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)
Sequence
MRRLTRRLVLPVFGVLWITVLLFFWVTKRKLEVPTGPEVQTPKPSDADWDDLWDQFDERRYLNAKKWRVGDDPYKLYAFNQRESERISSNRAIPDTRHLRCTLLVYCTDLPPTSIIITFHNEARSTLLRTIRSVLNRTPTHLIREIILVDDFSNDPDDCKQLIKLPKVKCLRNNERQGLVRSRIRGADIAQGTTLTFLDSHCEVNRDWLQPLLHRVKEDYTRVVCPVIDIINLDTFTYIESASELRGGFDWSLHFQWEQLSPEQKARRLDPTEPIRTPIIAGGLFVIDKAWFDYLGKYDMDMDIWGGENFEISFRVWMCGGSLEIVPCSRVGHVFRKKHPYVFPDGNANTYIKNTKRTAEVWMDEYKQYYYAARPFALERPFGNVESRLDLRKNLRCQSFKWYLENIYPELSIPKESSIQKGNIRQRQKCLESQRQNNQETPNLKLSPCAKVKGEDAKSQVWAFTYTQQILQEELCLSVITLFPGAPVVLVLCKNGDDRQQWTKTGSHIEHIASHLCLDTDMFGDGTENGKEIVVNPCESSLMSQHWDMVSS
Glycosylation Sites
Displaying all 3 entries
Position Description PubMed ID GlyTouCan ID Source
19
41
45
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Pathway
Displaying 1 entry
Pathway Name Organism
O-linked glycosylation of mucins Homo sapiens
Disease
Displaying entries 1 - 10 of 62 in total
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

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024