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Phenotype ontology term - FYPO:0008216 - abnormal DNA N-glycosylase activity

Term summary

ID
FYPO:0008216
Name
abnormal DNA N-glycosylase activity
Ontology or CV name
Phenotype
Definition
A molecular function phenotype in which the observed rate of DNA N-glycosylase activity is abnormal.

Parents

Annotation

Single locus phenotype

FYPO:0000699 - abolished DNA-7-methylguanine glycosylase activity

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FYPO:0004677 - abolished purine-specific mismatch base pair DNA N-glycosylase activity

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FYPO:0000693 - decreased DNA-1,N6-ethenoadenine N-glycosylase activity

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FYPO:0000698 - decreased DNA-7-methylguanine glycosylase activity

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FYPO:0004280 - decreased hypoxanthine DNA N-glycosylase activity

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FYPO:0004284 - decreased oxanine DNA N-glycosylase activity

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FYPO:0004278 - decreased uracil DNA N-glycosylase activity

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FYPO:0004282 - decreased xanthine DNA N-glycosylase activity

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FYPO:0000695 - increased DNA-1,N6-ethenoadenine N-glycosylase activity

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