WSCD1
Sialate:O-sulfotransferase 1
Also known as: KIAA0523, WSCD1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q658N2
- Gene
- WSCD1
- Ensembl
- ENSG00000179314
- Chromosome
- 17
- Canonical length
- 575 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Golgi apparatus
OverviewNCBI Gene
Predicted to enable sulfotransferase activity. Predicted to be located in Golgi membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
575 residues, UniProt reviewed canonical sequence.
>Q658N2|WSCD1
1 MAKPFFRLQK FLRRTQFLLF FLTAAYLMTG SLLLLQRVRV ALPQGPRAPG PLQTLPVAAV
61 ALGVGLLDSR ALHDPRVSPE LLLGVDMLQS PLTRPRPGPR WLRSRNSELR QLRRRWFHHF
121 MSDSQGPPAL GPEAARPAIH SRGTYIGCFS DDGHERTLKG AVFYDLRKMT VSHCQDACAE
181 RSYVYAGLEA GAECYCGNRL PAVSVGLEEC NHECKGEKGS VCGAVDRLSV YRVDELQPGS
241 RKRRTATYRG CFRLPENITH AFPSSLIQAN VTVGTCSGFC SQKEFPLAIL RGWECYCAYP
301 TPRFNLRDAM DSSVCGQDPE AQRLAEYCEV YQTPVQDTRC TDRRFLPNKS KVFVALSSFP
361 GAGNTWARHL IEHATGFYTG SYYFDGTLYN KGFKGEKDHW RSRRTICVKT HESGRREIEM
421 FDSAILLIRN PYRSLVAEFN RKCAGHLGYA ADRNWKSKEW PDFVNSYASW WSSHVLDWLK
481 YGKRLLVVHY EELRRSLVPT LREMVAFLNV SVSEERLLCV ENNKEGSFRR RGRRSHDPEP
541 FTPEMKDLIN GYIRTVDQAL RDHNWTGLPR EYVPRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against WSCD1 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)
- 0.35
- Highest tissue expression
- 19 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 19 nTPM
- cerebral cortex: 16 nTPM
- spinal cord: 15 nTPM
- midbrain: 14 nTPM
- amygdala: 13 nTPM
- hippocampal formation: 13 nTPM
Single-cell type
- late spermatids: 172 nCPM
- oligodendrocyte progenitor cells: 168 nCPM
- early spermatids: 162 nCPM
- bergmann glia: 62 nCPM
- lactotrophs: 52 nCPM
- retinal bipolar cells: 50 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- cerebellum: 51 nTPM
- medulla oblongata: 50 nTPM
- white matter: 44 nTPM
- pons: 42 nTPM
- midbrain: 39 nTPM
- thalamus: 37 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)
- 0.68
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.54
- DepMap mean gene effect
- 0.11
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads WSCD1 as an antibody target. Whether an autoantibody or antibody against WSCD1 could matter depends on whether native WSCD1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
WSCD1 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 WSCD1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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