2024-05-06 10:41:23, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_024040 1100 bp mRNA linear PRI 25-DEC-2022 DEFINITION Homo sapiens CUE domain containing 2 (CUEDC2), mRNA. ACCESSION NM_024040 VERSION NM_024040.3 KEYWORDS RefSeq; MANE Select. 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 1100) AUTHORS Roy S, Saha S, Dhar D, Chakraborty P, Singha Roy K, Mukherjee C, Gupta A, Bhattacharyya S, Roy A, Sengupta S, Roychoudhury S and Nath S. TITLE Molecular crosstalk between CUEDC2 and ERalpha influences the clinical outcome by regulating mitosis in breast cancer JOURNAL Cancer Gene Ther 29 (11), 1697-1706 (2022) PUBMED 35732909 REMARK GeneRIF: Molecular crosstalk between CUEDC2 and ERalpha influences the clinical outcome by regulating mitosis in breast cancer. REFERENCE 2 (bases 1 to 1100) AUTHORS Ghatak D, Datta A, Roychowdhury T, Chattopadhyay S and Roychoudhury S. TITLE MicroRNA-324-5p-CUEDC2 Axis Mediates Gain-of-Function Mutant p53-Driven Cancer Stemness JOURNAL Mol Cancer Res 19 (10), 1635-1650 (2021) PUBMED 34257080 REMARK GeneRIF: MicroRNA-324-5p-CUEDC2 Axis Mediates Gain-of-Function Mutant p53-Driven Cancer Stemness. REFERENCE 3 (bases 1 to 1100) AUTHORS Mu M, Niu W, Zhang X, Hu S and Niu C. TITLE LncRNA BCYRN1 inhibits glioma tumorigenesis by competitively binding with miR-619-5p to regulate CUEDC2 expression and the PTEN/AKT/p21 pathway JOURNAL Oncogene 39 (45), 6879-6892 (2020) PUBMED 32978519 REMARK GeneRIF: LncRNA BCYRN1 inhibits glioma tumorigenesis by competitively binding with miR-619-5p to regulate CUEDC2 expression and the PTEN/AKT/p21 pathway. Erratum:[Oncogene. 2021 Oct;40(40):5972-5973. PMID: 34400767] REFERENCE 4 (bases 1 to 1100) AUTHORS Xu S, Huang S, Li D, Zou Q, Yuan Y and Yang Z. TITLE Comparison of ADAM19 and CUEDC2 expression in EHCC and their clinicopathological significance JOURNAL Biomark Med 14 (16), 1573-1584 (2020) PUBMED 32960074 REMARK GeneRIF: Comparison of ADAM19 and CUEDC2 expression in EHCC and their clinicopathological significance. REFERENCE 5 (bases 1 to 1100) AUTHORS Lingyun H, Ailing L, Yali L, Yanqin Y and Jing N. TITLE Expression of CUE domain containing 2 protein in serous ovarian cancer tissue: predicting disease-free and overall survival of patients JOURNAL J Int Med Res 48 (9), 300060520954770 (2020) PUBMED 32967504 REMARK GeneRIF: Expression of CUE domain containing 2 protein in serous ovarian cancer tissue: predicting disease-free and overall survival of patients. REFERENCE 6 (bases 1 to 1100) AUTHORS Pan X, Zhou T, Tai YH, Wang C, Zhao J, Cao Y, Chen Y, Zhang PJ, Yu M, Zhen C, Mu R, Bai ZF, Li HY, Li AL, Liang B, Jian Z, Zhang WN, Man JH, Gao YF, Gong WL, Wei LX and Zhang XM. TITLE Elevated expression of CUEDC2 protein confers endocrine resistance in breast cancer JOURNAL Nat Med 17 (6), 708-714 (2011) PUBMED 21572428 REMARK GeneRIF: key factor in endocrine resistance in breast cancer REFERENCE 7 (bases 1 to 1100) AUTHORS Zhang PJ, Zhao J, Li HY, Man JH, He K, Zhou T, Pan X, Li AL, Gong WL, Jin BF, Xia Q, Yu M, Shen BF and Zhang XM. TITLE CUE domain containing 2 regulates degradation of progesterone receptor by ubiquitin-proteasome JOURNAL EMBO J 26 (7), 1831-1842 (2007) PUBMED 17347654 REMARK GeneRIF: These results identify a key post-translational mechanism that controls progesterone receptor protein levels and for the first time provide an important insight into the function of CUEDC2 in breast cancer proliferation. REFERENCE 8 (bases 1 to 1100) AUTHORS Grupe A, Li Y, Rowland C, Nowotny P, Hinrichs AL, Smemo S, Kauwe JS, Maxwell TJ, Cherny S, Doil L, Tacey K, van Luchene R, Myers A, Wavrant-De Vrieze F, Kaleem M, Hollingworth P, Jehu L, Foy C, Archer N, Hamilton G, Holmans P, Morris CM, Catanese J, Sninsky J, White TJ, Powell J, Hardy J, O'Donovan M, Lovestone S, Jones L, Morris JC, Thal L, Owen M, Williams J and Goate A. TITLE A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease JOURNAL Am J Hum Genet 78 (1), 78-88 (2006) PUBMED 16385451 REMARK GeneRIF: Observational study of gene-disease association. (HuGE Navigator) REFERENCE 9 (bases 1 to 1100) AUTHORS Oh JH, Yang JO, Hahn Y, Kim MR, Byun SS, Jeon YJ, Kim JM, Song KS, Noh SM, Kim S, Yoo HS, Kim YS and Kim NS. TITLE Transcriptome analysis of human gastric cancer JOURNAL Mamm Genome 16 (12), 942-954 (2005) PUBMED 16341674 REFERENCE 10 (bases 1 to 1100) AUTHORS Deloukas P, Earthrowl ME, Grafham DV, Rubenfield M, French L, Steward CA, Sims SK, Jones MC, Searle S, Scott C, Howe K, Hunt SE, Andrews TD, Gilbert JG, Swarbreck D, Ashurst JL, Taylor A, Battles J, Bird CP, Ainscough R, Almeida JP, Ashwell RI, Ambrose KD, Babbage AK, Bagguley CL, Bailey J, Banerjee R, Bates K, Beasley H, Bray-Allen S, Brown AJ, Brown JY, Burford DC, Burrill W, Burton J, Cahill P, Camire D, Carter NP, Chapman JC, Clark SY, Clarke G, Clee CM, Clegg S, Corby N, Coulson A, Dhami P, Dutta I, Dunn M, Faulkner L, Frankish A, Frankland JA, Garner P, Garnett J, Gribble S, Griffiths C, Grocock R, Gustafson E, Hammond S, Harley JL, Hart E, Heath PD, Ho TP, Hopkins B, Horne J, Howden PJ, Huckle E, Hynds C, Johnson C, Johnson D, Kana A, Kay M, Kimberley AM, Kershaw JK, Kokkinaki M, Laird GK, Lawlor S, Lee HM, Leongamornlert DA, Laird G, Lloyd C, Lloyd DM, Loveland J, Lovell J, McLaren S, McLay KE, McMurray A, Mashreghi-Mohammadi M, Matthews L, Milne S, Nickerson T, Nguyen M, Overton-Larty E, Palmer SA, Pearce AV, Peck AI, Pelan S, Phillimore B, Porter K, Rice CM, Rogosin A, Ross MT, Sarafidou T, Sehra HK, Shownkeen R, Skuce CD, Smith M, Standring L, Sycamore N, Tester J, Thorpe A, Torcasso W, Tracey A, Tromans A, Tsolas J, Wall M, Walsh J, Wang H, Weinstock K, West AP, Willey DL, Whitehead SL, Wilming L, Wray PW, Young L, Chen Y, Lovering RC, Moschonas NK, Siebert R, Fechtel K, Bentley D, Durbin R, Hubbard T, Doucette-Stamm L, Beck S, Smith DR and Rogers J. TITLE The DNA sequence and comparative analysis of human chromosome 10 JOURNAL Nature 429 (6990), 375-381 (2004) PUBMED 15164054 COMMENT VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from BC000262.1 and CX165866.1. On Nov 23, 2018 this sequence version replaced NM_024040.2. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## Transcript exon combination :: SRR1163655.50918.1, SRR1163655.367980.1 [ECO:0000332] RNAseq introns :: mixed sample support SAMEA1965299, SAMEA1966682 [ECO:0006172] ##Evidence-Data-END## ##RefSeq-Attributes-START## MANE Ensembl match :: ENST00000369937.5/ ENSP00000358953.4 RefSeq Select criteria :: based on single protein-coding transcript ##RefSeq-Attributes-END## COMPLETENESS: full length. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-737 BC000262.1 23-759 738-812 CX165866.1 714-788 813-1100 BC000262.1 835-1122 FEATURES Location/Qualifiers source 1..1100 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="10" /map="10q24.32" gene 1..1100 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /note="CUE domain containing 2" /db_xref="GeneID:79004" /db_xref="HGNC:HGNC:28352" /db_xref="MIM:614142" exon 1..49 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /inference="alignment:Splign:2.1.0" variation 1 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="g" /replace="t" /db_xref="dbSNP:945007780" variation 3 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:2061620609" variation 5 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1230695804" variation 7 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:1469014629" variation 8 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:573169242" variation 9 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="g" /db_xref="dbSNP:2061620571" variation 10 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="c" /db_xref="dbSNP:2061620562" variation 12 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:368222846" variation 13 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:2061620529" variation 15 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="g" /db_xref="dbSNP:2061620522" variation 16 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:2061620516" variation 17 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:1396252851" variation 18 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="g" /db_xref="dbSNP:2061620501" variation 19..22 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="gaca" /replace="gacagaca" /db_xref="dbSNP:2061620476" variation 19 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:1298169117" variation 21 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:1462932871" variation 22 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:1374909915" variation 23 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="c" /db_xref="dbSNP:1024072193" variation 24 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:1372567525" variation 26 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:2061620435" variation 28 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="c" /db_xref="dbSNP:2061620420" variation 30 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:554940634" variation 31 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:2061620389" variation 32 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1328207911" variation 33 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="g" /replace="t" /db_xref="dbSNP:1334085928" variation 34 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:2061620341" variation 40 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:1438748432" variation 42 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="c" /db_xref="dbSNP:921041855" variation 43 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:1370228228" exon 50..133 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /inference="alignment:Splign:2.1.0" variation 50 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:1284777445" variation 52 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="" /replace="g" /db_xref="dbSNP:2061591705" variation 52 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="g" /db_xref="dbSNP:11597439" variation 56 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="g" /db_xref="dbSNP:367656275" variation 59 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:1048603949" CDS 60..923 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /codon_start=1 /product="CUE domain-containing protein 2" /protein_id="NP_076945.2" /db_xref="CCDS:CCDS41566.1" /db_xref="GeneID:79004" /db_xref="HGNC:HGNC:28352" /db_xref="MIM:614142" /translation="
MELERIVSAALLAFVQTHLPEADLSGLDEVIFSYVLGVLEDLGPSGPSEENFDMEAFTEMMEAYVPGFAHIPRGTIGDMMQKLSGQLSDARNKENLQPQSSGVQGQVPISPEPLQRPEMLKEETRSSAAAAADTQDEATGAEEELLPGVDVLLEVFPTCSVEQAQWVLAKARGDLEEAVQMLVEGKEEGPAAWEGPNQDLPRRLRGPQKDELKSFILQKYMMVDSAEDQKIHRPMAPKEAPKKLIRYIDNQVVSTKGERFKDVRNPEAEEMKATYINLKPARKYRFH"
misc_feature 333..482 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /note="propagated from UniProtKB/Swiss-Prot (Q9H467.1); Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite" misc_feature 387..389 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /note="Phosphoserine. /evidence=ECO:0007744|PubMed:20068231; propagated from UniProtKB/Swiss-Prot (Q9H467.1); phosphorylation site" misc_feature 498..617 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /note="CUE domain found in CUE domain-containing protein 2 (CUED2) and similar proteins; Region: CUE_CUED2; cd14367" /db_xref="CDD:270550" variation 62 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:1329358405" variation 66 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:759596094" variation 72 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:776855352" variation 75 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="c" /db_xref="dbSNP:2061591619" variation 77 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:1433292132" variation 78 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:771132275" variation 82 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:2061591583" variation 83 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="g" /replace="t" /db_xref="dbSNP:2135471056" variation 84 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:1337608179" variation 85 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:1471019718" variation 86 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1400151284" variation 93 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:1565236954" variation 103 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:1171984613" variation 104 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="g" /db_xref="dbSNP:199727426" variation 111 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:1374658234" variation 113 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:772959797" variation 115 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="t" /db_xref="dbSNP:1589907223" variation 116 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:1448598112" variation 118 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:562865002" variation 119..120 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="g" /replace="gg" /db_xref="dbSNP:767805099" variation 119 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:200755540" variation 125 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:377444631" variation 126 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:532839181" variation 128 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="g" /db_xref="dbSNP:1589907211" variation 131 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="g" /db_xref="dbSNP:748773100" exon 134..277 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /inference="alignment:Splign:2.1.0" variation 136 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:556077135" variation 140 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:779358967" variation 142 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="t" /db_xref="dbSNP:2061589874" variation 144 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:1403337970" variation 146 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:1565236812" variation 147 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="g" /db_xref="dbSNP:1412678621" variation 148..152 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="tc" /replace="tcatc" /db_xref="dbSNP:1470915464" variation 149 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:2061589829" variation 150 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="c" /db_xref="dbSNP:1158754396" variation 155 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:755483104" variation 157 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:1379906944" variation 159 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:1308546068" variation 161 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="t" /db_xref="dbSNP:1177735968" variation 167 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:1180754911" variation 169 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="g" /replace="t" /db_xref="dbSNP:1009621265" variation 171 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:2061589725" variation 176 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:893461359" variation 182 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:753968673" variation 183 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:2061589694" variation 185 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:1255641563" variation 188..193 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="cccctc" /replace="cccctccccctc" /db_xref="dbSNP:899616329" variation 188 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:1270180230" variation 191 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:766470053" variation 193 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:201349133" variation 194 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:996594383" variation 204..209 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="gag" /replace="gaggag" /db_xref="dbSNP:1286551063" variation 204 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="g" /db_xref="dbSNP:917018551" variation 208 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:1224539667" variation 209 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1331387636" variation 212 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:1565236782" variation 215 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:750651141" variation 216 /gene="CUEDC2" /gene_synonym="bA18I14.5; 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C10orf66" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:543941583" variation 864 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:761445800" variation 867 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="g" /db_xref="dbSNP:774440274" variation 869 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:764106858" variation 871 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="g" /replace="t" /db_xref="dbSNP:762618761" variation 873 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:775108901" variation 878 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:1373415564" variation 881 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:532258513" variation 882 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="g" /replace="t" /db_xref="dbSNP:1451559593" variation 884 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:558596412" variation 887 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="c" /db_xref="dbSNP:2061582930" variation 891 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:1565236123" variation 900 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:2061582889" variation 904 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:1363106206" variation 908 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:962507618" variation 912 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:745555678" variation 913 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:776083598" variation 920 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:2061582817" variation 926 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:772500057" variation 928 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:1034172002" variation 929 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:1324569886" variation 930 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:148904455" variation 931 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:779466393" variation 933 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:755450757" variation 934 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:749421817" variation 935 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:780208468" variation 940 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:1234480325" variation 944 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="g" /db_xref="dbSNP:2061582674" variation 945 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1314295112" variation 946 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:756104194" variation 948 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:1301606234" variation 952 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:12558" variation 954 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:767573620" variation 958 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:1437556684" variation 964 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:1589905977" variation 969 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="c" /db_xref="dbSNP:1322667678" variation 970 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:2061582569" variation 971..975 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="g" /replace="ggatg" /db_xref="dbSNP:2061582547" variation 974 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:2061582559" variation 976 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:907165161" variation 978 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:1046356773" variation 979 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:1565236077" variation 981 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="g" /replace="t" /db_xref="dbSNP:1272620735" variation 983 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:538399204" variation 984 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:1487578844" variation 985 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="g" /replace="t" /db_xref="dbSNP:2061582456" variation 986 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:2061582441" variation 990 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:891558309" variation 996 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1262393952" variation 999 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:1427882259" variation 1005 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1589905940" variation 1009 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:2061582372" variation 1016 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:2061582360" variation 1018 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:1191178447" variation 1022 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:2061582341" variation 1027 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="g" /db_xref="dbSNP:2135469688" variation 1028 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:1589905933" variation 1029 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:2061582322" variation 1031 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="g" /replace="t" /db_xref="dbSNP:1196962234" variation 1033 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:2061582289" variation 1040 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:1437060774" variation 1044 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:1419776004" variation 1050..1051 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="aa" /replace="aaa" /db_xref="dbSNP:1475294910" variation 1053 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="g" /db_xref="dbSNP:540278954" variation 1057 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="t" /db_xref="dbSNP:1273492057" variation 1060 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:1197287270" variation 1061 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:1040746157" variation 1062 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:1454941941" variation 1064 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:2061582167" variation 1065 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:2061582159" variation 1074 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="t" /db_xref="dbSNP:892525670" variation 1079 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:2061582129" variation 1080 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="c" /replace="g" /db_xref="dbSNP:2061582110" regulatory 1081..1086 /regulatory_class="polyA_signal_sequence" /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /note="hexamer: AGTAAA" variation 1087 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:2061582100" variation 1088 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="g" /db_xref="dbSNP:1386247758" variation 1092 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="a" /replace="c" /db_xref="dbSNP:1382166592" variation 1097..1098 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /replace="g" /replace="gg" /db_xref="dbSNP:2061582061" polyA_site 1100 /gene="CUEDC2" /gene_synonym="bA18I14.5; C10orf66" /note="major polyA site" ORIGIN
gagagctgcaccgcgcgggacaagtcgccggcggcgcccgacggagcagaagagagagcatggagctggagaggatcgtcagtgcagccctccttgcctttgtccagacacacctcccggaggccgacctcagtggcttggatgaggtcatcttctcctatgtgcttggggtcctggaggacctgggcccctcgggcccatcagaggagaacttcgatatggaggctttcactgagatgatggaggcctatgtgcctggcttcgcccacatccccaggggcacaataggggacatgatgcagaagctctcagggcagctgagcgatgccaggaacaaagagaacctgcaaccgcagagctctggtgtccaaggtcaggtgcccatctccccagagcccctgcagcggcccgaaatgctcaaagaagagactaggtcttcggctgctgctgctgcagacacccaagatgaggcaactggcgctgaggaggagcttctgccaggggtggatgtactcctggaggtgttccctacctgttcggtggagcaggcccagtgggtgctggccaaagctcggggggacttggaagaagctgtgcagatgctggtagagggaaaggaagaggggcctgcagcctgggagggccccaaccaggacctgcccagacgcctcagaggcccccaaaaggatgagctgaagtccttcatcctgcagaagtacatgatggtggatagcgcagaggatcagaagattcaccggcccatggctcccaaggaggcccccaagaagctgatccgatacatcgacaaccaggtagtgagcaccaaaggggagcgattcaaagatgtgcggaaccctgaggccgaggagatgaaggccacatacatcaacctcaagccagccagaaagtaccgcttccattgaggcactcgccggactctgcccgagccttctaggctcagatcccagagggatgcaggagccctatacccctacacaggggccccctaactcctgtcccccttctctactcctttgctccatagtgttaacctactctcggagctgcctccatgggcacagtaaaggtggcccaaggaa
//
by
@meso_cacase at
DBCLS
This page is licensed under a
Creative Commons Attribution 4.0 International License (CC BY 4.0).
If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596.
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