GO Term | Evidence Code | PMID |
---|---|---|
mismatch repair | ||
negative regulation of necroptotic process | ||
base-excision repair | ||
DNA repair | ||
depurination |
GO Term | Evidence Code | PMID |
---|---|---|
nucleus | ||
mitochondrion | ||
nucleoplasm |
GO Term | Evidence Code | PMID |
---|---|---|
metal ion binding | ||
MutSbeta complex binding | ||
MutLalpha complex binding | ||
protein binding | ||
purine-specific mismatch base pair DNA N-glycosylase activity |
DO ID | Disease Name | Source |
---|---|---|
DOID:0050424 | familial adenomatous polyposis | |
DOID:0050465 | Muir-Torre syndrome | |
DOID:0050589 | inflammatory bowel disease | |
DOID:0050638 | transthyretin amyloidosis | |
DOID:0050646 | distal arthrogryposis | |
DOID:0050657 | Bannayan-Riley-Ruvalcaba syndrome | |
DOID:0050757 | deafness-dystonia-optic neuronopathy syndrome | |
DOID:0050787 | juvenile polyposis syndrome | |
DOID:0060389 | chromosome 10q23 deletion syndrome | |
DOID:0080144 | childhood acute lymphocytic leukemia |
HPO ID | HPO Term |
---|---|
HP:0002027 | Abdominal pain |
HP:0002076 | Migraine |
HP:0002167 | Abnormality of speech or vocalization |
HP:0002239 | Gastrointestinal hemorrhage |
HP:0002354 | Memory impairment |
HP:0002376 | Developmental regression |
HP:0002516 | Increased intracranial pressure |
HP:0002671 | Basal cell carcinoma |
HP:0002893 | Pituitary adenoma |
HP:0002894 | Neoplasm of the pancreas |
Disease ID | Disease Name |
---|---|
OMIM:613659 |
|
ORPHA:440437 |
|
ORPHA:247798 |
|
OMIM:608456 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
109083710 | CYPCA73072 | ||
103259761 | CARSF24599 | ||
108312749 | CEBIM14782 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024