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Previous release (v1)
2024-04-30 12:26:56, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_001401361 1108 bp mRNA linear PRI 22-MAR-2023
DEFINITION Homo sapiens ADP ribosylation factor like GTPase 9 (ARL9),
transcript variant 7, mRNA.
ACCESSION NM_001401361
VERSION NM_001401361.1
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 1108)
AUTHORS Yang HD, Jin XX, Gu BB, Yu-Zhang, Li D and Yan LL.
TITLE ARL9 is upregulated and serves as a biomarker for a poor prognosis
in colon adenocarcinoma
JOURNAL BMC Gastroenterol 23 (1), 48 (2023)
PUBMED 36823542
REMARK GeneRIF: ARL9 is upregulated and serves as a biomarker for a poor
prognosis in colon adenocarcinoma.
Publication Status: Online-Only
REFERENCE 2 (bases 1 to 1108)
AUTHORS Tan Y, Zhang S, Xiao Q, Wang J, Zhao K, Liu W, Huang K, Tian W, Niu
H, Lei T and Shu K.
TITLE Prognostic significance of ARL9 and its methylation in low-grade
glioma
JOURNAL Genomics 112 (6), 4808-4816 (2020)
PUBMED 32882327
REMARK GeneRIF: Prognostic significance of ARL9 and its methylation in
low-grade glioma.
REFERENCE 3 (bases 1 to 1108)
AUTHORS Louro R, Nakaya HI, Paquola AC, Martins EA, da Silva AM,
Verjovski-Almeida S and Reis EM.
TITLE RASL11A, member of a novel small monomeric GTPase gene family, is
down-regulated in prostate tumors
JOURNAL Biochem Biophys Res Commun 316 (3), 618-627 (2004)
PUBMED 15033445
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
AC114766.5 and AC108215.4.
Summary: ARL9 is a member of the small GTPase protein family with a
high degree of similarity to ARF (MIM 103180) proteins of the RAS
superfamily.[supplied by OMIM, Nov 2008].
Sequence Note: The RefSeq transcript and protein were derived from
genomic sequence to make the sequence consistent with the reference
genome assembly. The genomic coordinates used for the transcript
record were based on alignments.
##Evidence-Data-START##
RNAseq introns :: single sample supports all introns SAMEA2146982,
SAMEA2154665 [ECO:0000348]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-351 AC114766.5 63763-64113
352-1108 AC108215.4 5789-6545
FEATURES Location/Qualifiers
source 1..1108
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="4"
/map="4q12"
gene 1..1108
/gene="ARL9"
/note="ADP ribosylation factor like GTPase 9"
/db_xref="GeneID:132946"
/db_xref="HGNC:HGNC:23592"
/db_xref="MIM:612405"
exon 1..351
/gene="ARL9"
/inference="alignment:Splign:2.1.0"
variation 8
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:911969770"
variation 10..15
/gene="ARL9"
/replace="gcccag"
/replace="gcccagcccag"
/db_xref="dbSNP:1199109255"
variation 11
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1453017266"
variation 13
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1721439016"
variation 14
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1255797984"
variation 17
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1560694351"
variation 18
/gene="ARL9"
/replace="c"
/replace="g"
/db_xref="dbSNP:1721439227"
variation 22
/gene="ARL9"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:766937966"
variation 25
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1039424949"
variation 28..43
/gene="ARL9"
/replace="gcacgcgggcacgcgg"
/replace="gcacgcgggcacgcgggcacgcgg"
/db_xref="dbSNP:2110139004"
variation 31
/gene="ARL9"
/replace="a"
/replace="c"
/db_xref="dbSNP:1217473240"
variation 32
/gene="ARL9"
/replace="c"
/replace="g"
/db_xref="dbSNP:1366614494"
variation 35
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1239995489"
variation 39
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:904788471"
variation 40
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:972941526"
variation 41
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1025809735"
variation 42
/gene="ARL9"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1334154170"
variation 43
/gene="ARL9"
/replace="g"
/replace="t"
/db_xref="dbSNP:1330945004"
variation 44
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1466141662"
variation 45
/gene="ARL9"
/replace="g"
/replace="t"
/db_xref="dbSNP:2110139040"
variation 48
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1402629190"
variation 49
/gene="ARL9"
/replace="c"
/replace="g"
/db_xref="dbSNP:952904923"
variation 52
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1442511548"
variation 59
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1578204986"
variation 60
/gene="ARL9"
/replace="c"
/replace="g"
/db_xref="dbSNP:1414452388"
variation 65
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:984663725"
variation 66
/gene="ARL9"
/replace="g"
/replace="t"
/db_xref="dbSNP:1473053015"
variation 70
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1578204999"
variation 72
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1426276269"
CDS 73..531
/gene="ARL9"
/note="isoform 6 is encoded by transcript variant 7;
ADP-ribosylation factor-like protein 9; ADP-ribosylation
factor-like 9"
/codon_start=1
/product="ADP-ribosylation factor-like protein 9 isoform
6"
/protein_id="NP_001388290.1"
/db_xref="GeneID:132946"
/db_xref="HGNC:HGNC:23592"
/db_xref="MIM:612405"
/translation="
MERGKVKKKEKEKETQEEKIGEKGREEKVKRKEVEQKIKQKQEKQERRKGKEKEEKRTKQGKETNKEKEQFKGQEEKGENKDSTLTRTPLEPLDLEAAYHITDIHEALALSEVGNDRKMFLFGTYLTKNGSEIPSTMQDAKDLIAQLAADVQ"
misc_feature <352..522
/gene="ARL9"
/note="P-loop containing Nucleoside Triphosphate
Hydrolases; Region: P-loop_NTPase; cl38936"
/db_xref="CDD:453896"
misc_feature 445..453
/gene="ARL9"
/note="G5 box; other site"
/db_xref="CDD:206648"
variation 74
/gene="ARL9"
/replace="a"
/replace="t"
/db_xref="dbSNP:1578205005"
variation 75..96
/gene="ARL9"
/replace="ggagagggggaaagtgaagaag"
/replace="ggagagggggaaagtgaagaagggagagggggaaagtgaagaag"
/db_xref="dbSNP:1721440779"
variation 75
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:2110139067"
variation 76
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:752209750"
variation 80
/gene="ARL9"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:375726523"
variation 84
/gene="ARL9"
/replace="g"
/replace="t"
/db_xref="dbSNP:1721441038"
variation 85..87
/gene="ARL9"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1235918359"
variation 85
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1578205013"
variation 89
/gene="ARL9"
/replace="g"
/replace="t"
/db_xref="dbSNP:1721441256"
variation 90..98
/gene="ARL9"
/replace="gaagaa"
/replace="gaagaagaa"
/db_xref="dbSNP:562013756"
variation 90
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1721441339"
variation 94..101
/gene="ARL9"
/replace="aaga"
/replace="aagaaaga"
/db_xref="dbSNP:1167885461"
variation 95
/gene="ARL9"
/replace="a"
/replace="c"
/db_xref="dbSNP:867667355"
variation 96
/gene="ARL9"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1465711878"
variation 98..105
/gene="ARL9"
/replace="aag"
/replace="aagagaag"
/db_xref="dbSNP:1279271465"
variation 99..103
/gene="ARL9"
/replace="aga"
/replace="agaga"
/db_xref="dbSNP:760881473"
variation 101
/gene="ARL9"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1578205031"
variation 106
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1333930590"
variation 107..110
/gene="ARL9"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:1351235676"
variation 109
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1308793124"
variation 111
/gene="ARL9"
/replace="c"
/replace="g"
/db_xref="dbSNP:892004187"
variation 114
/gene="ARL9"
/replace="g"
/replace="t"
/db_xref="dbSNP:551711540"
variation 115
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1301213028"
variation 116
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1452371236"
variation 119..126
/gene="ARL9"
/replace="ag"
/replace="aggag"
/replace="aggaggag"
/db_xref="dbSNP:1360205274"
variation 121
/gene="ARL9"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:6841856"
variation 123..140
/gene="ARL9"
/replace="ggagaaaa"
/replace="ggagaaaatcggagaaaa"
/db_xref="dbSNP:1721443876"
variation 123
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1721443786"
variation 129..132
/gene="ARL9"
/replace=""
/replace="aatc"
/db_xref="dbSNP:1721443963"
variation 130
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1721444067"
variation 133
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:2110139159"
variation 142
/gene="ARL9"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:113886246"
variation 144
/gene="ARL9"
/replace="g"
/replace="t"
/db_xref="dbSNP:1721444404"
variation 147
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1721444502"
variation 151
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:150294934"
variation 153
/gene="ARL9"
/replace="c"
/replace="g"
/db_xref="dbSNP:1016982086"
variation 154..156
/gene="ARL9"
/replace="a"
/replace="aaa"
/db_xref="dbSNP:1721444917"
variation 156
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:2110139178"
variation 157
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:962664176"
variation 158
/gene="ARL9"
/replace="g"
/replace="t"
/db_xref="dbSNP:572144198"
variation 159
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1308128133"
variation 160..163
/gene="ARL9"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:1721445471"
variation 160
/gene="ARL9"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1179559735"
variation 161..168
/gene="ARL9"
/replace="aaag"
/replace="aaagaaag"
/db_xref="dbSNP:568667239"
variation 163
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:2110139193"
variation 164
/gene="ARL9"
/replace=""
/replace="g"
/db_xref="dbSNP:764062588"
variation 166..170
/gene="ARL9"
/replace="a"
/replace="aagga"
/db_xref="dbSNP:1721445704"
variation 167..172
/gene="ARL9"
/replace="agg"
/replace="aggagg"
/db_xref="dbSNP:1259909058"
variation 169
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1487177065"
variation 171
/gene="ARL9"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1578205110"
variation 172
/gene="ARL9"
/replace="g"
/replace="t"
/db_xref="dbSNP:1721446021"
variation 178
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1459971002"
variation 179
/gene="ARL9"
/replace=""
/replace="a"
/db_xref="dbSNP:1721446178"
variation 182
/gene="ARL9"
/replace="a"
/replace="t"
/db_xref="dbSNP:1578205115"
variation 186..189
/gene="ARL9"
/replace=""
/replace="taaa"
/db_xref="dbSNP:761870782"
variation 186..187
/gene="ARL9"
/replace=""
/replace="ta"
/db_xref="dbSNP:753023397"
variation 187..193
/gene="ARL9"
/replace="aaa"
/replace="aaacaaa"
/replace="aaacaaacaaa"
/db_xref="dbSNP:200616211"
variation 187..189
/gene="ARL9"
/replace="aa"
/replace="aaa"
/replace="aaaaaa"
/db_xref="dbSNP:1560694446"
variation 190
/gene="ARL9"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:112278450"
variation 191..192
/gene="ARL9"
/replace="aa"
/replace="aagaa"
/db_xref="dbSNP:59024435"
variation 193..199
/gene="ARL9"
/replace="aag"
/replace="aagcaag"
/db_xref="dbSNP:1721447003"
variation 193
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:113001363"
variation 194..195
/gene="ARL9"
/replace="ag"
/replace="agag"
/db_xref="dbSNP:1227757982"
variation 196
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1721447142"
variation 207
/gene="ARL9"
/replace="c"
/replace="g"
/db_xref="dbSNP:1484130958"
variation 208
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1379990571"
variation 210
/gene="ARL9"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1578205157"
variation 211..224
/gene="ARL9"
/replace="a"
/replace="aggagaaagggaaa"
/db_xref="dbSNP:1305107797"
variation 212
/gene="ARL9"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1578205160"
variation 213
/gene="ARL9"
/replace="g"
/replace="t"
/db_xref="dbSNP:1398761100"
variation 222..225
/gene="ARL9"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:1721447661"
variation 226
/gene="ARL9"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:567510312"
variation 227..233
/gene="ARL9"
/replace="aga"
/replace="agaaaga"
/db_xref="dbSNP:1299142939"
variation 229..244
/gene="ARL9"
/replace="aaagaggaaaagagga"
/replace="aaagaggaaaagaggaaaagagga"
/db_xref="dbSNP:1721448347"
variation 229..231
/gene="ARL9"
/replace="a"
/replace="aaa"
/db_xref="dbSNP:986615200"
variation 229
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1346539265"
variation 231..234
/gene="ARL9"
/replace="ag"
/replace="agag"
/db_xref="dbSNP:1162258901"
variation 231
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1721448504"
variation 232..235
/gene="ARL9"
/replace="gagg"
/replace="gagggagg"
/db_xref="dbSNP:2110139292"
variation 232
/gene="ARL9"
/replace=""
/replace="g"
/db_xref="dbSNP:1721448840"
variation 234..235
/gene="ARL9"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1422720729"
variation 234
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:904955417"
variation 235
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1183500050"
variation 239..242
/gene="ARL9"
/replace="ag"
/replace="agag"
/db_xref="dbSNP:1721449234"
variation 240..244
/gene="ARL9"
/replace="ga"
/replace="gagga"
/replace="gaggagga"
/db_xref="dbSNP:151023416"
variation 240
/gene="ARL9"
/replace="c"
/replace="g"
/db_xref="dbSNP:1003234988"
variation 241
/gene="ARL9"
/replace="a"
/replace="c"
/db_xref="dbSNP:1034672187"
variation 242
/gene="ARL9"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:112010666"
variation 246
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:535987208"
variation 253
/gene="ARL9"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:113810069"
variation 255..258
/gene="ARL9"
/replace="g"
/replace="gaag"
/db_xref="dbSNP:1469675482"
variation 255
/gene="ARL9"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1721450020"
variation 256
/gene="ARL9"
/replace="a"
/replace="acaaacaacaaacaa"
/db_xref="dbSNP:1263836146"
variation 258
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1221199792"
variation 259
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1721450492"
variation 262..270
/gene="ARL9"
/replace="acaaa"
/replace="acaaacaaa"
/db_xref="dbSNP:368342138"
variation 264..270
/gene="ARL9"
/replace="a"
/replace="aaacaaa"
/db_xref="dbSNP:1361210260"
variation 265
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:74665438"
variation 266
/gene="ARL9"
/replace="a"
/replace="t"
/db_xref="dbSNP:1721450963"
variation 268..272
/gene="ARL9"
/replace="a"
/replace="aaaga"
/db_xref="dbSNP:1053813904"
variation 268..270
/gene="ARL9"
/replace="a"
/replace="aaa"
/db_xref="dbSNP:150827751"
variation 268
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1279404223"
variation 269
/gene="ARL9"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1578205243"
variation 271
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1402164211"
variation 277
/gene="ARL9"
/replace="c"
/replace="g"
/db_xref="dbSNP:1721451467"
variation 287
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:6824893"
variation 293..299
/gene="ARL9"
/replace="aaga"
/replace="aagaaga"
/db_xref="dbSNP:2110139381"
variation 295
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1291413645"
variation 297
/gene="ARL9"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:558500943"
variation 298
/gene="ARL9"
/replace="c"
/replace="g"
/db_xref="dbSNP:1457135068"
variation 301..303
/gene="ARL9"
/replace="a"
/replace="aaa"
/db_xref="dbSNP:1721451883"
variation 304
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1721451959"
variation 306
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1005738951"
variation 307
/gene="ARL9"
/replace="c"
/replace="g"
/db_xref="dbSNP:1018843222"
variation 309
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1166419685"
variation 311
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1721452355"
variation 312
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1463629085"
variation 314
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1422766265"
variation 315
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1721452543"
variation 316
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1401908690"
variation 318
/gene="ARL9"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1478677962"
variation 319
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1721452896"
variation 320
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1721452969"
variation 321
/gene="ARL9"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1265076612"
variation 324
/gene="ARL9"
/replace="c"
/replace="g"
/db_xref="dbSNP:575640725"
variation 326
/gene="ARL9"
/replace="g"
/replace="t"
/db_xref="dbSNP:964182689"
variation 327
/gene="ARL9"
/replace="c"
/replace="g"
/db_xref="dbSNP:976828393"
variation 332
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:2110139447"
variation 335
/gene="ARL9"
/replace="a"
/replace="c"
/db_xref="dbSNP:1721453337"
variation 336
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:548593924"
variation 338
/gene="ARL9"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1218534710"
variation 339
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:905632665"
variation 342
/gene="ARL9"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1259256984"
variation 346..347
/gene="ARL9"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1721453817"
variation 346
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1721453739"
exon 352..1108
/gene="ARL9"
/inference="alignment:Splign:2.1.0"
variation 354
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1280099745"
variation 355
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:779105544"
variation 358
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1385756422"
variation 359..360
/gene="ARL9"
/replace=""
/replace="tccgg"
/db_xref="dbSNP:1400403414"
variation 360..361
/gene="ARL9"
/replace=""
/replace="t"
/db_xref="dbSNP:1316461472"
variation 360
/gene="ARL9"
/replace="a"
/replace="t"
/db_xref="dbSNP:1030702659"
variation 361
/gene="ARL9"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:960385280"
variation 362
/gene="ARL9"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1408524870"
variation 363
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:992504048"
variation 364..365
/gene="ARL9"
/replace=""
/replace="atgaaggata"
/replace="gata"
/db_xref="dbSNP:1453135082"
variation 365
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1314035658"
variation 370
/gene="ARL9"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:192409324"
variation 371
/gene="ARL9"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1241097593"
variation 372
/gene="ARL9"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:772424781"
variation 376
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:773668030"
variation 380
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:185554089"
variation 383
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:771468801"
variation 384
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:539572636"
variation 386
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:201809806"
variation 394
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1046537853"
variation 396
/gene="ARL9"
/replace="c"
/replace="g"
/db_xref="dbSNP:909049292"
variation 403
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1430370201"
variation 411
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:552400289"
variation 412
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1721998651"
variation 416
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1193093231"
variation 417
/gene="ARL9"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1455055191"
variation 421
/gene="ARL9"
/replace="a"
/replace="c"
/db_xref="dbSNP:940732567"
variation 422
/gene="ARL9"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:371408202"
variation 424
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:375064985"
variation 425
/gene="ARL9"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:201807967"
variation 426
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1469722621"
variation 427
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:367820708"
variation 434
/gene="ARL9"
/replace="g"
/replace="t"
/db_xref="dbSNP:2110158592"
variation 437
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1275843312"
variation 440
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1051789984"
variation 443
/gene="ARL9"
/replace="c"
/replace="g"
/db_xref="dbSNP:994716901"
variation 444
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:757024205"
variation 445
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1722000189"
variation 448..453
/gene="ARL9"
/replace="ct"
/replace="ctgact"
/db_xref="dbSNP:746797315"
variation 449
/gene="ARL9"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:767411788"
variation 451
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1722000611"
variation 452
/gene="ARL9"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:190431762"
variation 454
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1722000792"
variation 462
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:750314548"
variation 465
/gene="ARL9"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1444307970"
variation 466
/gene="ARL9"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1560701010"
variation 467
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1393118945"
variation 468
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1722001368"
variation 472
/gene="ARL9"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1329423411"
variation 474
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:756089755"
variation 476..477
/gene="ARL9"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:34211533"
variation 476
/gene="ARL9"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1236278692"
variation 477
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1722001786"
variation 478
/gene="ARL9"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1722001988"
variation 478
/gene="ARL9"
/replace="a"
/replace="c"
/db_xref="dbSNP:1050270465"
variation 481
/gene="ARL9"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1284574801"
variation 483
/gene="ARL9"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:534989111"
variation 485
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1722002412"
variation 492
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1722002519"
variation 493
/gene="ARL9"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1323807725"
variation 499
/gene="ARL9"
/replace="g"
/replace="t"
/db_xref="dbSNP:778790148"
variation 501
/gene="ARL9"
/replace="g"
/replace="t"
/db_xref="dbSNP:1262972795"
variation 503
/gene="ARL9"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:752852658"
variation 507
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1198119455"
variation 508
/gene="ARL9"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:758642714"
variation 509
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:888967521"
variation 511
/gene="ARL9"
/replace="c"
/replace="g"
/db_xref="dbSNP:1722003533"
variation 515
/gene="ARL9"
/replace="a"
/replace="c"
/db_xref="dbSNP:778114642"
variation 519
/gene="ARL9"
/replace="a"
/replace="c"
/db_xref="dbSNP:747270340"
variation 520
/gene="ARL9"
/replace="g"
/replace="t"
/db_xref="dbSNP:771421840"
variation 529
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1722003938"
variation 531
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1397424807"
variation 534..535
/gene="ARL9"
/replace=""
/replace="ctgtgcggctcacgactgat"
/db_xref="dbSNP:1180115239"
variation 536
/gene="ARL9"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:781665242"
variation 537
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:768272130"
variation 538
/gene="ARL9"
/replace=""
/replace="c"
/db_xref="dbSNP:1419017603"
variation 538
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1175951849"
variation 539
/gene="ARL9"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:770340214"
variation 540
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:2110158840"
variation 545..547
/gene="ARL9"
/replace="c"
/replace="cac"
/db_xref="dbSNP:1179350238"
variation 546
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1722004774"
variation 548
/gene="ARL9"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:774824321"
variation 549..550
/gene="ARL9"
/replace=""
/replace="gtc"
/db_xref="dbSNP:1722005155"
variation 549
/gene="ARL9"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1722005034"
variation 550..551
/gene="ARL9"
/replace=""
/replace="ca"
/db_xref="dbSNP:1722005390"
variation 550
/gene="ARL9"
/replace="a"
/replace="t"
/db_xref="dbSNP:1722005271"
variation 552
/gene="ARL9"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:537875607"
variation 553
/gene="ARL9"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:181851273"
variation 557
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:2110158878"
variation 558
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1560701125"
variation 559
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:773988126"
variation 560
/gene="ARL9"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:373601518"
variation 562
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:750236269"
variation 563
/gene="ARL9"
/replace="g"
/replace="t"
/db_xref="dbSNP:760487412"
variation 565
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1404003973"
variation 572
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:766360815"
variation 575
/gene="ARL9"
/replace="a"
/replace="c"
/db_xref="dbSNP:368044929"
variation 578
/gene="ARL9"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1230090740"
variation 581
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1252183397"
variation 586
/gene="ARL9"
/replace="g"
/replace="t"
/db_xref="dbSNP:1316278890"
variation 591
/gene="ARL9"
/replace="a"
/replace="c"
/db_xref="dbSNP:1722007445"
variation 592
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1722007564"
variation 594
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:751818590"
variation 598
/gene="ARL9"
/replace="a"
/replace="c"
/db_xref="dbSNP:1449029856"
variation 603
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:554456785"
variation 605
/gene="ARL9"
/replace="g"
/replace="t"
/db_xref="dbSNP:1578217696"
variation 610
/gene="ARL9"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:577371326"
regulatory 616..621
/regulatory_class="polyA_signal_sequence"
/gene="ARL9"
/note="hexamer: AATAAA"
variation 616
/gene="ARL9"
/replace="a"
/replace="c"
/db_xref="dbSNP:1722008380"
variation 622
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1722008493"
variation 625
/gene="ARL9"
/replace="g"
/replace="t"
/db_xref="dbSNP:1560701192"
variation 628
/gene="ARL9"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:571501795"
variation 629
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:2110158981"
variation 636
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1722008971"
polyA_site 638
/gene="ARL9"
/note="major polyA site"
variation 639
/gene="ARL9"
/replace="g"
/replace="t"
/db_xref="dbSNP:1722009102"
variation 645
/gene="ARL9"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:969569863"
variation 656
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1290320489"
variation 657
/gene="ARL9"
/replace="g"
/replace="t"
/db_xref="dbSNP:984666390"
variation 661
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1722009591"
variation 663
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:982264788"
variation 665
/gene="ARL9"
/replace="c"
/replace="g"
/db_xref="dbSNP:928106437"
variation 674
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1722009953"
variation 676
/gene="ARL9"
/replace="a"
/replace="c"
/db_xref="dbSNP:1722010087"
variation 677
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1364900425"
variation 680
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1722010295"
variation 681..694
/gene="ARL9"
/replace="cat"
/replace="catgggttccacat"
/db_xref="dbSNP:1722010406"
variation 682
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1722010529"
variation 684..686
/gene="ARL9"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1161702703"
variation 685
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:556004586"
variation 686
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415206961"
variation 687
/gene="ARL9"
/replace="g"
/replace="t"
/db_xref="dbSNP:1036410142"
variation 688
/gene="ARL9"
/replace="g"
/replace="t"
/db_xref="dbSNP:1722011098"
variation 689
/gene="ARL9"
/replace="a"
/replace="c"
/db_xref="dbSNP:1560701245"
variation 690
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1722011285"
variation 700
/gene="ARL9"
/replace="g"
/replace="t"
/db_xref="dbSNP:111411599"
variation 708
/gene="ARL9"
/replace="a"
/replace="t"
/db_xref="dbSNP:1722011454"
variation 711
/gene="ARL9"
/replace="a"
/replace="t"
/db_xref="dbSNP:1485802430"
variation 715
/gene="ARL9"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1722011583"
variation 719
/gene="ARL9"
/replace="a"
/replace="c"
/db_xref="dbSNP:2110159067"
variation 729..733
/gene="ARL9"
/replace="aaaaa"
/replace="aaaaaa"
/db_xref="dbSNP:1722011658"
variation 733
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:972803035"
variation 738
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:371720343"
variation 739
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:541457441"
variation 740
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:930621965"
variation 757
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1050326887"
variation 759
/gene="ARL9"
/replace="c"
/replace="g"
/db_xref="dbSNP:1261294841"
variation 761
/gene="ARL9"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1240908793"
variation 770
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1292458417"
variation 771
/gene="ARL9"
/replace=""
/replace="t"
/db_xref="dbSNP:2110159101"
regulatory 772..777
/regulatory_class="polyA_signal_sequence"
/gene="ARL9"
/note="hexamer: AATACA"
variation 773
/gene="ARL9"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1179935749"
variation 776
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1722012295"
variation 778
/gene="ARL9"
/replace="c"
/replace="g"
/db_xref="dbSNP:1722012341"
variation 780
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1722012420"
variation 783
/gene="ARL9"
/replace="a"
/replace="t"
/db_xref="dbSNP:1722012477"
variation 786
/gene="ARL9"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:933985526"
variation 790
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:561337454"
polyA_site 792
/gene="ARL9"
variation 793
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1051142235"
variation 794
/gene="ARL9"
/replace="a"
/replace="t"
/db_xref="dbSNP:1553950746"
variation 795
/gene="ARL9"
/replace=""
/replace="t"
/db_xref="dbSNP:1381769563"
variation 796
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1386275966"
variation 799..800
/gene="ARL9"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1722012994"
variation 801
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1722013115"
variation 802
/gene="ARL9"
/replace="a"
/replace="t"
/db_xref="dbSNP:1291215083"
variation 807
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1578217803"
variation 809
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:184474793"
variation 810
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:942993381"
variation 812
/gene="ARL9"
/replace="c"
/replace="g"
/db_xref="dbSNP:1008718268"
variation 822
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1722013804"
variation 828
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1722013910"
variation 830
/gene="ARL9"
/replace="g"
/replace="t"
/db_xref="dbSNP:1722014078"
variation 835
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:540930126"
variation 836
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1164854398"
variation 839
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1043983641"
variation 844
/gene="ARL9"
/replace="a"
/replace="c"
/db_xref="dbSNP:1419605481"
variation 852
/gene="ARL9"
/replace="g"
/replace="t"
/db_xref="dbSNP:2110159189"
variation 853
/gene="ARL9"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1190373823"
variation 854
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:2110159197"
variation 857..860
/gene="ARL9"
/replace="a"
/replace="aaaa"
/db_xref="dbSNP:2110159206"
variation 857
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1416601137"
variation 860
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1040606196"
variation 861
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:753195489"
variation 863
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1722014679"
variation 865
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:563998286"
variation 866
/gene="ARL9"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1170223148"
variation 868
/gene="ARL9"
/replace="g"
/replace="t"
/db_xref="dbSNP:117702751"
variation 873
/gene="ARL9"
/replace="a"
/replace="t"
/db_xref="dbSNP:2110159240"
variation 875
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1722015022"
variation 876
/gene="ARL9"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1272269311"
variation 878
/gene="ARL9"
/replace="c"
/replace="g"
/db_xref="dbSNP:1578217885"
variation 882
/gene="ARL9"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:538848438"
variation 885
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:114105293"
variation 888
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:146602954"
variation 893
/gene="ARL9"
/replace="a"
/replace="t"
/db_xref="dbSNP:1560701364"
variation 896
/gene="ARL9"
/replace="a"
/replace="t"
/db_xref="dbSNP:1722015619"
variation 897
/gene="ARL9"
/replace="g"
/replace="t"
/db_xref="dbSNP:1453476976"
variation 901
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1722015745"
variation 904
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1722015808"
variation 907
/gene="ARL9"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:756243516"
variation 916
/gene="ARL9"
/replace="g"
/replace="t"
/db_xref="dbSNP:1722015969"
variation 918
/gene="ARL9"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1722016043"
variation 921
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:969622122"
variation 922
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1722016212"
variation 926
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:969448295"
variation 928
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1297836980"
variation 933
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1439258809"
variation 936
/gene="ARL9"
/replace="c"
/replace="g"
/db_xref="dbSNP:1394440942"
variation 941
/gene="ARL9"
/replace="g"
/replace="t"
/db_xref="dbSNP:141360697"
variation 944
/gene="ARL9"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1722016627"
variation 956
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1722016710"
variation 960
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:2110159330"
variation 961
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1463392954"
variation 962
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1016104168"
variation 964
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1165848884"
variation 965..968
/gene="ARL9"
/replace="a"
/replace="aata"
/db_xref="dbSNP:1284649786"
variation 969
/gene="ARL9"
/replace="a"
/replace="c"
/db_xref="dbSNP:1560701389"
variation 972
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1381276943"
variation 973
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:79958106"
variation 974
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1373083034"
variation 978
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:971830203"
variation 980
/gene="ARL9"
/replace="a"
/replace="c"
/db_xref="dbSNP:1452445016"
variation 981
/gene="ARL9"
/replace="g"
/replace="t"
/db_xref="dbSNP:1035601574"
variation 982
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:962202599"
variation 983
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1469705820"
variation 984
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1411680296"
variation 985
/gene="ARL9"
/replace="a"
/replace="c"
/db_xref="dbSNP:972571450"
variation 990
/gene="ARL9"
/replace="a"
/replace="t"
/db_xref="dbSNP:1722018010"
variation 997
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1722018081"
variation 1000
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1195386000"
variation 1002
/gene="ARL9"
/replace="a"
/replace="t"
/db_xref="dbSNP:1722018315"
variation 1004
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:568464270"
variation 1006
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:930674092"
variation 1010
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1722018725"
variation 1012
/gene="ARL9"
/replace="a"
/replace="aaa"
/db_xref="dbSNP:1318140557"
variation 1012
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1722018835"
variation 1014..1015
/gene="ARL9"
/replace=""
/replace="caaaa"
/db_xref="dbSNP:1200204295"
variation 1016
/gene="ARL9"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:777770597"
variation 1018
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:556597288"
variation 1019
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:942655764"
variation 1022
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:2110159460"
variation 1023
/gene="ARL9"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1323986965"
variation 1027
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1130196"
variation 1033
/gene="ARL9"
/replace="g"
/replace="t"
/db_xref="dbSNP:1722019580"
variation 1037
/gene="ARL9"
/replace="a"
/replace="c"
/db_xref="dbSNP:944626472"
variation 1039..1040
/gene="ARL9"
/replace=""
/replace="t"
/db_xref="dbSNP:1722019758"
variation 1040
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1396794090"
variation 1051..1053
/gene="ARL9"
/replace="a"
/replace="aca"
/db_xref="dbSNP:1169121746"
variation 1057
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:935489625"
variation 1061
/gene="ARL9"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1474733495"
variation 1063
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1722020189"
variation 1065
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:188483784"
variation 1070
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1722020351"
variation 1078
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1578218030"
regulatory 1083..1088
/regulatory_class="polyA_signal_sequence"
/gene="ARL9"
/note="hexamer: AACAAA"
variation 1084
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1420735909"
variation 1087
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:554516435"
variation 1095
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1722020671"
variation 1100
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:896641655"
variation 1101
/gene="ARL9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1478920608"
variation 1106
/gene="ARL9"
/replace="c"
/replace="t"
/db_xref="dbSNP:903026911"
polyA_site 1108
/gene="ARL9"
ORIGIN
acacctggggcccagagccaccgctcagcacgcgggcacgcggcgggagggaaggaaaccgcggcgctggggatggagagggggaaagtgaagaagaaagagaaggaaaaggagacgcaggaggagaaaatcggagaaaagggtagggaagagaaagtgaaaagaaaggaggtggagcagaaaattaaacaaaagcaagagaagcaggagaggagaaagggaaaagagaaagaggaaaagaggacaaagcaagggaaggagacaaacaaagagaaggaacaatttaagggacaagaagagaaaggggagaacaaggacagcaccttgacaaggaccccgctcgagccgctggatcttgaagcagcctatcacattacagatatccatgaagctttggcattatctgaagtgggaaatgacaggaagatgttcttgtttggaacctacctgactaagaatggctcagagataccctccaccatgcaagatgccaaagacttgattgcacagctggctgcagatgtgcagtgaccaggactcagcccactgtgcggctcacgactgagatgtcatcagtgttgaatggcaggcttgaagccaaaggtttccacctcaaataaaaattaagccatttcctattttctcagtgcatgggatgtatatagttagccctccatatccatgggttccacatctggggattcaagaactgtggatccaaaacattcaaaaagtaaacccactgaagaataataacacaacaataaaaataatacacattttaaaatacaatataacaactatttacatagcattttcattgtattaggtattataagtaatctaaagatgatttaaaatacacgagtagaagtgtgtaggttatatgtaaatatgccattttccatcaggagcttgagcatccacatttgcctgtgaggatcttggaatcagtctccctgagaataccaacggacaactgtacaaagataatgctaacataataacagcatctctatttggattttgaatgttaaaaatatttgtaaaacagtgtattgggggtattgggatttttaatcaacaaaggtaaaatgaacattagcaa
//
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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