ST6GALNAC2
Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2
Also known as: SIA7B_HUMAN, SIAT7, SIAT7B, SIATL1, ST6GalNAII, STHM
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9UJ37
- Gene
- ST6GALNAC2
- Ensembl
- ENSG00000070731
- Chromosome
- 17
- Canonical length
- 374 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
OverviewNCBI Gene
ST6GALNAC2 belongs to a family of sialyltransferases that add sialic acids to the nonreducing ends of glycoconjugates. At the cell surface, these modifications have roles in cell-cell and cell-substrate interactions, bacterial adhesion, and protein targeting (Samyn-Petit et al., 2000 [PubMed 10742600]).[supplied by OMIM, Mar 2008]
Canonical amino-acid sequenceUniProt
374 residues, UniProt reviewed canonical sequence.
>Q9UJ37|ST6GALNAC2
1 MGLPRGSFFW LLLLLTAACS GLLFALYFSA VQRYPGPAAG ARDTTSFEAF FQSKASNSWT
61 GKGQACRHLL HLAIQRHPHF RGLFNLSIPV LLWGDLFTPA LWDRLSQHKA PYGWRGLSHQ
121 VIASTLSLLN GSESAKLFAP PRDTPPKCIR CAVVGNGGIL NGSRQGPNID AHDYVFRLNG
181 AVIKGFERDV GTKTSFYGFT VNTMKNSLVS YWNLGFTSVP QGQDLQYIFI PSDIRDYVML
241 RSAILGVPVP EGLDKGDRPH AYFGPEASAS KFKLLHPDFI SYLTERFLKS KLINTHFGDL
301 YMPSTGALML LTALHTCDQV SAYGFITSNY WKFSDHYFER KMKPLIFYAN HDLSLEAALW
361 RDLHKAGILQ LYQRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ST6GALNAC2 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)
- 0.31
- Highest tissue expression
- 123 nTPM
Expression across tissuesHPA
Tissue
- choroid plexus: 123 nTPM
- retina: 49 nTPM
- skin: 49 nTPM
- fallopian tube: 48 nTPM
- testis: 41 nTPM
- thyroid gland: 24 nTPM
Single-cell type
- rod photoreceptor cells: 207 nCPM
- neutrophils: 115 nCPM
- schwann cells: 101 nCPM
- retinal pigment epithelial cells: 90 nCPM
- respiratory ciliated cells: 85 nCPM
- müller glia: 76 nCPM
Immune cell
- neutrophil: 47 nTPM
- eosinophil: 5.2 nTPM
- classical monocyte: 3 nTPM
- intermediate monocyte: 1.8 nTPM
- myeloid DC: 0.4 nTPM
- non-classical monocyte: 0.4 nTPM
Brain region
- choroid plexus: 70 nTPM
- midbrain: 13 nTPM
- medulla oblongata: 11 nTPM
- spinal cord: 7.7 nTPM
- white matter: 4.7 nTPM
- thalamus: 4.6 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)
- 1.68
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.24
- DepMap mean gene effect
- 0.02
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- glycoprotein biosynthetic process
- protein O-linked glycosylation
- protein O-linked glycosylation via N-acetyl-galactosamine
- protein sialylation
- viral protein processing
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ST6GALNAC2 as an antibody target. Whether an autoantibody or antibody against ST6GALNAC2 could matter depends on whether native ST6GALNAC2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ST6GALNAC2 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 ST6GALNAC2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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