Gene: [19p131/RFX1] regulatory factor (trans-acting) 1 (influences HLA class II expression); bare lymphocyte syndrome (combined immunodeficiency with lack of HLA-II; MIM:209920); [BLS ]


REL

GEM:19p133/RFX2; GEM:00.0/RFX3; GEM:00.0/RFX4; GEM:01q21/RFX5.

REF

CLO,LOC "Brandriff BF &: Genomics, 23, 582-591, 1994
LOC,MAF "Doyle J &: Genomics, 35, 227-230, 1996
CLO,LOC "Pugliatti L &: Genomics, 13, 1307-1310, 1992
PRO,LOC "Pugliatti L &: CCG, 51, (HGM10), 1069, 1989
CLO,SEQ,STR,EXP "Reith W &: Mol Cell Biol, 14, 1230-1244, 1994
CLO,SEQ "Reith W &: Genes Dev, 4, 1528-1540, 1990

KEY

trc, imm

CLA

coding, basic

LOC

19 p13.1

MIM

MIM: 600006

SYN

BLS

Смотрите также:

  • Gene: [00.0/MHC2TA] MHC class II transactivator; MHC class II deficiency, complementation group A; bare lymphocyte syndrome, complementation group A (BLS; MIM:209920); [CIITA C2TA ]