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 |
