GO Term |
---|
negative regulation of intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediator |
GO Term |
---|
Golgi apparatus |
plasma membrane |
microvillus |
secretory granule membrane |
cell projection |
extracellular exosome |
basolateral plasma membrane |
apical plasma membrane |
lamellipodium membrane |
cytosol |
GO Term |
---|
transmembrane signaling receptor activity |
cytokine receptor activity |
collagen binding |
hyaluronic acid binding |
Position | Description | PubMed ID | GlyTouCan ID | Source |
---|---|---|---|---|
583 |
|
|||
595 |
|
|
||
597 |
|
|
||
599 | N-linked (GlcNAc...) asparagine | |||
627 |
|
|||
636 | N-linked (GlcNAc...) asparagine | |||
637 |
|
|||
638 |
|
|||
|
Pathway Name | Organism |
---|---|
Cell surface interactions at the vascular wall | Homo sapiens |
Degradation of the extracellular matrix | Homo sapiens |
Hyaluronan uptake and degradation | Homo sapiens |
Integrin cell surface interactions | Homo sapiens |
Interferon gamma signaling | Homo sapiens |
Neutrophil degranulation | Homo sapiens |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0060600 | obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum | |
DOID:0060642 | recessive dystrophic epidermolysis bullosa | |
DOID:0060707 | lymphoproliferative syndrome 1 | |
DOID:0060708 | lymphoproliferative syndrome 2 | |
DOID:0060713 | autosomal recessive congenital ichthyosis 4B | |
DOID:0060843 | hereditary neuropathy with liability to pressure palsies | |
DOID:0060857 | septooptic dysplasia | |
DOID:0060870 | isolated growth hormone deficiency | |
DOID:0060872 | isolated growth hormone deficiency type II | |
DOID:0060873 | isolated growth hormone deficiency type IA |
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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