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Previous release (v1)
2024-04-29 03:23:29, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NR_110882 624 bp RNA linear PRI 27-APR-2021
DEFINITION Homo sapiens ZNF652 antisense RNA 1 (ZNF652-AS1), transcript
variant 1, long non-coding RNA.
ACCESSION NR_110882 XR_424846 XR_429994 XR_433414
VERSION NR_110882.1
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 624)
AUTHORS Coviello AD, Haring R, Wellons M, Vaidya D, Lehtimaki T, Keildson
S, Lunetta KL, He C, Fornage M, Lagou V, Mangino M, Onland-Moret
NC, Chen B, Eriksson J, Garcia M, Liu YM, Koster A, Lohman K,
Lyytikainen LP, Petersen AK, Prescott J, Stolk L, Vandenput L, Wood
AR, Zhuang WV, Ruokonen A, Hartikainen AL, Pouta A, Bandinelli S,
Biffar R, Brabant G, Cox DG, Chen Y, Cummings S, Ferrucci L, Gunter
MJ, Hankinson SE, Martikainen H, Hofman A, Homuth G, Illig T,
Jansson JO, Johnson AD, Karasik D, Karlsson M, Kettunen J, Kiel DP,
Kraft P, Liu J, Ljunggren O, Lorentzon M, Maggio M, Markus MR,
Mellstrom D, Miljkovic I, Mirel D, Nelson S, Morin Papunen L,
Peeters PH, Prokopenko I, Raffel L, Reincke M, Reiner AP, Rexrode
K, Rivadeneira F, Schwartz SM, Siscovick D, Soranzo N, Stockl D,
Tworoger S, Uitterlinden AG, van Gils CH, Vasan RS, Wichmann HE,
Zhai G, Bhasin S, Bidlingmaier M, Chanock SJ, De Vivo I, Harris TB,
Hunter DJ, Kahonen M, Liu S, Ouyang P, Spector TD, van der Schouw
YT, Viikari J, Wallaschofski H, McCarthy MI, Frayling TM, Murray A,
Franks S, Jarvelin MR, de Jong FH, Raitakari O, Teumer A, Ohlsson
C, Murabito JM and Perry JR.
TITLE A genome-wide association meta-analysis of circulating sex
hormone-binding globulin reveals multiple Loci implicated in sex
steroid hormone regulation
JOURNAL PLoS Genet 8 (7), e1002805 (2012)
PUBMED 22829776
REFERENCE 2 (bases 1 to 624)
AUTHORS Haiman CA, Chen GK, Blot WJ, Strom SS, Berndt SI, Kittles RA,
Rybicki BA, Isaacs WB, Ingles SA, Stanford JL, Diver WR, Witte JS,
Hsing AW, Nemesure B, Rebbeck TR, Cooney KA, Xu J, Kibel AS, Hu JJ,
John EM, Gueye SM, Watya S, Signorello LB, Hayes RB, Wang Z, Yeboah
E, Tettey Y, Cai Q, Kolb S, Ostrander EA, Zeigler-Johnson C,
Yamamura Y, Neslund-Dudas C, Haslag-Minoff J, Wu W, Thomas V, Allen
GO, Murphy A, Chang BL, Zheng SL, Leske MC, Wu SY, Ray AM, Hennis
AJ, Thun MJ, Carpten J, Casey G, Carter EN, Duarte ER, Xia LY,
Sheng X, Wan P, Pooler LC, Cheng I, Monroe KR, Schumacher F, Le
Marchand L, Kolonel LN, Chanock SJ, Van Den Berg D, Stram DO and
Henderson BE.
TITLE Genome-wide association study of prostate cancer in men of African
ancestry identifies a susceptibility locus at 17q21
JOURNAL Nat Genet 43 (6), 570-573 (2011)
PUBMED 21602798
REFERENCE 3 (bases 1 to 624)
AUTHORS Newton-Cheh C, Johnson T, Gateva V, Tobin MD, Bochud M, Coin L,
Najjar SS, Zhao JH, Heath SC, Eyheramendy S, Papadakis K, Voight
BF, Scott LJ, Zhang F, Farrall M, Tanaka T, Wallace C, Chambers JC,
Khaw KT, Nilsson P, van der Harst P, Polidoro S, Grobbee DE,
Onland-Moret NC, Bots ML, Wain LV, Elliott KS, Teumer A, Luan J,
Lucas G, Kuusisto J, Burton PR, Hadley D, McArdle WL, Brown M,
Dominiczak A, Newhouse SJ, Samani NJ, Webster J, Zeggini E,
Beckmann JS, Bergmann S, Lim N, Song K, Vollenweider P, Waeber G,
Waterworth DM, Yuan X, Groop L, Orho-Melander M, Allione A, Di
Gregorio A, Guarrera S, Panico S, Ricceri F, Romanazzi V, Sacerdote
C, Vineis P, Barroso I, Sandhu MS, Luben RN, Crawford GJ,
Jousilahti P, Perola M, Boehnke M, Bonnycastle LL, Collins FS,
Jackson AU, Mohlke KL, Stringham HM, Valle TT, Willer CJ, Bergman
RN, Morken MA, Doring A, Gieger C, Illig T, Meitinger T, Org E,
Pfeufer A, Wichmann HE, Kathiresan S, Marrugat J, O'Donnell CJ,
Schwartz SM, Siscovick DS, Subirana I, Freimer NB, Hartikainen AL,
McCarthy MI, O'Reilly PF, Peltonen L, Pouta A, de Jong PE, Snieder
H, van Gilst WH, Clarke R, Goel A, Hamsten A, Peden JF, Seedorf U,
Syvanen AC, Tognoni G, Lakatta EG, Sanna S, Scheet P, Schlessinger
D, Scuteri A, Dorr M, Ernst F, Felix SB, Homuth G, Lorbeer R,
Reffelmann T, Rettig R, Volker U, Galan P, Gut IG, Hercberg S,
Lathrop GM, Zelenika D, Deloukas P, Soranzo N, Williams FM, Zhai G,
Salomaa V, Laakso M, Elosua R, Forouhi NG, Volzke H, Uiterwaal CS,
van der Schouw YT, Numans ME, Matullo G, Navis G, Berglund G,
Bingham SA, Kooner JS, Connell JM, Bandinelli S, Ferrucci L,
Watkins H, Spector TD, Tuomilehto J, Altshuler D, Strachan DP, Laan
M, Meneton P, Wareham NJ, Uda M, Jarvelin MR, Mooser V, Melander O,
Loos RJ, Elliott P, Abecasis GR, Caulfield M and Munroe PB.
CONSRTM Wellcome Trust Case Control Consortium
TITLE Genome-wide association study identifies eight loci associated with
blood pressure
JOURNAL Nat Genet 41 (6), 666-676 (2009)
PUBMED 19430483
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
DA167001.1 and DA017831.1.
On or before Mar 1, 2014 this sequence version replaced
XR_429994.1, XR_424846.1, XR_433414.1.
Transcript Variant: This variant (1) represents the longest
transcript.
##Evidence-Data-START##
Transcript exon combination :: DA167001.1, SRR1803617.263679.1
[ECO:0000332]
RNAseq introns :: single sample supports all introns
SAMEA1968968, SAMEA2151119
[ECO:0000348]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-558 DA167001.1 1-558
559-624 DA017831.1 480-545
FEATURES Location/Qualifiers
source 1..624
/organism="Homo sapiens"
/mol_type="transcribed RNA"
/db_xref="taxon:9606"
/chromosome="17"
/map="17q21.33"
gene 1..624
/gene="ZNF652-AS1"
/note="ZNF652 antisense RNA 1"
/db_xref="GeneID:102724596"
/db_xref="HGNC:HGNC:55582"
ncRNA 1..624
/ncRNA_class="lncRNA"
/gene="ZNF652-AS1"
/product="ZNF652 antisense RNA 1, transcript variant 1"
/db_xref="GeneID:102724596"
/db_xref="HGNC:HGNC:55582"
exon 1..136
/gene="ZNF652-AS1"
/inference="alignment:Splign:2.1.0"
variation 1
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2070411452"
variation 2
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2143177489"
variation 3
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:944776024"
variation 6..18
/gene="ZNF652-AS1"
/replace="c"
/replace="cagccctcgggcc"
/db_xref="dbSNP:2143177554"
variation 6
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070411516"
variation 7
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2070411556"
variation 8
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1036441970"
variation 9
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1259440625"
variation 10
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1179932163"
variation 11
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1598324876"
variation 12..15
/gene="ZNF652-AS1"
/replace="tcgg"
/replace="tcggtcgg"
/db_xref="dbSNP:2070411769"
variation 12
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:933270899"
variation 13
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2143177670"
variation 14
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070411793"
variation 15..22
/gene="ZNF652-AS1"
/replace="ggcc"
/replace="ggccggcc"
/db_xref="dbSNP:2070411849"
variation 15
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2070411823"
variation 16
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070411882"
variation 18
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2143177740"
variation 19
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070411914"
variation 20
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2070411948"
variation 21
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070411974"
variation 22
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070412003"
variation 23
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1238001164"
variation 24
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1212230150"
variation 25
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070412084"
variation 26
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070412116"
variation 27
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:897951960"
variation 28
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070412190"
variation 31
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1284018902"
variation 33
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070412257"
variation 34
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2044013985"
variation 38
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070412292"
variation 39
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070412326"
variation 41
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1354713736"
variation 42
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:930280767"
variation 44
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2143178095"
variation 47
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070412432"
variation 49
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1485279382"
variation 51
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070412510"
variation 52
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2070412549"
variation 53
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:994985970"
variation 55
/gene="ZNF652-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1027853435"
variation 57
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1303776891"
variation 58
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:894697045"
variation 59..70
/gene="ZNF652-AS1"
/replace="c"
/replace="cgctccgccgcc"
/db_xref="dbSNP:2070412728"
variation 60
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1013602786"
variation 61
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1359161864"
variation 64..99
/gene="ZNF652-AS1"
/replace="cgccgccc"
/replace="cgccgcccagataaccgccggctccccgcgccgccc"
/db_xref="dbSNP:1598324917"
variation 64
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:888627753"
variation 65
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1023260240"
variation 67
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:970806068"
variation 68
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:527988827"
variation 69..71
/gene="ZNF652-AS1"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1256685331"
variation 69
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:764236384"
variation 70
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:186057296"
variation 71
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070413232"
variation 72
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1030985727"
variation 73
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1262728013"
variation 74
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070413340"
variation 75
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1242958598"
variation 76..77
/gene="ZNF652-AS1"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2070413400"
variation 77
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2143178597"
variation 79
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:989247047"
variation 80
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070413449"
variation 81
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070413478"
variation 82
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1321345767"
variation 83
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070413512"
variation 84
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070413557"
variation 85
/gene="ZNF652-AS1"
/replace=""
/replace="c"
/db_xref="dbSNP:2070413591"
variation 86
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:915080569"
variation 87
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070413648"
variation 88..111
/gene="ZNF652-AS1"
/replace="ccc"
/replace="cccgcgccgcccccgccttctccc"
/db_xref="dbSNP:2143178731"
variation 88
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1598324955"
variation 90
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:891705837"
variation 92
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070413753"
variation 93
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1235472347"
variation 94
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070413816"
variation 97..101
/gene="ZNF652-AS1"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:2070413867"
variation 97
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070413841"
variation 101
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1598324965"
variation 102
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1598324970"
variation 105
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:953283507"
variation 106
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:986462411"
variation 110
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:911847895"
variation 111
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1298056138"
variation 113
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:944687518"
variation 115
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1415901428"
variation 117
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070414121"
variation 118
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2143178929"
variation 121
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070414146"
variation 126
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1036387705"
variation 127
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1010189476"
variation 129..130
/gene="ZNF652-AS1"
/replace=""
/replace="t"
/db_xref="dbSNP:34995208"
variation 130
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1021842946"
variation 132
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070414253"
variation 133
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1344492677"
variation 135
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:968583702"
variation 136
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1567705702"
exon 137..207
/gene="ZNF652-AS1"
/inference="alignment:Splign:2.1.0"
variation 137
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2143187474"
variation 140
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1279696726"
variation 142
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070431965"
variation 144
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1676505241"
variation 151
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070431985"
variation 152
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070432011"
variation 158
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1597809534"
variation 160
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070432054"
variation 161
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1211909554"
variation 163
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2070432093"
variation 168
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2070432119"
variation 173
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2070432137"
variation 174
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:62076449"
variation 175
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:751691029"
variation 176
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1035667021"
variation 180
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1374703565"
variation 183
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070432281"
variation 196
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070432302"
variation 197..198
/gene="ZNF652-AS1"
/replace="c"
/replace="cc"
/db_xref="dbSNP:2070432343"
variation 197
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070432326"
variation 200
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:956101436"
variation 201
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1281725470"
variation 202
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1010280011"
variation 206
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070432434"
exon 208..624
/gene="ZNF652-AS1"
/inference="alignment:Splign:2.1.0"
variation 212
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:905466009"
variation 215
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070440446"
variation 225
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:978219459"
variation 229
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1284462241"
variation 232
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070440518"
variation 236
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1205488458"
variation 237
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1343792582"
variation 238
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1336215255"
variation 243
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1232176024"
variation 250
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070440602"
variation 252
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2143190692"
variation 255
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070440615"
variation 258
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070440633"
variation 261
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070440652"
variation 265
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1331626200"
variation 266
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070440692"
variation 267
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070440709"
variation 270
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1303394561"
variation 272
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1001594035"
variation 273
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1348754881"
variation 277
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:957797532"
variation 279
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070440796"
variation 281
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070440811"
variation 282
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1033988919"
variation 294
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:974404808"
variation 300
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070440867"
variation 301
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:921633552"
variation 302
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:933519301"
variation 303
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:987758280"
variation 305
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070440939"
variation 308
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070440956"
variation 312
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1378566373"
variation 318
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:959758613"
variation 323
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:879703397"
variation 324
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1250454146"
variation 325..326
/gene="ZNF652-AS1"
/replace=""
/replace="a"
/db_xref="dbSNP:35862262"
variation 325
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070441104"
variation 328
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1182219509"
variation 329
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2070441148"
variation 331
/gene="ZNF652-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1597810001"
variation 333
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2143190894"
variation 334..336
/gene="ZNF652-AS1"
/replace="tgt"
/replace="tgtgt"
/db_xref="dbSNP:2070441184"
variation 339
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2143190905"
variation 349
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1257183509"
variation 350
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2143190922"
variation 355
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:908006715"
variation 360..362
/gene="ZNF652-AS1"
/replace=""
/replace="cca"
/db_xref="dbSNP:1197510371"
variation 362..363
/gene="ZNF652-AS1"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:2070441268"
variation 365
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1276373279"
variation 367
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1199516656"
variation 369
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1345534493"
variation 373
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1440813987"
variation 375
/gene="ZNF652-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2070441360"
variation 376
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1209479896"
variation 377
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070441402"
variation 386
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1013958666"
variation 390..398
/gene="ZNF652-AS1"
/replace="agagggctg"
/replace="agagggctgagagggctg"
/db_xref="dbSNP:2070441456"
variation 390
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070441443"
variation 394
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1258556996"
variation 395
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:940855518"
variation 398..399
/gene="ZNF652-AS1"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:2070441509"
variation 399
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070441529"
variation 400
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1287847648"
variation 405
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2143191021"
variation 409
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1410447647"
variation 416
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070441572"
variation 420
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070441589"
variation 424
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070441603"
variation 427
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1020039862"
variation 430
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1332515730"
variation 433
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070441645"
variation 435
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1191696486"
variation 441
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070441688"
variation 449
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1395634477"
variation 453
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070441709"
variation 454
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:967607281"
variation 456
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1478324545"
variation 458
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2143191129"
variation 459
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:755422394"
variation 463
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070441803"
variation 465
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1304907500"
variation 466
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1456141120"
variation 467
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:978643313"
variation 468
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070441871"
variation 471
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:899250740"
variation 473
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1159278090"
variation 474
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070441920"
variation 478
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2070441939"
variation 480
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1473321378"
variation 485
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415014465"
variation 490
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070441995"
variation 493
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1186450846"
variation 495
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:937459472"
variation 501..506
/gene="ZNF652-AS1"
/replace="gtc"
/replace="gtcgtc"
/db_xref="dbSNP:2070442045"
variation 503
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:9903556"
variation 504
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:530454855"
variation 520
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070442144"
variation 523
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1836749782"
variation 525
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:766612819"
variation 526..530
/gene="ZNF652-AS1"
/replace="tagtt"
/replace="tagttagtt"
/db_xref="dbSNP:2070442186"
variation 527
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1268753848"
variation 534
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1413456203"
variation 535
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070442245"
variation 536
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1597810054"
variation 540
/gene="ZNF652-AS1"
/replace=""
/replace="c"
/db_xref="dbSNP:2070442304"
variation 540
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2070442286"
variation 541..544
/gene="ZNF652-AS1"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:2070442334"
variation 541
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2070442318"
variation 546
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2143191377"
variation 553
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070442349"
variation 557
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2070442366"
variation 559
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1230144193"
variation 560
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1334228746"
variation 565
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070442412"
variation 566..567
/gene="ZNF652-AS1"
/replace=""
/replace="tg"
/db_xref="dbSNP:2070442432"
variation 567
/gene="ZNF652-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2070442442"
variation 573
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070442454"
variation 575
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1282475193"
variation 576
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1244359600"
variation 579
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070442485"
variation 581
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:975390511"
variation 583..596
/gene="ZNF652-AS1"
/replace="tttt"
/replace="ttttttcttttttt"
/db_xref="dbSNP:2070442561"
variation 583
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070442541"
variation 589
/gene="ZNF652-AS1"
/replace=""
/replace="c"
/db_xref="dbSNP:2070442596"
variation 589
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070442584"
variation 590..596
/gene="ZNF652-AS1"
/replace="tttttt"
/replace="ttttttt"
/replace="tttttttt"
/db_xref="dbSNP:1024907772"
variation 595
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:550550265"
variation 596
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:77101414"
variation 597
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2070442678"
variation 598
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070442693"
variation 599..600
/gene="ZNF652-AS1"
/replace=""
/replace="ttttt"
/db_xref="dbSNP:76269324"
variation 599
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:539705846"
variation 600..602
/gene="ZNF652-AS1"
/replace="gtt"
/replace="gttgtt"
/replace="gttgtttttgtt"
/db_xref="dbSNP:2070442757"
variation 600
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1459258844"
variation 602..603
/gene="ZNF652-AS1"
/replace=""
/replace="g"
/db_xref="dbSNP:2070442782"
variation 603
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:79645723"
variation 604..606
/gene="ZNF652-AS1"
/replace="ttg"
/replace="ttgctgttg"
/db_xref="dbSNP:2143191600"
variation 604
/gene="ZNF652-AS1"
/replace="t"
/replace="tgt"
/replace="tgttgt"
/db_xref="dbSNP:2070442820"
variation 605..609
/gene="ZNF652-AS1"
/replace="tgttg"
/replace="tgttgctgttg"
/db_xref="dbSNP:1467045457"
variation 606
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2070442930"
variation 607..611
/gene="ZNF652-AS1"
/replace="ttgtt"
/replace="ttgttttgtt"
/db_xref="dbSNP:2143191657"
variation 607
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:879034747"
variation 611..615
/gene="ZNF652-AS1"
/replace="tgttg"
/replace="tgttgctgttg"
/db_xref="dbSNP:1287850207"
variation 613..617
/gene="ZNF652-AS1"
/replace="ttgtt"
/replace="ttgttattgtt"
/db_xref="dbSNP:1340933321"
variation 616..620
/gene="ZNF652-AS1"
/replace="ttgtt"
/replace="ttgtttttgtt"
/db_xref="dbSNP:2070442970"
variation 618..624
/gene="ZNF652-AS1"
/replace=""
/replace="gttgttg"
/db_xref="dbSNP:2070443004"
variation 618
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070442991"
variation 619..623
/gene="ZNF652-AS1"
/replace="ttgtt"
/replace="ttgttattgtt"
/db_xref="dbSNP:2070443016"
variation 621..624
/gene="ZNF652-AS1"
/replace=""
/replace="gttg"
/db_xref="dbSNP:1357336412"
variation 621
/gene="ZNF652-AS1"
/replace=""
/replace="g"
/db_xref="dbSNP:1229298248"
variation 622
/gene="ZNF652-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2070443055"
variation 624
/gene="ZNF652-AS1"
/replace=""
/replace="g"
/db_xref="dbSNP:374051404"
variation 624
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:144621505"
ORIGIN
atgcgcagccctcgggccggcccgggcgcaccttttctgtctcctgccacattgtgagcgctccgccgcccagataaccgccggctccccgcgccgcccccgccttctcccactccgcccactgccgggagcccaggggatgatgcagcaagaagacccacaccagatgagggcgccttgatattggatttcccagcctccagaactaagcctgggacttgcctctgtgatctggtgctttggagggccttgggcctcagggctagcaaggtccctttctggagattccagttcctctgcccgccctcctttacctctttctcctcacacatctgtctgagggatggggatgagggctgccaaccaatgttaccacttgacagaccacaagagggctggttccagtgcctcccttgttcagctgctgacactgcagcttggcagtcattgaaggcaatatttagctcctacatctgacctgattggaagatcaggcttctgtcgtcctggtttcctggccttggatagttcttcactaacttttattcattaaggcagtgggcagaaagcagcagaaccctgttttttctttttttggggtttttgttgttgttgttgttgttg
//
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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