| GENE NAME | IGF1 |
| CHROMOSOME | 12 |
| ENSEMBL ID | ENSG00000017427 |
| ENTREZ ID | 3479 |
| UNIPROT ACCESSION NUMBER | P05019 |
| GO MOLECULAR FUNCTION | insulin-like growth factor receptor binding; integrin binding |
| ESSENTIAL IN MOUSE | Essential |
| PATHWAYS | hsa04935; R-HSA-2428924; hsa04151; R-HSA-381426; R-HSA-2428933; hsa05410; R-HSA-9006934; R-HSA-76002; hsa04150; R-HSA-109582; hsa04015; hsa04114; hsa04914; R-HSA-114608; hsa04730; hsa05224; hsa05200; hsa04152; hsa04750; hsa05414; hsa04010; R-HSA-162582; hsa05214; R-HSA-76005; hsa04550; hsa05215; hsa01522; hsa05205; R-HSA-422085; hsa04014; hsa04115; hsa04960; hsa04066; R-HSA-2428928; hsa05202; R-HSA-2980736; R-HSA-392499; hsa04211; hsa04913; hsa04068; hsa01521; R-HSA-2404192; hsa04510; hsa04213; hsa05218 |
| 3 combinations linked to IGF1 | OLI879; OLI871; OLI880 |
| 1 variant linked to IGF1 | IGF1:c.476G>A, p.Gly159Glu |
| 1 disease linked to IGF1 | Kallmann syndrome |