更多...
收起
The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It is strongly expressed in the cell lines of promyelocytic leukemia and Burkitt's lymphoma. In addition, it and another family member, the WNT6 gene, are strongly coexpressed in colorectal cancer cell lines. The gene overexpression may play key roles in carcinogenesis through activation of the WNT-beta-catenin-TCF signaling pathway. This gene and the WNT6 gene are clustered in the chromosome 2q35 region. [provided by RefSeq, Jul 2008]
[中文简述(自动翻译):]  Wnt信号基因家族由结构相关基因,其编码分泌信号蛋白。这些蛋白质有牵连肿瘤发生并在几个发育过程,包括胚胎发育过程中细胞命运和图案化的调节。此基因是WNT基因家族的一个成员。它在早幼粒细胞白血病和伯基特淋巴瘤的细胞系中强烈表达。此外,它和其他家庭成员,WNT6基因,强烈结肠癌细胞系中共表达。基因表达可能癌变通过WNT-β-连环蛋白的TCF信号转导通路的活化中起关键作用。此基因和WNT6基因都聚集在染色体2q35区域。 [由RefSeq的,2008年7月提供]
WNT10A基因(以及对应的蛋白质)的细胞分布位置:
WNT10A基因的本体(GO)信息:
疾病名称 | 关系值 | NofPmids | NofSnps | 来源 |
SCHOPF-SCHULZ-PASSARGE SYNDROME (disorder) | 0.361628651 | 6 | 1 | BeFree_CLINVAR_CTD_human_ORPHANET |
Odontoonychodermal dysplasia | 0.36 | 1 | 6 | CLINVAR_CTD_human_UNIPROT |
TOOTH AGENESIS, SELECTIVE, 4 (disorder) | 0.24 | 3 | 6 | CLINVAR_UNIPROT |
Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse | 0.12272435 | 1 | 0 | CTD_human_LHGDN |
Odonto-onycho-dermal dysplasia | 0.121628651 | 6 | 0 | BeFree_ORPHANET |
Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive | 0.12 | 0 | 0 | ORPHANET |
Ectodermal Dysplasia | 0.005167327 | 9 | 0 | BeFree_LHGDN |
Hypodontia | 0.003257302 | 12 | 0 | BeFree |
Malignant neoplasm of stomach | 0.000814326 | 3 | 0 | BeFree |
Tooth Loss | 0.000814326 | 3 | 0 | BeFree |
Christ-Siemens-Touraine syndrome | 0.000814326 | 3 | 0 | BeFree |
Developmental absence of tooth | 0.000814326 | 3 | 0 | BeFree |
Stomach Carcinoma | 0.000814326 | 3 | 0 | BeFree |
Increased sweating | 0.000542884 | 2 | 0 | BeFree |
Anhydrotic Ectodermal Dysplasias | 0.000542884 | 2 | 0 | BeFree |
Zlotogora-Ogur syndrome | 0.000542884 | 2 | 0 | BeFree |
Congenital Abnormality | 0.000271442 | 1 | 0 | BeFree |
Renal Cell Carcinoma | 0.000271442 | 1 | 0 | BeFree |
Colorectal Carcinoma | 0.000271442 | 1 | 0 | BeFree |
Cyst | 0.000271442 | 1 | 0 | BeFree |
Esophageal Neoplasms | 0.000271442 | 1 | 0 | BeFree |
Kidney Diseases | 0.000271442 | 1 | 0 | BeFree |
Skin Neoplasms | 0.000271442 | 1 | 0 | BeFree |
Acute interstitial nephritis | 0.000271442 | 1 | 0 | BeFree |
Renal fibrosis | 0.000271442 | 1 | 0 | BeFree |
Esophageal carcinoma | 0.000271442 | 1 | 0 | BeFree |
Teratocarcinoma | 0.000271442 | 1 | 0 | BeFree |
Congenital anomaly of face | 0.000271442 | 1 | 0 | BeFree |
Squamous cell carcinoma of esophagus | 0.000271442 | 1 | 0 | BeFree |
Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site | 0.000271442 | 1 | 0 | BeFree |
Associated symptom | 0.000271442 | 1 | 0 | BeFree |
Malignant neoplasm of esophagus | 0.000271442 | 1 | 0 | BeFree |
Colorectal Cancer | 0.000271442 | 1 | 0 | BeFree |
Tooth Agenesis, Familial | 0.000271442 | 1 | 0 | BeFree |
忘记密码? 点击找回密码.
扫一扫右方二维码,关注微信订阅号,实时查看信息,关注医学生物学动态。