Cwc22 Phenotype Annotations

About Help FAQ

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Cwc22
CWC22 spliceosome-associated protein
MGI:2136773

16 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Cwc22^em1(IMPC)Mbp/Cwc22⁺ C57BL/6NCrl-Cwc22^em1(IMPC)Mbp/Mmucd	abnormal liver morphology	J:211773
	abnormal spleen morphology	J:211773
	anophthalmia	J:211773
	cystolithiasis	J:211773
	hemorrhage	J:211773
	increased bone mineral content	J:211773
	increased circulating aspartate transaminase level	J:211773
	microcephaly	J:211773
	microphthalmia	J:211773
	polydactyly	J:211773
	spina bifida	J:211773
	syndactyly	J:211773
	urinary bladder obstruction	J:211773
Cwc22^em1(IMPC)Mbp/Cwc22^em1(IMPC)Mbp C57BL/6NCrl-Cwc22^em1(IMPC)Mbp/Mmucd	embryonic lethality prior to organogenesis	J:211773
	prenatal lethality prior to heart atrial septation	J:211773
	preweaning lethality, complete penetrance	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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/30/2024 MGI 6.23