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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Polypeptide N-acetylgalactosaminyltransferase 14
Summary
- UniProt ID
- Q96FL9
- Gene Symbol
-
- GALNT14
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- Q96FL9
- PubChem
- Q96FL9
- The Human Metabolome Database
- HMDBP01005
- The O-GlcNAc Database
- Q96FL9
- O-GlcNAcAtlas
- Q96FL9
Annotation
- Keyword
-
- Alternative splicing
- Disulfide bond
- Glycosyltransferase
- Golgi apparatus
- Lectin
- Manganese
- Metal-binding
- Reference proteome
- Signal-anchor
- Transmembrane helix
- Gene Ontology (GO)
| GO Term |
|---|
| O-glycan processing |
| protein O-linked glycosylation |
| GO Term |
|---|
| Golgi membrane |
| Golgi apparatus |
| GO Term |
|---|
| metal ion binding |
| carbohydrate binding |
| polypeptide N-acetylgalactosaminyltransferase activity |
Sequence
MRRLTRRLVLPVFGVLWITVLLFFWVTKRKLEVPTGPEVQTPKPSDADWDDLWDQFDERRYLNAKKWRVGDDPYKLYAFNQRESERISSNRAIPDTRHLRCTLLVYCTDLPPTSIIITFHNEARSTLLRTIRSVLNRTPTHLIREIILVDDFSNDPDDCKQLIKLPKVKCLRNNERQGLVRSRIRGADIAQGTTLTFLDSHCEVNRDWLQPLLHRVKEDYTRVVCPVIDIINLDTFTYIESASELRGGFDWSLHFQWEQLSPEQKARRLDPTEPIRTPIIAGGLFVIDKAWFDYLGKYDMDMDIWGGENFEISFRVWMCGGSLEIVPCSRVGHVFRKKHPYVFPDGNANTYIKNTKRTAEVWMDEYKQYYYAARPFALERPFGNVESRLDLRKNLRCQSFKWYLENIYPELSIPKESSIQKGNIRQRQKCLESQRQNNQETPNLKLSPCAKVKGEDAKSQVWAFTYTQQILQEELCLSVITLFPGAPVVLVLCKNGDDRQQWTKTGSHIEHIASHLCLDTDMFGDGTENGKEIVVNPCESSLMSQHWDMVSS
Glycosylation Sites
G49108TO
G53434XO
G43417UB
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| O-linked glycosylation of mucins | Homo sapiens |
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050569 | Seckel syndrome | |
| DOID:0060215 | Balo concentric sclerosis | |
| DOID:0060254 | Robinow syndrome | |
| DOID:0060578 | Noonan syndrome 1 | |
| DOID:0060580 | Noonan syndrome 2 | |
| DOID:0060581 | Noonan syndrome 3 | |
| DOID:0060582 | Noonan syndrome 4 | |
| DOID:0060583 | Noonan syndrome 5 | |
| DOID:0060584 | Noonan syndrome 6 | |
| DOID:0060585 | Noonan syndrome 7 |
