2024-04-27 04:28:28, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001127389 1380 bp mRNA linear PRI 07-MAY-2013 DEFINITION Homo sapiens double homeobox 4 like 5 (DUX4L5), mRNA. ACCESSION NM_001127389 XM_928008 VERSION NM_001127389.2 GI:489406872 KEYWORDS RefSeq. SOURCE Homo sapiens (human) ORGANISM Homo sapiens Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo. REFERENCE 1 (bases 1 to 1380) AUTHORS Dixit,M., Ansseau,E., Tassin,A., Winokur,S., Shi,R., Qian,H., Sauvage,S., Matteotti,C., van Acker,A.M., Leo,O., Figlewicz,D., Barro,M., Laoudj-Chenivesse,D., Belayew,A., Coppee,F. and Chen,Y.W. TITLE DUX4, a candidate gene of facioscapulohumeral muscular dystrophy, encodes a transcriptional activator of PITX1 JOURNAL Proc. Natl. Acad. Sci. U.S.A. 104 (46), 18157-18162 (2007) PUBMED 17984056 REFERENCE 2 (bases 1 to 1380) AUTHORS Clapp,J., Mitchell,L.M., Bolland,D.J., Fantes,J., Corcoran,A.E., Scotting,P.J., Armour,J.A. and Hewitt,J.E. TITLE Evolutionary conservation of a coding function for D4Z4, the tandem DNA repeat mutated in facioscapulohumeral muscular dystrophy JOURNAL Am. J. Hum. Genet. 81 (2), 264-279 (2007) PUBMED 17668377 REFERENCE 3 (bases 1 to 1380) AUTHORS Kowaljow,V., Marcowycz,A., Ansseau,E., Conde,C.B., Sauvage,S., Matteotti,C., Arias,C., Corona,E.D., Nunez,N.G., Leo,O., Wattiez,R., Figlewicz,D., Laoudj-Chenivesse,D., Belayew,A., Coppee,F. and Rosa,A.L. TITLE The DUX4 gene at the FSHD1A locus encodes a pro-apoptotic protein JOURNAL Neuromuscul. Disord. 17 (8), 611-623 (2007) PUBMED 17588759 REFERENCE 4 (bases 1 to 1380) AUTHORS Beckers,M., Gabriels,J., van der Maarel,S., De Vriese,A., Frants,R.R., Collen,D. and Belayew,A. TITLE Active genes in junk DNA? Characterization of DUX genes embedded within 3.3 kb repeated elements JOURNAL Gene 264 (1), 51-57 (2001) PUBMED 11245978 REFERENCE 5 (bases 1 to 1380) AUTHORS Gabriels,J., Beckers,M.C., Ding,H., De Vriese,A., Plaisance,S., van der Maarel,S.M., Padberg,G.W., Frants,R.R., Hewitt,J.E., Collen,D. and Belayew,A. TITLE Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element JOURNAL Gene 236 (1), 25-32 (1999) PUBMED 10433963 REFERENCE 6 (bases 1 to 1380) AUTHORS Lee,J.H., Goto,K., Matsuda,C. and Arahata,K. TITLE Characterization of a tandemly repeated 3.3-kb KpnI unit in the facioscapulohumeral muscular dystrophy (FSHD) gene region on chromosome 4q35 JOURNAL Muscle Nerve Suppl 2, S6-S13 (1995) PUBMED 7739628 COMMENT VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from AC126281.3. On May 7, 2013 this sequence version replaced gi:188497733. Sequence Note: This RefSeq record was created from genomic sequence data because no transcripts are available to represent this gene. The extent of this RefSeq is supported by similar human loci. PubMedID: 17588759 shows some evidence that this locus is transcribed and is protein-coding. COMPLETENESS: complete on the 5' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-1380 AC126281.3 9480-10859 FEATURES Location/Qualifiers source 1..1380 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="4" /map="4q35.2" gene 1..1380 /gene="DUX4L5" /note="double homeobox 4 like 5" /db_xref="GeneID:653545" /db_xref="HGNC:38689" exon 1..1380 /gene="DUX4L5" /inference="alignment:Splign:1.39.8" CDS 98..1372 /gene="DUX4L5" /codon_start=1 /product="double homeobox protein 4-like protein 5" /protein_id="NP_001120861.3" /db_xref="GI:489406873" /db_xref="GeneID:653545" /db_xref="HGNC:38689" /translation="
MALPTPSDSTLPAEARGRGRRRRLVWTPSQSEALRACFERNPYPGIATRERLAQAIGIPEPRVQIWFQNERSRQLRQHRRESRPWPGRRGPPEGRRKRTAVTGSQTALLLRAFEKDRFPGIAAREELARETGLPESRIQIWFQNRRARHPGQGGRAPAQAGGLCSAAPGGGHPAPSWVAFAHTGAWGTGLPAPHVPCAPGALPQGAFVSQAARAAPALQPSQAAPAEGVSQPAPARGDFAYAAPAPPDGALSHPQAPRWPPHPGKSREDRDPQRDGLPGPCAVAQPGPAQAGPQGQGVLAPPTSQGSPWWGWGRGPQVAGAAWEPQAGAAPPPQPAPPDASASARQGQMQGIPAPSQALQEPAPWSALPCGLLLDELLASPEFLQQAQPLLETEAPGELEASEEAASLEAPLSEEEYRALLEEL
" misc_feature 170..331 /gene="DUX4L5" /note="Homeodomain; DNA binding domains involved in the transcriptional regulation of key eukaryotic developmental processes; may bind to DNA as monomers or as homo- and/or heterodimers, in a sequence-specific manner; Region: homeodomain; cd00086" /db_xref="CDD:238039" misc_feature order(170..172,290..292,299..304,311..313) /gene="DUX4L5" /note="specific DNA base contacts [nucleotide binding]; other site" /db_xref="CDD:238039" misc_feature order(173..175,224..226,242..244,281..283,287..292, 299..304,308..316,320..325) /gene="DUX4L5" /note="DNA binding site [nucleotide binding]" /db_xref="CDD:238039" misc_feature 401..544 /gene="DUX4L5" /note="Homeodomain; DNA binding domains involved in the transcriptional regulation of key eukaryotic developmental processes; may bind to DNA as monomers or as homo- and/or heterodimers, in a sequence-specific manner; Region: homeodomain; cd00086" /db_xref="CDD:238039" misc_feature order(449..451,467..469,506..508,512..517,524..529, 533..541) /gene="DUX4L5" /note="DNA binding site [nucleotide binding]" /db_xref="CDD:238039" misc_feature order(515..517,524..529,536..538) /gene="DUX4L5" /note="specific DNA base contacts [nucleotide binding]; other site" /db_xref="CDD:238039" variation 546 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:1001841" variation 667 /gene="DUX4L5" /replace="g" /replace="t" /db_xref="dbSNP:3927872" variation 688 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:78098781" variation 691 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:75532223" variation 693 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:78034460" variation 729 /gene="DUX4L5" /replace="c" /replace="g" /db_xref="dbSNP:80113703" variation 731 /gene="DUX4L5" /replace="g" /replace="t" /db_xref="dbSNP:76950501" variation 741 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:75602111" variation 745 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:75378282" variation 747 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:79787961" variation 751 /gene="DUX4L5" /replace="c" /replace="g" /db_xref="dbSNP:78876729" variation 766 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:75429164" variation 838 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:3885294" variation 897 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:2078365" variation 959 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:36167667" variation 962 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:4073816" variation 996 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:2336886" variation 998 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:1533571" variation 1001 /gene="DUX4L5" /replace="g" /replace="t" /db_xref="dbSNP:36151648" variation 1020 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:74198705" variation 1035..1036 /gene="DUX4L5" /replace="" /replace="c" /db_xref="dbSNP:36126854" variation 1041 /gene="DUX4L5" /replace="a" /replace="c" /db_xref="dbSNP:36189223" variation 1062 /gene="DUX4L5" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:4072648" variation 1066 /gene="DUX4L5" /replace="c" /replace="g" /db_xref="dbSNP:36130291" variation 1071 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36148840" variation 1079..1080 /gene="DUX4L5" /replace="c" /replace="g" /db_xref="dbSNP:36156691" variation 1086..1087 /gene="DUX4L5" /replace="g" /replace="t" /db_xref="dbSNP:36127411" variation 1094..1096 /gene="DUX4L5" /replace="c" /replace="g" /db_xref="dbSNP:36143292" variation 1095..1096 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36182096" variation 1095..1096 /gene="DUX4L5" /replace="ccagccgt" /replace="tcagctgg" /db_xref="dbSNP:74222403" variation 1095 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36136318" variation 1098 /gene="DUX4L5" /replace="a" /replace="t" /db_xref="dbSNP:36133002" variation 1101..1102 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36154473" variation 1102..1103 /gene="DUX4L5" /replace="a" /replace="c" /db_xref="dbSNP:36160149" variation 1102 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:71214797" variation 1103 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36131718" variation 1104 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:36176569" variation 1104 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:36183463" variation 1106 /gene="DUX4L5" /replace="g" /replace="t" /db_xref="dbSNP:36165213" variation 1110 /gene="DUX4L5" /replace="" /replace="g" /db_xref="dbSNP:36138289" variation 1111 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36162857" variation 1112 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:36174656" variation 1114..1119 /gene="DUX4L5" /replace="" /replace="cgcctc" /db_xref="dbSNP:71265617" variation 1117 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:36197830" variation 1123..1129 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36148040" variation 1123 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:36147765" variation 1130..1131 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36165499" variation 1130 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36175519" variation 1130 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:74187058" variation 1131 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36178803" variation 1136 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:4075715" variation 1137 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:4073815" variation 1138 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:36135732" variation 1139..1140 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36140034" variation 1141..1142 /gene="DUX4L5" /replace="" /replace="a" /db_xref="dbSNP:36174150" variation 1148 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:71283414" variation 1150 /gene="DUX4L5" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:36150813" variation 1150 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36153856" variation 1153 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36192296" variation 1156 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36159331" variation 1156 /gene="DUX4L5" /replace="" /replace="g" /db_xref="dbSNP:36183587" variation 1157..1158 /gene="DUX4L5" /replace="" /replace="t" /db_xref="dbSNP:36130133" variation 1159 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:3885293" variation 1159 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:36146406" variation 1160 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36137486" variation 1162 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:71217007" variation 1167 /gene="DUX4L5" /replace="a" /replace="t" /db_xref="dbSNP:36130447" variation 1168 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36173725" variation 1168 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:71190237" variation 1170 /gene="DUX4L5" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:36131572" variation 1171 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:74185826" variation 1171 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:3885301" variation 1171 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:36185212" variation 1177 /gene="DUX4L5" /replace="c" /replace="g" /db_xref="dbSNP:36165366" variation 1182..1183 /gene="DUX4L5" /replace="" /replace="g" /db_xref="dbSNP:36151107" variation 1182 /gene="DUX4L5" /replace="" /replace="g" /db_xref="dbSNP:36135461" variation 1183..1185 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36172872" variation 1183 /gene="DUX4L5" /replace="a" /replace="c" /db_xref="dbSNP:74216378" variation 1183 /gene="DUX4L5" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:36144110" variation 1183 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:36154521" variation 1183 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:36165293" variation 1185..1186 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36179412" variation 1185 /gene="DUX4L5" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:36163675" variation 1185 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:36145703" variation 1187..1188 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:36152748" variation 1187..1188 /gene="DUX4L5" /replace="g" /replace="t" /db_xref="dbSNP:36137352" variation 1191 /gene="DUX4L5" /replace="a" /replace="c" /db_xref="dbSNP:71217420" variation 1191 /gene="DUX4L5" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:36158615" variation 1191 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:36168464" variation 1196 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:36141674" variation 1199..1200 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:77495790" variation 1200..1201 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36178400" variation 1200..1201 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:79083258" variation 1203 /gene="DUX4L5" /replace="a" /replace="c" /db_xref="dbSNP:80081518" variation 1204 /gene="DUX4L5" /replace="a" /replace="c" /db_xref="dbSNP:78542547" variation 1206..1216 /gene="DUX4L5" /replace="cagcaggccg" /replace="tagcaggcca" /db_xref="dbSNP:74209687" variation 1206..1207 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36195896" variation 1206..1207 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:71271246" variation 1206 /gene="DUX4L5" /replace="c" /replace="g" /db_xref="dbSNP:77324699" variation 1206 /gene="DUX4L5" /replace="c" /replace="g" /db_xref="dbSNP:78709147" variation 1207 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:79370186" variation 1208 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:76210389" variation 1209 /gene="DUX4L5" /replace="g" /replace="t" /db_xref="dbSNP:77638190" variation 1210 /gene="DUX4L5" /replace="g" /replace="t" /db_xref="dbSNP:36174708" variation 1211 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:36171484" variation 1213 /gene="DUX4L5" /replace="a" /replace="c" /db_xref="dbSNP:71214796" variation 1214 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:36162930" variation 1214 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:80174686" variation 1215 /gene="DUX4L5" /replace="a" /replace="t" /db_xref="dbSNP:36189063" variation 1216 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36147580" variation 1217 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:36136565" variation 1219 /gene="DUX4L5" /replace="g" /replace="t" /db_xref="dbSNP:36129442" variation 1229 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36187837" variation 1229 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:36182028" variation 1229 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:79169724" variation 1231 /gene="DUX4L5" /replace="g" /replace="t" /db_xref="dbSNP:79133889" variation 1232 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:74186626" variation 1233 /gene="DUX4L5" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:75230145" variation 1233 /gene="DUX4L5" /replace="c" /replace="g" /db_xref="dbSNP:36127666" variation 1235 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:36145677" variation 1236 /gene="DUX4L5" /replace="c" /replace="g" /db_xref="dbSNP:76247614" variation 1237 /gene="DUX4L5" /replace="a" /replace="c" /db_xref="dbSNP:74629767" variation 1239..1241 /gene="DUX4L5" /replace="a" /replace="c" /db_xref="dbSNP:36185951" variation 1240 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:36151642" variation 1240 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:71211169" variation 1241 /gene="DUX4L5" /replace="c" /replace="g" /db_xref="dbSNP:36151813" variation 1253 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:36192229" variation 1254 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36174332" variation 1257 /gene="DUX4L5" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:36159640" variation 1257 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36161596" variation 1257 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36172956" variation 1258 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36193803" variation 1258 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:71193703" variation 1259 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:36179367" variation 1262..1263 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:74213964" variation 1264..1265 /gene="DUX4L5" /replace="a" /replace="t" /db_xref="dbSNP:36165689" variation 1265 /gene="DUX4L5" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:36172692" variation 1268..1269 /gene="DUX4L5" /replace="a" /replace="c" /db_xref="dbSNP:36151313" variation 1268 /gene="DUX4L5" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:36156653" variation 1268 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:36150308" variation 1275 /gene="DUX4L5" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:36140073" variation 1275 /gene="DUX4L5" /replace="c" /replace="g" /db_xref="dbSNP:36187301" variation 1280..1281 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:36151010" variation 1280 /gene="DUX4L5" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:74222218" variation 1285 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:74185329" variation 1288 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36135145" variation 1289 /gene="DUX4L5" /replace="c" /replace="g" /db_xref="dbSNP:36192357" variation 1295 /gene="DUX4L5" /replace="c" /replace="g" /db_xref="dbSNP:36136747" variation 1312 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:36169604" variation 1313..1314 /gene="DUX4L5" /replace="g" /replace="t" /db_xref="dbSNP:36155942" variation 1313 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:74216664" variation 1313 /gene="DUX4L5" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:3885278" variation 1313 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:36182886" variation 1315 /gene="DUX4L5" /replace="c" /replace="g" /db_xref="dbSNP:36176167" variation 1317 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:36173132" variation 1318 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36164553" variation 1323 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:4077005" variation 1327 /gene="DUX4L5" /replace="a" /replace="t" /db_xref="dbSNP:36132822" variation 1328 /gene="DUX4L5" /replace="g" /replace="t" /db_xref="dbSNP:34566145" variation 1331 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36128401" variation 1332 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:36142895" variation 1335..1336 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36167609" variation 1338..1340 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:36161478" variation 1349 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36176392" variation 1350 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:71193704" variation 1353 /gene="DUX4L5" /replace="g" /replace="t" /db_xref="dbSNP:36146433" variation 1355 /gene="DUX4L5" /replace="c" /replace="g" /db_xref="dbSNP:36136100" variation 1357 /gene="DUX4L5" /replace="c" /replace="t" /db_xref="dbSNP:36184679" variation 1366..1367 /gene="DUX4L5" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:36127633" variation 1367 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:4077628" variation 1376..1377 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36157409" variation 1376 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36128322" variation 1376 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36173546" variation 1376 /gene="DUX4L5" /replace="a" /replace="g" /db_xref="dbSNP:36181680" ORIGIN
acctgccgcagtgcacagtccggctgaggtgcacgggagcccgccggcctctctctgcccgcgtccgtccgtgaaattccggccggggctcaccgcgatggccctcccgacaccctcggacagcaccctccccgcggaagcccggggacgaggacggcgacggagactcgtttggaccccgagccaaagcgaggccctgcgagcctgctttgagcggaacccgtacccgggcatcgccaccagagaacggctggcccaggccatcggcattccggagcccagggtccagatttggtttcagaatgagaggtcacgccagctgaggcagcaccggcgggaatctcggccctggcccgggagacgcggcccgccagaaggccggcgaaagcggaccgccgtcaccggatcccagaccgccctgctcctccgagcctttgagaaggatcgctttccaggcatcgccgcccgggaggagctggccagagagacgggcctcccggagtccaggattcagatctggtttcagaatcgaagggccaggcacccgggacagggtggcagggcgcccgcgcaggcaggcggcctgtgcagcgcggcccccggcgggggtcaccctgctccctcgtgggtcgccttcgcccacaccggcgcgtggggaacggggcttcccgcaccccacgtgccctgcgcgcctggggctctcccacagggggctttcgtgagccaggcagcgagggccgcccccgcgctgcagcccagccaggccgcgccggcagagggggtctcccaacctgccccggcgcgcggggatttcgcctacgccgccccggctcctccggacggggcgctctcccaccctcaggctcctcggtggcctccgcacccgggcaaaagccgggaggaccgggacccgcagcgcgacggcctgccgggcccctgcgcggtggcacagcctgggcccgctcaagcggggccgcagggccaaggggtgcttgcgccacccacgtcccaggggagtccgtggtggggctggggccggggtccccaggtcgccggggcggcgtgggaaccccaagccggggcagctccacctccccagcccgcgcccccggacgcctccgcctccgcgcggcaggggcagatgcaaggcatcccggcgccctcccaggcgctccaggagccggcgccctggtctgcactcccctgcggcctgctgctggatgagctcctggcgagcccggagtttctgcagcaggcgcaacctctcctagaaacggaggccccgggggagctggaggcctcggaagaggccgcctcgctggaagcacccctcagcgaggaagaataccgggctctgctggaggagctttaggacgcggg
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:653545 -> Molecular function: GO:0000976 [transcription regulatory region sequence-specific DNA binding] evidence: IEA GeneID:653545 -> Molecular function: GO:0003700 [sequence-specific DNA binding transcription factor activity] evidence: IEA GeneID:653545 -> Biological process: GO:0006351 [transcription, DNA-dependent] evidence: IEA GeneID:653545 -> Cellular component: GO:0005634 [nucleus] evidence: IEA
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