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Glycan Structure Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
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Repository for lectin-assisted multimodality data
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MIRAGE
Kit ligand
Summary
- UniProt ID
- P21583
- Gene Symbol
-
- KITLG
- MGF
- SCF
- Gene ID
- 4254
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- P21583
- PubChem
- P21583
- The Human Metabolome Database
- HMDBP12111
- RaftProt
- P21583
- Re-Glyco
- P21583
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Cell adhesion
- Cell membrane
- Cell projection
- Cytoskeleton
- Direct protein sequencing
- Disease variant
- Disulfide bond
- Glycoprotein
- Growth factor
- Non-syndromic deafness
- Reference proteome
- Secreted
- Signal
- Transmembrane helix
- Waardenburg syndrome
- Gene Ontology (GO)
| GO Term |
|---|
| extracellular region |
| extracellular space |
| cytoplasm |
| cytoskeleton |
| plasma membrane |
| lamellipodium |
| filopodium |
| GO Term |
|---|
| stem cell factor receptor binding |
| cytokine activity |
| growth factor activity |
- Site Annotations
| Position | Description |
|---|---|
| 97 | Not glycosylated |
Sequence
MKKTQTWILTCIYLQLLLFNPLVKTEGICRNRVTNNVKDVTKLVANLPKDYMITLKYVPGMDVLPSHCWISEMVVQLSDSLTDLLDKFSNISEGLSNYSIIDKLVNIVDDLVECVKENSSKDLKKSFKSPEPRLFTPEEFFRIFNRSIDAFKDFVVASETSDCVVSSTLSPEKDSRVSVTKPFMLPPVAASSLRNDSSSSNRKAKNPPGDSSLHWAAMALPALFSLIIGFAFGALYWKKRQPSLTRAVENIQINEEDNEISMLQEKEREFQEV
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 90 | N-linked (GlcNAc...) asparagine; partial | |||
| 118 | N-linked (GlcNAc...) asparagine; partial |
|
||
| 145 | N-linked (GlcNAc...) asparagine |
|
||
| 147 |
|
|||
| 167 | O-linked (GalNAc...) serine | |||
| 168 | O-linked (GalNAc...) threonine |
|
||
| 170 |
|
|||
| 178 |
|
|||
| 180 | O-linked (GalNAc...) threonine | |||
| 195 | N-linked (GlcNAc...) asparagine |
|
G45395BF
G23719VF
G57321FI
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110590 | autosomal dominant nonsyndromic deafness 69 | |
| DOID:0111373 | familial progressive hyperpigmentation with or without hypopigmentation | |
| DOID:10123 | pigmentation disease | |
| DOID:9258 | Waardenburg syndrome |
