Gene Gene information from NCBI Gene database.
Entrez ID 79805
Gene name Vasohibin 2
Gene symbol VASH2
Synonyms (NCBI Gene)
-
Chromosome 1
Chromosome location 1q32.3
miRNA miRNA information provided by mirtarbase database.
68
miRTarBase ID miRNA Experiments Reference
MIRT024439 hsa-miR-215-5p Microarray 19074876
MIRT026913 hsa-miR-192-5p Microarray 19074876
MIRT031071 hsa-miR-21-5p Microarray 19253296
MIRT031071 hsa-miR-21-5p Microarray 19342589
MIRT646158 hsa-miR-6734-3p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
31
GO ID Ontology Definition Evidence Reference
GO:0000768 Process Syncytium formation by plasma membrane fusion IEA
GO:0001938 Process Positive regulation of endothelial cell proliferation IDA 19204325
GO:0003779 Function Actin binding IDA 29146869
GO:0003779 Function Actin binding IEA
GO:0004180 Function Carboxypeptidase activity IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
610471 25723 ENSG00000143494
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q86V25
Protein name Tubulinyl-Tyr carboxypeptidase 2 (EC 3.4.17.17) (Vasohibin-2) (Vasohibin-like protein)
Protein function Tyrosine carboxypeptidase that removes the C-terminal tyrosine residue of alpha-tubulin, thereby regulating microtubule dynamics and function (PubMed:29146869). Critical for spindle function and accurate chromosome segregation during mitosis sin
PDB 6J4O , 6J4P , 6J4Q , 6J4S , 6J4V , 6QBY , 7ZCW
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14822 Vasohibin 47 291 Vasohibin Domain
Sequence
Sequence length 355
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
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
CARCINOMA, BASAL CELL CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
TYPE 2 DIABETES MELLITUS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
UTERINE CERVIX CARCINOMA IN SITU 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
ANOPHTHALMIA AND PULMONARY HYPOPLASIA Syndromic microphthalmia BEFREE 31074083
★☆☆☆☆
Found in Text Mining only
Aortic Aneurysm Abdominal Aortic aneurysm Pubtator 35922907 Associate
★☆☆☆☆
Found in Text Mining only
Atherosclerosis Atherosclerosis Pubtator 35922907 Associate
★☆☆☆☆
Found in Text Mining only
Breast Carcinoma Breast Carcinoma BEFREE 24920244, 27702660, 27867016, 29039601
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Hepatocellular carcinoma Pubtator 37430466 Associate
★☆☆☆☆
Found in Text Mining only
Carcinoma, Ovarian Epithelial Ovarian Epithelial carcinoma BEFREE 24118388
★☆☆☆☆
Found in Text Mining only
Color Vision Defects Color vision deficiency Pubtator 23548203 Associate
★☆☆☆☆
Found in Text Mining only
Diabetes Diabetes BEFREE 29641565
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus Diabetes Mellitus BEFREE 29641565
★☆☆☆☆
Found in Text Mining only
Diabetic Nephropathy Diabetic Nephropathy BEFREE 29641565
★☆☆☆☆
Found in Text Mining only