| GENE NAME | VCL |
| CHROMOSOME | 10 |
| ENSEMBL ID | ENSG00000035403 |
| ENTREZ ID | 7414 |
| UNIPROT ACCESSION NUMBER | P18206 |
| GO MOLECULAR FUNCTION | protein binding; structural molecule activity |
| ESSENTIAL IN MOUSE | Essential |
| PATHWAYS | R-HSA-6802948; R-HSA-76005; R-HSA-5683057; R-HSA-6798695; R-HSA-9656223; hsa05131; hsa04670; R-HSA-5663202; R-HSA-5673001; R-HSA-6802955; R-HSA-162582; R-HSA-9649948; R-HSA-5684996; R-HSA-6802952; R-HSA-168256; R-HSA-6802946; R-HSA-76002; hsa05100; R-HSA-114608; hsa04520; hsa05146; R-HSA-5674135; R-HSA-6802957; R-HSA-109582; R-HSA-397014; R-HSA-1643685; R-HSA-445355; hsa04810; R-HSA-168249; R-HSA-6802949; hsa04510 |
| 1 combination linked to VCL | OLI647 |
| 1 variant linked to VCL | VCL:c.2046A>T, p.Leu682Phe |
| 1 disease linked to VCL | Sudden infant death syndrome |