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The protein encoded by this gene is a beta isoform of tubulin, which binds GTP and is a major component of microtubules. This gene is highly similar to TUBB2A and TUBB2C. Defects in this gene are a cause of asymmetric polymicrogyria. [provided by RefSeq, Mar 2010]
[中文简述(自动翻译):]  由该基因编码的蛋白质是微管蛋白的beta同种型,其结合GTP和是微管的主要组成部分。这种基因是高度相似TUBB2A和TUBB2C。在这个基因的缺陷是不对称多小脑的起因。 [由RefSeq的,2010年3月提供]
TUBB2B基因(以及对应的蛋白质)的细胞分布位置:
TUBB2B基因的本体(GO)信息:
疾病名称 | 关系值 | NofPmids | NofSnps | 来源 |
POLYMICROGYRIA, SYMMETRIC OR ASYMMETRIC | 0.44 | 1 | 0 | CTD_human_MGD_ORPHANET_UNIPROT |
Malformations of Cortical Development | 0.120542884 | 3 | 0 | BeFree_CTD_human |
Animal Mammary Neoplasms | 0.12 | 1 | 0 | CTD_human |
Mammary Neoplasms, Experimental | 0.12 | 1 | 0 | CTD_human |
Polymicrogyria, Asymmetric | 0.12 | 0 | 10 | CLINVAR |
Schizophrenia | 0.00272435 | 1 | 0 | LHGDN |
Mammary Neoplasms | 0.00272435 | 1 | 0 | LHGDN |
Polymicrogyria | 0.001628651 | 6 | 0 | BeFree |
Congenital Abnormality | 0.000542884 | 2 | 0 | BeFree |
Microcephaly | 0.000542884 | 2 | 0 | BeFree |
Ocular Motility Disorders | 0.000271442 | 1 | 0 | BeFree |
Scoliosis, unspecified | 0.000271442 | 1 | 0 | BeFree |
Agenesis of corpus callosum | 0.000271442 | 1 | 0 | BeFree |
Congenital anomaly of brain | 0.000271442 | 1 | 0 | BeFree |
Lissencephaly | 0.000271442 | 1 | 0 | BeFree |
Congenital scoliosis | 0.000271442 | 1 | 0 | BeFree |
Acquired scoliosis | 0.000271442 | 1 | 0 | BeFree |
Congenital Fibrosis of the Extraocular Muscles | 0.000271442 | 1 | 1 | BeFree |
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