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Immunogen sequence: KNGAGLSKS KGSRIGFDST QWRAVKKFIM LTSNQNVPVF LIDPLILELI NKNFEQVKNT SHGSTSQCKF FCVPRDFTAF ALQYHLWKNE EGWFRIAENM GFQCLKIESK DPRLDGIDSL SGTEIPLHYI CKLATHAIHL VVFHERSGNY LWHGHLRLKE HIDRKFVPFR KLQFGRYPGA FDRPELQQVT VDGLEVLIPK DPMHFVEEVP HSRFIECRYK EARAFFQQYL DDNTVEAVAF RKSAKELLQL AAKTLNKLGV PFWLSSGTCL GWYRQCNIIP YSKDVDLGIF IQDYKSDIIL AFQDAGLPLK HKFGKVEDSL ELSFQGKDDV KLDVFFFYEE TDHMWNGGTQ AKTGKKFKYL FPKFTLCWTE FVDMKVHVPC ETLEYIEANY GKTWKIPVKT WDWKRSPPNV QPNGIWPISE WDEVIQLY (35-461 aa encoded by BC101808 )
FKTN regulates the migration and assembly of neurons during cortical histogenesis. Fukuyama congenital muscular dystrophy results from mutations in its gene.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: Fukutin; Fukuyama type congenital muscular dystrophy (fukutin); Fukuyama type congenital muscular dystrophy homolog; Fukuyama type congenital muscular dystrophy protein; Fukuyama-type congenital muscular dystrophy protein; patient fukutin; Ribitol-5-phosphate transferase; Ribitol-5-phosphate transferase FKTN; RP11-235C23.1
基因别名: CMD1X; D830030O17Rik; FCMD; FKTN; LGMD2M; MDDGA4; MDDGB4; MDDGC4
UniProt ID: (Human) O75072, (Mouse) Q8R507
Entrez Gene ID: (Human) 2218, (Rat) 362520, (Mouse) 246179