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2025-05-09 17:10:22, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001013439 8911 bp mRNA linear PRI 07-JUL-2013
DEFINITION Homo sapiens fragile X mental retardation, autosomal homolog 1
(FXR1), transcript variant 3, mRNA.
ACCESSION NM_001013439
VERSION NM_001013439.2 GI:298231193
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 8911)
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 8911)
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 8911)
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 8911)
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 8911)
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 8911)
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 8911)
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 8911)
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 8911)
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 8911)
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 VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
DC352767.1, AU280585.1, AK292633.1 and AC008009.5.
On Jun 13, 2010 this sequence version replaced gi:61835171.
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 (3) contains an alternate exon
compared to variant 1. The resulting isoform (c) is shorter at the
N-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##
CDS exon combination :: AY341428.1 [ECO:0000331]
RNAseq introns :: single sample supports all introns
ERS025084, ERS025088 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-242 DC352767.1 1-242
243-798 AU280585.1 18-573
799-2562 AK292633.1 231-1994
2563-8911 AC008009.5 72297-78645
FEATURES Location/Qualifiers
source 1..8911
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="3"
/map="3q28"
gene 1..8911
/gene="FXR1"
/gene_synonym="FXR1P"
/note="fragile X mental retardation, autosomal homolog 1"
/db_xref="GeneID:8087"
/db_xref="HGNC:4023"
/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"
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..635
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 485
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:139202315"
variation 513
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:182031741"
misc_feature 633..635
/gene="FXR1"
/gene_synonym="FXR1P"
/note="upstream in-frame stop codon"
exon 636..688
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
exon 689..782
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 708
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:375255336"
variation 755
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:371183000"
exon 783..854
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 808
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:199903473"
variation 812
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:144304502"
CDS 840..2450
/gene="FXR1"
/gene_synonym="FXR1P"
/note="isoform c is encoded by transcript variant 3;
fragile X mental retardation syndrome-related protein 1;
hFXR1p"
/codon_start=1
/product="fragile X mental retardation syndrome-related
protein 1 isoform c"
/protein_id="NP_001013457.1"
/db_xref="GI:61835172"
/db_xref="CCDS:CCDS33894.1"
/db_xref="GeneID:8087"
/db_xref="HGNC:4023"
/db_xref="MIM:600819"
/translation="
MMKGEFYVIEYAACDATYNEIVTFERLRPVNQNKTVKKNTFFKCTVDVPEDLREACANENAHKDFKKAVGACRIFYHPETTQLMILSASEATVKRVNILSDMHLRSIRTKLMLMSRNEEATKHLECTKQLAAAFHEEFVVREDLMGLAIGTHGSNIQQARKVPGVTAIELDEDTGTFRIYGESADAVKKARGFLEFVEDFIQVPRNLVGKVIGKNGKVIQEIVDKSGVVRVRIEGDNENKLPREDGMVPFVFVGTKESIGNVQVLLEYHIAYLKEVEQLRMERLQIDEQLRQIGSRSYSGRGRGRRGPNYTSGYGTNSELSNPSETESERKDELSDWSLAGEDDRDSRHQRDSRRRPGGRGRSVSGGRGRGGPRGGKSSISSVLKDPDSNPYSLLDNTESDQTADTDASESHHSTNRRRRSRRRRTDEDAVLMDGMTESDTASVNENGLVTVADYISRAESQSRQRNLPRETLAKNKKEMAKDVIEEHGPSEKAINGPTSASGDDISKLQRTPGEEKINTLKEENTQEAAVLNGVS
"
misc_feature 1242..1424
/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(1266..1268,1272..1280,1284..1298,1305..1310,
1317..1322,1335..1343)
/gene="FXR1"
/gene_synonym="FXR1P"
/note="nucleic acid binding region [nucleotide binding];
other site"
/db_xref="CDD:29002"
misc_feature 1287..1298
/gene="FXR1"
/gene_synonym="FXR1P"
/note="G-X-X-G motif; other site"
/db_xref="CDD:29002"
misc_feature 1440..1640
/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(1455..1457,1461..1469,1473..1487,1494..1499,
1506..1511,1527..1538)
/gene="FXR1"
/gene_synonym="FXR1P"
/note="nucleic acid binding region [nucleotide binding];
other site"
/db_xref="CDD:29002"
misc_feature 1476..1487
/gene="FXR1"
/gene_synonym="FXR1P"
/note="G-X-X-G motif; other site"
/db_xref="CDD:29002"
misc_feature 1665..>1718
/gene="FXR1"
/gene_synonym="FXR1P"
/note="Fragile X-related 1 protein C terminal; Region:
FXR1P_C; pfam12235"
/db_xref="CDD:152670"
misc_feature 1785..1787
/gene="FXR1"
/gene_synonym="FXR1P"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1791..1793
/gene="FXR1"
/gene_synonym="FXR1P"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1800..1802
/gene="FXR1"
/gene_synonym="FXR1P"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1809..1811
/gene="FXR1"
/gene_synonym="FXR1P"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1815..1817
/gene="FXR1"
/gene_synonym="FXR1P"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1821..1823
/gene="FXR1"
/gene_synonym="FXR1P"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1917..1919
/gene="FXR1"
/gene_synonym="FXR1P"
/experiment="experimental evidence, no additional details
recorded"
/note="methylation site"
misc_feature 1941..1943
/gene="FXR1"
/gene_synonym="FXR1P"
/experiment="experimental evidence, no additional details
recorded"
/note="methylation site"
misc_feature 2013..2015
/gene="FXR1"
/gene_synonym="FXR1P"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 2037..2039
/gene="FXR1"
/gene_synonym="FXR1P"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 2046..2048
/gene="FXR1"
/gene_synonym="FXR1P"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 2064..2066
/gene="FXR1"
/gene_synonym="FXR1P"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
exon 855..1003
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 872
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:145159450"
variation 878
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:369357473"
variation 971
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:139008118"
STS 972..1086
/gene="FXR1"
/gene_synonym="FXR1P"
/standard_name="FXR1"
/db_xref="UniSTS:505522"
STS 980..1063
/gene="FXR1"
/gene_synonym="FXR1P"
/standard_name="RH123299"
/db_xref="UniSTS:135676"
exon 1004..1097
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 1046
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:377389758"
variation 1052
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:3026195"
exon 1098..1214
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 1101
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:143250917"
variation 1110
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:201512027"
variation 1157
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:148268040"
variation 1205
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:370062138"
exon 1215..1385
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 1268
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:374396414"
variation 1337
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:73176330"
variation 1365
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:200507471"
variation 1371
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:142641159"
exon 1386..1464
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 1406
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="g"
/db_xref="dbSNP:371122085"
STS 1413..1619
/gene="FXR1"
/gene_synonym="FXR1P"
/standard_name="Fxr1h"
/db_xref="UniSTS:498301"
variation 1440
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:200358370"
exon 1465..1574
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 1476
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:76531300"
exon 1575..1661
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 1635
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="g"
/db_xref="dbSNP:376660925"
variation 1646
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1805617"
exon 1662..1719
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 1673
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:369969651"
exon 1720..1782
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 1736
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:202004870"
variation 1775
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:370623678"
variation 1776
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:372792772"
exon 1783..1986
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 1792
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:199510994"
variation 1815
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:199504601"
variation 1816
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:201616183"
variation 1820
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:200492892"
variation 1869
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1051080"
variation 1882
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:371485992"
variation 1891
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:374389670"
variation 1959
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:199785386"
exon 1987..2187
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 1993
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:138120810"
variation 2075
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:201665512"
variation 2080
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:371778667"
variation 2092
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:143480969"
STS 2180..2378
/gene="FXR1"
/gene_synonym="FXR1P"
/standard_name="BI281166"
/db_xref="UniSTS:249408"
exon 2188..2279
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 2203
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:377706871"
variation 2228..2229
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="t"
/db_xref="dbSNP:11435319"
STS 2233..2437
/gene="FXR1"
/gene_synonym="FXR1P"
/standard_name="BI274570"
/db_xref="UniSTS:249125"
variation 2236..2237
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="t"
/db_xref="dbSNP:11435320"
variation 2251
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:201230703"
variation 2269
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:201838203"
exon 2280..8911
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 2302
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:147171380"
variation 2303
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:367886303"
variation 2305
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:138367563"
variation 2313
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:149239435"
variation 2315
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:201161602"
variation 2316
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:111774718"
variation 2335
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:371671972"
variation 2343
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:201637634"
variation 2352
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:148795102"
variation 2373
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:55637125"
variation 2376
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:143951672"
variation 2398
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:146350316"
variation 2419
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:3026204"
variation 2422
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:112134282"
variation 2425
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:11499"
variation 2438
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:139713512"
variation 2455
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:376366097"
variation 2460
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:371231893"
variation 2496
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:199650094"
variation 2537
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:368937602"
variation 2600
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="g"
/db_xref="dbSNP:138323510"
polyA_signal 2683..2688
/gene="FXR1"
/gene_synonym="FXR1P"
polyA_site 2711
/gene="FXR1"
/gene_synonym="FXR1P"
variation 2754
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="g"
/db_xref="dbSNP:77451926"
variation 2820
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:3026205"
variation 2944
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:372825020"
variation 2951
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:377201428"
variation 2962
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:188550393"
variation 2965
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:117037927"
variation 2980
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:191923790"
variation 3167
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:145591161"
variation 3232
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:200701459"
variation 3235..3236
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="a"
/db_xref="dbSNP:201501227"
variation 3236
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:138114654"
variation 3245..3247
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="ttt"
/db_xref="dbSNP:79881434"
polyA_signal 3293..3298
/gene="FXR1"
/gene_synonym="FXR1P"
variation 3302
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:183311734"
polyA_site 3320
/gene="FXR1"
/gene_synonym="FXR1P"
variation 3560..3561
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="aa"
/db_xref="dbSNP:146154883"
variation 3593..3594
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="gg"
/db_xref="dbSNP:201594378"
variation 3665
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:187223562"
variation 3668
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:191718661"
variation 3811
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:183888010"
variation 3862
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="g"
/db_xref="dbSNP:370717702"
variation 3952
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:3026206"
variation 3956
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:113426020"
variation 4001
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:149096577"
variation 4229
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:186780056"
variation 4339..4340
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="a"
/db_xref="dbSNP:35250215"
variation 4340
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="a"
/db_xref="dbSNP:67565008"
variation 4359
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:143130417"
variation 4361
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1805627"
variation 4375
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1805628"
variation 4387
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:193140070"
STS 4415..4576
/gene="FXR1"
/gene_synonym="FXR1P"
/standard_name="D3S2910E"
/db_xref="UniSTS:150894"
variation 4449
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="ta"
/db_xref="dbSNP:200214928"
variation 4450..4451
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="tt"
/db_xref="dbSNP:67477912"
variation 4577
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:185723329"
variation 4706
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="g"
/db_xref="dbSNP:190201524"
variation 4760
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="g"
/db_xref="dbSNP:182067416"
variation 4840
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:148220661"
variation 4920
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:62291435"
variation 4950
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:141181334"
variation 4978
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:112349907"
variation 5143
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:114145770"
STS 5236..5386
/gene="FXR1"
/gene_synonym="FXR1P"
/standard_name="RH98363"
/db_xref="UniSTS:89700"
variation 5375
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:184223404"
variation 5392
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:147356292"
variation 5403
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:370998297"
variation 5496
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1465374"
variation 5504
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="g"
/db_xref="dbSNP:188684032"
variation 5568
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:3026207"
variation 5591
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1008412"
variation 5626
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1805629"
STS 5635..5834
/gene="FXR1"
/gene_synonym="FXR1P"
/standard_name="D3S3105"
/db_xref="UniSTS:61824"
STS 5640..5790
/gene="FXR1"
/gene_synonym="FXR1P"
/standard_name="Cda01e11"
/db_xref="UniSTS:64869"
variation 5658
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:374633367"
variation 5687
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:181123657"
variation 5711
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:116043654"
variation 5742
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:3026208"
variation 5775
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:137877459"
variation 5797
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:189429564"
polyA_signal 5823..5828
/gene="FXR1"
/gene_synonym="FXR1P"
variation 5835
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:114677034"
polyA_site 5854
/gene="FXR1"
/gene_synonym="FXR1P"
variation 5881
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:143392613"
variation 6105
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:180725645"
variation 6201
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:147544455"
variation 6353
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:187502719"
STS 6370..6499
/gene="FXR1"
/gene_synonym="FXR1P"
/standard_name="A006P45"
/db_xref="UniSTS:58844"
variation 6498
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:1058382"
variation 6500
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:6799476"
variation 6542..6543
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="t"
/db_xref="dbSNP:201242121"
variation 6551
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:16832224"
variation 6558..6559
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="t"
/db_xref="dbSNP:144707771"
variation 6610..6613
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="atta"
/db_xref="dbSNP:373289717"
variation 6612
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:3026209"
variation 6626
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:191834999"
variation 6681
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:140179467"
variation 6786
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:183796587"
variation 6808
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:79629055"
variation 6836
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:185999941"
variation 6918
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:373868693"
variation 6919
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:190427919"
variation 7036
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:150037153"
variation 7086..7087
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="t"
/db_xref="dbSNP:151155261"
variation 7087..7088
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="t"
/db_xref="dbSNP:11448946"
variation 7151
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:182639763"
variation 7369
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:7646508"
variation 7499
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:368717976"
variation 7534
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:148748584"
variation 7544
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1805630"
variation 7595
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:202106534"
variation 7662
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:142318810"
variation 7666
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:187015735"
variation 7691
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1805607"
variation 7779
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="g"
/db_xref="dbSNP:146809695"
variation 7791
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="a"
/db_xref="dbSNP:199927975"
variation 7825
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:192718619"
variation 7864
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:73046170"
variation 7910
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:201358029"
variation 7955
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:189118011"
variation 7971
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1805631"
variation 8001..8015
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="tttacctggcttctg"
/db_xref="dbSNP:368024256"
variation 8084
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:193073756"
variation 8085
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1805632"
variation 8181
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:184439182"
variation 8275
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:369747203"
variation 8324
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:144198197"
variation 8345
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:188933563"
variation 8369
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="g"
/db_xref="dbSNP:191855515"
variation 8429
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1805633"
variation 8453
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="g"
/db_xref="dbSNP:117800767"
STS 8466..8565
/gene="FXR1"
/gene_synonym="FXR1P"
/standard_name="SHGC-77579"
/db_xref="UniSTS:32551"
STS 8467..8565
/gene="FXR1"
/gene_synonym="FXR1P"
/standard_name="G60386"
/db_xref="UniSTS:137492"
variation 8495..8496
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:2602"
variation 8508
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:184031096"
variation 8520
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:2601"
variation 8563
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:368901111"
variation 8571
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:76288512"
variation 8596
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:189394362"
variation 8683
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:62291436"
variation 8729
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:146531694"
variation 8857
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:11548477"
polyA_signal 8889..8894
/gene="FXR1"
/gene_synonym="FXR1P"
polyA_site 8911
/gene="FXR1"
/gene_synonym="FXR1P"
ORIGIN
aggcaaatccgacgtagacggcggcaggcggagcccaaagccggtgatgcagggtgcgcagggatcccacctggagagtcggggcggcacgttgagaccccaggggtgaagggcgggggatcccaatcccagccctgttttcccctcccctttccccgcctccttctcgcccctcccccctcctcccctctggttggaaagtttctagaatctcttcccagcggcctttgcggttccaacatggcggagctgacggtggaggttcgcggctctaacggggctttctacaagtcaattcacaatgaatcaaatgtccccattttggaactctgaagtatttataattgatctctatacatatctacaatctactgcttgtttctacttagactttgactccattactcattttgcctcacaaagtgagttggtactttgacaaaggttggaaaggacactagccacctgtgtgtgcactgaaatcatgtacgcttgaacatttggaattttatgtccagccataatccacttgcatatgcactttgtggaaactgtggtcttcagaactctggaagaatgagaatggcggagtggaaaagagtcctggatttgaagtaaacagatgagaattctagggatttatcaaagatgttcatgaagactcccttacagttgtttttgaaaataattggcaaccagaacgccaggttccatttaatgaagttagattaccaccaccacctgatataaaaaaagaaattagtgaaggagatgaagtagaggtatattcaagagcaaatgaccaagagccatgtgggtggtggttggctaaagttcggatgatgaaaggagaattttatgtcattgaatatgctgcttgtgacgctacttacaatgaaatagtcacatttgaacgacttcggcctgtcaatcaaaataaaactgtcaaaaaaaataccttctttaaatgcacagtggatgttcctgaggatttgagagaggcgtgtgctaatgaaaatgcacataaagattttaagaaagcagtaggagcatgcagaattttttaccatccagaaacaacacagctaatgatactgtctgccagtgaagcaactgtgaagagagtaaacatcttaagtgacatgcatttgcgaagtattcgtacgaagttgatgcttatgtccagaaatgaagaggccactaagcatttagaatgcacaaaacaacttgcagcagcttttcatgaggaatttgttgtgagagaagatttaatgggcctggcaataggaacacatggtagtaacatccagcaagctaggaaggttcctggagttaccgccattgagctagatgaagatactggaacattcagaatctacggagagagtgctgatgctgtaaaaaaggctagaggtttcttggaatttgtggaggattttattcaggttcctaggaatctcgttggaaaagtaattggaaaaaatggcaaagttattcaagaaatagtggacaaatctggtgtggttcgagtgagaattgaaggggacaatgaaaataaattacccagagaagacggtatggttccatttgtatttgttggcactaaagaaagcattggaaatgtgcaggttcttctagagtatcatattgcctatctaaaggaagtagaacagctaagaatggaacgcctacagattgatgaacagctgcgacagattggttctaggtcttatagcggaagaggcagaggtcgtcggggacctaattacacctccggttatggtacaaattctgagctgtctaacccctctgaaacggaatctgagcgtaaagacgagctgagtgattggtcattggcaggagaagatgatcgagacagccgacatcagcgtgacagcaggagacgcccaggaggaagaggcagaagtgtttcagggggtcgaggtcgtggtggaccacgtggtggcaaatcctccatcagttctgtgctcaaagatccagacagcaatccatacagcttacttgataatacagaatcagatcagactgcagacactgatgccagcgaatctcatcacagtactaaccgtcgtaggcggtctcgtagacgaaggactgatgaagatgctgttctgatggatggaatgactgaatctgatacagcttcagttaatgaaaatgggctagtcacagttgcagattatatttctagagctgagtctcagagcagacaaagaaacctcccaagggaaactttggctaaaaacaagaaagaaatggcaaaagatgtgattgaagagcatggtccttcagaaaaggcaataaacggcccaactagtgcttctggcgatgacatttctaagctacagcgtactccaggagaagaaaagattaataccttaaaagaagaaaacactcaagaagcagcagtcctgaatggtgtttcataaactgaagaagttcctagtttacagttcttttacattacatttacaatagtgcttgtacaagcttgccaaagatagaatatggatcgccagtctttacatcgcactttcagttcctccatttggaattcaaaaaggggagggatcctgaagaaatcatatgttaaacatactttgacacctactgtgttataaaatatatcatcagatgtgccttgagaatagtatatgtaacattaaaaaaaagttgctggctataggaaatgttattttgttttcaaaatatggcagagatggggggtggtgggtggggtgggatccctaacgtaatattctttatgaaagcattagctgcttttgttacatttttaatatgcaaccacttcttcacctgaggaaaactagaatgaaatgcagtctaaaatattttgcactgaattgtaatttcttcattagtttagtctggaaactggtctgttttaatgtgttttttaaatgctgtatgtagaggaaaatctgcagaccactggaatacatttgttaaactctcatctgcagggacactgggcgatacttggcagtgactgttctaccttgaggctttgtttggtttatttattaaagtgtacagtatttaaaaatcaaacatagctttagttaaaacactaagctgaattagtcatgtccattcagacataacctgaactactgaaaagatcaatttccagaaggtttattctgtataaactacatgttagtcttcagtagagtatcttttttttttccttttttttttttttatttcggttgtttgatgtgcaatatgtttttgtatgcaggtagtaaataaactttgatcttccatttgctgaatttttttaactttctactttttacaccaattgttgcaaaatagttggagctattaataggcttaggatagtatactttgctttttaaaaagcatttatacttgctcataaatagcattaaaatgtcagttggccatttaatcattttgtaatgaatcatctgaaatctttacacaagtttaggctgttagatgcataggtaattaataatacatgtgataattagcaaaaaaacctaacaaaattctaatcaaaggcaactttggaagacaatgggggatagaagggatgacaagcaatttttaaataataggccaatgatttgctttattcattctcaacttattttgaaggctctcatatcagtgaccaaaaatcagttattaaactttatgtatatattttagccagagcttaatttttatgaagataaagacatgaagtttaacaatggacaacagttagtacagctaattgtgaggtcaagtaattgttagacataggggaaggctttgttccacaatattatatggaccactgaacaagaatgacagccctttgttatcacttggcatatgaaaagtgttgtgtgcatagtttgtgttaattttttatgtgcataaaaatgtgattttaatttatatgctctgaaggataattcagggtatagttaaaaatgtacaatgtgccagttcagtatatataaccctagccctcaaattattctgattaaggttaaaatgtgctggtattacgtgctttttcctgaggccttctgattggttcttggtaacagaattttaaagtaaggtgtgagtagtgcaactcctgtcctttatatataaagatatcaagtaatttcatgtcctgatatttaaaaaaattacccacaaatgtgtttttttaaatcgatcaaagctagcaacaggttaaattgtctcagttctcttacataattgggttaaaaattataaggtattagaagaattttaattaatgccaaattggtaaatatggtgtaaaaaaaaaaaaaaagacttttcattttctcccacatagaatagtcagatatattaaacatcccttttccataaagatggtttcaatgggaatggaagaaacaaaatcttaaaagagtgagtatagctgaaccaattcttcattctagcaataaccacactaagttcattactttacaaatgactaaacccaatgtcttgtcctttaaaaaatataggtagtgcagaattgtgataaatacgcatttgtttttttagagagccccactccccaaagggtagccattaattcaggtagccttttaaatgtatttgagagggttccgtctttttggctgctatcctagttaggtgagatgttgctatgggaagaacttgccactatacactaaacagacacttaagcaaaagatgtattctggagcctggcacagtagcttatgtctttggttctagctactcaggagcctgaggtgggagcatcatttgaactcagttctgggccactgagaccctctttaaagagaaggaaaaaaaggtattctggaagatcttgtgcagttgcaacaatgtttcagcatatatatgtgaattcatatatgacacctgaacggaatcatgaagtaacagctgagattatatggtggcaaaaatgacctgcttttcctgaagctttgggaggcctaggattcttgctttaggcatcacctttgttaagccttaaagggggctacaacttgtgcaaaatggtgtctctggtaacacttcagaaataattggcaaaagtgtaataggaatacacaaatctttattttgaaataatcttgtattttaatgtggaattagaagcagcacatcaaactggtgagttcacagaaacttacctgagatgatgctgggttccattgctgttgtgctaagtcacgtatttttgtagctgctgttagctgtgtctagcgttttgtaacctaaggagggtcttatagaagttggtatgttaactaaatcttggactgggaaacagcaccatttgtatcctctgcaaacagatttacgcttttgaggctcaaaccaactagtgttctcatgggctgttgcctaaggacagataaacatggaaaacaggctatgtccagggacagatgattggtggttaagaattacagtaaaggaaaattacacctggattttcttctgtaaagtttcaaggaacttggatttgaactgtgaatctactgttttggcaaaaaatctcaaagaaaaggatgtttgttactgtctcagtcttcctgtctttgctacacgatttggatcccttacgctttttcgttaagaatatctgtctgctatagtgaatttgctagccccttatttttttttttaattttagttctttattagaacgtgtacttgaatggactgtagttgctcataacccatgttaatctctgatagtatttgggttttatttcaggagcttttgcaataaagcagtaactgcaatctgctaaagtcagactgttagcaagtggtgttaaaactgatttaagtccattacactgaacagtaggaaattaccacttttgtaaggctcaaaaatgatcaactattaacagtttcttatggttcagtctaattacaaatttttaaaaagtttatcagtgtatcatttcagattcatctgtatcttctgtaatattatttccagtactgaggtaaggtacacaaaaattcccctggaaaaactatattctagttttgtaagatgatttcccacagtccatttgcttatttcttcctttgataattcaaaaagatgctttaggtaatggtacagaattagaagctgctattttagctctattaactttttctctatggtttcaattttatccaaccagagagggctggcctagttggtatctttaaggcccttccagtagtaatttgagtctagtcacatgtcagaccctgagcaacacctaaccaaatgcccaagtattctcataaggagtatgctgaatttaagtggtgtttgttttacatatgtatccatcccagacattttcaactatgctgaatgcaatctataagatattccaaacaaggacaaagtaatttttcacaagtcttacagccccactattaagtatgctactaattagcttcttgaatttctttgtatttcagtgattgggatgttctttttttttgggaaagtttttttacccctttgtaccctcttaattggattaactgtaaaatgtacatattaattttctagttttagagaccattttcattaaaaatattttccaatagtttttctagataaacaatttatacttaattgttgcttggttgcttacatttcaacctctaggcttcctttttcagctaacttggctgtcttcaggttgtaaagaaaaatgtaaacatatatttgaaatttcattaactgaaactgctgtaaggtgttagcaaatgttaaccataacagattatcccatatcattggactgttctattattgggtcaggaataataggtgacacaggatagaagctcttcctatatatatcttgttgctaaggcagtagttggctctaagctgataaacagcacactgtacagcagtccaaaaactaaaaccagagcttaggtcattcaagttaactggtactcaaggttactcattccaggatactttacataaccaaaaacctaggagagcattctacattgtaattttttttttactttgtttacataaaatttacagggttttgtttttttaagcttagtctgttctttgacattgttgattcatgttctaaattttcatcagatttaacatgtttggaggttcttgtgcactcaatgtgaacctactacaagcttctgaactgcaaaaccttttttttaggtcactgtcaacagaaagatgccttatagaatttctcatgattgaaacagaactctgcattctaacctaaaacccctctaaccctttaaatgaagcattatgcctgcgtgaaattttatttttagacatttctgatactaggttttctttacgggggggcatacatattcagtatactgaatttatacagctttcagtgtggcaatatattaagaagctagttccctaatttttctcagttctcattggttttccatttaaatgtttccgtaagtactctcatcatttggaaaatacttgatggcaggagaacttgcttaaaactaaaggtggagaaagagttaacttccaggacaacccattatagctcacttcttaccaacaaagcagtttttatacagcaccttaggactcatttctaatgtcaacccagatggccagtaaaggcaagggaagaggctaagtgactcacaaaaatctctgatattgaggtctaatgtgaaggctatagataggaattccccacaaacttctaatgaggactaatatgaacagcaaattggagaagacaccaaggacctaattttagtttcactagccgtgggaccttagaaaaaagaccatttgctctggacttttgtttcccaagccataaaatgtggaagaatcttcacaatttcaagttggtcatgtatatttcccttttacagagaaagctgaagcctcgaggctcagatttacctggcttctgtttacctggcttctgcagaagtttaacttgtaacctacctctcattcccaaagtgtgtttaatcatgccgccttctttaaaatatatctggaagcaccaatgagtaaagacaaaggccccaagctagatctgtagagataagtactagactcacatctcagtactatcaaggaaaacatgcttaggttatcagaattgtgaaggccatagtacaaaaagttaagagaacggaactcaggatctgagaaagatcagccattctcagcatgttgccttggctgcttaaccttactaaacttccatttcctcacatgtaaaatgtacatcataataactagtctactgagataagggaagaatacttagcacagtgctagtacactgtaagtactcaaatgttacagatccaagtattttgtaagaaaataccagcaaaagataaaagtttttttatggatcgtatttgtatcaatcacctacatgatctagagccctcacatggataacatttaaatgttcagtttgcctaatagccttcaatgaaacacggattcttctacttaaaaaaggtaagcctggagaaaataaaactgattactatgcaagaaaaaaatgtgctctgctgtgctccttggtatttttaagtggtttccattgtcttaacacctgtcttaaaacgggtatgttgtttgcactgaaccctcaaaagtatttatacctattaagttaaatttccctttttagagttaatgcttcattgcctgtcggcatattatcactatctgtctttgaaaaattttcttttaagtctcaactatttcttcataaagctcttgttcagagaaacattttttgatttgtccaatggactgaaataaaaggttagtaaaccaaaa
//
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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