970
	decreased neuronal precursor cell number	J:344970
	decreased neuronal precursor proliferation	J:344970
	increased neuron apoptosis	J:344970
	premature death	J:344970
	thin cerebral cortex	J:344970

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 12/17/2024 MGI 6.24