Gene Gene information from NCBI Gene database.
Entrez ID 340706
Gene name Von Willebrand factor A domain containing 2
Gene symbol VWA2
Synonyms (NCBI Gene)
AMACOCCSP-2CCSP2NET42
Chromosome 10
Chromosome location 10q25.3
Summary This gene encodes a member of the von Willebrand factor A-like domain protein superfamily. The encoded protein is localized to the extracellular matrix and may serve as a structural component in basement membranes or in anchoring structures on scaffolds o
miRNA miRNA information provided by mirtarbase database.
84
miRTarBase ID miRNA Experiments Reference
MIRT709452 hsa-miR-512-5p HITS-CLIP 19536157
MIRT709451 hsa-miR-6769a-3p HITS-CLIP 19536157
MIRT709450 hsa-miR-4690-3p HITS-CLIP 19536157
MIRT709449 hsa-miR-5685 HITS-CLIP 19536157
MIRT709448 hsa-miR-361-3p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
15
GO ID Ontology Definition Evidence Reference
GO:0005509 Function Calcium ion binding IEA
GO:0005515 Function Protein binding IPI 25416956, 32296183
GO:0005576 Component Extracellular region IEA
GO:0005604 Component Basement membrane IBA
GO:0005604 Component Basement membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
618281 24709 ENSG00000165816
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q5GFL6
Protein name von Willebrand factor A domain-containing protein 2 (A domain-containing protein similar to matrilin and collagen) (AMACO) (Colon cancer secreted protein 2) (CCSP-2)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00092 VWA 51 221 von Willebrand factor type A domain Domain
PF00008 EGF 299 329 EGF-like domain Domain
PF00092 VWA 343 512 von Willebrand factor type A domain Domain
PF00092 VWA 531 698 von Willebrand factor type A domain Domain
PF00008 EGF 716 746 EGF-like domain Domain
Tissue specificity TISSUE SPECIFICITY: Expression is generally absent in normal colon and other normal body tissues, but it is induced an average of 78-fold in Stage II, III, and IV colon cancers, as well as in colon adenomas and colon cancer cell lines. {ECO:0000269|PubMed
Sequence
Sequence length 755
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
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Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Vesicoureteral reflux Likely pathogenic rs148731211 RCV000845170
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Cervical cancer Benign rs34806476, rs75028145 RCV005905052
RCV005907318
Clear cell carcinoma of kidney Benign rs34806476, rs62640959 RCV005905053
RCV005913408
Colon adenocarcinoma Benign rs75028145 RCV005907317
Familial cancer of breast Benign rs75028145 RCV005907316
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Alzheimer Disease Associate 33023779
Colorectal Neoplasms Associate 26474385, 33572952
Colorectal Neoplasms Stimulate 30038405