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Protein-coding gene in the species Homo sapiens
of Differentiation 42b), is a protein that in humans is encoded by the GP1BA gene. Glycoprotein Ib (GP Ib) is a platelet surface membrane glycoprotein
GP1BA
Medical condition
Unusual menstrual periods In regards to mechanism, there are three genes, GP1BA, GP1BB and GP9 that are involved (due to mutations). These mutations do
Bernard–Soulier_syndrome
Protein found in platelets
can be produced in immune thrombocytopenic purpura. Components include GP1BA and GP1BB. It complexes with Glycoprotein IX. Bode AP, Read MS, Reddick
Glycoprotein_Ib
Process of formation of blood clots
platelet to bind to vWF, which is exposed upon damage to vasculature. The vWF A1 domain (yellow) interacts with the extracellular domain of GP1ba (blue).
Coagulation
Mammalian protein involved in blood clotting
platelet to bind to VWF, which is exposed upon damage to vasculature. The VWF A1 domain (yellow) interacts with the extracellular domain of GP1ba (blue).
Von_Willebrand_factor
Protein-coding gene in the species Homo sapiens
receptor is a heterodimer composed of 2 polypeptide chains, an alpha chain (GP1BA; MIM 606672) and a beta chain (GP1BB; MIM 138720), that are linked by disulfide
GP5_(gene)
a vWF-independent manner. It binds specifically to platelet GPIbalpha (GP1BA) to a distinct binding site from that of flavocetin-A. It is isolated from
Mucrocetin
Protein complex found in mammals
neutrophils and deposited on vessel walls. Platelet glycoprotein Ib alpha (GP1BA;GPIbα) is the receptor for S100A8/A9 on platelets. In vitro, platelets adhere
Calprotectin
the GP9 gene. CD42b Platelet glycoprotein Ib alpha chain encoded by the GP1BA gene. CD42c Platelet glycoprotein Ib beta chain encoded by the GP1BB gene
List of human clusters of differentiation
List_of_human_clusters_of_differentiation
Protein-coding gene in the species Homo sapiens
receptor is a heterodimer composed of 2 polypeptide chains, an alpha chain (GP1BA; MIM 606672) and a beta chain (GP1BB; MIM 138720), that are linked by disulfide
Glycoprotein_IX
Protein-coding gene in the species Homo sapiens
dysplasia and atelosteogenesis type I. FLNB has been shown to interact with GP1BA, Filamin-A, FBLIM1, PSEN1, CD29 and PSEN2. Larsen syndrome GRCh38: Ensembl
Filamin-B
Bernard–Soulier syndrome, benign autosomal dominant; 153670; GP1BA Bernard–Soulier syndrome, type A; 231200; GP1BA Bernard–Soulier syndrome, type B; 231200; GP1BB
List_of_OMIM_disorder_codes
P17174 6457 GOT1L1 HGNC:28487; Q8NHS2 6458 GOT2 HGNC:4433; P00505 6459 GP1BA HGNC:4439; P07359 6460 GP1BB HGNC:4440; P13224 6461 GP2 HGNC:4441; P55259
List of human protein-coding genes 3
List_of_human_protein-coding_genes_3
Protein-coding gene in the species Homo sapiens
phosphatase 1, BIS, ATG9A, NOXA, AKT1, BCAR1, BAX, BAD, C-Raf, CDC25B, GP1BA, GP1BB, HMGN1, IL9R, LIMK1, P53, PRKCE PRKCZ, TNFAIP3, TSC2, Tau protein
YWHAZ
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