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2025-05-09 16:10:39, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_005087 8567 bp mRNA linear PRI 07-JUL-2013
DEFINITION Homo sapiens fragile X mental retardation, autosomal homolog 1
(FXR1), transcript variant 1, mRNA.
ACCESSION NM_005087
VERSION NM_005087.3 GI:298231191
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 8567)
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 8567)
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 8567)
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 8567)
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 8567)
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 8567)
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 8567)
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 8567)
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 8567)
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 8567)
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, AK292633.1 and
AC008009.5.
On Jun 13, 2010 this sequence version replaced gi:61835147.
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 (1) encodes the longest 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 :: U25165.1, AK292633.1 [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
1-319 DC352767.1 1-319
320-2218 AK292633.1 96-1994
2219-8567 AC008009.5 72297-78645
FEATURES Location/Qualifiers
source 1..8567
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="3"
/map="3q28"
gene 1..8567
/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"
CDS 241..2106
/gene="FXR1"
/gene_synonym="FXR1P"
/note="isoform a is encoded by transcript variant 1;
fragile X mental retardation syndrome-related protein 1;
hFXR1p"
/codon_start=1
/product="fragile X mental retardation syndrome-related
protein 1 isoform a"
/protein_id="NP_005078.2"
/db_xref="GI:61835148"
/db_xref="CCDS:CCDS3238.1"
/db_xref="GeneID:8087"
/db_xref="HGNC:4023"
/db_xref="MIM:600819"
/translation="
MAELTVEVRGSNGAFYKGFIKDVHEDSLTVVFENNWQPERQVPFNEVRLPPPPDIKKEISEGDEVEVYSRANDQEPCGWWLAKVRMMKGEFYVIEYAACDATYNEIVTFERLRPVNQNKTVKKNTFFKCTVDVPEDLREACANENAHKDFKKAVGACRIFYHPETTQLMILSASEATVKRVNILSDMHLRSIRTKLMLMSRNEEATKHLECTKQLAAAFHEEFVVREDLMGLAIGTHGSNIQQARKVPGVTAIELDEDTGTFRIYGESADAVKKARGFLEFVEDFIQVPRNLVGKVIGKNGKVIQEIVDKSGVVRVRIEGDNENKLPREDGMVPFVFVGTKESIGNVQVLLEYHIAYLKEVEQLRMERLQIDEQLRQIGSRSYSGRGRGRRGPNYTSGYGTNSELSNPSETESERKDELSDWSLAGEDDRDSRHQRDSRRRPGGRGRSVSGGRGRGGPRGGKSSISSVLKDPDSNPYSLLDNTESDQTADTDASESHHSTNRRRRSRRRRTDEDAVLMDGMTESDTASVNENGLVTVADYISRAESQSRQRNLPRETLAKNKKEMAKDVIEEHGPSEKAINGPTSASGDDISKLQRTPGEEKINTLKEENTQEAAVLNGVS
"
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"
misc_feature 1999..2001
/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 2071..2073
/gene="FXR1"
/gene_synonym="FXR1P"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphothreonine; propagated from
UniProtKB/Swiss-Prot (P51114.3); 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"
STS 1836..2034
/gene="FXR1"
/gene_synonym="FXR1P"
/standard_name="BI281166"
/db_xref="UniSTS:249408"
exon 1844..1935
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 1859
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:377706871"
variation 1884..1885
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="t"
/db_xref="dbSNP:11435319"
STS 1889..2093
/gene="FXR1"
/gene_synonym="FXR1P"
/standard_name="BI274570"
/db_xref="UniSTS:249125"
variation 1892..1893
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="t"
/db_xref="dbSNP:11435320"
variation 1907
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:201230703"
variation 1925
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:201838203"
exon 1936..8567
/gene="FXR1"
/gene_synonym="FXR1P"
/inference="alignment:Splign:1.39.8"
variation 1958
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:147171380"
variation 1959
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:367886303"
variation 1961
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:138367563"
variation 1969
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:149239435"
variation 1971
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:201161602"
variation 1972
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:111774718"
variation 1991
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:371671972"
variation 1999
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:201637634"
variation 2008
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:148795102"
variation 2029
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:55637125"
variation 2032
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:143951672"
variation 2054
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:146350316"
variation 2075
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:3026204"
variation 2078
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:112134282"
variation 2081
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:11499"
variation 2094
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:139713512"
variation 2111
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:376366097"
variation 2116
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:371231893"
variation 2152
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:199650094"
variation 2193
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:368937602"
variation 2256
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="g"
/db_xref="dbSNP:138323510"
polyA_signal 2339..2344
/gene="FXR1"
/gene_synonym="FXR1P"
polyA_site 2367
/gene="FXR1"
/gene_synonym="FXR1P"
variation 2410
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="g"
/db_xref="dbSNP:77451926"
variation 2476
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:3026205"
variation 2600
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:372825020"
variation 2607
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:377201428"
variation 2618
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:188550393"
variation 2621
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:117037927"
variation 2636
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:191923790"
variation 2823
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:145591161"
variation 2888
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:200701459"
variation 2891..2892
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="a"
/db_xref="dbSNP:201501227"
variation 2892
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:138114654"
variation 2901..2903
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="ttt"
/db_xref="dbSNP:79881434"
polyA_signal 2949..2954
/gene="FXR1"
/gene_synonym="FXR1P"
variation 2958
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:183311734"
polyA_site 2976
/gene="FXR1"
/gene_synonym="FXR1P"
variation 3216..3217
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="aa"
/db_xref="dbSNP:146154883"
variation 3249..3250
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="gg"
/db_xref="dbSNP:201594378"
variation 3321
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:187223562"
variation 3324
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:191718661"
variation 3467
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:183888010"
variation 3518
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="g"
/db_xref="dbSNP:370717702"
variation 3608
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:3026206"
variation 3612
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:113426020"
variation 3657
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:149096577"
variation 3885
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:186780056"
variation 3995..3996
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="a"
/db_xref="dbSNP:35250215"
variation 3996
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="a"
/db_xref="dbSNP:67565008"
variation 4015
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:143130417"
variation 4017
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1805627"
variation 4031
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1805628"
variation 4043
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:193140070"
STS 4071..4232
/gene="FXR1"
/gene_synonym="FXR1P"
/standard_name="D3S2910E"
/db_xref="UniSTS:150894"
variation 4105
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="ta"
/db_xref="dbSNP:200214928"
variation 4106..4107
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="tt"
/db_xref="dbSNP:67477912"
variation 4233
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:185723329"
variation 4362
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="g"
/db_xref="dbSNP:190201524"
variation 4416
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="g"
/db_xref="dbSNP:182067416"
variation 4496
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:148220661"
variation 4576
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:62291435"
variation 4606
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:141181334"
variation 4634
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:112349907"
variation 4799
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:114145770"
STS 4892..5042
/gene="FXR1"
/gene_synonym="FXR1P"
/standard_name="RH98363"
/db_xref="UniSTS:89700"
variation 5031
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:184223404"
variation 5048
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:147356292"
variation 5059
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:370998297"
variation 5152
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1465374"
variation 5160
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="g"
/db_xref="dbSNP:188684032"
variation 5224
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:3026207"
variation 5247
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1008412"
variation 5282
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1805629"
STS 5291..5490
/gene="FXR1"
/gene_synonym="FXR1P"
/standard_name="D3S3105"
/db_xref="UniSTS:61824"
STS 5296..5446
/gene="FXR1"
/gene_synonym="FXR1P"
/standard_name="Cda01e11"
/db_xref="UniSTS:64869"
variation 5314
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:374633367"
variation 5343
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:181123657"
variation 5367
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:116043654"
variation 5398
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:3026208"
variation 5431
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:137877459"
variation 5453
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:189429564"
polyA_signal 5479..5484
/gene="FXR1"
/gene_synonym="FXR1P"
variation 5491
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:114677034"
polyA_site 5510
/gene="FXR1"
/gene_synonym="FXR1P"
variation 5537
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:143392613"
variation 5761
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:180725645"
variation 5857
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:147544455"
variation 6009
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:187502719"
STS 6026..6155
/gene="FXR1"
/gene_synonym="FXR1P"
/standard_name="A006P45"
/db_xref="UniSTS:58844"
variation 6154
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:1058382"
variation 6156
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:6799476"
variation 6198..6199
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="t"
/db_xref="dbSNP:201242121"
variation 6207
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:16832224"
variation 6214..6215
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="t"
/db_xref="dbSNP:144707771"
variation 6266..6269
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="atta"
/db_xref="dbSNP:373289717"
variation 6268
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:3026209"
variation 6282
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:191834999"
variation 6337
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:140179467"
variation 6442
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:183796587"
variation 6464
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:79629055"
variation 6492
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:185999941"
variation 6574
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:373868693"
variation 6575
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:190427919"
variation 6692
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:150037153"
variation 6742..6743
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="t"
/db_xref="dbSNP:151155261"
variation 6743..6744
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="t"
/db_xref="dbSNP:11448946"
variation 6807
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:182639763"
variation 7025
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:7646508"
variation 7155
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:368717976"
variation 7190
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:148748584"
variation 7200
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1805630"
variation 7251
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:202106534"
variation 7318
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:142318810"
variation 7322
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:187015735"
variation 7347
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1805607"
variation 7435
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="g"
/db_xref="dbSNP:146809695"
variation 7447
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="a"
/db_xref="dbSNP:199927975"
variation 7481
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:192718619"
variation 7520
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:73046170"
variation 7566
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:201358029"
variation 7611
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:189118011"
variation 7627
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1805631"
variation 7657..7671
/gene="FXR1"
/gene_synonym="FXR1P"
/replace=""
/replace="tttacctggcttctg"
/db_xref="dbSNP:368024256"
variation 7740
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:193073756"
variation 7741
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1805632"
variation 7837
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:184439182"
variation 7931
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:369747203"
variation 7980
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:144198197"
variation 8001
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="c"
/db_xref="dbSNP:188933563"
variation 8025
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="g"
/db_xref="dbSNP:191855515"
variation 8085
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1805633"
variation 8109
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="g"
/db_xref="dbSNP:117800767"
STS 8122..8221
/gene="FXR1"
/gene_synonym="FXR1P"
/standard_name="SHGC-77579"
/db_xref="UniSTS:32551"
STS 8123..8221
/gene="FXR1"
/gene_synonym="FXR1P"
/standard_name="G60386"
/db_xref="UniSTS:137492"
variation 8151..8152
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:2602"
variation 8164
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:184031096"
variation 8176
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="g"
/db_xref="dbSNP:2601"
variation 8219
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:368901111"
variation 8227
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="a"
/replace="t"
/db_xref="dbSNP:76288512"
variation 8252
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:189394362"
variation 8339
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="g"
/replace="t"
/db_xref="dbSNP:62291436"
variation 8385
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:146531694"
variation 8513
/gene="FXR1"
/gene_synonym="FXR1P"
/replace="c"
/replace="t"
/db_xref="dbSNP:11548477"
polyA_signal 8545..8550
/gene="FXR1"
/gene_synonym="FXR1P"
polyA_site 8567
/gene="FXR1"
/gene_synonym="FXR1P"
ORIGIN
aggcaaatccgacgtagacggcggcaggcggagcccaaagccggtgatgcagggtgcgcagggatcccacctggagagtcggggcggcacgttgagaccccaggggtgaagggcgggggatcccaatcccagccctgttttcccctcccctttccccgcctccttctcgcccctcccccctcctcccctctggttggaaagtttctagaatctcttcccagcggcctttgcggttccaacatggcggagctgacggtggaggttcgcggctctaacggggctttctacaagggatttatcaaagatgttcatgaagactcccttacagttgtttttgaaaataattggcaaccagaacgccaggttccatttaatgaagttagattaccaccaccacctgatataaaaaaagaaattagtgaaggagatgaagtagaggtatattcaagagcaaatgaccaagagccatgtgggtggtggttggctaaagttcggatgatgaaaggagaattttatgtcattgaatatgctgcttgtgacgctacttacaatgaaatagtcacatttgaacgacttcggcctgtcaatcaaaataaaactgtcaaaaaaaataccttctttaaatgcacagtggatgttcctgaggatttgagagaggcgtgtgctaatgaaaatgcacataaagattttaagaaagcagtaggagcatgcagaattttttaccatccagaaacaacacagctaatgatactgtctgccagtgaagcaactgtgaagagagtaaacatcttaagtgacatgcatttgcgaagtattcgtacgaagttgatgcttatgtccagaaatgaagaggccactaagcatttagaatgcacaaaacaacttgcagcagcttttcatgaggaatttgttgtgagagaagatttaatgggcctggcaataggaacacatggtagtaacatccagcaagctaggaaggttcctggagttaccgccattgagctagatgaagatactggaacattcagaatctacggagagagtgctgatgctgtaaaaaaggctagaggtttcttggaatttgtggaggattttattcaggttcctaggaatctcgttggaaaagtaattggaaaaaatggcaaagttattcaagaaatagtggacaaatctggtgtggttcgagtgagaattgaaggggacaatgaaaataaattacccagagaagacggtatggttccatttgtatttgttggcactaaagaaagcattggaaatgtgcaggttcttctagagtatcatattgcctatctaaaggaagtagaacagctaagaatggaacgcctacagattgatgaacagctgcgacagattggttctaggtcttatagcggaagaggcagaggtcgtcggggacctaattacacctccggttatggtacaaattctgagctgtctaacccctctgaaacggaatctgagcgtaaagacgagctgagtgattggtcattggcaggagaagatgatcgagacagccgacatcagcgtgacagcaggagacgcccaggaggaagaggcagaagtgtttcagggggtcgaggtcgtggtggaccacgtggtggcaaatcctccatcagttctgtgctcaaagatccagacagcaatccatacagcttacttgataatacagaatcagatcagactgcagacactgatgccagcgaatctcatcacagtactaaccgtcgtaggcggtctcgtagacgaaggactgatgaagatgctgttctgatggatggaatgactgaatctgatacagcttcagttaatgaaaatgggctagtcacagttgcagattatatttctagagctgagtctcagagcagacaaagaaacctcccaagggaaactttggctaaaaacaagaaagaaatggcaaaagatgtgattgaagagcatggtccttcagaaaaggcaataaacggcccaactagtgcttctggcgatgacatttctaagctacagcgtactccaggagaagaaaagattaataccttaaaagaagaaaacactcaagaagcagcagtcctgaatggtgtttcataaactgaagaagttcctagtttacagttcttttacattacatttacaatagtgcttgtacaagcttgccaaagatagaatatggatcgccagtctttacatcgcactttcagttcctccatttggaattcaaaaaggggagggatcctgaagaaatcatatgttaaacatactttgacacctactgtgttataaaatatatcatcagatgtgccttgagaatagtatatgtaacattaaaaaaaagttgctggctataggaaatgttattttgttttcaaaatatggcagagatggggggtggtgggtggggtgggatccctaacgtaatattctttatgaaagcattagctgcttttgttacatttttaatatgcaaccacttcttcacctgaggaaaactagaatgaaatgcagtctaaaatattttgcactgaattgtaatttcttcattagtttagtctggaaactggtctgttttaatgtgttttttaaatgctgtatgtagaggaaaatctgcagaccactggaatacatttgttaaactctcatctgcagggacactgggcgatacttggcagtgactgttctaccttgaggctttgtttggtttatttattaaagtgtacagtatttaaaaatcaaacatagctttagttaaaacactaagctgaattagtcatgtccattcagacataacctgaactactgaaaagatcaatttccagaaggtttattctgtataaactacatgttagtcttcagtagagtatcttttttttttccttttttttttttttatttcggttgtttgatgtgcaatatgtttttgtatgcaggtagtaaataaactttgatcttccatttgctgaatttttttaactttctactttttacaccaattgttgcaaaatagttggagctattaataggcttaggatagtatactttgctttttaaaaagcatttatacttgctcataaatagcattaaaatgtcagttggccatttaatcattttgtaatgaatcatctgaaatctttacacaagtttaggctgttagatgcataggtaattaataatacatgtgataattagcaaaaaaacctaacaaaattctaatcaaaggcaactttggaagacaatgggggatagaagggatgacaagcaatttttaaataataggccaatgatttgctttattcattctcaacttattttgaaggctctcatatcagtgaccaaaaatcagttattaaactttatgtatatattttagccagagcttaatttttatgaagataaagacatgaagtttaacaatggacaacagttagtacagctaattgtgaggtcaagtaattgttagacataggggaaggctttgttccacaatattatatggaccactgaacaagaatgacagccctttgttatcacttggcatatgaaaagtgttgtgtgcatagtttgtgttaattttttatgtgcataaaaatgtgattttaatttatatgctctgaaggataattcagggtatagttaaaaatgtacaatgtgccagttcagtatatataaccctagccctcaaattattctgattaaggttaaaatgtgctggtattacgtgctttttcctgaggccttctgattggttcttggtaacagaattttaaagtaaggtgtgagtagtgcaactcctgtcctttatatataaagatatcaagtaatttcatgtcctgatatttaaaaaaattacccacaaatgtgtttttttaaatcgatcaaagctagcaacaggttaaattgtctcagttctcttacataattgggttaaaaattataaggtattagaagaattttaattaatgccaaattggtaaatatggtgtaaaaaaaaaaaaaaagacttttcattttctcccacatagaatagtcagatatattaaacatcccttttccataaagatggtttcaatgggaatggaagaaacaaaatcttaaaagagtgagtatagctgaaccaattcttcattctagcaataaccacactaagttcattactttacaaatgactaaacccaatgtcttgtcctttaaaaaatataggtagtgcagaattgtgataaatacgcatttgtttttttagagagccccactccccaaagggtagccattaattcaggtagccttttaaatgtatttgagagggttccgtctttttggctgctatcctagttaggtgagatgttgctatgggaagaacttgccactatacactaaacagacacttaagcaaaagatgtattctggagcctggcacagtagcttatgtctttggttctagctactcaggagcctgaggtgggagcatcatttgaactcagttctgggccactgagaccctctttaaagagaaggaaaaaaaggtattctggaagatcttgtgcagttgcaacaatgtttcagcatatatatgtgaattcatatatgacacctgaacggaatcatgaagtaacagctgagattatatggtggcaaaaatgacctgcttttcctgaagctttgggaggcctaggattcttgctttaggcatcacctttgttaagccttaaagggggctacaacttgtgcaaaatggtgtctctggtaacacttcagaaataattggcaaaagtgtaataggaatacacaaatctttattttgaaataatcttgtattttaatgtggaattagaagcagcacatcaaactggtgagttcacagaaacttacctgagatgatgctgggttccattgctgttgtgctaagtcacgtatttttgtagctgctgttagctgtgtctagcgttttgtaacctaaggagggtcttatagaagttggtatgttaactaaatcttggactgggaaacagcaccatttgtatcctctgcaaacagatttacgcttttgaggctcaaaccaactagtgttctcatgggctgttgcctaaggacagataaacatggaaaacaggctatgtccagggacagatgattggtggttaagaattacagtaaaggaaaattacacctggattttcttctgtaaagtttcaaggaacttggatttgaactgtgaatctactgttttggcaaaaaatctcaaagaaaaggatgtttgttactgtctcagtcttcctgtctttgctacacgatttggatcccttacgctttttcgttaagaatatctgtctgctatagtgaatttgctagccccttatttttttttttaattttagttctttattagaacgtgtacttgaatggactgtagttgctcataacccatgttaatctctgatagtatttgggttttatttcaggagcttttgcaataaagcagtaactgcaatctgctaaagtcagactgttagcaagtggtgttaaaactgatttaagtccattacactgaacagtaggaaattaccacttttgtaaggctcaaaaatgatcaactattaacagtttcttatggttcagtctaattacaaatttttaaaaagtttatcagtgtatcatttcagattcatctgtatcttctgtaatattatttccagtactgaggtaaggtacacaaaaattcccctggaaaaactatattctagttttgtaagatgatttcccacagtccatttgcttatttcttcctttgataattcaaaaagatgctttaggtaatggtacagaattagaagctgctattttagctctattaactttttctctatggtttcaattttatccaaccagagagggctggcctagttggtatctttaaggcccttccagtagtaatttgagtctagtcacatgtcagaccctgagcaacacctaaccaaatgcccaagtattctcataaggagtatgctgaatttaagtggtgtttgttttacatatgtatccatcccagacattttcaactatgctgaatgcaatctataagatattccaaacaaggacaaagtaatttttcacaagtcttacagccccactattaagtatgctactaattagcttcttgaatttctttgtatttcagtgattgggatgttctttttttttgggaaagtttttttacccctttgtaccctcttaattggattaactgtaaaatgtacatattaattttctagttttagagaccattttcattaaaaatattttccaatagtttttctagataaacaatttatacttaattgttgcttggttgcttacatttcaacctctaggcttcctttttcagctaacttggctgtcttcaggttgtaaagaaaaatgtaaacatatatttgaaatttcattaactgaaactgctgtaaggtgttagcaaatgttaaccataacagattatcccatatcattggactgttctattattgggtcaggaataataggtgacacaggatagaagctcttcctatatatatcttgttgctaaggcagtagttggctctaagctgataaacagcacactgtacagcagtccaaaaactaaaaccagagcttaggtcattcaagttaactggtactcaaggttactcattccaggatactttacataaccaaaaacctaggagagcattctacattgtaattttttttttactttgtttacataaaatttacagggttttgtttttttaagcttagtctgttctttgacattgttgattcatgttctaaattttcatcagatttaacatgtttggaggttcttgtgcactcaatgtgaacctactacaagcttctgaactgcaaaaccttttttttaggtcactgtcaacagaaagatgccttatagaatttctcatgattgaaacagaactctgcattctaacctaaaacccctctaaccctttaaatgaagcattatgcctgcgtgaaattttatttttagacatttctgatactaggttttctttacgggggggcatacatattcagtatactgaatttatacagctttcagtgtggcaatatattaagaagctagttccctaatttttctcagttctcattggttttccatttaaatgtttccgtaagtactctcatcatttggaaaatacttgatggcaggagaacttgcttaaaactaaaggtggagaaagagttaacttccaggacaacccattatagctcacttcttaccaacaaagcagtttttatacagcaccttaggactcatttctaatgtcaacccagatggccagtaaaggcaagggaagaggctaagtgactcacaaaaatctctgatattgaggtctaatgtgaaggctatagataggaattccccacaaacttctaatgaggactaatatgaacagcaaattggagaagacaccaaggacctaattttagtttcactagccgtgggaccttagaaaaaagaccatttgctctggacttttgtttcccaagccataaaatgtggaagaatcttcacaatttcaagttggtcatgtatatttcccttttacagagaaagctgaagcctcgaggctcagatttacctggcttctgtttacctggcttctgcagaagtttaacttgtaacctacctctcattcccaaagtgtgtttaatcatgccgccttctttaaaatatatctggaagcaccaatgagtaaagacaaaggccccaagctagatctgtagagataagtactagactcacatctcagtactatcaaggaaaacatgcttaggttatcagaattgtgaaggccatagtacaaaaagttaagagaacggaactcaggatctgagaaagatcagccattctcagcatgttgccttggctgcttaaccttactaaacttccatttcctcacatgtaaaatgtacatcataataactagtctactgagataagggaagaatacttagcacagtgctagtacactgtaagtactcaaatgttacagatccaagtattttgtaagaaaataccagcaaaagataaaagtttttttatggatcgtatttgtatcaatcacctacatgatctagagccctcacatggataacatttaaatgttcagtttgcctaatagccttcaatgaaacacggattcttctacttaaaaaaggtaagcctggagaaaataaaactgattactatgcaagaaaaaaatgtgctctgctgtgctccttggtatttttaagtggtttccattgtcttaacacctgtcttaaaacgggtatgttgtttgcactgaaccctcaaaagtatttatacctattaagttaaatttccctttttagagttaatgcttcattgcctgtcggcatattatcactatctgtctttgaaaaattttcttttaagtctcaactatttcttcataaagctcttgttcagagaaacattttttgatttgtccaatggactgaaataaaaggttagtaaaccaaaa
//
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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