Details for Gene TNXB

GENE NAME TNXB
CHROMOSOME 6
ENSEMBL ID None
ENTREZ ID ENSG00000168477
UNIPROT ACCESSION NUMBER A0A140T8Z8
GO MOLECULAR FUNCTION ['integrin binding', 'heparin binding', 'collagen fibril binding', 'protein binding', 'collagen binding', 'extracellular matrix structural constituent']
ESSENTIAL IN MOUSE Non-essential
PATHWAYS hsa04151; hsa04510; hsa04512; hsa05165; hsa05206; R-HSA-1474244; R-HSA-3000178; hsa04151; hsa04510; hsa04512; hsa05165; hsa05206; R-HSA-1474244; R-HSA-3000178; hsa04151; hsa04510; hsa04512; hsa05165; hsa05206; R-HSA-1474244; R-HSA-3000178; hsa04151; hsa04510; hsa04512; hsa05165; hsa05206; R-HSA-1474244; R-HSA-3000178; hsa04151; hsa04510; hsa04512; hsa05165; hsa05206; R-HSA-1474244; R-HSA-3000178; hsa04151; hsa04510; hsa04512; hsa05165; hsa05206; R-HSA-1474244; R-HSA-3000178; hsa04151; hsa04510; hsa04512; hsa05165; hsa05206; R-HSA-1474244; R-HSA-3000178; hsa04151; hsa04510; hsa04512; hsa05165; hsa05206; R-HSA-1474244; R-HSA-3000178
1 combination linked to TNXB OLI1676
1 variant linked to TNXB TNXB:c.4010G>A, p.Arg1337His
1 disease linked to TNXB Syndromic genetic keratoconus
Found any issues with the data on this page? Report this entry.