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Previous release (v1)
2024-04-30 14:51:15, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NR_144386 901 bp RNA linear PRI 27-DEC-2023
DEFINITION Homo sapiens fibronectin leucine rich transmembrane protein 2
(FLRT2), transcript variant 8, non-coding RNA.
ACCESSION NR_144386
VERSION NR_144386.2
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 901)
AUTHORS Bae H, Kim B, Lee H, Lee S, Kang HS and Kim SJ.
TITLE Epigenetically regulated Fibronectin leucine rich transmembrane
protein 2 (FLRT2) shows tumor suppressor activity in breast cancer
cells
JOURNAL Sci Rep 7 (1), 272 (2017)
PUBMED 28325946
REMARK GeneRIF: Taken together, these results provide insights into the
role of FLRT2 as a novel tumor suppressor in the breast, which is
inactivated by hypermethylation during tumor development.
Publication Status: Online-Only
REFERENCE 2 (bases 1 to 901)
AUTHORS Jackson VA, Mehmood S, Chavent M, Roversi P, Carrasquero M, Del
Toro D, Seyit-Bremer G, Ranaivoson FM, Comoletti D, Sansom MS,
Robinson CV, Klein R and Seiradake E.
TITLE Super-complexes of adhesion GPCRs and neural guidance receptors
JOURNAL Nat Commun 7, 11184 (2016)
PUBMED 27091502
REMARK Publication Status: Online-Only
REFERENCE 3 (bases 1 to 901)
AUTHORS Wu Y, Davison J, Qu X, Morrissey C, Storer B, Brown L, Vessella R,
Nelson P and Fang M.
TITLE Methylation profiling identified novel differentially methylated
markers including OPCML and FLRT2 in prostate cancer
JOURNAL Epigenetics 11 (4), 247-258 (2016)
PUBMED 26890304
REMARK GeneRIF: OPCML and FLRT2 were further validated in an independent
cohort consisting of 20 low-Gleason and 33 high-Gleason tissues. We
then compared patients with biochemical recurrence (n=70) vs. those
without (n=86) in a third cohort, and they showed no difference in
methylation at these DMR loci
REFERENCE 4 (bases 1 to 901)
AUTHORS Visser JJ, Cheng Y, Perry SC, Chastain AB, Parsa B, Masri SS, Ray
TA, Kay JN and Wojtowicz WM.
TITLE An extracellular biochemical screen reveals that FLRTs and Unc5s
mediate neuronal subtype recognition in the retina
JOURNAL Elife 4, e08149 (2015)
PUBMED 26633812
REMARK Publication Status: Online-Only
REFERENCE 5 (bases 1 to 901)
AUTHORS Jackson VA, del Toro D, Carrasquero M, Roversi P, Harlos K, Klein R
and Seiradake E.
TITLE Structural basis of latrophilin-FLRT interaction
JOURNAL Structure 23 (4), 774-781 (2015)
PUBMED 25728924
REFERENCE 6 (bases 1 to 901)
AUTHORS Kuo JC, Han X, Hsiao CT, Yates JR 3rd and Waterman CM.
TITLE Analysis of the myosin-II-responsive focal adhesion proteome
reveals a role for beta-Pix in negative regulation of focal
adhesion maturation
JOURNAL Nat Cell Biol 13 (4), 383-393 (2011)
PUBMED 21423176
REFERENCE 7 (bases 1 to 901)
AUTHORS Wheeler HE, Metter EJ, Tanaka T, Absher D, Higgins J, Zahn JM,
Wilhelmy J, Davis RW, Singleton A, Myers RM, Ferrucci L and Kim SK.
TITLE Sequential use of transcriptional profiling, expression
quantitative trait mapping, and gene association implicates MMP20
in human kidney aging
JOURNAL PLoS Genet 5 (10), e1000685 (2009)
PUBMED 19834535
REMARK GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
REFERENCE 8 (bases 1 to 901)
AUTHORS Haines BP, Wheldon LM, Summerbell D, Heath JK and Rigby PW.
TITLE Regulated expression of FLRT genes implies a functional role in the
regulation of FGF signalling during mouse development
JOURNAL Dev Biol 297 (1), 14-25 (2006)
PUBMED 16872596
REFERENCE 9 (bases 1 to 901)
AUTHORS Zhang Z and Henzel WJ.
TITLE Signal peptide prediction based on analysis of experimentally
verified cleavage sites
JOURNAL Protein Sci 13 (10), 2819-2824 (2004)
PUBMED 15340161
REFERENCE 10 (bases 1 to 901)
AUTHORS Lacy SE, Bonnemann CG, Buzney EA and Kunkel LM.
TITLE Identification of FLRT1, FLRT2, and FLRT3: a novel family of
transmembrane leucine-rich repeat proteins
JOURNAL Genomics 62 (3), 417-426 (1999)
PUBMED 10644439
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from AL049775.2 and BX119446.1.
On Aug 14, 2020 this sequence version replaced NR_144386.1.
Summary: This gene encodes a member of the fibronectin leucine rich
transmembrane (FLRT) family of cell adhesion molecules, which
regulate early embryonic vascular and neural development. The
encoded type I transmembrane protein has an extracellular region
consisting of an N-terminal leucine-rich repeat domain and a type 3
fibronectin domain, followed by a transmembrane domain and a short
C-terminal cytoplasmic tail domain. It functions as both a
homophilic cell adhesion molecule and a heterophilic chemorepellent
through its interaction with members of the uncoordinated-5
receptor family. Proteolytic removal of the extracellular region
controls the migration of neurons in the developing cortex.
Alternative splicing results in multiple transcript variants.
[provided by RefSeq, Sep 2016].
Transcript Variant: This variant (8) uses an alternate exon
structure compared to variant 1 and lacks the coding region found
in variant 1. This variant is represented as non-coding because it
lacks the entire coding region found in variant 1.
Sequence Note: This RefSeq record was created from transcript and
genomic sequence data to make the sequence consistent with the
reference genome assembly. The genomic coordinates used for the
transcript record were based on transcript alignments.
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 :: DA777437.1, DA487741.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
SAMEA1968968, SAMEA2147920
[ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-391 AL049775.2 95847-96237
392-419 AL049775.2 126893-126920
420-901 BX119446.1 1-482
FEATURES Location/Qualifiers
source 1..901
/organism="Homo sapiens"
/mol_type="transcribed RNA"
/db_xref="taxon:9606"
/chromosome="14"
/map="14q31.3"
gene 1..901
/gene="FLRT2"
/note="fibronectin leucine rich transmembrane protein 2"
/db_xref="GeneID:23768"
/db_xref="HGNC:HGNC:3761"
/db_xref="MIM:604807"
misc_RNA 1..901
/gene="FLRT2"
/product="fibronectin leucine rich transmembrane protein
2, transcript variant 8"
/db_xref="GeneID:23768"
/db_xref="HGNC:HGNC:3761"
/db_xref="MIM:604807"
exon 1..391
/gene="FLRT2"
/inference="alignment:Splign:2.1.0"
variation 1
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1888180495"
variation 3
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:775726523"
variation 4
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:887157230"
variation 6
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1888180732"
variation 8
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1281900910"
variation 9
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:974461203"
variation 12
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1319728529"
variation 19
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1432821843"
variation 25
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1346690866"
variation 26
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888181503"
variation 30
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1888181634"
variation 31..32
/gene="FLRT2"
/replace=""
/replace="tt"
/db_xref="dbSNP:1488906559"
variation 34
/gene="FLRT2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1159598297"
variation 36
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1401484231"
variation 39
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1413420693"
variation 42
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1888182438"
variation 43
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:919965514"
variation 44
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888182793"
variation 46
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1888182917"
variation 48
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1888183034"
variation 49
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1446455214"
variation 51
/gene="FLRT2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1057339717"
variation 52
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1888183329"
variation 53
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2139786646"
variation 60
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:150485276"
variation 62
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1265282513"
variation 63
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1888183806"
variation 67
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:982837263"
variation 70
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:912688720"
variation 73
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1888184286"
variation 74
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1450670428"
variation 77
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:944219944"
variation 78
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1566709351"
variation 79
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888184657"
variation 80
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888184786"
variation 81
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:895761087"
variation 88
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1247721490"
variation 95
/gene="FLRT2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1888185171"
variation 96
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:573586763"
variation 97
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1182429349"
variation 102
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1039926925"
variation 105
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1888185970"
variation 106
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1888186175"
variation 107
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1411232560"
variation 108
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566709372"
variation 109
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1888186828"
variation 110
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1888186999"
variation 112
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1364035282"
variation 115
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1455427007"
variation 116
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1435583532"
variation 117
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2139786802"
variation 120
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2139786810"
variation 121
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:796457612"
variation 125..129
/gene="FLRT2"
/replace="ct"
/replace="ctcct"
/db_xref="dbSNP:1394988750"
variation 126
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1022622846"
variation 127
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2139786825"
variation 128
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1301466591"
variation 131
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1888188768"
variation 133
/gene="FLRT2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1426814507"
variation 134
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:543945882"
variation 135
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1168084849"
variation 139
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1448182839"
variation 140
/gene="FLRT2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1422342907"
variation 141
/gene="FLRT2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1187465545"
variation 143
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:947688646"
variation 144
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1888190262"
variation 146
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2139786895"
variation 147
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1457055010"
variation 148
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1888190669"
variation 150
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1594972542"
variation 151
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1888190884"
variation 152
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1042744587"
variation 154
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:902887542"
variation 155
/gene="FLRT2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:998571175"
variation 157
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1035442666"
variation 158
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1888192005"
variation 160
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2139786950"
variation 161
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1309184983"
variation 164
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888192451"
variation 169
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888192667"
variation 170
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1296128445"
variation 172
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2139786979"
variation 174
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888193066"
variation 175
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:895627417"
variation 176
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1594972583"
variation 177
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888193623"
variation 179
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1365164677"
variation 182
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:999781230"
variation 184
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:113033644"
variation 185
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:56105610"
variation 186
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1460588007"
variation 190
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1022820245"
variation 191
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1171664289"
variation 192
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1414419072"
variation 193
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1594972642"
variation 196
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1427586538"
variation 203
/gene="FLRT2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1350455864"
variation 204
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:988342472"
variation 206
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:963622059"
variation 210
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1295447985"
variation 211
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1322707560"
variation 214
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:531114003"
variation 221
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:546450205"
variation 222
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1026908377"
variation 223
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1888196334"
variation 224
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1263966815"
variation 228
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:564768939"
variation 232
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:528825348"
variation 237
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1594972721"
variation 239
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1888196816"
variation 240
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888196924"
variation 242
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1888197020"
variation 243
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1223954310"
variation 248
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888197239"
variation 251
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888197363"
variation 252
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1206022443"
variation 253
/gene="FLRT2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:376621464"
variation 258
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1888197747"
variation 262
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888197869"
variation 264
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:912657780"
variation 267
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1888198134"
variation 268
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:931310231"
variation 269
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1414178422"
variation 271
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:751097239"
variation 273
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1423033197"
variation 275
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:965517807"
variation 276
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:984083142"
variation 278
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:547279808"
variation 281
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1470471181"
variation 283
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1594972790"
variation 285
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1888199421"
variation 289..292
/gene="FLRT2"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:1888199565"
variation 293
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1355976787"
variation 301
/gene="FLRT2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:975969774"
variation 305
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:754553949"
variation 308
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:895634398"
variation 311
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1250579776"
variation 313
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888200395"
variation 318
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:948671605"
variation 319
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:118107793"
variation 324
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1888200903"
variation 325
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2139787291"
variation 326
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1888201042"
variation 333
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1244962100"
variation 335
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1888201155"
variation 336
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:904407174"
variation 338
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1328156236"
variation 342..344
/gene="FLRT2"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1888201675"
variation 342
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:561884493"
variation 348
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:529307953"
variation 349..350
/gene="FLRT2"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1318993624"
variation 354
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1380339426"
variation 355
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888202267"
variation 357
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888202459"
variation 359
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1395581317"
variation 360
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1888202911"
variation 362
/gene="FLRT2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1339206104"
variation 363
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1888203281"
variation 364
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1888203400"
variation 366
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1031727861"
variation 367
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1888203672"
variation 370
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1388317923"
variation 372
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888203907"
variation 374
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888204037"
variation 377
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1287530347"
variation 378
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:947620442"
variation 380
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1009046187"
variation 381
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1163458319"
variation 382
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:776772455"
variation 384..385
/gene="FLRT2"
/replace=""
/replace="gtaa"
/db_xref="dbSNP:1888204724"
variation 385
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:924235174"
variation 387
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1310816648"
variation 388
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:934333959"
variation 389
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1888205272"
exon 392..491
/gene="FLRT2"
/inference="alignment:Splign:2.1.0"
variation 393
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2139844815"
variation 395
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1890296807"
variation 403
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:952479748"
variation 404
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1890297167"
variation 407
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:755589217"
variation 411
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:908367733"
variation 412
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1890297628"
variation 415
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1299066340"
variation 416
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1316786846"
variation 417
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2139844862"
variation 423..424
/gene="FLRT2"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1890298073"
variation 428
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2139844870"
variation 443
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1890298240"
variation 444
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:187873507"
variation 447
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1167075369"
variation 450
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1890298680"
variation 453
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1890298848"
variation 454
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1890299000"
variation 457
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1424468957"
variation 460
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:879456951"
variation 461
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:767246801"
variation 462
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1294014707"
variation 463
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1890299838"
variation 466
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1890299976"
variation 467
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1185226191"
variation 473
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:193018774"
variation 474
/gene="FLRT2"
/replace=""
/replace="a"
/db_xref="dbSNP:1264294890"
variation 479
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2139844944"
variation 481
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1199125474"
variation 486
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1890300749"
variation 487
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1040948130"
variation 490
/gene="FLRT2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1890301206"
exon 492..901
/gene="FLRT2"
/inference="alignment:Splign:2.1.0"
variation 493
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2139847685"
variation 495
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:987218903"
variation 497
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1169888477"
variation 501
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1890418284"
variation 503
/gene="FLRT2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1018252140"
variation 505
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1890418651"
variation 509
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1321091764"
variation 513
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1387939130"
variation 516
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:770070687"
variation 520
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:964119982"
variation 521
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1595027794"
variation 523
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2139847742"
variation 529
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1890419506"
variation 532
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1890419670"
variation 542
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1890419835"
variation 546..560
/gene="FLRT2"
/replace="agg"
/replace="agggcagtattcagg"
/db_xref="dbSNP:1890420134"
variation 546
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1595027801"
variation 550
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:777990680"
variation 555
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:974115504"
variation 561
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1425564082"
variation 566
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:749298971"
variation 567
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1377276003"
variation 568
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1196847725"
variation 577
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:770744618"
variation 578
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1054252875"
variation 583
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1890421759"
variation 586
/gene="FLRT2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:535414728"
variation 587
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1198524321"
variation 589
/gene="FLRT2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1377261277"
variation 590
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1415338241"
variation 591
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:137873561"
variation 600
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1890423365"
variation 603
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1890423594"
variation 608
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1890423839"
variation 609
/gene="FLRT2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1890424078"
variation 620
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:539784298"
variation 628
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1010101157"
variation 630
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1272660114"
variation 634
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1595027935"
variation 635
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1890425415"
variation 636
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1020140923"
variation 637
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:928552403"
variation 638
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1270452644"
variation 645
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:938585564"
variation 646
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1890426680"
variation 652
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1890426925"
variation 655
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1890427178"
variation 656
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:907106316"
variation 659
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:894130240"
variation 664
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1890427801"
variation 666..682
/gene="FLRT2"
/replace="aat"
/replace="aatgacctgggggaaat"
/db_xref="dbSNP:1352150121"
variation 668
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1890428099"
variation 671
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1329367242"
variation 672
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1413627510"
variation 674..678
/gene="FLRT2"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1566729611"
variation 674
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:774306944"
variation 676
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1281864993"
variation 678
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:112458751"
variation 684
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1170985510"
variation 688
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:575303911"
variation 693
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:947152323"
variation 697..704
/gene="FLRT2"
/replace="aag"
/replace="aagcaaag"
/db_xref="dbSNP:1890429767"
variation 697
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:539937698"
variation 702
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1890429935"
variation 704
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1890430090"
variation 707
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2139848018"
variation 709
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1890430299"
variation 711
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1178075714"
variation 716
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1890430810"
variation 717
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1002758519"
variation 718
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:187574706"
variation 720
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1441092249"
variation 723
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1183004537"
variation 725..728
/gene="FLRT2"
/replace="aaaa"
/replace="aaaaa"
/db_xref="dbSNP:1000109268"
variation 725
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1216469403"
variation 730
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1276106897"
variation 732
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:959402849"
variation 733
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1212631264"
variation 743
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:991308854"
variation 744
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1284765311"
variation 753
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1890433804"
variation 754
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:558412946"
variation 763
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1375444592"
variation 769..771
/gene="FLRT2"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:1280005989"
variation 771
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1447040972"
variation 777
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1890435131"
variation 781
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1890435365"
variation 782
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:189447924"
variation 785
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1475117434"
variation 790
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2139848120"
variation 794
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1335901808"
variation 798
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1890436312"
variation 799
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1890436579"
variation 804
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1890436813"
variation 806
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1436870871"
variation 809
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1008461176"
variation 810
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1158128526"
variation 813
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:866319884"
variation 814
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1890438005"
variation 824
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1890438246"
variation 825
/gene="FLRT2"
/replace=""
/replace="c"
/db_xref="dbSNP:1166171479"
variation 828
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:963189164"
variation 830
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1890438998"
variation 831
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1890439238"
variation 833..844
/gene="FLRT2"
/replace="tctacttatcta"
/replace="tctacttatctacttatcta"
/db_xref="dbSNP:561145817"
variation 836
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1890439756"
variation 838..844
/gene="FLRT2"
/replace=""
/replace="ttatcta"
/db_xref="dbSNP:1890440089"
variation 838
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1018720168"
variation 840
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:964006488"
variation 841
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1435214732"
variation 843
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1890440238"
variation 846
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:972918389"
variation 847
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:562004715"
variation 851..854
/gene="FLRT2"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:1485835171"
variation 852
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1890440957"
variation 855
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2139848222"
variation 857
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1890441117"
variation 858
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:934199559"
variation 859
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1261929846"
variation 860
/gene="FLRT2"
/replace=""
/replace="t"
/db_xref="dbSNP:1213837506"
variation 862
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1318146602"
variation 864
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:573993910"
variation 868
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1383776939"
variation 872
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1027030889"
variation 877..884
/gene="FLRT2"
/replace="aataa"
/replace="aataataa"
/db_xref="dbSNP:1325433013"
variation 879
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1890442730"
variation 892
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1294963248"
variation 899
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1890443117"
variation 900..901
/gene="FLRT2"
/replace=""
/replace="g"
/replace="t"
/db_xref="dbSNP:1356352378"
variation 901
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:987055995"
ORIGIN
agttgtacgttcgaaacctgtcgccgtcacttgcgcgtttggcattatccattgtcaccgcggaggaacgagcgctcgagatatcatcagtgcccgcaaatctccgcgccaaggcgctgagctactcctttccgaggtgcgcctctggtcctccgtccctggtgcccagcagcggcgaggcggcatctccgctcccgccgccgtgtccaccgagccctgggatcagggtggcagttctcaacgatgggcaggagggacctcggcggcgacccctaaaacaataccatgccccgggatccccgctgctgccgcgccagcgtcttccctttccacctccctgaccctgtcggattcggatgagcccattgcaaggagaagacgcagccgtcagtttcagaagctatctcctgagcagtgtgtaattctctcctggctgtttgatggtaatgggagctgtacatgtatctggagagaggagaaccagcctggggactcaagatatattaaagactatgctcatggacatcaattctttcctgtcctttagggcagtattcaggccacacggttcaataacgggaaagaatgtcgtcacatgattgcatcatgttcttcaaaatgaaatctattgaacagtataaacaacaaagaacatcatttgtcagaatgacctgggggaaatagtccagtgaaactaagcaaagggaactttataccgtgagggaaaatcaatggattgtaacagaaccctgcaagaagagacatagctttcaagttccagagacctagaggtgactgagaagcaggatgtaccagaaactgggcttcttgttctacttatctagcgcccttttcacagtgttgtatatgtaaataaataataaagcagtgtgatttttaa
//
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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