GO Term |
---|
GABA-ergic synapse |
basolateral plasma membrane |
lamellipodium |
filopodium |
sarcolemma |
costamere |
cytosol |
dystrophin-associated glycoprotein complex |
dystroglycan complex |
nuclear periphery |
GO Term |
---|
dystroglycan binding |
actin binding |
Position | Description | PubMed ID | GlyTouCan ID | Source |
---|---|---|---|---|
33 |
|
|||
49 |
|
|||
52 |
|
|||
63 | O-linked (GalNAc...) threonine | |||
141 | N-linked (GlcNAc...) asparagine | |||
169 |
|
|||
171 |
|
|||
317 | O-linked (Man6P...) threonine |
|
||
319 | O-linked (Man6P...) threonine |
|
||
343 |
|
Pathway Name | Organism |
---|---|
Defective POMGNT1 causes MDDGA3, MDDGB3 and MDDGC3 | Homo sapiens |
Defective POMT1 causes MDDGA1, MDDGB1 and MDDGC1 | Homo sapiens |
Defective POMT2 causes MDDGA2, MDDGB2 and MDDGC2 | Homo sapiens |
ECM proteoglycans | Homo sapiens |
EGR2 and SOX10-mediated initiation of Schwann cell myelination | Homo sapiens |
Non-integrin membrane-ECM interactions | Homo sapiens |
O-linked glycosylation | Homo sapiens |
Regulation of expression of SLITs and ROBOs | Homo sapiens |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0110459 | dilated cardiomyopathy 1FF | |
DOID:0110460 | dilated cardiomyopathy 2A | |
DOID:0110461 | X-linked dilated cardiomyopathy | |
DOID:0110635 | muscular dystrophy-dystroglycanopathy type B5 | |
DOID:0110892 | inflammatory bowel disease 1 | |
DOID:0111232 | congenital muscular dystrophy-dystroglycanopathy type A9 | |
DOID:0111237 | congenital muscular dystrophy-dystroglycanopathy type A1 | |
DOID:0111338 | isolated elevated serum creatine phosphokinase levels | |
DOID:10223 | dermatomyositis | |
DOID:10283 | prostate cancer |
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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