Gene Gene information from NCBI Gene database.
Entrez ID 149708
Gene name WAP four-disulfide core domain 5
Gene symbol WFDC5
Synonyms (NCBI Gene)
PRG5WAP1dJ211D12.5
Chromosome 20
Chromosome location 20q13.12
Summary This gene encodes a member of the WAP-type four-disulfide core (WFDC) domain family. Most WFDC proteins contain only one WFDC domain, and this encoded protein contains two WFDC domains. The WFDC domain, or WAP signature motif, contains eight cysteines for
miRNA miRNA information provided by mirtarbase database.
9
miRTarBase ID miRNA Experiments Reference
MIRT2148428 hsa-miR-1587 CLIP-seq
MIRT2148429 hsa-miR-3147 CLIP-seq
MIRT2148430 hsa-miR-4492 CLIP-seq
MIRT2148431 hsa-miR-4498 CLIP-seq
MIRT2148432 hsa-miR-4656 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
8
GO ID Ontology Definition Evidence Reference
GO:0004867 Function Serine-type endopeptidase inhibitor activity IBA
GO:0004867 Function Serine-type endopeptidase inhibitor activity IEA
GO:0005515 Function Protein binding IPI 32296183, 32814053
GO:0005576 Component Extracellular region IEA
GO:0005615 Component Extracellular space IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
605161 20477 ENSG00000175121
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8TCV5
Protein name WAP four-disulfide core domain protein 5 (Putative protease inhibitor WAP1) (p53-responsive gene 5 protein)
Protein function Putative acid-stable proteinase inhibitor.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00095 WAP 30 73 Domain
PF00095 WAP 77 120 Domain
Sequence
MRTQSLLLLGALLAVGSQLPAVFGRKKGEKSGGCPPDDGPCLLSVPDQCVEDSQCPLTRK
CCYRACFRQCVPR
VSVKLGSCPEDQLRCLSPMNHLCHKDSDCSGKKRCCHSACGRDCRDP
ARGTAPGCPGQANSDLGSVALHLSWGPTERVHDGRPGALPAGQHYLYQRWFQPSDNHWPA
DTSLQPIHPWFLLLGVKVHSLSSEEGLCITPVLCTTAIRASHPS
Sequence length 224
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
BIPOLAR DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Melanoma Melanoma Pubtator 36553569 Associate
★☆☆☆☆
Found in Text Mining only
Neoplasms Neoplasms BEFREE 10656678
★☆☆☆☆
Found in Text Mining only