tubulin, beta 2C, isoform CRA_b [Homo sapiens]

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TUBB4B gene mutation in Leber phenotype of congenital amaurosis syndrome associated with early-onset deafness. [Eur J Med Genet. 2022]
TUBB4B gene mutation in Leber phenotype of congenital amaurosis syndrome associated with early-onset deafness.
Maasz A, Hadzsiev K, Ripszam R, Zsigmond A, Maka E, Knezy K, Lesch B, Nemeth A, Bene J, Galik B, et al. Eur J Med Genet. 2022 Apr; 65(4):104471. Epub 2022 Feb 28.
TUBB4B Downregulation Is Critical for Increasing Migration of Metastatic Colon Cancer Cells. [Cells. 2019]
TUBB4B Downregulation Is Critical for Increasing Migration of Metastatic Colon Cancer Cells.
Sobierajska K, Ciszewski WM, Wawro ME, Wieczorek-Szukała K, Boncela J, Papiewska-Pajak I, Niewiarowska J, Kowalska MA. Cells. 2019 Aug 1; 8(8). Epub 2019 Aug 1.
Mutations in TUBB4B Cause a Distinctive Sensorineural Disease. [Am J Hum Genet. 2017]
Mutations in TUBB4B Cause a Distinctive Sensorineural Disease.
Luscan R, Mechaussier S, Paul A, Tian G, Gérard X, Defoort-Dellhemmes S, Loundon N, Audo I, Bonnin S, LeGargasson JF, et al. Am J Hum Genet. 2017 Dec 7; 101(6):1006-1012. Epub 2017 Nov 30.

RefSeq protein
See the reference protein sequence for tubulin beta-4B chain (NP_006079.1).

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tubulin, beta 2C, isoform CRA_b [Homo sapiens]
tubulin, beta 2C, isoform CRA_b [Homo sapiens]
gi|119608775|gb|EAW88369.1||gnl|WGS |hCP1796043

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