LOCUS X71342 1466 bp DNA linear HUM 14-NOV-2006
DEFINITION Homo sapiens partial XPGC gene, exon 2.
ACCESSION X71342
VERSION X71342.1
KEYWORDS DNA repair; RAD2 protein; Xeroderma Pigmentosum Group G
Complementing Factor (XPGC).
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
REFERENCE 1
AUTHORS Samec S., Jones T.A., Corlet J., Scherly D., Sheer D., Wood R.D.,
Clarkson S.G.
TITLE The human gene for xeroderma pigmentosum complementation group G
(XPG) maps to 13q33 by fluorescence in situ hybridization
JOURNAL Genomics 21(1), 283-285(1994).
PUBMED 8088806
REFERENCE 2 (bases 1 to 1466)
AUTHORS Clarkson S.G.
JOURNAL Submitted (06-APR-1993) to the INSDC. S.G. Clarkson, University of
Geneva, Dept of Genetics and Microbiology, Centre Medical
Universitaire, 9 avenue de Champel, 1211 Geneva 4, SWITZERLAND
REFERENCE 3 (bases 1 to 1466)
AUTHORS Scherly D., Nouspikel T., Corlet J., Ucla C., Bairoch A.,
Clarkson S.G.
TITLE Complementation of the DNA repair defect in xeroderma pigmentosum
group G cells by a human cDNA related to yeast RAD2
JOURNAL Nature 363(6425), 182-185(1993).
PUBMED 8483504
COMMENT Related sequence: X69978
FEATURES Location/Qualifiers
source 1..1466
/organism="Homo sapiens"
/chromosome="13"
/map="13q32-33"
/isolate="XY boy with fragile X"
/mol_type="genomic DNA"
/clone_lib="genomic DNA in EMBL3"
/clone="20"
/cell_type="lymphocyte"
/db_xref="taxon:9606"
intron <1..1248
/gene="XPGC"
/number=1
exon 1249..1424
/gene="XPGC"
/number=2
misc_difference 1296..1298
/replace="cat"
/note="conflict"
/citation=[3]
variation 1298
/replace="t"
/note="polymorphism"
intron 1425..>1466
/gene="XPGC"
/number=2
BASE COUNT 430 a 250 c 278 g 508 t
ORIGIN
1 aagaagaggg cctgagaaag atcactgatg aagtgaatac tttaacagtg ttacaggagc
61 tggcaaagag tctgagagca ggaaaaccag cagagcgcgg tatcactctt tcttttggac
121 aaatataaca ttttttgaga agcacttttt agaaaagttt aaaaatataa gaaaacttca
181 agatgaaaat ataagttatc tttagtctca gcagacataa tatctacttt aatattttgg
241 tatgtgaact agttttttat atttaacata tatactgtat cagaaaatgg agttatactt
301 tatatggttt tatagcctgt tttactatct ttaataatat ttaatgacta tcttccttat
361 cacacatgct cctgcaactt ccatttttaa gggctttttg gtattccagc aaataggtct
421 gccataatta gtttttcttt tttgagacgg agtcttgctc tgtcaccagg ctggagtgca
481 gtggcgcgat ctcggctcac tgcaacctct gcctcctggg ttcaagcgat tctcctgcct
541 cagcctcctg agtagctggg actacaggtg cgcaccacca tgcccagcca atttttgtat
601 ttttagtaga gatggggttt caccatgttg gccaggatgg tctcgatctc ttgatctcgt
661 gatccacctg cctcggcctc ccaaagtgct gggattacag gtgtgagcca ccgcgcccgg
721 cctatgatta gttttttaaa aagacctgct ggaaaacttt taagttgatt tttatatttt
781 cattattata aacaagcatt ctgtaaataa ctctcattat atatccatga tgattttctg
841 aagatcaatg tctggaagtg gtaaaataga ctgcaaagtt ttaaaaagtt tttttcacta
901 tgaattgtca aattgtcctc cagaaaattt gtgctaattc atgaaaattc tttagcaatc
961 acttattttt tttttaaaga agcaattctt tgcaatgaga cttcttaaaa ggatatgtct
1021 gtctttgtat gattttaaaa tgcagtatgt gaataggggt aacaagagtt caactaaaag
1081 ttaactgact ttaggtagat cccatgagag ctaaatgttt ttcaatttta aatgaatagt
1141 gataagtatt tagtgttcaa cgtttggata atatcagtta ttaggaaatt gaagttgtga
1201 ggatgaagag aaaaatcccg gagttttttc cattaacaat tctcccagat attagcattt
1261 ggttaaacca agcacttaaa ggagtccggg atcgccacgg gaactcaata gaaaatcctc
1321 atcttctcac tttgtttcat cggctctgca aactcttatt ttttcgaatt cgtcctattt
1381 ttgtgtttga tggggatgct ccactattga agaaacagac tttggtaagt gtcgtatagt
1441 ttttagtaag tgtcaaataa tttttt
//