GALNT1
Polypeptide N-acetylgalactosaminyltransferase 1
Also known as: GalNAc-T1, GALT1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q10472
- Gene
- GALNT1
- Ensembl
- ENSG00000141429
- Chromosome
- 18
- Canonical length
- 559 aa
- Protein class
- Enzymes, Metabolic proteins, Plasma proteins, Predicted intracellular proteins, Predicted membrane proteins
- Secretome location
- Intracellular and membrane
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. Transcript variants derived from this gene that utilize alternative polyA signals have been described in the literature. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
559 residues, UniProt reviewed canonical sequence.
>Q10472|GALNT1
1 MRKFAYCKVV LATSLIWVLL DMFLLLYFSE CNKCDEKKER GLPAGDVLEP VQKPHEGPGE
61 MGKPVVIPKE DQEKMKEMFK INQFNLMASE MIALNRSLPD VRLEGCKTKV YPDNLPTTSV
121 VIVFHNEAWS TLLRTVHSVI NRSPRHMIEE IVLVDDASER DFLKRPLESY VKKLKVPVHV
181 IRMEQRSGLI RARLKGAAVS KGQVITFLDA HCECTVGWLE PLLARIKHDR RTVVCPIIDV
241 ISDDTFEYMA GSDMTYGGFN WKLNFRWYPV PQREMDRRKG DRTLPVRTPT MAGGLFSIDR
301 DYFQEIGTYD AGMDIWGGEN LEISFRIWQC GGTLEIVTCS HVGHVFRKAT PYTFPGGTGQ
361 IINKNNRRLA EVWMDEFKNF FYIISPGVTK VDYGDISSRV GLRHKLQCKP FSWYLENIYP
421 DSQIPRHYFS LGEIRNVETN QCLDNMARKE NEKVGIFNCH GMGGNQVFSY TANKEIRTDD
481 LCLDVSKLNG PVTMLKCHHL KGNQLWEYDP VKLTLQHVNS NQCLDKATEE DSQVPSIRDC
541 NGSRSQQWLL RNVTLPEIFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against GALNT1 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
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.25
- Highest tissue expression
- 57 nTPM
Expression across tissuesHPA
Tissue
- urinary bladder: 57 nTPM
- esophagus: 47 nTPM
- skin: 46 nTPM
- placenta: 44 nTPM
- small intestine: 41 nTPM
- liver: 40 nTPM
Single-cell type
- esophageal apical cells: 646 nCPM
- retinal pigment epithelial cells: 431 nCPM
- urothelial cells: 363 nCPM
- lacrimal acinar cells: 334 nCPM
- neutrophil progenitors: 324 nCPM
- salivary acinar cells: 295 nCPM
Immune cell
- basophil: 6.5 nTPM
- non-classical monocyte: 6.1 nTPM
- eosinophil: 6 nTPM
- plasmacytoid DC: 4.1 nTPM
- intermediate monocyte: 3.9 nTPM
- NK-cell: 3.9 nTPM
Brain region
- choroid plexus: 18 nTPM
- hypothalamus: 17 nTPM
- medulla oblongata: 15 nTPM
- midbrain: 15 nTPM
- white matter: 15 nTPM
- thalamus: 15 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)
- 0.59
- gnomAD pLI
- 0
- gnomAD missense Z
- 2.52
- DepMap mean gene effect
- 0.1
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- protein O-linked glycosylation
- protein O-linked glycosylation via N-acetyl-galactosamine
- viral protein processing
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads GALNT1 as an antibody target. Whether an autoantibody or antibody against GALNT1 could matter depends on whether native GALNT1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
GALNT1 is annotated as secreted, so native GALNT1 circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label GALNT1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...