Cmah Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

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

20 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Cmah^tm1Ykoz/Cmah⁺ B6.129P2-Cmah^tm1Ykoz	premature death	J:121365
Cmah^tm1Ykoz/Cmah^tm1Ykoz B6.129P2-Cmah^tm1Ykoz	abnormal B cell physiology	J:121365
	abnormal humoral immune response	J:121365
	abnormal inner ear morphology	J:122351
	abnormal interleukin secretion	J:121365
	abnormal organ of Corti morphology	J:122351
	abnormal semicircular canal morphology	J:122351
	abnormal sensorimotor gating	J:122351
	abnormal startle reflex	J:122351
	abnormal T cell physiology	J:121365
	cochlear outer hair cell degeneration	J:122351
	decreased interferon-gamma secretion	J:121365
	normal hematopoietic system phenotype	J:121365
	normal immune system phenotype	J:121365
	impaired coordination	J:122351
	impaired hearing	J:122351
	impaired wound healing	J:122351
	increased B cell proliferation	J:121365
	increased IgG1 level	J:121365
	increased vertical activity	J:122351
	premature death	J:121365

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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