更多...
收起
The protein encoded by this gene is a keratan sulfate proteoglycan that is involved in corneal transparency. Defects in this gene are a cause of autosomal recessive cornea plana 2 (CNA2).[provided by RefSeq, May 2010]
[中文简述(自动翻译):]  由该基因编码的蛋白质是参与角膜透明度的硫酸角质素蛋白多糖。这种基因缺陷。[由RefSeq的,2010年5月提供]常染色体隐性遗传扁平角膜2(CNA2)的原因
KERA基因(以及对应的蛋白质)的细胞分布位置:
KERA基因的本体(GO)信息:
| 疾病名称 | 关系值 | NofPmids | NofSnps | 来源 |
| CORNEA PLANA 2 | 0.44 | 2 | 7 | CLINVAR_CTD_human_MGD_UNIPROT |
| Cornea plana | 0.002714419 | 10 | 1 | BeFree |
| Hematocrit level | 0.002367032 | 1 | 1 | GAD |
| Severe myopia | 0.000542884 | 2 | 0 | BeFree |
| CORNEAL DYSTROPHY, POSTERIOR AMORPHOUS | 0.000542884 | 2 | 0 | BeFree |
| Arteriosclerosis | 0.000271442 | 1 | 0 | BeFree |
| Atherosclerosis | 0.000271442 | 1 | 0 | BeFree |
| Keratoconus | 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。