GO Term |
---|
nuclear replication fork |
chromosome, telomeric region |
mitochondrion |
cytosol |
nucleoplasm |
transcription regulator complex |
protein-DNA complex |
nuclear body |
site of double-strand break |
site of DNA damage |
GO Term |
---|
damaged DNA binding |
NAD+ ADP-ribosyltransferase activity |
nucleotidyltransferase activity |
zinc ion binding |
DNA binding |
chromatin binding |
RNA binding |
enzyme binding |
protein kinase binding |
histone deacetylase binding |
Position | Description | PubMed ID | GlyTouCan ID | Source |
---|---|---|---|---|
|
Pathway Name | Organism |
---|---|
DNA Damage Recognition in GG-NER | Homo sapiens |
Downregulation of SMAD2/3:SMAD4 transcriptional activity | Homo sapiens |
Dual Incision in GG-NER | Homo sapiens |
Formation of Incision Complex in GG-NER | Homo sapiens |
HDR through MMEJ (alt-NHEJ) | Homo sapiens |
POLB-Dependent Long Patch Base Excision Repair | Homo sapiens |
SUMOylation of DNA damage response and repair proteins | Homo sapiens |
vRNA Synthesis | Homo sapiens |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0110280 | autosomal recessive limb-girdle muscular dystrophy type 2F | |
DOID:0110281 | autosomal recessive limb-girdle muscular dystrophy type 2G | |
DOID:0110282 | autosomal recessive limb-girdle muscular dystrophy type 2H | |
DOID:0110283 | autosomal recessive limb-girdle muscular dystrophy type 2J | |
DOID:0110284 | autosomal recessive limb-girdle muscular dystrophy type 2L | |
DOID:0110285 | autosomal recessive limb-girdle muscular dystrophy type 2Q | |
DOID:0110286 | obsolete autosomal recessive limb-girdle muscular dystrophy type 2R | |
DOID:0110287 | autosomal recessive limb-girdle muscular dystrophy type 2S | |
DOID:0110289 | autosomal recessive limb-girdle muscular dystrophy type 2Y | |
DOID:0110292 | autosomal recessive limb-girdle muscular dystrophy type 2O |
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Last updated: August 19, 2024