GlyCosmos Portal

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GO Term	Evidence Code	PMID
DNA N-glycosylase activity	TAS
MutLbeta complex binding	IDA	11801590
adenine/guanine mispair binding	IBA
4 iron, 4 sulfur cluster binding	IEA
MutSalpha complex binding	IDA	11801590

GO Hierarchy

molecular function

catalytic activity [inference]

hydrolase activity [inference]

hydrolase activity, acting on glycosyl bonds [inference]

hydrolase activity, hydrolyzing N-glycosyl compounds [inference]

DNA N-glycosylase activity

mismatch base pair DNA N-glycosylase activity [inference]

purine-specific mismatch base pair DNA N-glycosylase activity

oxidized base lesion DNA N-glycosylase activity [inference]

oxidized purine nucleobase lesion DNA N-glycosylase activity [inference]

8-oxo-7,8-dihydroguanine DNA N-glycosylase activity

catalytic activity, acting on a nucleic acid [inference]

catalytic activity, acting on DNA [inference]

DNA N-glycosylase activity

mismatch base pair DNA N-glycosylase activity [inference]

purine-specific mismatch base pair DNA N-glycosylase activity

oxidized base lesion DNA N-glycosylase activity [inference]

oxidized purine nucleobase lesion DNA N-glycosylase activity [inference]

8-oxo-7,8-dihydroguanine DNA N-glycosylase activity

binding [inference]

protein binding

ion binding [inference]

cation binding [inference]

metal ion binding

protein-containing complex binding [inference]

mismatch repair complex binding [inference]

metal cluster binding [inference]

iron-sulfur cluster binding [inference]

4 iron, 4 sulfur cluster binding

organic cyclic compound binding [inference]

nucleic acid binding [inference]

DNA binding [inference]

damaged DNA binding [inference]

oxidized DNA binding [inference]

oxidized purine DNA binding

double-stranded DNA binding [inference]

mismatched DNA binding [inference]

adenine/guanine mispair binding

Gene Ontology information from NCBI Gene and UniProt.

Disease

Disease Ontology

Displaying entries **1 - 10** of **150** in total

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DO ID	Disease Name	Source
DOID:0050424	familial adenomatous polyposis	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:0050465	Muir-Torre syndrome	DisGeNET
DOID:0050589	inflammatory bowel disease	DisGeNET
DOID:0050638	transthyretin amyloidosis	DisGeNET
DOID:0050646	distal arthrogryposis	DisGeNET
DOID:0050657	Bannayan-Riley-Ruvalcaba syndrome	DisGeNET
DOID:0050757	deafness-dystonia-optic neuronopathy syndrome	DisGeNET
DOID:0050787	juvenile polyposis syndrome	DisGeNET
DOID:0060389	chromosome 10q23 deletion syndrome	DisGeNET
DOID:0080144	childhood acute lymphocytic leukemia	DisGeNET

The Human Phenotype Ontology

Displaying entries **41 - 50** of 61 in total

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HPO ID	HPO Term
HP:0010524	Disturbed sensory perception
HP:0010526	Dysgraphia
HP:0010622	Neoplasm of the skeletal system
HP:0010784	Uterine neoplasm
HP:0010786	Urinary tract neoplasm
HP:0012113	Abnormal circulating creatine concentration
HP:0012126	Stomach cancer
HP:0012174	Glioblastoma multiforme
HP:0012378	Fatigue
HP:0100013	Neoplasm of the breast

Displaying **all 4** entries
Disease ID	Disease Name
OMIM:613659	gastric cancer
ORPHA:440437	familial colorectal cancer type X
ORPHA:247798	familial adenomatous polyposis 2
OMIM:608456	familial adenomatous polyposis 2

PubChem Disease

GHR Health Conditions

Familial adenomatous polyposis

MedGen Diseases

OMIM Phenotypes

KEGG Diseases

Gene-Disease-Co-Occurrences-in-Literature (PubChem)

Ortholog

Displaying entries **11 - 20** of 63 in total

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Species	Gene ID	Alliance of Genome Resources	Orthologous MAtrix
Oreochromis niloticus	100708864		ORENI43121
Haplochromis burtoni	102302415		HAPBU28344
Xenopus laevis	108714269	Xenbase:XB-GENE-6487001
Xenopus tropicalis	780292	Xenbase:XB-GENE-998137
Serinus canaria	103815172		SERCA08385
Callithrix jacchus	100397524		CALJA41663
Cercocebus atys	105594590		CERAT05670
Macaca mulatta	705651		MACMU25552
Macaca nemestrina	105494936		MACNE02171
Papio anubis	101025544		PAPAN21074