GALNT6
Polypeptide N-acetylgalactosaminyltransferase 6
Also known as: GalNAc-T6, GALT6_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8NCL4
- Gene
- GALNT6
- Ensembl
- ENSG00000139629
- Chromosome
- 12
- Canonical length
- 622 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Golgi apparatus
OverviewNCBI Gene
This gene encodes a member of the UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase (GalNAc-T) family of enzymes. GalNAc-Ts initiate mucin-type O-linked glycosylation in the Golgi apparatus by catalyzing the transfer of GalNAc to serine and threonine residues on target proteins. They are characterized by an N-terminal transmembrane domain, a stem region, a lumenal catalytic domain containing a GT1 motif and Gal/GalNAc transferase motif, and a C-terminal ricin/lectin-like domain. GalNAc-Ts have different, but overlapping, substrate specificities and patterns of expression. The encoded protein is capable of glycosylating fibronectin peptide in vitro and is expressed in a fibroblast cell line, indicating that it may be involved in the synthesis of oncofetal fibronectin. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
622 residues, UniProt reviewed canonical sequence.
>Q8NCL4|GALNT6
1 MRLLRRRHMP LRLAMVGCAF VLFLFLLHRD VSSREEATEK PWLKSLVSRK DHVLDLMLEA
61 MNNLRDSMPK LQIRAPEAQQ TLFSINQSCL PGFYTPAELK PFWERPPQDP NAPGADGKAF
121 QKSKWTPLET QEKEEGYKKH CFNAFASDRI SLQRSLGPDT RPPECVDQKF RRCPPLATTS
181 VIIVFHNEAW STLLRTVYSV LHTTPAILLK EIILVDDAST EEHLKEKLEQ YVKQLQVVRV
241 VRQEERKGLI TARLLGASVA QAEVLTFLDA HCECFHGWLE PLLARIAEDK TVVVSPDIVT
301 IDLNTFEFAK PVQRGRVHSR GNFDWSLTFG WETLPPHEKQ RRKDETYPIK SPTFAGGLFS
361 ISKSYFEHIG TYDNQMEIWG GENVEMSFRV WQCGGQLEII PCSVVGHVFR TKSPHTFPKG
421 TSVIARNQVR LAEVWMDSYK KIFYRRNLQA AKMAQEKSFG DISERLQLRE QLHCHNFSWY
481 LHNVYPEMFV PDLTPTFYGA IKNLGTNQCL DVGENNRGGK PLIMYSCHGL GGNQYFEYTT
541 QRDLRHNIAK QLCLHVSKGA LGLGSCHFTG KNSQVPKDEE WELAQDQLIR NSGSGTCLTS
601 QDKKPAMAPC NPSDPHQLWL FVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against GALNT6 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Other membrane
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.28
- Highest tissue expression
- 59 nTPM
Expression across tissuesHPA
Tissue
- stomach: 59 nTPM
- cervix: 30 nTPM
- salivary gland: 29 nTPM
- epididymis: 23 nTPM
- small intestine: 20 nTPM
- duodenum: 20 nTPM
Single-cell type
- foveolar cells: 328 nCPM
- mast cells: 178 nCPM
- lacrimal acinar cells: 113 nCPM
- respiratory secretory cells: 107 nCPM
- respiratory deuterosomal cells: 104 nCPM
- salivary acinar cells: 95 nCPM
Immune cell
- eosinophil: 29 nTPM
- NK-cell: 16 nTPM
- non-classical monocyte: 9.8 nTPM
- basophil: 7.2 nTPM
- classical monocyte: 5.8 nTPM
- intermediate monocyte: 5.2 nTPM
Brain region
- white matter: 42 nTPM
- basal ganglia: 29 nTPM
- midbrain: 28 nTPM
- pons: 28 nTPM
- thalamus: 25 nTPM
- cerebral cortex: 25 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.9
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.35
- DepMap mean gene effect
- -0.02
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads GALNT6 as an antibody target. Whether an autoantibody or antibody against GALNT6 could matter depends on whether native GALNT6 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
GALNT6 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label GALNT6 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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