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The protein encoded by this gene is erythrocyte-specific and is thought to be part of a membrane channel that transports ammonium and carbon dioxide across the blood cell membrane. The encoded protein appears to interact with Rh blood group antigens and Rh30 polypeptides. Defects in this gene are a cause of regulator type Rh-null hemolytic anemia (RHN), or Rh-deficiency syndrome.[provided by RefSeq, Mar 2009]
[中文简述(自动翻译):]  由该基因编码的蛋白质是红细胞特异性,被认为是在整个细胞膜运输铵和二氧化碳的膜通道的一部分。所编码的蛋白质似乎与Rh血型抗原和RH30多肽相互作用。这种基因缺陷是调节型的Rh空溶血性贫血的原因(RHN),或Rh缺陷综合征。[由RefSeq的,2009年03月提供]
RHAG基因(以及对应的蛋白质)的细胞分布位置:
RHAG基因的本位(GO)信息:
疾病名称 | 关系值 | NofPmids | NofSnps | 来源 |
STOMATOCYTOSIS I | 0.240542884 | 2 | 2 | BeFree_CLINVAR_ORPHANET |
Rh-Null, Regulator Type | 0.24 | 3 | 2 | CTD_human_UNIPROT |
Rh Deficiency Syndrome | 0.12 | 0 | 0 | ORPHANET |
Migraine Disorders | 0.002638474 | 1 | 0 | BeFree_GAD |
Hereditary stomatocytosis | 0.000271442 | 1 | 0 | BeFree |
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