This intronless gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. The protein may function in the developing nervous system and play a role in tumorigenesis. [provided by RefSeq, Jul 2008]
此内含子基因编码SOX的成员(SRY相关HMG盒)家族参与胚胎发育的调节,并在细胞命运的决心转录因子。所编码的蛋白质也可以在形成与其他蛋白质的蛋白复合物后充当转录调节。蛋白质可以在发育中的神经系统的功能和在肿瘤发生中发挥作用。 [由RefSeq的,2008年7月提供]
SOX11基因(以及对应的蛋白质)的细胞分布位置:
SOX11基因的本体(GO)信息:
疾病名称 | 关系值 | NofPmids | NofSnps | 来源 |
Coffin-Siris syndrome | 0.120271442 | 1 | 0 | BeFree_ORPHANET |
Salivary Gland Neoplasms | 0.12 | 1 | 0 | CTD_human |
Neoplasm Invasiveness | 0.12 | 1 | 0 | CTD_human |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 27 | 0.12 | 1 | 0 | UNIPROT |
Adenoid Cystic Carcinoma | 0.12 | 1 | 0 | CTD_human |
Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse | 0.006786047 | 25 | 0 | BeFree |
Male infertility | 0.00272435 | 1 | 0 | LHGDN |
Creatinine finding | 0.002367032 | 1 | 1 | GAD |
Kidney Diseases | 0.002367032 | 1 | 1 | GAD |
Blood pressure finding | 0.002367032 | 1 | 1 | GAD |
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