Gene: [13q32/ERCC5] excision repair cross-complementing rodent repair deficiency, complementation group 5; xeroderma pigmentosum, complementation group G (MIM:278780); [ERCM2 UVDR ]
HIS | [1] ERCC5
gene was demonstrated to be identical to marker ERCM2, which was previously
mapped to Chr 13 (Hori-1983). By virtue of this, the latter was excluded
from HGM. [2] ERCC5 localization 13q was refined (Gersen-1989 and Warburton-1991) as 13q33." |
REL | GEM:19q133/ERCC1. |
REF | LOC,CYG "Gersen &:
CCG, 51, (HGM10), 1003, 1989 REV "Hoeijmakers JHJ: J Cell Sci Suppl, 6, 111-125, 1987 COM,LIN "Hori &: PNAS, 80, 5655-5659, 1983 PRO,EXP,GEN "Mudgett JS, MacInnes: Genomics, 8, 623-633, 1990 PRO,EXP,GEN "Mudgett JS &: J Cell Biol, 107, 520A, 1988 LOC,CYG "Siciliano &: CCG, 46, (HGM9), 691-692, 1987 LOC,CYG "Thompson LH &: Somat Cell Mol Genet, 13, N5, 539-551, 1987 HIS,FUN "Thompson LH &: Mutation Res, 95, 427-440, 1982 LOC,CYG "Warburton &: CCG, 58, (HGM11), 1984, 1991 |
SWI | SWISSPROT: P28715 |
KEY | repr |
CLA | coding, basic |
LOC | 13 q32 |
MIM | MIM: 133530 |
SYN | ERCM2 UVDR |
