Position | Description |
---|---|
523 | Not glycosylated |
1225 | Not glycosylated |
Position | Description | PubMed ID | GlyTouCan ID | Source |
---|---|---|---|---|
38 | N-linked (GlcNAc...) asparagine |
|
||
54 | N-linked (GlcNAc...) asparagine |
|
||
74 | N-linked (GlcNAc...) asparagine |
|
||
103 | N-linked (GlcNAc...) asparagine |
|
||
111 | N-linked (GlcNAc...) asparagine |
|
||
121 | N-linked (GlcNAc...) asparagine |
|
||
140 | N-linked (GlcNAc...) asparagine |
|
||
146 | N-linked (GlcNAc...) asparagine | |||
160 | N-linked (GlcNAc...) asparagine |
|
||
318 | N-linked (GlcNAc...) asparagine |
|
Pathway Name | Organism |
---|---|
Metabolism of Angiotensinogen to Angiotensins | Homo sapiens |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
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 | |
DOID:0110293 | autosomal recessive limb-girdle muscular dystrophy type 2P | |
DOID:0110294 | autosomal recessive limb-girdle muscular dystrophy type 2T | |
DOID:0110295 | autosomal recessive limb-girdle muscular dystrophy type 2U | |
DOID:0110296 | autosomal recessive limb-girdle muscular dystrophy type 2M | |
DOID:0110297 | autosomal recessive limb-girdle muscular dystrophy type 2K | |
DOID:0110298 | autosomal recessive limb-girdle muscular dystrophy type 2N |
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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