VWF

Summary

VWF is a gene^[1].

Key Facts

• VWF's instance of is recorded as gene^[2].
• VWF is a type of protein-coding gene^[3].
• VWF's HomoloGene ID is recorded as 466^[4].
• VWF's genomic start is recorded as 6058040^[5].
• VWF's genomic start is recorded as 5948877^[6].
• VWF's genomic end is recorded as 6124770^[7].
• VWF's genomic end is recorded as 6233936^[8].
• VWF's ortholog is recorded as Vwf^[9].
• VWF's ortholog is recorded as Vwf^[10].
• VWF's ortholog is recorded as vwf^[11].
• VWF's encodes is recorded as Von Willebrand factor^[12].
• VWF's found in taxon is recorded as Homo sapiens^[13].
• VWF's chromosome is recorded as human chromosome 12^[14].
• VWF's genetic association is recorded as von willebrand disease type 2B^[15].
• VWF's genetic association is recorded as von Willebrand's disease 1^[16].
• VWF's genetic association is recorded as von Willebrand's disease 2^[17].
• VWF's strand orientation is recorded as reverse strand^[18].
• VWF's exact match is recorded as http://identifiers.org/ncbigene/7450^[19].
• VWF's cytogenetic location is recorded as 12p13.31^[20].
• VWF's expressed in is recorded as urethra^[21].
• VWF's expressed in is recorded as tendon of biceps brachii^[22].
• VWF's expressed in is recorded as apex of heart^[23].
• VWF's expressed in is recorded as right lung^[24].
• VWF's expressed in is recorded as upper lobe of left lung^[25].
• VWF's expressed in is recorded as pericardium^[26].