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2024-04-17 05:41:28, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001080415 7464 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens U2 snRNP-associated SURP domain containing (U2SURP),
mRNA.
ACCESSION NM_001080415 XM_031553
VERSION NM_001080415.1 GI:122937226
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 7464)
AUTHORS Will,C.L., Urlaub,H., Achsel,T., Gentzel,M., Wilm,M. and
Luhrmann,R.
TITLE Characterization of novel SF3b and 17S U2 snRNP proteins, including
a human Prp5p homologue and an SF3b DEAD-box protein
JOURNAL EMBO J. 21 (18), 4978-4988 (2002)
PUBMED 12234937
COMMENT PROVISIONAL REFSEQ: This record has not yet been subject to final
NCBI review. The reference sequence was derived from AC026304.19
and AC018450.26.
On Jan 18, 2007 this sequence version replaced gi:113414702.
Sequence Note: The RefSeq transcript and protein were derived from
genomic sequence to make the sequence consistent with the reference
genome assembly. The genomic coordinates used for the transcript
record were based on alignments.
##Evidence-Data-START##
Transcript exon combination :: AB002330.1, BK000564.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025083, ERS025084 [ECO:0000348]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-144 AC026304.19 1717-1860 c
145-189 AC018450.26 182003-182047 c
190-321 AC018450.26 180509-180640 c
322-420 AC018450.26 178453-178551 c
421-535 AC018450.26 176491-176605 c
536-669 AC018450.26 175887-176020 c
670-737 AC018450.26 172826-172893 c
738-832 AC018450.26 172169-172263 c
833-868 AC018450.26 171477-171512 c
869-951 AC018450.26 171307-171389 c
952-1117 AC018450.26 170200-170365 c
1118-1329 AC018450.26 169798-170009 c
1330-1373 AC018450.26 168844-168887 c
1374-1478 AC018450.26 165609-165713 c
1479-1545 AC018450.26 164456-164522 c
1546-1709 AC018450.26 164216-164379 c
1710-1872 AC018450.26 159916-160078 c
1873-1952 AC018450.26 159512-159591 c
1953-2040 AC018450.26 157887-157974 c
2041-2163 AC018450.26 156758-156880 c
2164-2320 AC018450.26 155527-155683 c
2321-2416 AC018450.26 154659-154754 c
2417-2483 AC018450.26 153902-153968 c
2484-2643 AC018450.26 149586-149745 c
2644-2754 AC018450.26 141813-141923 c
2755-2873 AC018450.26 139068-139186 c
2874-3050 AC018450.26 137743-137919 c
3051-7464 AC018450.26 132137-136550 c
FEATURES Location/Qualifiers
source 1..7464
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="3"
/map="3q23"
gene 1..7464
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/note="U2 snRNP-associated SURP domain containing"
/db_xref="GeneID:23350"
/db_xref="HGNC:30855"
exon 1..144
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/inference="alignment:Splign:1.39.8"
variation 34
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="c"
/db_xref="dbSNP:191623793"
variation 57
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="g"
/db_xref="dbSNP:375855390"
variation 72
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="g"
/db_xref="dbSNP:111340020"
variation 89
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:372971680"
variation 99
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:376927803"
CDS 100..3189
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/note="Ser/Arg-rich domain protein, 140 kDa; U2 associated
SR140 protein; functional spliceosome-associated protein
a; U2-associated protein SR140; U2-associated SR140
protein; 140 kDa Ser/Arg-rich domain protein"
/codon_start=1
/product="U2 snRNP-associated SURP motif-containing
protein"
/protein_id="NP_001073884.1"
/db_xref="GI:122937227"
/db_xref="CCDS:CCDS46928.1"
/db_xref="GeneID:23350"
/db_xref="HGNC:30855"
/translation="
MADKTPGGSQKASSKTRSSDVHSSGSSDAHMDASGPSDSDMPSRTRPKSPRKHNYRNESARESLCDSPHQNLSRPLLENKLKAFSIGKMSTAKRTLSKKEQEELKKKEDEKAAAEIYEEFLAAFEGSDGNKVKTFVRGGVVNAAKEEHETDEKRGKIYKPSSRFADQKNPPNQSSNERPPSLLVIETKKPPLKKGEKEKKKSNLELFKEELKQIQEERDERHKTKGRLSRFEPPQSDSDGQRRSMDAPSRRNRSSGVLDDYAPGSHDVGDPSTTNLYLGNINPQMNEEMLCQEFGRFGPLASVKIMWPRTDEERARERNCGFVAFMNRRDAERALKNLNGKMIMSFEMKLGWGKAVPIPPHPIYIPPSMMEHTLPPPPSGLPFNAQPRERLKNPNAPMLPPPKNKEDFEKTLSQAIVKVVIPTERNLLALIHRMIEFVVREGPMFEAMIMNREINNPMFRFLFENQTPAHVYYRWKLYSILQGDSPTKWRTEDFRMFKNGSFWRPPPLNPYLHGMSEEQETEAFVEEPSKKGALKEEQRDKLEEILRGLTPRKNDIGDAMVFCLNNAEAAEEIVDCITESLSILKTPLPKKIARLYLVSDVLYNSSAKVANASYYRKFFETKLCQIFSDLNATYRTIQGHLQSENFKQRVMTCFRAWEDWAIYPEPFLIKLQNIFLGLVNIIEEKETEDVPDDLDGAPIEEELDGAPLEDVDGIPIDATPIDDLDGVPIKSLDDDLDGVPLDATEDSKKNEPIFKVAPSKWEAVDESELEAQAVTTSKWELFDQHEESEEEENQNQEEESEDEEDTQSSKSEEHHLYSNPIKEEMTESKFSKYSEMSEEKRAKLREIELKVMKFQDELESGKRPKKPGQSFQEQVEHYRDKLLQREKEKELERERERDKKDKEKLESRSKDKKEKDECTPTRKERKRRHSTSPSPSRSSSGRRVKSPSPKSERSERSERSHKESSRSRSSHKDSPRDVSKKAKRSPSGSRTPKRSRRSRSRSPKKSGKKSRSQSRSPHRSHKKSKKNKH
"
misc_feature 703..705
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(O15042.2); phosphorylation site"
misc_feature 922..1155
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/note="RRM (RNA recognition motif), also known as RBD (RNA
binding domain) or RNP (ribonucleoprotein domain), is a
highly abundant domain in eukaryotes found in proteins
involved in post-transcriptional gene expression processes
including mRNA and rRNA...; Region: RRM; cd00590"
/db_xref="CDD:100104"
misc_feature order(928..930,1057..1059,1063..1065)
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/note="RNA/DNA binding site [nucleotide binding]; other
site"
/db_xref="CDD:100104"
misc_feature 1147..1155
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/note="RRM dimerization site [polypeptide binding]; other
site"
/db_xref="CDD:100104"
misc_feature 1381..1542
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/note="Surp module; Region: Surp; pfam01805"
/db_xref="CDD:201983"
misc_feature 1387..1518
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (O15042.2);
Region: SURP motif"
misc_feature 1552..1554
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(O15042.2); phosphorylation site"
misc_feature 1720..2127
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/note="domain present in proteins, which are involved in
regulation of nuclear pre-mRNA; Region: RPR; smart00582"
/db_xref="CDD:197799"
misc_feature 2377..2379
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/experiment="experimental evidence, no additional details
recorded"
/note="N6-acetyllysine; propagated from
UniProtKB/Swiss-Prot (O15042.2); acetylation site"
misc_feature 2461..2463
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(O15042.2); phosphorylation site"
misc_feature 2497..2499
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(O15042.2); phosphorylation site"
misc_feature 2530..2532
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(O15042.2); phosphorylation site"
misc_feature 2626..>2733
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/note="cwf21 domain; Region: cwf21; pfam08312"
/db_xref="CDD:203903"
misc_feature 2890..2892
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphothreonine; propagated from
UniProtKB/Swiss-Prot (O15042.2); phosphorylation site"
misc_feature 2935..2937
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(O15042.2); phosphorylation site"
misc_feature 2941..2943
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(O15042.2); phosphorylation site"
variation 117
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="c"
/db_xref="dbSNP:370308369"
variation 137
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:183628705"
exon 145..189
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/inference="alignment:Splign:1.39.8"
variation 160
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:367592203"
variation 170
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:186856142"
exon 190..321
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/inference="alignment:Splign:1.39.8"
variation 205
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:369933477"
variation 213
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:202048164"
variation 229
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:200575639"
variation 230
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:185429890"
variation 242
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:141570501"
variation 254
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="c"
/db_xref="dbSNP:369610759"
variation 256
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:372782950"
variation 257
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:368122040"
STS 315..917
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/standard_name="2610101N10Rik"
/db_xref="UniSTS:479055"
variation 318
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:377198844"
exon 322..420
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/inference="alignment:Splign:1.39.8"
variation 390
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:202018152"
variation 401
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:372614386"
variation 403
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="g"
/replace="t"
/db_xref="dbSNP:78259926"
exon 421..535
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/inference="alignment:Splign:1.39.8"
STS 534..665
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/standard_name="EST17D12"
/db_xref="UniSTS:263160"
exon 536..669
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/inference="alignment:Splign:1.39.8"
variation 579
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:375152362"
variation 651
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="g"
/replace="t"
/db_xref="dbSNP:370084492"
exon 670..737
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/inference="alignment:Splign:1.39.8"
variation 698
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:374916152"
exon 738..832
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/inference="alignment:Splign:1.39.8"
variation 822
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:183411991"
exon 833..868
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/inference="alignment:Splign:1.39.8"
variation 837
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:371988575"
variation 838
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:201384657"
variation 846
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="c"
/db_xref="dbSNP:200124980"
exon 869..951
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/inference="alignment:Splign:1.39.8"
exon 952..1117
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/inference="alignment:Splign:1.39.8"
variation 963
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:201558817"
variation 1048
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="g"
/db_xref="dbSNP:200439948"
variation 1117
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="g"
/db_xref="dbSNP:370839077"
exon 1118..1329
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/inference="alignment:Splign:1.39.8"
variation 1197
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:370500835"
variation 1218
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:374871094"
variation 1224
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:367649132"
variation 1236
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:190778086"
variation 1298
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:374471161"
variation 1299
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:368643846"
exon 1330..1373
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/inference="alignment:Splign:1.39.8"
variation 1339
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="g"
/replace="t"
/db_xref="dbSNP:199673101"
variation 1345
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:369925488"
exon 1374..1478
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/inference="alignment:Splign:1.39.8"
variation 1404
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="t"
/db_xref="dbSNP:145720949"
exon 1479..1545
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/inference="alignment:Splign:1.39.8"
variation 1489
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="g"
/replace="t"
/db_xref="dbSNP:76332901"
variation 1527
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:80238215"
variation 1539
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="t"
/db_xref="dbSNP:201510232"
exon 1546..1709
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/inference="alignment:Splign:1.39.8"
variation 1567
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:376693702"
variation 1620
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:141375076"
variation 1629
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:373867396"
variation 1668
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:376021154"
exon 1710..1872
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/inference="alignment:Splign:1.39.8"
exon 1873..1952
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/inference="alignment:Splign:1.39.8"
variation 1917
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="t"
/db_xref="dbSNP:77794774"
exon 1953..2040
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/inference="alignment:Splign:1.39.8"
variation 1964
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:200396401"
variation 1995
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:199769158"
variation 2003
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:372196737"
exon 2041..2163
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/inference="alignment:Splign:1.39.8"
variation 2124
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:376762965"
exon 2164..2320
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/inference="alignment:Splign:1.39.8"
variation 2178
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:376506538"
variation 2202
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:374496642"
variation 2223
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:368850919"
variation 2255
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:370077868"
variation 2262
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:370686170"
variation 2265
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:201356861"
variation 2278
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:373648103"
exon 2321..2416
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/inference="alignment:Splign:1.39.8"
variation 2334
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:371989668"
variation 2404
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:376920494"
exon 2417..2483
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/inference="alignment:Splign:1.39.8"
variation 2451
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="g"
/replace="t"
/db_xref="dbSNP:375705628"
exon 2484..2643
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/inference="alignment:Splign:1.39.8"
variation 2544
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:201514391"
variation 2586
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:372739578"
exon 2644..2754
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/inference="alignment:Splign:1.39.8"
variation 2754
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:376035119"
exon 2755..2873
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/inference="alignment:Splign:1.39.8"
variation 2791
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:370060610"
variation 2812
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:373100084"
variation 2858
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:376318821"
variation 2861
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:371501706"
variation 2865
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:376254231"
exon 2874..3050
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/inference="alignment:Splign:1.39.8"
variation 2940
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="t"
/db_xref="dbSNP:374301725"
variation 2944
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:200513999"
variation 2945
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:200000025"
variation 2958
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:367886781"
variation 2966
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:372157259"
STS 2983..3161
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/standard_name="MARC_23929-23930:1032289482:1"
/db_xref="UniSTS:268805"
variation 3031
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="g"
/replace="t"
/db_xref="dbSNP:375521999"
variation 3036
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="g"
/db_xref="dbSNP:182412631"
exon 3051..7464
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/inference="alignment:Splign:1.39.8"
variation 3135
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:371934749"
variation 3179
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:375140128"
variation 3212
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="t"
/db_xref="dbSNP:201223643"
variation 3213
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="g"
/db_xref="dbSNP:373003796"
variation 3226
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:376933947"
variation 3227
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:201644832"
STS 3240..3404
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/standard_name="STS-N93625"
/db_xref="UniSTS:40329"
variation 3385..3386
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace=""
/replace="c"
/db_xref="dbSNP:35706965"
variation 3401
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="c"
/db_xref="dbSNP:147882033"
variation 3456
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="c"
/db_xref="dbSNP:141610970"
variation 3464
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="t"
/db_xref="dbSNP:371418610"
variation 3575
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:184240580"
variation 3605
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:375690606"
variation 3655
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:150437605"
variation 3784
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="g"
/replace="t"
/db_xref="dbSNP:370550944"
variation 3817
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="c"
/db_xref="dbSNP:373943493"
variation 3838
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:187309558"
variation 3943
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace=""
/replace="a"
/db_xref="dbSNP:370423541"
variation 4048
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:1043898"
variation 4089
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="g"
/db_xref="dbSNP:138272199"
variation 4109
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:191842970"
variation 4138..4141
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace=""
/replace="cc"
/db_xref="dbSNP:10655158"
variation 4147..4148
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace=""
/replace="cc"
/db_xref="dbSNP:369094886"
variation 4184
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:184067845"
STS 4199..4321
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/standard_name="RH66197"
/db_xref="UniSTS:82037"
variation 4304
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="g"
/replace="t"
/db_xref="dbSNP:149625881"
variation 4306
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:77943591"
variation 4425
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:370562641"
variation 4585
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:138992033"
variation 4626..4627
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace=""
/replace="g"
/db_xref="dbSNP:143332183"
variation 4675
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="g"
/db_xref="dbSNP:75845909"
variation 4707
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:112485071"
variation 4714
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:192879844"
variation 4752
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="g"
/replace="t"
/db_xref="dbSNP:111916583"
variation 4817
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="c"
/db_xref="dbSNP:368298057"
variation 4861
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:114747828"
variation 4913
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:372568456"
variation 4944
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:142270080"
variation 5080
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:145930029"
variation 5319
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:3088201"
variation 5326
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="g"
/replace="t"
/db_xref="dbSNP:11549146"
variation 5333
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:199662686"
variation 5405
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="c"
/db_xref="dbSNP:7623532"
variation 5406
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="c"
/db_xref="dbSNP:139831543"
variation 5424
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="g"
/replace="t"
/db_xref="dbSNP:141613900"
variation 5521
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:185865282"
variation 5534
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:150757578"
variation 5612
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:7635468"
variation 5615
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="c"
/db_xref="dbSNP:115091996"
variation 5658
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:139142135"
variation 5756
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="g"
/replace="t"
/db_xref="dbSNP:149920065"
variation 5771..5772
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace=""
/replace="t"
/db_xref="dbSNP:150892230"
variation 5797
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:190293233"
variation 5865..5866
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace=""
/replace="c"
/db_xref="dbSNP:34680345"
variation 5882
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:181026571"
variation 6211
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="g"
/replace="t"
/db_xref="dbSNP:186013558"
variation 6252
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:17633378"
STS 6271..7113
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/standard_name="SR140__5311"
/db_xref="UniSTS:464564"
variation 6271
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="t"
/db_xref="dbSNP:377442417"
variation 6293
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="g"
/db_xref="dbSNP:188040338"
variation 6314
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:374011529"
variation 6416
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:140580112"
variation 6563
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:10790"
variation 6616
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:111440951"
variation 6659
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:62276908"
STS 6682..6913
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/standard_name="A006A24"
/db_xref="UniSTS:16438"
STS 6682..6913
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/standard_name="G20651"
/db_xref="UniSTS:16437"
STS 6728..6849
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/standard_name="RH12741"
/db_xref="UniSTS:21031"
variation 6892
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:8831"
variation 6929
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:13715"
variation 6969
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:144530445"
variation 6970
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:369681099"
STS 6979..7177
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/standard_name="STS-N23755"
/db_xref="UniSTS:5087"
variation 6987
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:147871863"
STS 7091..7226
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/standard_name="G62100"
/db_xref="UniSTS:139125"
variation 7132
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:141570395"
variation 7191
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="a"
/replace="g"
/db_xref="dbSNP:10413"
variation 7437
/gene="U2SURP"
/gene_synonym="fSAPa; SR140"
/replace="c"
/replace="t"
/db_xref="dbSNP:3821646"
ORIGIN
gccttgcaggcgcctctggcgggcttcactgagatccgctctttcggtgctcgactcgcccgtgctgctgccgccgccgaaggaggggcaaagctcaagatggcggacaaaacgccaggcggatctcagaaggccagttcaaagacgagatcatcagatgttcattcatctggatcttcagatgcacatatggatgcatctggaccctcagatagtgatatgccaagtcggacacgacctaagagcccaagaaaacataattataggaatgaaagtgcccgtgaaagcctttgtgattctcctcatcagaatctctcaagacctcttctggaaaacaaacttaaagcattcagtattggaaaaatgagtacagctaagcgaactttaagtaaaaaggaacaggaagaattaaagaaaaaggaggatgaaaaggcagctgctgagatttatgaggagtttcttgctgcttttgaaggaagtgatggtaataaagtgaaaacatttgtgcgagggggtgttgttaatgcagctaaagaagaacatgaaacagatgaaaaaagaggtaaaatctataagccatcttcaagatttgcagatcaaaaaaatcctccaaatcagtcttccaatgaaagaccaccatctcttcttgtgatagaaaccaaaaaacctccacttaaaaaaggagagaaagaaaagaaaaaaagcaatttggaactcttcaaagaagaattaaagcaaattcaagaggaacgtgatgagagacataaaacaaaaggcagattaagtcgatttgaacctcctcagtcagattctgatggtcagcgtcgttctatggacgcgccttcaagaagaaatagatcatctggtgttcttgatgattacgcacctggctcacatgatgtaggagatccaagcactactaatttataccttggaaacattaatccacagatgaatgaagaaatgctgtgccaagaatttggaagatttggaccgttagccagtgtgaaaatcatgtggcctagaactgatgaagaaagagccagagagagaaattgcggctttgtggcctttatgaatagaagagatgctgaaagagctttaaaaaatttgaatggaaaaatgattatgtcttttgaaatgaagttaggttggggtaaagctgtacctattcctccacatccaatatacattccgccttctatgatggaacatacgcttcccccacctccatccggactgccttttaatgcgcagcctagagagcggttaaaaaaccctaatgctcctatgttaccgccacctaaaaacaaagaggattttgagaagactctgtcgcaagccatagtcaaagtggttatcccaacagaaaggaatttgctcgccctgatacatcgaatgatagagtttgttgtacgtgaagggccaatgtttgaagctatgattatgaacagagaaatcaacaatcctatgttcaggttcttatttgaaaaccagacaccagcccatgtttactataggtggaagctttattctattctgcagggagattctccaactaaatggcggacggaagattttcgtatgttcaaaaatggatctttttggaggccaccaccattaaatccgtacttgcatggaatgtcagaagagcaagaaacagaagcttttgtagaggaacctagtaaaaagggagcacttaaggaagaacagagggataaattggaagaaatcttgcggggattaactccaaggaaaaatgatattggagatgcaatggttttctgtcttaataatgctgaagctgctgaagaaatagtggattgcattactgagtcgttgtccatcttaaagacaccccttcctaaaaagattgccagattatatttggtttctgatgttttgtacaactcttcagccaaagttgctaatgcttcatattatagaaaattttttgaaacaaagttatgtcagatattttcagacctcaatgccacctatcgtacaattcaaggccatttacaatctgaaaactttaagcaacgggtaatgacttgcttcagagcatgggaagattgggcaatttatccagaaccatttttgatcaaactacaaaatattttcttaggacttgtaaatattattgaagaaaaggaaacagaggatgttccagatgaccttgatggtgcccccatcgaggaagagcttgatggtgcacctctggaagatgtagatggaattcctattgatgctactcccatcgatgatcttgatggagtccctataaaaagtcttgatgatgatcttgatggagtgcctttggatgcaactgaagactcaaaaaagaatgagcctatatttaaagttgccccatcaaaatgggaagctgtggatgaatctgaattggaagcacaggctgttacaacttctaaatgggaattatttgaccagcatgaagaatcagaagaagaagaaaatcaaaatcaagaagaagaaagtgaagatgaagaagatactcaaagttccaaatctgaagaacatcatttgtactctaatccaatcaaagaagaaatgactgagtctaagttctctaagtactctgaaatgagtgaggaaaaacgagccaaacttcgtgaaattgagctcaaagttatgaagtttcaggatgaattggaatctgggaaaagacctaaaaaaccaggccagagttttcaggagcaagtagaacactacagagataaacttcttcaacgagagaaagagaaagagttagaaagagaacgagaaagagacaagaaagataaagaaaaattggaatctcgctccaaagacaagaaggaaaaagatgagtgtactccgacaaggaaggaaaggaagaggcgacacagtacatcccccagcccatctcgcagtagcagtggtagacgagtgaaatccccatcaccaaaatcggagcgatcagagcgttcagaaagatctcataaagagagctcacggtccaggtcatctcacaaagattctcctagagatgttagcaaaaaagccaaaagatcaccatctggttcaaggacacctaaaaggtctaggcgatcacggtctagatctcctaaaaaatcaggaaagaagtccagatcccagtccagatctccacacaggtctcataaaaagtcaaagaaaaacaaacactgacgtaaatttttaagatgctgtcacttattggaaatgcgatttgttttgtgcctgaacggtctgttttttaaaaaaacaaaaaatcaaatgaaagagcattcctggggttttttgtttgtttgtgtatgcatgtgtaaactcatgagcaactgcatctgtagatctgtcattgttttatattgtgtaaattactttcattgtggctatttctcaagatgaaatttttattgttctaatggatttcatcagaaatgtgtataatggatctgctgacagtagtagtattttgttttaggatgttgtgacttagcaaaaataatacagatgtcttccccccttttgtagctttgacaatttgaattagatttcaaataaaatctgaacagaaaactataatgttgtttttttgccccaccggtgatattaagtcccttaaagtcctactgagtttcacactactgttgtgcttcttatacctgatgcactttataagccccagtgttcaagtagcttaagttttatatttactaagatgactatccaaattaagggacctgagactcctatttggtggtttgctaaccatttgcttttgataagtttctcttgggtaatactaatacccagatatcaaagactaggtagatatggcatggcgttttgttagtggaatgcctggctaaaacatttttttcacagaagcaatatgatttccatacatccaacccatgttctgagcaactacttacttttagggggaaattaaatatcttttcatttcctcttctattatgaaagaagtttatttgtaaaacaaattttctaacaaggtttggccatagaattctcttgtatgatcgttgaccttttataatcttctgtaggctatctttcaaacactggcatcagaatattttttataagtttgtgtttaaacagcttagttggtccccccccactcccaagagacttgggtttagttatagctttaagtaaaatttaaaaataaaatgtttttcaggaaacttcgtatctaatggtttgtaaattcaaggtgcaaaaagttgatttaaaccatttgcagagttgaactctattatgaaaataaatttgctacggtatgaggaagaaataaaacttgtgtaatgttggtcataatactgctataaatataataaagggttatgtagaattgaactgacactattatttgtgaatcttgatttcagttttttatgtaggcacttcatacactggtttgatgggttttttttttcctccctaaaagagaaagtagaaaactattctaacaatggattattttgatttagcttgctttttaaaaaaatcttttcaacttgttttacttaatcttgcctagtcacaaaataagatgtgcacccatggtttggagagttcctatattagctgagcagtgagatacactatttccaaacggtgcacacctacagtagctttggaaatgagccaatcactgttttacttaatggttcttatcagcatgcaaatattgcttgaaagttatttccttattcactgttttgttagtccattttgttaggaaacattaattcctaaaaatttgttcagaataattaaaagtgaacatttggtgctgatactcaaaaacctacaaatgtagccatttaaaaagtaacatgtttttctcccctgctcattgcctgggagaatggaattttatataactacctttctttgcaaaaataacggtcgtgtcgagttggtggtgattttggcattccatcttgcactggtttctagtataggcttagaaataattggtcaggtaataatctttccagtcaagttgcaagggatgcttatttctcttcaaaaaaagacatcctgcgggattgagtagaaaattttaggtcagttttgggtgcttatttgtaatatttttcctactacattggagtttagcagttctttttttctggatccagatacaagtgtcatggtttatcttacagtgggtgaaactgactttcttttggttgggtgggtgaggatttcttaggcctgatagaatatatattctgtgaagtttgttaatgtacatattagattgtattggatttttttttcttgaattgcaaatggtattattagataggttatttccagttttacttcatgacaaattacctagagtaaacctacttaatactcccatggattctatgaaagtttaatgggatcagaaattggtgacttataagggggaagatattctaccatatttttataatagcttattattcatgtttcttgtctgaaggacactcaagttacagagcaaaatttctataggttgactagaatgttcataagcatggtcttccagttgcaggaaagatcatgttctatctgtggacacttactgtcctctaccacagctacgtgccagagttgttttccacagttcttataaagggcatgacttaggctctttaccctccaacttaatgtttatacacagggattgtttactaggttaatgacatttaactcccctctcttctgtaggtgagagaaaataagtaagtcttgatctgtttcttaccaaagagagacagacctatgatggaaaatgatcacgtctctgaattttttctttaacgttatagttccttattacagatagtaagcatatgggaatttctgagctataacatgttgagaagttagaaattaaaactaacacaacaaaaggcgctgaatcaaaagatctttgcttttatttggctcagaatgtttttggcttttctgctaaagatggcagaaattactctacacagacctgatttttctttattgcagaccattcttgtgggcttaccctgagacttttatcccaattagtgaatcttggagggaatacttgcttatttatgacttaggtatttccccccaaactttaatattcttgagcacttgaaaatacttttgagaaattttaactgtgattaaatttaggtttattagaaatattctgtacacatttgcctccatggtggcgtaagttctgaaaaattatatgaccgtgacaatagtttatcatcatcattattgttattcaaaataagggtaaataaatctctgtattgccaaagtgacttaaactgttctgatgaccacacagtgtgatttctttagcagagaaagttggttttaaaaataaatagtaccacttttctaagactgtacagtttacaaataaggtttttttctttgttgttttcctcttctattaagttttagtgaaaagcctaattacagaaaattgtgcagatactagtgaagatactagtataagtttaaaggaacacgtgactgtaaaatctcacatttacaaagtgcttgatctcttcatatttcacacgcatgttttagaatagattttagggagtgtttaattcattatccttttgacttaaaatttttgttaccaacttcctaggacttagataatatataaataagtacaaatcccaggggaagtgttgtgatgctagactaaaaggtgggaatgtgctgctgttccgtgagccttgttccattgttgaaaatttgatgcctcagtgtttattcagtaccacctcatggagcttcaatgtaaatggattatatgtataattggtaatttgtatagttttgtagattgtagattaaatgcactcatcatgtcacatgtaattgtgcttggagtatttgtgttttattcttttacttcaacgggttcttgtctgttacatctctggtgatttgaaatatcaggaaagacagtttgtcagaaatgagaataatatagttgaaatcagttgggctaaaatattctacagcaagacaatttcttttgggtgaactgattctataatttacttacttttaatgtaaggattagatttattgttgagctgctttccagatcagactgtcactttatagtttttctacataaagattatatagttgcaaacaaaggttgtgaaatttcccttttgttgtttttgacttttaattaataaaagtacattgttttcatagcaaacttagactgtccatgtaattttctccatattgtttttccgatgcaagcccagttaataattagttttttagcagctttctctcaagtgaaataagtgatgtgacatgtttatcagttatggctaaaatgttacactttacatgtttaaactataatcatatgttttcatgctagatggt
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:23350 -> Molecular function: GO:0000166 [nucleotide binding] evidence: IEA
GeneID:23350 -> Molecular function: GO:0003723 [RNA binding] evidence: IEA
GeneID:23350 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
GeneID:23350 -> Biological process: GO:0006396 [RNA processing] evidence: IEA
GeneID:23350 -> Cellular component: GO:0005634 [nucleus] evidence: IDA
GeneID:23350 -> Cellular component: GO:0005730 [nucleolus] evidence: IDA
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