闈舵爣锛欬p style="text-indent: 2em;">Tmem242

浜у搧鍒悕锛欬p style="text-indent: 2em;">1110008A10Rik锛 2310046K16Rik锛 5730437N04Rik锛 Tmem242锛 transmembrane protein 242锛 transmembrane protein 242锛 transmembrane protein 242锛 UPF0463 transmembrane protein C6orf35 homolog锛 6鍙锋煋鑹蹭綋寮€鏀鹃槄璇绘35锛

鑳屾櫙淇℃伅锛欬div style="text-indent: 2em;">Making up nearly 6% of the human genome, chromosome 6 contains around 1,200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf35 gene product has been provisionally designated C6orf35 pending further characterization.