Homo sapiens integrin subunit alpha 2b (ITGA2B), RefSeqGene (LRG_479) - Nucleotide

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[Pedigree Analysis and Molecular Mechanism Study of Hereditary Glanzmann Thrombasthenia Caused by Compound Heterozygous Mutation of the ITGA2B Gene]. [Zhonghua Xue Ye Xue Za Zhi. 2024]
[Pedigree Analysis and Molecular Mechanism Study of Hereditary Glanzmann Thrombasthenia Caused by Compound Heterozygous Mutation of the ITGA2B Gene].
Lu XM, Fu DY, Zhang YF, Zhao LD, Wang L, Yang J, Liu J, Zheng JW, Yang LH, Wang G. Zhonghua Xue Ye Xue Za Zhi. 2024 Apr 14; 45(4):370-377.
Full-length αIIbβ3 cryo-EM structure reveals intact integrin initiate-activation intrinsic architecture. [Structure. 2024]
Full-length αIIbβ3 cryo-EM structure reveals intact integrin initiate-activation intrinsic architecture.
Huo T, Wu H, Moussa Z, Sen M, Dalton V, Wang Z. Structure. 2024 Jul 11; 32(7):899-906.e3. Epub 2024 Apr 4.
Molecular dynamics simulations corroborate recombinant expression studies carried out on three αIIb β-propeller mutations reported in Indian Glanzmann thrombasthenia patients. [J Cell Biochem. 2023]
Molecular dynamics simulations corroborate recombinant expression studies carried out on three αIIb β-propeller mutations reported in Indian Glanzmann thrombasthenia patients.
Chandrasekaran FP, Vishal A, Arora U, Kumar S U, George C PD, Nelson EJR. J Cell Biochem. 2023 Jul; 124(7):989-1001. Epub 2023 May 21.

RefSeq alternative splicing
See 5 reference mRNA sequence splice variants for the ITGA2B gene.

Protein
Protein sequence from Nucleotide coding region
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Nucleotide