Gene Gene information from NCBI Gene database.
Entrez ID 5212
Gene name Vitrin
Gene symbol VIT
Synonyms (NCBI Gene)
VIT1
Chromosome 2
Chromosome location 2p22.2
Summary This gene encodes an extracellular matrix (ECM) protein. The protein may be associated with cell adhesion and migration. High levels of expression of the protein in specific parts of the brain suggest its likely role in neural development. [provided by Re
miRNA miRNA information provided by mirtarbase database.
27
miRTarBase ID miRNA Experiments Reference
MIRT022689 hsa-miR-124-3p Microarray 18668037
MIRT1485080 hsa-miR-4663 CLIP-seq
MIRT1485081 hsa-miR-4738-3p CLIP-seq
MIRT1485082 hsa-miR-4797-5p CLIP-seq
MIRT1485083 hsa-miR-628-5p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
12
GO ID Ontology Definition Evidence Reference
GO:0005539 Function Glycosaminoglycan binding IEA
GO:0005576 Component Extracellular region IEA
GO:0005614 Component Interstitial matrix IBA
GO:0005614 Component Interstitial matrix IEA
GO:0007399 Process Nervous system development IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
617693 12697 ENSG00000205221
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6UXI7
Protein name Vitrin
Protein function Promotes matrix assembly and cell adhesiveness. Plays a role in spinal cord formation by regulating the proliferation and differentiation of neural stem cells.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03815 LCCL 38 133 LCCL domain Domain
PF00092 VWA 293 472 von Willebrand factor type A domain Domain
PF00092 VWA 495 663 von Willebrand factor type A domain Domain
Sequence
Sequence length 678
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Sarcoma Likely benign rs141908607 RCV005902708
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Alveolar capillary dysplasia Associate 38029923
Osteoarthritis Associate 25575966