Cmah Phenotype Annotations - Multigenic Genotypes

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Cmah
cytidine monophospho-N-acetylneuraminic acid hydroxylase
MGI:103227

23 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Cmah^tm1Avrk/Cmah^tm1Avrk Dmd^mdx/Dmd^mdx involves: 129X1/SvJ * C57BL/10ScSn	abnormal gait	J:164594
	cardiac muscle necrosis	J:164594
	dystrophic muscle	J:164594
	impaired coordination	J:164594
	increased macrophage cell number	J:164594
	increased monocyte cell number	J:164594
	muscle weakness	J:164594
	premature death	J:164594
	skeletal muscle fibrosis	J:164594
Cmah^tm1Avrk/Cmah^tm1Avrk Dock2^m1Hsd/Dock2^m1Hsd B6NHsd.Cg-Dock2^m1Hsd Cmah^tm1Avrk	abnormal B cell activation	J:144035
	abnormal cochlear sensory epithelium morphology	J:122351
	abnormal inner ear morphology	J:122351
	abnormal organ of Corti morphology	J:122351
	abnormal otolithic membrane morphology	J:122351
	abnormal semicircular canal morphology	J:122351
	abnormal sensorimotor gating	J:122351
	abnormal startle reflex	J:122351
	cochlear outer hair cell degeneration	J:122351
	decreased follicular B cell number	J:144035
	decreased marginal zone B cell number	J:144035
	impaired coordination	J:122351
	impaired hearing	J:122351
	impaired wound healing	J:122351
	increased vertical activity	J:122351
Cmah^tm1Avrk/Cmah^tm1Avrk Dock2^m1Hsd/Dock2^m1Hsd Siae^tm1.2Avrk/Siae^tm1.2Avrk B6NHsd.Cg-Siae^tm1.2Avrk Dock2^m1Hsd Cmah^tm1Avrk	abnormal B cell activation	J:144035
	decreased follicular B cell number	J:144035
	decreased marginal zone B cell number	J:144035

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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