Seroatlas · Human Serome Atlas

SPRR1B

Cornifin-B

Also known as: GADD33, SPR1B_HUMAN, SPRR1

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
P22528
Gene
SPRR1B
Ensembl
ENSG00000169469
Chromosome
1
Canonical length
89 aa
Protein class
Cancer-related genes, Predicted intracellular proteins

OverviewNCBI Gene

The protein encoded by this gene is an envelope protein of keratinocytes. The encoded protein is crosslinked to membrane proteins by transglutaminase, forming an insoluble layer under the plasma membrane. This protein is proline-rich and contains several tandem amino acid repeats. [provided by RefSeq, Nov 2015]

Canonical amino-acid sequenceUniProt

89 residues, UniProt reviewed canonical sequence.

>P22528|SPRR1B
     1  MSSQQQKQPC TPPPQLQQQQ VKQPCQPPPQ EPCIPKTKEP CHPKVPEPCH PKVPEPCQPK
    61  VPEPCHPKVP EPCPSIVTPA PAQQKTKQK

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against SPRR1B 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
Intracellular
Secreted
No
Transmembrane segments
0
Mean surface accessibility (rSASA)
0.73
Highest tissue expression
2,177 nTPM

Expression across tissuesHPA

Tissue

  • esophagus: 2,177 nTPM
  • vagina: 1,767 nTPM
  • cervix: 1,541 nTPM
  • salivary gland: 664 nTPM
  • skin: 517 nTPM
  • tonsil: 374 nTPM

Single-cell type

  • esophageal apical cells: 37,247 nCPM
  • esophageal suprabasal cells: 8,162 nCPM
  • suprabasal keratinocytes: 1,839 nCPM
  • esophageal basal cells: 769 nCPM
  • ocular epithelial cells: 216 nCPM
  • basal keratinocytes: 88 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

  • amygdala: 0 nTPM
  • basal ganglia: 0 nTPM
  • cerebellum: 0 nTPM
  • cerebral cortex: 0 nTPM
  • choroid plexus: 0 nTPM
  • hippocampal formation: 0 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)
1.93
gnomAD pLI
0
gnomAD missense Z
-0.64
DepMap mean gene effect
-0.58
DepMap dependency class
common

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

Biological processes

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads SPRR1B as an antibody target. Whether an autoantibody or antibody against SPRR1B could matter depends on whether native SPRR1B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

SPRR1B 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 SPRR1B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/SPRR1B. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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