The protein encoded by this gene is a plasma membrane protein whose function is to transport creatine into and out of cells. Defects in this gene can result in X-linked creatine deficiency syndrome. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]
由该基因编码的蛋白质是一个质膜蛋白,其功能是肌酸输送到进出细胞。这种基因缺陷可能会导致X连锁肌酸缺乏综合征。已发现该基因编码不同亚型的多个抄本变形。 [由RefSeq的,2008年12月提供]
SLC6A8基因(以及对应的蛋白质)的细胞分布位置:
SLC6A8基因的本体(GO)信息:
疾病名称 | 关系值 | NofPmids | NofSnps | 来源 |
Creatine deficiency, X-linked | 0.565157396 | 25 | 10 | BeFree_CLINVAR_CTD_human_MGD_ORPHANET_UNIPROT |
Mental Retardation, X-Linked | 0.127348794 | 8 | 0 | BeFree_CTD_human_LHGDN |
Autistic Disorder | 0.122909916 | 2 | 0 | BeFree_CTD_human_GAD |
Developmental Disabilities | 0.120271442 | 2 | 0 | BeFree_CTD_human |
Intellectual Disability | 0.004353001 | 7 | 0 | BeFree_LHGDN |
Mental Retardation | 0.003181358 | 3 | 0 | BeFree_GAD |
Seizures | 0.002995792 | 1 | 0 | BeFree_LHGDN |
Premature ventricular contractions | 0.00272435 | 1 | 0 | LHGDN |
Arginine:Glycine Amidinotransferase Deficiency | 0.000814326 | 3 | 0 | BeFree |
Mild Mental Retardation | 0.000814326 | 3 | 0 | BeFree |
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