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.