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2025-05-09 16:42:48, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001013438 8475 bp mRNA linear PRI 07-JUL-2013
DEFINITION Homo sapiens fragile X mental retardation, autosomal homolog 1
(FXR1), transcript variant 2, mRNA.
ACCESSION NM_001013438
VERSION NM_001013438.2 GI:298231192
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 8475)
AUTHORS Davidovic,L., Durand,N., Khalfallah,O., Tabet,R., Barbry,P.,
Mari,B., Sacconi,S., Moine,H. and Bardoni,B.
TITLE A novel role for the RNA-binding protein FXR1P in myoblasts
cell-cycle progression by modulating p21/Cdkn1a/Cip1/Waf1 mRNA
stability
JOURNAL PLoS Genet. 9 (3), E1003367 (2013)
PUBMED 23555284
REMARK GeneRIF: Our study describes a novel role of FXR1P that has crucial
implications for the understanding of its role during myogenesis
and muscle development
REFERENCE 2 (bases 1 to 8475)
AUTHORS Coffee,R.L. Jr., Tessier,C.R., Woodruff,E.A. III and Broadie,K.
TITLE Fragile X mental retardation protein has a unique, evolutionarily
conserved neuronal function not shared with FXR1P or FXR2P
JOURNAL Dis Model Mech 3 (7-8), 471-485 (2010)
PUBMED 20442204
REMARK GeneRIF: These results indicate that FMR1 gene function is
evolutionarily conserved in neural mechanisms and cannot be
compensated by either FXR1 or FXR2, but that all three proteins can
substitute for each other in non-neuronal requirements.
REFERENCE 3 (bases 1 to 8475)
AUTHORS Adams-Cioaba,M.A., Guo,Y., Bian,C., Amaya,M.F., Lam,R.,
Wasney,G.A., Vedadi,M., Xu,C. and Min,J.
TITLE Structural studies of the tandem Tudor domains of fragile X mental
retardation related proteins FXR1 and FXR2
JOURNAL PLoS ONE 5 (11), E13559 (2010)
PUBMED 21072162
REMARK GeneRIF: Data show that the nuclear localization signals of the
FXR1 and FXR2 comprise tandem Tudor domain architectures.
Publication Status: Online-Only
REFERENCE 4 (bases 1 to 8475)
AUTHORS Darnell,J.C., Fraser,C.E., Mostovetsky,O. and Darnell,R.B.
TITLE Discrimination of common and unique RNA-binding activities among
Fragile X mental retardation protein paralogs
JOURNAL Hum. Mol. Genet. 18 (17), 3164-3177 (2009)
PUBMED 19487368
REMARK GeneRIF: FXR1P and FXR2P KH2 domains bind G-quadruplex and kissing
complex RNA with the same affinity as the FMRP KH2 domain.
REFERENCE 5 (bases 1 to 8475)
AUTHORS Purcell SM, Wray NR, Stone JL, Visscher PM, O'Donovan MC, Sullivan
PF and Sklar P.
CONSRTM International Schizophrenia Consortium
TITLE Common polygenic variation contributes to risk of schizophrenia and
bipolar disorder
JOURNAL Nature 460 (7256), 748-752 (2009)
PUBMED 19571811
REFERENCE 6 (bases 1 to 8475)
AUTHORS Tamanini,F., Willemsen,R., van Unen,L., Bontekoe,C., Galjaard,H.,
Oostra,B.A. and Hoogeveen,A.T.
TITLE Differential expression of FMR1, FXR1 and FXR2 proteins in human
brain and testis
JOURNAL Hum. Mol. Genet. 6 (8), 1315-1322 (1997)
PUBMED 9259278
REFERENCE 7 (bases 1 to 8475)
AUTHORS Siomi,M.C., Zhang,Y., Siomi,H. and Dreyfuss,G.
TITLE Specific sequences in the fragile X syndrome protein FMR1 and the
FXR proteins mediate their binding to 60S ribosomal subunits and
the interactions among them
JOURNAL Mol. Cell. Biol. 16 (7), 3825-3832 (1996)
PUBMED 8668200
REFERENCE 8 (bases 1 to 8475)
AUTHORS Coy,J.F., Sedlacek,Z., Bachner,D., Hameister,H., Joos,S.,
Lichter,P., Delius,H. and Poustka,A.
TITLE Highly conserved 3' UTR and expression pattern of FXR1 points to a
divergent gene regulation of FXR1 and FMR1
JOURNAL Hum. Mol. Genet. 4 (12), 2209-2218 (1995)
PUBMED 8634689
REFERENCE 9 (bases 1 to 8475)
AUTHORS Zhang,Y., O'Connor,J.P., Siomi,M.C., Srinivasan,S., Dutra,A.,
Nussbaum,R.L. and Dreyfuss,G.
TITLE The fragile X mental retardation syndrome protein interacts with
novel homologs FXR1 and FXR2
JOURNAL EMBO J. 14 (21), 5358-5366 (1995)
PUBMED 7489725
REFERENCE 10 (bases 1 to 8475)
AUTHORS Siomi,M.C., Siomi,H., Sauer,W.H., Srinivasan,S., Nussbaum,R.L. and
Dreyfuss,G.
TITLE FXR1, an autosomal homolog of the fragile X mental retardation gene
JOURNAL EMBO J. 14 (11), 2401-2408 (1995)
PUBMED 7781595
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from DC352767.1, AK225334.1 and
AC008009.5.
On Jun 13, 2010 this sequence version replaced gi:61835163.
Summary: The protein encoded by this gene is an RNA binding protein
that interacts with the functionally-similar proteins FMR1 and
FXR2. These proteins shuttle between the nucleus and cytoplasm and
associate with polyribosomes, predominantly with the 60S ribosomal
subunit. Three transcript variants encoding different isoforms have
been found for this gene. [provided by RefSeq, Jul 2008].
Transcript Variant: This variant (2) lacks an alternate exon
compared to variant 1, that causes a frameshift. The resulting
isoform (b) is shorter and has a distinct C-terminus compared to
isoform a.
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 :: BC028983.1, AK225334.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025081, ERS025082 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-226 DC352767.1 1-226
227-783 AK225334.1 3-559
784-784 AC008009.5 45149-45149
785-2268 AK225334.1 561-2044
2269-8475 AC008009.5 72439-78645
FEATURES Location/Qualifiers
source 1..8475
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="3"
/map="3q28"
gene 1..8475
/gene="FXR1"
/gene_synonym="FXR1P"
/note="fragile X mental retardation, autosomal homolog 1"
/db_xref="GeneID:8087"
/db_xref="HGNC:4023"
/db_xref="HPRD:02892"
/db_xref="MIM:600819"
exon 1..291
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 17
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:13072332"
variation 111
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:189076195"
variation 194
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:376999929"
variation 214
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:371117434"
variation 232
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:375850195"
CDS 241..1860
/gene="FXR1"
/gene_synonym="FXR1P"
/note="isoform b is encoded by transcript variant 2;
fragile X mental retardation syndrome-related protein 1;
hFXR1p"
/codon_start=1
/product="fragile X mental retardation syndrome-related
protein 1 isoform b"
/protein_id="NP_001013456.1"
/db_xref="GI:61835164"
/db_xref="CCDS:CCDS46965.1"
/db_xref="GeneID:8087"
/db_xref="HGNC:4023"
/db_xref="HPRD:02892"
/db_xref="MIM:600819"
/translation="
MAELTVEVRGSNGAFYKGFIKDVHEDSLTVVFENNWQPERQVPFNEVRLPPPPDIKKEISEGDEVEVYSRANDQEPCGWWLAKVRMMKGEFYVIEYAACDATYNEIVTFERLRPVNQNKTVKKNTFFKCTVDVPEDLREACANENAHKDFKKAVGACRIFYHPETTQLMILSASEATVKRVNILSDMHLRSIRTKLMLMSRNEEATKHLECTKQLAAAFHEEFVVREDLMGLAIGTHGSNIQQARKVPGVTAIELDEDTGTFRIYGESADAVKKARGFLEFVEDFIQVPRNLVGKVIGKNGKVIQEIVDKSGVVRVRIEGDNENKLPREDGMVPFVFVGTKESIGNVQVLLEYHIAYLKEVEQLRMERLQIDEQLRQIGSRSYSGRGRGRRGPNYTSGYGTNSELSNPSETESERKDELSDWSLAGEDDRDSRHQRDSRRRPGGRGRSVSGGRGRGGPRGGKSSISSVLKDPDSNPYSLLDNTESDQTADTDASESHHSTNRRRRSRRRRTDEDAVLMDGMTESDTASVNENGLGKRCD
"
misc_feature 244..246
/gene="FXR1"
/gene_synonym="FXR1P"
/experiment="experimental evidence, no additional details
recorded"
/note="N-acetylalanine; propagated from
UniProtKB/Swiss-Prot (P51114.3); acetylation site"
misc_feature 415..585
/gene="FXR1"
/gene_synonym="FXR1P"
/note="Agenet domain; Region: Agenet; pfam05641"
/db_xref="CDD:191330"
misc_feature 898..1080
/gene="FXR1"
/gene_synonym="FXR1P"
/note="K homology RNA-binding domain, type I. KH binds
single-stranded RNA or DNA. It is found in a wide variety
of proteins including ribosomal proteins, transcription
factors and post-transcriptional modifiers of mRNA. There
are two different KH domains that...; Region: KH-I;
cd00105"
/db_xref="CDD:29002"
misc_feature order(922..924,928..936,940..954,961..966,973..978,
991..999)
/gene="FXR1"
/gene_synonym="FXR1P"
/note="nucleic acid binding region [nucleotide binding];
other site"
/db_xref="CDD:29002"
misc_feature 943..954
/gene="FXR1"
/gene_synonym="FXR1P"
/note="G-X-X-G motif; other site"
/db_xref="CDD:29002"
misc_feature 1096..1296
/gene="FXR1"
/gene_synonym="FXR1P"
/note="K homology RNA-binding domain, type I. KH binds
single-stranded RNA or DNA. It is found in a wide variety
of proteins including ribosomal proteins, transcription
factors and post-transcriptional modifiers of mRNA. There
are two different KH domains that...; Region: KH-I;
cd00105"
/db_xref="CDD:29002"
misc_feature order(1111..1113,1117..1125,1129..1143,1150..1155,
1162..1167,1183..1194)
/gene="FXR1"
/gene_synonym="FXR1P"
/note="nucleic acid binding region [nucleotide binding];
other site"
/db_xref="CDD:29002"
misc_feature 1132..1143
/gene="FXR1"
/gene_synonym="FXR1P"
/note="G-X-X-G motif; other site"
/db_xref="CDD:29002"
misc_feature 1321..>1374
/gene="FXR1"
/gene_synonym="FXR1P"
/note="Fragile X-related 1 protein C terminal; Region:
FXR1P_C; pfam12235"
/db_xref="CDD:152670"
misc_feature 1441..1443
/gene="FXR1"
/gene_synonym="FXR1P"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1447..1449
/gene="FXR1"
/gene_synonym="FXR1P"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1456..1458
/gene="FXR1"
/gene_synonym="FXR1P"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P51114.3); phosphorylation site"
misc_feature 1456..1458
/gene="FXR1"
/gene_synonym="FXR1P"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1465..1467
/gene="FXR1"
/gene_synonym="FXR1P"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P51114.3); phosphorylation site"
misc_feature 1465..1467
/gene="FXR1"
/gene_synonym="FXR1P"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1471..1473
/gene="FXR1"
/gene_synonym="FXR1P"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1477..1479
/gene="FXR1"
/gene_synonym="FXR1P"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1498..1500
/gene="FXR1"
/gene_synonym="FXR1P"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P51114.3); phosphorylation site"
misc_feature 1507..1509
/gene="FXR1"
/gene_synonym="FXR1P"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P51114.3); phosphorylation site"
misc_feature 1564..1611
/gene="FXR1"
/gene_synonym="FXR1P"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (P51114.3);
Region: RNA-binding RGG-box"
misc_feature 1573..1575
/gene="FXR1"
/gene_synonym="FXR1P"
/experiment="experimental evidence, no additional details
recorded"
/note="methylation site"
misc_feature 1597..1599
/gene="FXR1"
/gene_synonym="FXR1P"
/experiment="experimental evidence, no additional details
recorded"
/note="methylation site"
misc_feature 1669..1671
/gene="FXR1"
/gene_synonym="FXR1P"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1693..1695
/gene="FXR1"
/gene_synonym="FXR1P"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P51114.3); phosphorylation site"
misc_feature 1693..1695
/gene="FXR1"
/gene_synonym="FXR1P"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1702..1704
/gene="FXR1"
/gene_synonym="FXR1P"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1720..1722
/gene="FXR1"
/gene_synonym="FXR1P"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
variation 250
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="g"
/db_xref="dbSNP:377637427"
variation 267
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1805578"
variation 276
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:201247137"
exon 292..344
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
exon 345..438
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 364
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:375255336"
variation 411
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:371183000"
exon 439..510
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 464
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:199903473"
variation 468
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:144304502"
exon 511..659
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 528
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:145159450"
variation 534
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:369357473"
variation 627
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:139008118"
STS 628..742
/gene="FXR1"
/gene_synonym="FXR1P"
/standard_name="FXR1"
/db_xref="UniSTS:505522"
STS 636..719
/gene="FXR1"
/gene_synonym="FXR1P"
/standard_name="RH123299"
/db_xref="UniSTS:135676"
exon 660..753
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 702
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:377389758"
variation 708
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:3026195"
exon 754..870
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 757
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:143250917"
variation 766
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:201512027"
variation 813
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:148268040"
variation 861
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:370062138"
exon 871..1041
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 924
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:374396414"
variation 993
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:73176330"
variation 1021
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:200507471"
variation 1027
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:142641159"
exon 1042..1120
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 1062
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="g"
/db_xref="dbSNP:371122085"
STS 1069..1275
/gene="FXR1"
/gene_synonym="FXR1P"
/standard_name="Fxr1h"
/db_xref="UniSTS:498301"
variation 1096
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:200358370"
exon 1121..1230
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 1132
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:76531300"
exon 1231..1317
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 1291
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="g"
/db_xref="dbSNP:376660925"
variation 1302
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1805617"
exon 1318..1375
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 1329
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:369969651"
exon 1376..1438
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 1392
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:202004870"
variation 1431
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:370623678"
variation 1432
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:372792772"
exon 1439..1642
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 1448
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:199510994"
variation 1471
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:199504601"
variation 1472
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:201616183"
variation 1476
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:200492892"
variation 1525
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1051080"
variation 1538
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:371485992"
variation 1547
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:374389670"
variation 1615
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:199785386"
exon 1643..1843
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 1649
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:138120810"
variation 1731
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:201665512"
variation 1736
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:371778667"
variation 1748
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:143480969"
exon 1844..8475
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 1866
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:147171380"
variation 1867
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:367886303"
variation 1869
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:138367563"
variation 1877
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:149239435"
variation 1879
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:201161602"
variation 1880
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:111774718"
variation 1899
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:371671972"
variation 1907
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:201637634"
variation 1916
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:148795102"
variation 1937
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:55637125"
variation 1940
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:143951672"
variation 1962
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:146350316"
variation 1983
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:3026204"
variation 1986
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:112134282"
variation 1989
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:11499"
variation 2002
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:139713512"
variation 2019
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:376366097"
variation 2024
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:371231893"
variation 2060
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:199650094"
variation 2101
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:368937602"
variation 2164
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="g"
/db_xref="dbSNP:138323510"
polyA_signal 2247..2252
/gene="FXR1"
/gene_synonym="FXR1P"
polyA_site 2275
/gene="FXR1"
/gene_synonym="FXR1P"
variation 2318
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="g"
/db_xref="dbSNP:77451926"
variation 2384
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:3026205"
variation 2508
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:372825020"
variation 2515
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:377201428"
variation 2526
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:188550393"
variation 2529
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:117037927"
variation 2544
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:191923790"
variation 2731
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:145591161"
variation 2796
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:200701459"
variation 2799..2800
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="a"
/db_xref="dbSNP:201501227"
variation 2800
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:138114654"
variation 2809..2811
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="ttt"
/db_xref="dbSNP:79881434"
polyA_signal 2857..2862
/gene="FXR1"
/gene_synonym="FXR1P"
variation 2866
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:183311734"
polyA_site 2884
/gene="FXR1"
/gene_synonym="FXR1P"
variation 3124..3125
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="aa"
/db_xref="dbSNP:146154883"
variation 3157..3158
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="gg"
/db_xref="dbSNP:201594378"
variation 3229
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:187223562"
variation 3232
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:191718661"
variation 3375
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:183888010"
variation 3426
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="g"
/db_xref="dbSNP:370717702"
variation 3516
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:3026206"
variation 3520
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:113426020"
variation 3565
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:149096577"
variation 3793
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:186780056"
variation 3903..3904
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="a"
/db_xref="dbSNP:35250215"
variation 3904
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="a"
/db_xref="dbSNP:67565008"
variation 3923
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:143130417"
variation 3925
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1805627"
variation 3939
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1805628"
variation 3951
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:193140070"
STS 3979..4140
/gene="FXR1"
/gene_synonym="FXR1P"
/standard_name="D3S2910E"
/db_xref="UniSTS:150894"
variation 4013
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="ta"
/db_xref="dbSNP:200214928"
variation 4014..4015
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="tt"
/db_xref="dbSNP:67477912"
variation 4141
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:185723329"
variation 4270
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="g"
/db_xref="dbSNP:190201524"
variation 4324
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="g"
/db_xref="dbSNP:182067416"
variation 4404
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:148220661"
variation 4484
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:62291435"
variation 4514
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:141181334"
variation 4542
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:112349907"
variation 4707
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:114145770"
STS 4800..4950
/gene="FXR1"
/gene_synonym="FXR1P"
/standard_name="RH98363"
/db_xref="UniSTS:89700"
variation 4939
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:184223404"
variation 4956
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:147356292"
variation 4967
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:370998297"
variation 5060
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1465374"
variation 5068
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="g"
/db_xref="dbSNP:188684032"
variation 5132
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:3026207"
variation 5155
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1008412"
variation 5190
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1805629"
STS 5199..5398
/gene="FXR1"
/gene_synonym="FXR1P"
/standard_name="D3S3105"
/db_xref="UniSTS:61824"
STS 5204..5354
/gene="FXR1"
/gene_synonym="FXR1P"
/standard_name="Cda01e11"
/db_xref="UniSTS:64869"
variation 5222
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:374633367"
variation 5251
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:181123657"
variation 5275
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:116043654"
variation 5306
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:3026208"
variation 5339
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:137877459"
variation 5361
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:189429564"
polyA_signal 5387..5392
/gene="FXR1"
/gene_synonym="FXR1P"
variation 5399
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:114677034"
polyA_site 5418
/gene="FXR1"
/gene_synonym="FXR1P"
variation 5445
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:143392613"
variation 5669
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:180725645"
variation 5765
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:147544455"
variation 5917
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:187502719"
STS 5934..6063
/gene="FXR1"
/gene_synonym="FXR1P"
/standard_name="A006P45"
/db_xref="UniSTS:58844"
variation 6062
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:1058382"
variation 6064
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:6799476"
variation 6106..6107
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="t"
/db_xref="dbSNP:201242121"
variation 6115
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:16832224"
variation 6122..6123
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="t"
/db_xref="dbSNP:144707771"
variation 6174..6177
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="atta"
/db_xref="dbSNP:373289717"
variation 6176
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:3026209"
variation 6190
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:191834999"
variation 6245
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:140179467"
variation 6350
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:183796587"
variation 6372
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:79629055"
variation 6400
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:185999941"
variation 6482
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:373868693"
variation 6483
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:190427919"
variation 6600
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:150037153"
variation 6650..6651
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="t"
/db_xref="dbSNP:151155261"
variation 6651..6652
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="t"
/db_xref="dbSNP:11448946"
variation 6715
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:182639763"
variation 6933
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:7646508"
variation 7063
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:368717976"
variation 7098
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:148748584"
variation 7108
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1805630"
variation 7159
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:202106534"
variation 7226
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:142318810"
variation 7230
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:187015735"
variation 7255
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1805607"
variation 7343
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="g"
/db_xref="dbSNP:146809695"
variation 7355
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="a"
/db_xref="dbSNP:199927975"
variation 7389
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:192718619"
variation 7428
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:73046170"
variation 7474
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:201358029"
variation 7519
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:189118011"
variation 7535
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1805631"
variation 7565..7579
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="tttacctggcttctg"
/db_xref="dbSNP:368024256"
variation 7648
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:193073756"
variation 7649
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1805632"
variation 7745
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:184439182"
variation 7839
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:369747203"
variation 7888
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:144198197"
variation 7909
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:188933563"
variation 7933
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="g"
/db_xref="dbSNP:191855515"
variation 7993
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1805633"
variation 8017
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="g"
/db_xref="dbSNP:117800767"
STS 8030..8129
/gene="FXR1"
/gene_synonym="FXR1P"
/standard_name="SHGC-77579"
/db_xref="UniSTS:32551"
STS 8031..8129
/gene="FXR1"
/gene_synonym="FXR1P"
/standard_name="G60386"
/db_xref="UniSTS:137492"
variation 8059..8060
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:2602"
variation 8072
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:184031096"
variation 8084
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:2601"
variation 8127
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:368901111"
variation 8135
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:76288512"
variation 8160
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:189394362"
variation 8247
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:62291436"
variation 8293
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:146531694"
variation 8421
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:11548477"
polyA_signal 8453..8458
/gene="FXR1"
/gene_synonym="FXR1P"
polyA_site 8475
/gene="FXR1"
/gene_synonym="FXR1P"
ORIGIN
aggcaaatccgacgtagacggcggcaggcggagcccaaagccggtgatgcagggtgcgcagggatcccacctggagagtcggggcggcacgttgagaccccaggggtgaagggcgggggatcccaatcccagccctgttttcccctcccctttccccgcctccttctcgcccctcccccctcctcccctctggttggaaagtttctagaatctcttcccagcggcctttgcggttccaacatggcggagctgacggtggaggttcgcggctctaacggggctttctacaagggatttatcaaagatgttcatgaagactcccttacagttgtttttgaaaataattggcaaccagaacgccaggttccatttaatgaagttagattaccaccaccacctgatataaaaaaagaaattagtgaaggagatgaagtagaggtatattcaagagcaaatgaccaagagccatgtgggtggtggttggctaaagttcggatgatgaaaggagaattttatgtcattgaatatgctgcttgtgacgctacttacaatgaaatagtcacatttgaacgacttcggcctgtcaatcaaaataaaactgtcaaaaaaaataccttctttaaatgcacagtggatgttcctgaggatttgagagaggcgtgtgctaatgaaaatgcacataaagattttaagaaagcagtaggagcatgcagaattttttaccatccagaaacaacacagctaatgatactgtctgccagtgaagcaactgtgaagagagtaaacatcttaagtgacatgcatttgcgaagtattcgtacgaagttgatgcttatgtccagaaatgaagaggccactaagcatttagaatgcacaaaacaacttgcagcagcttttcatgaggaatttgttgtgagagaagatttaatgggcctggcaataggaacacatggtagtaacatccagcaagctaggaaggttcctggagttaccgccattgagctagatgaagatactggaacattcagaatctacggagagagtgctgatgctgtaaaaaaggctagaggtttcttggaatttgtggaggattttattcaggttcctaggaatctcgttggaaaagtaattggaaaaaatggcaaagttattcaagaaatagtggacaaatctggtgtggttcgagtgagaattgaaggggacaatgaaaataaattacccagagaagacggtatggttccatttgtatttgttggcactaaagaaagcattggaaatgtgcaggttcttctagagtatcatattgcctatctaaaggaagtagaacagctaagaatggaacgcctacagattgatgaacagctgcgacagattggttctaggtcttatagcggaagaggcagaggtcgtcggggacctaattacacctccggttatggtacaaattctgagctgtctaacccctctgaaacggaatctgagcgtaaagacgagctgagtgattggtcattggcaggagaagatgatcgagacagccgacatcagcgtgacagcaggagacgcccaggaggaagaggcagaagtgtttcagggggtcgaggtcgtggtggaccacgtggtggcaaatcctccatcagttctgtgctcaaagatccagacagcaatccatacagcttacttgataatacagaatcagatcagactgcagacactgatgccagcgaatctcatcacagtactaaccgtcgtaggcggtctcgtagacgaaggactgatgaagatgctgttctgatggatggaatgactgaatctgatacagcttcagttaatgaaaatgggctaggcaaaagatgtgattgaagagcatggtccttcagaaaaggcaataaacggcccaactagtgcttctggcgatgacatttctaagctacagcgtactccaggagaagaaaagattaataccttaaaagaagaaaacactcaagaagcagcagtcctgaatggtgtttcataaactgaagaagttcctagtttacagttcttttacattacatttacaatagtgcttgtacaagcttgccaaagatagaatatggatcgccagtctttacatcgcactttcagttcctccatttggaattcaaaaaggggagggatcctgaagaaatcatatgttaaacatactttgacacctactgtgttataaaatatatcatcagatgtgccttgagaatagtatatgtaacattaaaaaaaagttgctggctataggaaatgttattttgttttcaaaatatggcagagatggggggtggtgggtggggtgggatccctaacgtaatattctttatgaaagcattagctgcttttgttacatttttaatatgcaaccacttcttcacctgaggaaaactagaatgaaatgcagtctaaaatattttgcactgaattgtaatttcttcattagtttagtctggaaactggtctgttttaatgtgttttttaaatgctgtatgtagaggaaaatctgcagaccactggaatacatttgttaaactctcatctgcagggacactgggcgatacttggcagtgactgttctaccttgaggctttgtttggtttatttattaaagtgtacagtatttaaaaatcaaacatagctttagttaaaacactaagctgaattagtcatgtccattcagacataacctgaactactgaaaagatcaatttccagaaggtttattctgtataaactacatgttagtcttcagtagagtatcttttttttttccttttttttttttttatttcggttgtttgatgtgcaatatgtttttgtatgcaggtagtaaataaactttgatcttccatttgctgaatttttttaactttctactttttacaccaattgttgcaaaatagttggagctattaataggcttaggatagtatactttgctttttaaaaagcatttatacttgctcataaatagcattaaaatgtcagttggccatttaatcattttgtaatgaatcatctgaaatctttacacaagtttaggctgttagatgcataggtaattaataatacatgtgataattagcaaaaaaacctaacaaaattctaatcaaaggcaactttggaagacaatgggggatagaagggatgacaagcaatttttaaataataggccaatgatttgctttattcattctcaacttattttgaaggctctcatatcagtgaccaaaaatcagttattaaactttatgtatatattttagccagagcttaatttttatgaagataaagacatgaagtttaacaatggacaacagttagtacagctaattgtgaggtcaagtaattgttagacataggggaaggctttgttccacaatattatatggaccactgaacaagaatgacagccctttgttatcacttggcatatgaaaagtgttgtgtgcatagtttgtgttaattttttatgtgcataaaaatgtgattttaatttatatgctctgaaggataattcagggtatagttaaaaatgtacaatgtgccagttcagtatatataaccctagccctcaaattattctgattaaggttaaaatgtgctggtattacgtgctttttcctgaggccttctgattggttcttggtaacagaattttaaagtaaggtgtgagtagtgcaactcctgtcctttatatataaagatatcaagtaatttcatgtcctgatatttaaaaaaattacccacaaatgtgtttttttaaatcgatcaaagctagcaacaggttaaattgtctcagttctcttacataattgggttaaaaattataaggtattagaagaattttaattaatgccaaattggtaaatatggtgtaaaaaaaaaaaaaaagacttttcattttctcccacatagaatagtcagatatattaaacatcccttttccataaagatggtttcaatgggaatggaagaaacaaaatcttaaaagagtgagtatagctgaaccaattcttcattctagcaataaccacactaagttcattactttacaaatgactaaacccaatgtcttgtcctttaaaaaatataggtagtgcagaattgtgataaatacgcatttgtttttttagagagccccactccccaaagggtagccattaattcaggtagccttttaaatgtatttgagagggttccgtctttttggctgctatcctagttaggtgagatgttgctatgggaagaacttgccactatacactaaacagacacttaagcaaaagatgtattctggagcctggcacagtagcttatgtctttggttctagctactcaggagcctgaggtgggagcatcatttgaactcagttctgggccactgagaccctctttaaagagaaggaaaaaaaggtattctggaagatcttgtgcagttgcaacaatgtttcagcatatatatgtgaattcatatatgacacctgaacggaatcatgaagtaacagctgagattatatggtggcaaaaatgacctgcttttcctgaagctttgggaggcctaggattcttgctttaggcatcacctttgttaagccttaaagggggctacaacttgtgcaaaatggtgtctctggtaacacttcagaaataattggcaaaagtgtaataggaatacacaaatctttattttgaaataatcttgtattttaatgtggaattagaagcagcacatcaaactggtgagttcacagaaacttacctgagatgatgctgggttccattgctgttgtgctaagtcacgtatttttgtagctgctgttagctgtgtctagcgttttgtaacctaaggagggtcttatagaagttggtatgttaactaaatcttggactgggaaacagcaccatttgtatcctctgcaaacagatttacgcttttgaggctcaaaccaactagtgttctcatgggctgttgcctaaggacagataaacatggaaaacaggctatgtccagggacagatgattggtggttaagaattacagtaaaggaaaattacacctggattttcttctgtaaagtttcaaggaacttggatttgaactgtgaatctactgttttggcaaaaaatctcaaagaaaaggatgtttgttactgtctcagtcttcctgtctttgctacacgatttggatcccttacgctttttcgttaagaatatctgtctgctatagtgaatttgctagccccttatttttttttttaattttagttctttattagaacgtgtacttgaatggactgtagttgctcataacccatgttaatctctgatagtatttgggttttatttcaggagcttttgcaataaagcagtaactgcaatctgctaaagtcagactgttagcaagtggtgttaaaactgatttaagtccattacactgaacagtaggaaattaccacttttgtaaggctcaaaaatgatcaactattaacagtttcttatggttcagtctaattacaaatttttaaaaagtttatcagtgtatcatttcagattcatctgtatcttctgtaatattatttccagtactgaggtaaggtacacaaaaattcccctggaaaaactatattctagttttgtaagatgatttcccacagtccatttgcttatttcttcctttgataattcaaaaagatgctttaggtaatggtacagaattagaagctgctattttagctctattaactttttctctatggtttcaattttatccaaccagagagggctggcctagttggtatctttaaggcccttccagtagtaatttgagtctagtcacatgtcagaccctgagcaacacctaaccaaatgcccaagtattctcataaggagtatgctgaatttaagtggtgtttgttttacatatgtatccatcccagacattttcaactatgctgaatgcaatctataagatattccaaacaaggacaaagtaatttttcacaagtcttacagccccactattaagtatgctactaattagcttcttgaatttctttgtatttcagtgattgggatgttctttttttttgggaaagtttttttacccctttgtaccctcttaattggattaactgtaaaatgtacatattaattttctagttttagagaccattttcattaaaaatattttccaatagtttttctagataaacaatttatacttaattgttgcttggttgcttacatttcaacctctaggcttcctttttcagctaacttggctgtcttcaggttgtaaagaaaaatgtaaacatatatttgaaatttcattaactgaaactgctgtaaggtgttagcaaatgttaaccataacagattatcccatatcattggactgttctattattgggtcaggaataataggtgacacaggatagaagctcttcctatatatatcttgttgctaaggcagtagttggctctaagctgataaacagcacactgtacagcagtccaaaaactaaaaccagagcttaggtcattcaagttaactggtactcaaggttactcattccaggatactttacataaccaaaaacctaggagagcattctacattgtaattttttttttactttgtttacataaaatttacagggttttgtttttttaagcttagtctgttctttgacattgttgattcatgttctaaattttcatcagatttaacatgtttggaggttcttgtgcactcaatgtgaacctactacaagcttctgaactgcaaaaccttttttttaggtcactgtcaacagaaagatgccttatagaatttctcatgattgaaacagaactctgcattctaacctaaaacccctctaaccctttaaatgaagcattatgcctgcgtgaaattttatttttagacatttctgatactaggttttctttacgggggggcatacatattcagtatactgaatttatacagctttcagtgtggcaatatattaagaagctagttccctaatttttctcagttctcattggttttccatttaaatgtttccgtaagtactctcatcatttggaaaatacttgatggcaggagaacttgcttaaaactaaaggtggagaaagagttaacttccaggacaacccattatagctcacttcttaccaacaaagcagtttttatacagcaccttaggactcatttctaatgtcaacccagatggccagtaaaggcaagggaagaggctaagtgactcacaaaaatctctgatattgaggtctaatgtgaaggctatagataggaattccccacaaacttctaatgaggactaatatgaacagcaaattggagaagacaccaaggacctaattttagtttcactagccgtgggaccttagaaaaaagaccatttgctctggacttttgtttcccaagccataaaatgtggaagaatcttcacaatttcaagttggtcatgtatatttcccttttacagagaaagctgaagcctcgaggctcagatttacctggcttctgtttacctggcttctgcagaagtttaacttgtaacctacctctcattcccaaagtgtgtttaatcatgccgccttctttaaaatatatctggaagcaccaatgagtaaagacaaaggccccaagctagatctgtagagataagtactagactcacatctcagtactatcaaggaaaacatgcttaggttatcagaattgtgaaggccatagtacaaaaagttaagagaacggaactcaggatctgagaaagatcagccattctcagcatgttgccttggctgcttaaccttactaaacttccatttcctcacatgtaaaatgtacatcataataactagtctactgagataagggaagaatacttagcacagtgctagtacactgtaagtactcaaatgttacagatccaagtattttgtaagaaaataccagcaaaagataaaagtttttttatggatcgtatttgtatcaatcacctacatgatctagagccctcacatggataacatttaaatgttcagtttgcctaatagccttcaatgaaacacggattcttctacttaaaaaaggtaagcctggagaaaataaaactgattactatgcaagaaaaaaatgtgctctgctgtgctccttggtatttttaagtggtttccattgtcttaacacctgtcttaaaacgggtatgttgtttgcactgaaccctcaaaagtatttatacctattaagttaaatttccctttttagagttaatgcttcattgcctgtcggcatattatcactatctgtctttgaaaaattttcttttaagtctcaactatttcttcataaagctcttgttcagagaaacattttttgatttgtccaatggactgaaataaaaggttagtaaaccaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:8087 -> Molecular function: GO:0002151 [G-quadruplex RNA binding] evidence: IEA
GeneID:8087 -> Molecular function: GO:0003723 [RNA binding] evidence: TAS
GeneID:8087 -> Molecular function: GO:0003730 [mRNA 3'-UTR binding] evidence: IEA
GeneID:8087 -> Biological process: GO:0006915 [apoptotic process] evidence: TAS
GeneID:8087 -> Biological process: GO:0007517 [muscle organ development] evidence: IEA
GeneID:8087 -> Biological process: GO:0017148 [negative regulation of translation] evidence: IEA
GeneID:8087 -> Biological process: GO:0030154 [cell differentiation] evidence: IEA
GeneID:8087 -> Cellular component: GO:0005730 [nucleolus] evidence: TAS
GeneID:8087 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA
GeneID:8087 -> Cellular component: GO:0005844 [polysome] evidence: IEA
GeneID:8087 -> Cellular component: GO:0043034 [costamere] evidence: IEA
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