WFDC13
WAP four-disulfide core domain protein 13
Also known as: C20orf138, dJ601O1.3, WAP13, WFD13_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8IUB5
- Gene
- WFDC13
- Ensembl
- ENSG00000168634
- Chromosome
- 20
- Canonical length
- 93 aa
- Protein class
- Predicted secreted proteins
- Secretome location
- Secreted in male reproductive system
OverviewNCBI Gene
This gene encodes a member of the WAP-type four-disulfide core (WFDC) domain family. The WFDC domain, or WAP signature motif, contains eight cysteines forming four disulfide bonds at the core of the protein, and functions as a protease inhibitor. Most WFDC gene members are localized to chromosome 20q12-q13 in two clusters: centromeric and telomeric. This gene belongs to the telomeric cluster. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
93 residues, UniProt reviewed canonical sequence.
>Q8IUB5|WFDC13
1 MKPVLPLQFL VVFCLALQLV PGSPKQRVLK YILEPPPCIS APENCTHLCT MQEDCEKGFQ
61 CCSSFCGIVC SSETFQKRNR IKHKGSEVIM PANLocalizationUniProt · AlphaFold · HPA
Whether an antibody against WFDC13 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
- 0
- Mean surface accessibility (rSASA)
- 0.53
- Highest tissue expression
- 85 nTPM
Expression across tissuesHPA
Tissue
- epididymis: 85 nTPM
- retina: 2 nTPM
- urinary bladder: 0.3 nTPM
- seminal vesicle: 0.2 nTPM
- cerebral cortex: 0.1 nTPM
- lung: 0.1 nTPM
Single-cell type
- epididymal principal cells: 117 nCPM
- rod photoreceptor cells: 26 nCPM
- oocytes: 4.6 nCPM
- cone photoreceptor cells: 4.1 nCPM
- epididymal basal cells: 2.9 nCPM
- retinal amacrine cells: 2.1 nCPM
Immune cell
- naive CD4 T-cell: 0.6 nTPM
- total PBMC: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
Brain region
- medulla oblongata: 0.7 nTPM
- midbrain: 0.7 nTPM
- spinal cord: 0.4 nTPM
- white matter: 0.4 nTPM
- cerebral cortex: 0.3 nTPM
- hypothalamus: 0.3 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)
- 1.56
- gnomAD pLI
- 0.02
- gnomAD missense Z
- 0.27
- DepMap mean gene effect
- -0.03
- 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
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads WFDC13 as an antibody target. Whether an autoantibody or antibody against WFDC13 could matter depends on whether native WFDC13 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
WFDC13 is annotated as secreted, so native WFDC13 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 WFDC13 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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