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. Author manuscript; available in PMC: 2019 Mar 6.
Published in final edited form as: Methods Cell Biol. 2018;144:33–74. doi: 10.1016/bs.mcb.2018.03.040

Table 2. Human β-tubulin isotypes.

Gene Full name Alternative name Locus Transcript variants NCBI Reference Sequence Number of protein-coding transcribed from this gene https://www.proteinatlas.org/ Tissue-Expression Associated Human Diseases
TUBB Tubulin beta class I Tubb5 6p21.33 1 - NM_001293212.1
2 - NM_178014.3
3 - NM_001293213.1
4 - NM_001293214.1
5 - NM_001293215.1
6 - NM_001293216.1
4 (49.7, 41.7, 47.8, 41.7 kDa) Ubiquitous Cortical dysplasia, complex, with other brain malformations
TUBB1 Tubulin beta 1 class VI --- 20q13.32 1 - NM_030773.3 1 (50.3 kDa) Enriched in platelets and megakaryocytes Autosomal dominant macrothrombocytopenia
TUBB2A Tubulin beta 2A class IIa TUBB2 6p25.2 1 - NM_001069.2
2 - NM_001310315.1
1 (49.9 kDa) Ubiquitous Cortical dysplasia with other brain malformations
TUBB2B Tubulin beta 2B class IIb MGC8685 6p25.2 1 - NM_178012.4 1 (50.0 kDa) Ubiquitous Asymmetric polymicrogyria
TUBB3 Tubulin beta 3 class III beta-4 16q24.3 1 - NM_006086.3
2 - NM_001197181.1
8 (50.4, 42.4, 5, 20.7, 10.8, 13.6, 18.3, 16.4 kDa) Ubiquitous Congenital fibrosis of the extraocular muscles type 3
TUBB4A Tubulin beta 4A class IVa TUBB4 18p13.3 1 - NM_001289123.1
2 - NM_001289127.1
3 - NM_006087.3
4 - NM_001289129.1
5 - NM_001289130.1
6 - NM_001289131.1
11 (49.6, 11.8, 17.6, 16.6, 10.6, 11.7, 17.8, 17.4, 12.2, 7.8, 15.8 kDa) Ubiquitous Hypomyelinating leukodystrophy-6 and autosomal dominant torsion dystonia-4
TUBB4B Tubulin beta 4B class IVb TUBB2C 9q34.3 1 - NM_006088.5 1 (49.8 kDa) Ubiquitous ND
TUBB6 Tubulin beta 6 class V MGC4083 18p11.21 1 - NM_032525.2
2 - NM_001303524.1
3 - NM_001303525.1
4 - NM_001303526.1
5 - NM_001303527.1
6 - NM_001303528.1
7 - NM_001303529.1
8 - NM_001303530.1
10 (49.6, 11.8, 17.6, 16.6, 10.6, 11.7, 17.8, 17.4, 12.2, 7.8, 15.8 kDa) Ubiquitous ND
TUBB8 Tubulin beta 8 class VIII bA631M21.2 10p15.3 1 - NM_177987.2 5 (49.8, 7.8, 45.5, 13, 45.7 kDa) Ubiquitous low Defects in this gene are a cause of oocyte maturation defect 2 and infertility

ND: Not described.