Gene: [0Xp211/XK] Kell blood group precursor (McLeod phenotype); McLeod syndrome (Xk-related chronic granulomatous disease); [KX CGD ]


FAG

The gene encoding for Kell isoantigens is mapped to Chr 7q33 (GEM:07q33/KEL)."

REF

LOC "Bertelson CJ &: AJHG, 42, 703-711, 1988
CLO,SEQ,LOC "Davis MB &: CCG, 58, (HGM11), 2061, 1991
LOC "Francke U &: AJHG, 37, 250-267, 1985
LOC "Frey D &: Blood, 71, 252-255, 1988
CLO,SEQ,LOC "Ho MF &: Cell, 77, 869-880, 1994
CLO,SEQ,LOC "Ho MF &: AJHG, 50, 317-330, 1992
CLO,SEQ,LOC "Ho MF &: CCG, 58, (HGM11), 2067, 1991
CLO,SEQ,LOC "Musarella MA &: Genomics, 11, 263-272, 1991
CLO,SEQ,LOC "Pelham A &: Blood, 76, 820-824, 1990
CLO,SEQ,LOC "Uchida K &: Transfusion, 32, 691, 1992
CLO,SEQ,LOC "Witt TN &: J Neurol, 239, 302-306, 1992

SWI

SWISSPROT: P51811

KEY

hem, blgr, ant

CLA

coding, basic

LOC

0X p21.1

MIM

MIM: 314850

SYN

KX CGD

鸯铗痂蝈 蜞赕:

  • Kx 铃腙