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2024-04-24 11:00:47, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001169123 13716 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens AF4/FMR2 family, member 2 (AFF2), transcript variant
3, mRNA.
ACCESSION NM_001169123
VERSION NM_001169123.1 GI:282165692
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 13716)
AUTHORS Mondal,K., Ramachandran,D., Patel,V.C., Hagen,K.R., Bose,P.,
Cutler,D.J. and Zwick,M.E.
TITLE Excess variants in AFF2 detected by massively parallel sequencing
of males with autism spectrum disorder
JOURNAL Hum. Mol. Genet. 21 (19), 4356-4364 (2012)
PUBMED 22773736
REMARK GeneRIF: 2.5% of males Autism spectrum disorder patients had
missense mutations in AFF2 at highly conserved evolutionary sites.
REFERENCE 2 (bases 1 to 13716)
AUTHORS Sahoo,T., Theisen,A., Marble,M., Tervo,R., Rosenfeld,J.A.,
Torchia,B.S. and Shaffer,L.G.
TITLE Microdeletion of Xq28 involving the AFF2 (FMR2) gene in two
unrelated males with developmental delay
JOURNAL Am. J. Med. Genet. A 155A (12), 3110-3115 (2011)
PUBMED 22065534
REMARK GeneRIF: A report of novel deletions involving AFF2 provide
evidence for a new mutational spectrum, microdeletions, that are
responsible for Fragile X E in a small subset of patients.
REFERENCE 3 (bases 1 to 13716)
AUTHORS Melko,M., Douguet,D., Bensaid,M., Zongaro,S., Verheggen,C., Gecz,J.
and Bardoni,B.
TITLE Functional characterization of the AFF (AF4/FMR2) family of
RNA-binding proteins: insights into the molecular pathology of
FRAXE intellectual disability
JOURNAL Hum. Mol. Genet. 20 (10), 1873-1885 (2011)
PUBMED 21330300
REMARK GeneRIF: overexpression of AFF2/3/4 interferes with the
organization and/or biogenesis of nuclear speckles.
REFERENCE 4 (bases 1 to 13716)
AUTHORS Katikala,L., Guruju,M.R., Madireddi,S., Vallamkonda,O.,
Vallamkonda,N., Persha,A. and Spurgeon,A.M.
TITLE Distribution of CGG/GCC repeats at the FMR1 and FMR2 genes in an
Indian population with mental retardation of unknown etiology
JOURNAL Genet Test Mol Biomarkers 15 (4), 281-284 (2011)
PUBMED 21254876
REMARK GeneRIF: CGG/GCC repeat polymorphism at the FMR1 and FMR2 loci
observed in this study demonstrated a racial and ethnic variation
among the populations in India.
REFERENCE 5 (bases 1 to 13716)
AUTHORS Bensaid,M., Melko,M., Bechara,E.G., Davidovic,L., Berretta,A.,
Catania,M.V., Gecz,J., Lalli,E. and Bardoni,B.
TITLE FRAXE-associated mental retardation protein (FMR2) is an
RNA-binding protein with high affinity for G-quartet RNA forming
structure
JOURNAL Nucleic Acids Res. 37 (4), 1269-1279 (2009)
PUBMED 19136466
REFERENCE 6 (bases 1 to 13716)
AUTHORS Allingham-Hawkins,D.J. and Ray,P.N.
TITLE FRAXE expansion is not a common etiological factor among
developmentally delayed males
JOURNAL Am. J. Hum. Genet. 57 (1), 72-76 (1995)
PUBMED 7541938
REFERENCE 7 (bases 1 to 13716)
AUTHORS Mulley,J.C., Yu,S., Loesch,D.Z., Hay,D.A., Donnelly,A.,
Gedeon,A.K., Carbonell,P., Lopez,I., Glover,G., Gabarron,I. et al.
TITLE FRAXE and mental retardation
JOURNAL J. Med. Genet. 32 (3), 162-169 (1995)
PUBMED 7783162
REFERENCE 8 (bases 1 to 13716)
AUTHORS Knight,S.J., Voelckel,M.A., Hirst,M.C., Flannery,A.V., Moncla,A.
and Davies,K.E.
TITLE Triplet repeat expansion at the FRAXE locus and X-linked mild
mental handicap
JOURNAL Am. J. Hum. Genet. 55 (1), 81-86 (1994)
PUBMED 8023854
REFERENCE 9 (bases 1 to 13716)
AUTHORS Knight,S.J., Flannery,A.V., Hirst,M.C., Campbell,L.,
Christodoulou,Z., Phelps,S.R., Pointon,J., Middleton-Price,H.R.,
Barnicoat,A., Pembrey,M.E. et al.
TITLE Trinucleotide repeat amplification and hypermethylation of a CpG
island in FRAXE mental retardation
JOURNAL Cell 74 (1), 127-134 (1993)
PUBMED 8334699
REFERENCE 10 (bases 1 to 13716)
AUTHORS Sutherland,G.R. and Baker,E.
TITLE Characterisation of a new rare fragile site easily confused with
the fragile X
JOURNAL Hum. Mol. Genet. 1 (2), 111-113 (1992)
PUBMED 1301146
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from U48436.1, BC132683.1 and
AC231841.2.
Summary: This gene encodes a putative transcriptional activator
that is a member of the AF4\FMR2 gene family. This gene is
associated with the folate-sensitive fragile X E locus on
chromosome X. A repeat polymorphism in the fragile X E locus
results in silencing of this gene causing Fragile X E syndrome.
Fragile X E syndrome is a form of nonsyndromic X-linked mental
retardation. Alternate splicing results in multiple transcript
variants.[provided by RefSeq, Dec 2009].
Transcript Variant: This variant (3) has multiple differences,
compared to variant 1. The encoded isoform (3) is shorter than
isoform 1.
Sequence Note: This RefSeq record was created from transcript and
genomic sequence data to make the sequence consistent with the
reference genome assembly. The genomic coordinates used for the
transcript record were based on transcript alignments.
Publication Note: This RefSeq record includes a subset of the
publications that are available for this gene. Please see the Gene
record to access additional publications.
##Evidence-Data-START##
Transcript exon combination :: BC132683.1 [ECO:0000332]
RNAseq introns :: mixed/partial sample support
ERS025082, ERS025084 [ECO:0000350]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-428 U48436.1 1-428
429-3576 BC132683.1 1-3148
3577-3577 AC231841.2 36012-36012 c
3578-4455 BC132683.1 3150-4027
4456-13716 AC231841.2 2353-11613 c
FEATURES Location/Qualifiers
source 1..13716
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="X"
/map="Xq28"
gene 1..13716
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/note="AF4/FMR2 family, member 2"
/db_xref="GeneID:2334"
/db_xref="HGNC:3776"
/db_xref="MIM:300806"
exon 1..526
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/inference="alignment:Splign:1.39.8"
variation 20..64
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="(gcc(6_25))"
/db_xref="dbSNP:193922937"
misc_feature 357..359
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/note="upstream in-frame stop codon"
variation 378
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="g"
/db_xref="dbSNP:375327948"
variation 386
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:367920029"
variation 431
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="g"
/db_xref="dbSNP:375079978"
variation 433
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="g"
/replace="t"
/db_xref="dbSNP:200653079"
variation 441
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:372376276"
variation 456
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:375802594"
CDS 480..4385
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/note="isoform 3 is encoded by transcript variant 3;
fragile X E mental retardation syndrome protein; protein
FMR-2; fragile X mental retardation 2 protein"
/codon_start=1
/product="AF4/FMR2 family member 2 isoform 3"
/protein_id="NP_001162594.1"
/db_xref="GI:282165693"
/db_xref="GeneID:2334"
/db_xref="HGNC:3776"
/db_xref="MIM:300806"
/translation="
MDLFDFFRDWDLEQQCHYEQDRSALKKREWERRNQEVQQEDDLFSSGFDLFGEPYKTNKGDALANRVQNTLGNYDEMKNLLTNHSNQNHLVGIPKNSVPQNPNNKNEPSFFPEQKNRIIPPHQDNTHPSAPMPPPSVVILNSTLIHSNRKSKPEWSRDSHNPSTVLASQASGQPNKMQTLTQDQSQAKLEDFFVYPAEQPQIGEVEESNPSAKEDSNPNSSGEDAFKEIFQSNSPEESEFAVQAPGSPLVASSLLAPSSGLSVQNFPPGLYCKTSMGQQKPTAYVRPMDGQDQAPDISPTLKPSIEFENSFGNLSFGTLLDGKPSAASSKTKLPKFTILQTSEVSLPSDPSCVEEILREMTHSWPTPLTSMHTAGHSEQSTFSIPGQESQHLTPGFTLQKWNDPTTRASTKMLEDDLKLSSDEDDLEPVKTLTTQCTATELYQAVEKAKPRNNPVNPPLATPQPPPAVQASGGSGSSSESESSSESDSDTESSTTDSESNEAPRVATPEPEPPSTNKWQLDKWLNKVTSQNKSFICGQNETPMETISLPPPIIQPMEVQMKVKTNASQVPAEPKERPLLSLIREKARPRPTQKIPETKALKHKLSTTSETVSQRTIGKKQPKKVEKNTSTDEFTWPKPNITSSTPKEKESVELHDPPRGRNKATAHKPAPRKEPRPNIPLAPEKKKYRGPGKIVPKSREFIETDSSTSDSNTDQEETLQIKVLPPCIISGGNTAKSKEICGASLTLSTLMSSSGSNNNLSISNEEPTFSPIPVMQTEILSPLRDHENLKNLWVKIDLDLLSRVPGHSSLHAAPAKPDHKETATKPKRQTAVTAVEKPAPKGKRKHKPIEVAEKIPEKKQRLEEATTICLLPPCISPAPPHKPPNTRENNSSRRANRRKEEKLFPPPLSPLPEDPPRRRNVSGNNGPFGQDKNIAMTGQITSTKPKRTEGKFCATFKGISVNEGDTPKKASSATITVTNTAIATATVTATAIVTTTVTATATATATTTTTTTTISTITSTITTGLMDSSHLEMTSWAALPLLSSSSTNVRRPKLTFDDSVHNADYYMQEAKKLKHKADALFEKFGKAVNYADAALSFTECGNAMERDPLEAKSPYTMYSETVELLRYAMRLKNFASPLASDGDKKLAVLCYRCLSLLYLRMFKLKKDHAMKYSRSLMEYFKQNASKVAQIPSPWVSNGKNTPSPVSLNNVSPINAMGNCNNGPVTIPQRIHHMAASHVNITSNVLRGYEHWDMADKLTRENKEFFGDLDTLMGPLTQHSSMTNLVRYVRQGLCWLRIDAHLL
"
misc_feature 531..>3383
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/note="AF-4 proto-oncoprotein; Region: AF-4; pfam05110"
/db_xref="CDD:147338"
misc_feature 1737..1739
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P51816.4); phosphorylation site"
misc_feature 1740..1742
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P51816.4); phosphorylation site"
misc_feature 1998..2000
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphothreonine; propagated from
UniProtKB/Swiss-Prot (P51816.4); phosphorylation site"
misc_feature <3615..4376
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/note="AF-4 proto-oncoprotein; Region: AF-4; pfam05110"
/db_xref="CDD:147338"
exon 527..647
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/inference="alignment:Splign:1.39.8"
variation 543
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:372514798"
variation 573
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:143135907"
variation 584
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:144497911"
variation 616
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:376134557"
exon 648..1508
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/inference="alignment:Splign:1.39.8"
STS 688..756
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/standard_name="DXS7394"
/db_xref="UniSTS:78356"
variation 689
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:150713576"
variation 700
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:374628192"
variation 732
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="t"
/db_xref="dbSNP:188230009"
variation 744
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:200850740"
variation 750
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="g"
/replace="t"
/db_xref="dbSNP:376868984"
variation 761
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:370409032"
variation 812
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace=""
/replace="t"
/db_xref="dbSNP:36036992"
variation 860
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:148418993"
variation 960
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:142559324"
variation 963
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:150996735"
variation 1008
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:373610087"
variation 1028
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="c"
/db_xref="dbSNP:201152809"
variation 1072
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="c"
/db_xref="dbSNP:142149774"
variation 1084
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:144530268"
variation 1093
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:186434773"
variation 1152
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:201078458"
variation 1183
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:199567128"
variation 1199
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:370542676"
variation 1200
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:147842224"
variation 1203
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:141545529"
variation 1358
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:373944993"
variation 1363
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:368459122"
variation 1364
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:200832993"
variation 1403
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:150391518"
variation 1441
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="t"
/db_xref="dbSNP:371889759"
variation 1480..1481
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace=""
/replace="c"
/db_xref="dbSNP:34529029"
variation 1501
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="c"
/db_xref="dbSNP:199510763"
exon 1509..1553
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/inference="alignment:Splign:1.39.8"
variation 1528
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:376054184"
variation 1529
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:145185488"
variation 1552
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:368578550"
exon 1554..1640
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/inference="alignment:Splign:1.39.8"
variation 1564
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:199574795"
variation 1588
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="c"
/db_xref="dbSNP:200306870"
variation 1590
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:200737572"
variation 1627
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="c"
/db_xref="dbSNP:373013286"
exon 1641..1677
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/inference="alignment:Splign:1.39.8"
variation 1646
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:149177157"
exon 1678..1711
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/inference="alignment:Splign:1.39.8"
variation 1700
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:370129290"
exon 1712..1808
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/inference="alignment:Splign:1.39.8"
variation 1736
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="g"
/replace="t"
/db_xref="dbSNP:370821602"
variation 1779
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:143278161"
variation 1802
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="g"
/db_xref="dbSNP:138980868"
exon 1809..1846
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/inference="alignment:Splign:1.39.8"
variation 1842
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="g"
/replace="t"
/db_xref="dbSNP:375518863"
exon 1847..2006
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/inference="alignment:Splign:1.39.8"
variation 1872
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:199667824"
variation 1891
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:142107931"
variation 1894
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="g"
/db_xref="dbSNP:145907183"
variation 1919
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:202072020"
variation 1934
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="g"
/replace="t"
/db_xref="dbSNP:138454102"
variation 1937
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:12011040"
variation 1990
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:369100046"
exon 2007..3017
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/inference="alignment:Splign:1.39.8"
variation 2057
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:200788138"
variation 2089
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:147098255"
variation 2102
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:16994869"
variation 2126
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:368960902"
variation 2131
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="c"
/db_xref="dbSNP:201731285"
variation 2146
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:183626057"
variation 2170
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:200099351"
variation 2171
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:201846826"
variation 2174
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:370610365"
variation 2182
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:139036592"
variation 2237
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="c"
/db_xref="dbSNP:149492076"
variation 2244
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:373295539"
variation 2279
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="g"
/db_xref="dbSNP:200450195"
variation 2283
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="g"
/db_xref="dbSNP:376847375"
variation 2291
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="g"
/replace="t"
/db_xref="dbSNP:371160275"
variation 2307
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:143923852"
variation 2315
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:201939574"
variation 2339
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="c"
/db_xref="dbSNP:35481955"
variation 2373
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:374626798"
variation 2389
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:368412621"
variation 2391
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:370373395"
variation 2441
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:201552726"
variation 2490
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:188332287"
variation 2514
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:140525796"
variation 2545
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:374716787"
variation 2616
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:367644155"
variation 2630
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:143927826"
variation 2631
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:199773486"
variation 2645
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:202015083"
variation 2653
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:371781393"
variation 2786
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="c"
/db_xref="dbSNP:201075062"
variation 2800
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="g"
/replace="t"
/db_xref="dbSNP:147852345"
variation 2806
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="g"
/db_xref="dbSNP:376114319"
variation 2827
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:200490489"
variation 2873
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:139807832"
variation 2911
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="c"
/db_xref="dbSNP:368480543"
variation 2984
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:142686839"
variation 2994
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:372296594"
exon 3018..3139
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/inference="alignment:Splign:1.39.8"
variation 3029
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace=""
/replace="t"
/db_xref="dbSNP:56269792"
variation 3050
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:185675988"
variation 3105
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="g"
/db_xref="dbSNP:151043891"
variation 3124
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:189994494"
exon 3140..3362
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/inference="alignment:Splign:1.39.8"
variation 3161
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:373395605"
variation 3229
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:140927355"
variation 3237
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:150223404"
variation 3276
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="t"
/db_xref="dbSNP:374800841"
exon 3363..3652
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/inference="alignment:Splign:1.39.8"
variation 3385
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:146808155"
variation 3393
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:140666372"
variation 3424
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:145756055"
variation 3464
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:138406514"
variation 3482
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:201632076"
variation 3537
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="c"
/db_xref="dbSNP:149653283"
variation 3578
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:200301935"
variation 3602
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:143384205"
variation 3652
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:188208167"
exon 3653..3716
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/inference="alignment:Splign:1.39.8"
exon 3717..3853
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/inference="alignment:Splign:1.39.8"
variation 3717
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="t"
/db_xref="dbSNP:147991137"
variation 3719
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:371376716"
variation 3794
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:200225379"
exon 3854..3925
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/inference="alignment:Splign:1.39.8"
variation 3905
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:187306270"
variation 3920
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:372052962"
exon 3926..4019
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/inference="alignment:Splign:1.39.8"
variation 3992
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:141612728"
variation 4002
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:12858959"
exon 4020..4072
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/inference="alignment:Splign:1.39.8"
variation 4038
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:373659849"
variation 4048
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="c"
/db_xref="dbSNP:200360366"
exon 4073..4263
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/inference="alignment:Splign:1.39.8"
variation 4081..4082
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace=""
/replace="c"
/db_xref="dbSNP:34986113"
STS 4084..4216
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/standard_name="AFF2"
/db_xref="UniSTS:506659"
variation 4103
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:370206293"
variation 4104
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:147166674"
variation 4119
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:374197610"
variation 4142
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:140356860"
variation 4145
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="t"
/db_xref="dbSNP:35967616"
variation 4241
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:181570030"
exon 4264..13716
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/inference="alignment:Splign:1.39.8"
variation 4286
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:61743576"
variation 4352
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:139135283"
variation 4368
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:149966195"
variation 4431
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="t"
/db_xref="dbSNP:4636363"
variation 4438
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:370349898"
variation 4617
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:151228485"
variation 4822
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="g"
/replace="t"
/db_xref="dbSNP:376700540"
STS 4992..5224
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/standard_name="RH70649"
/db_xref="UniSTS:23918"
variation 5020
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:182335257"
variation 5026
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:186614933"
variation 5139
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:139176217"
variation 5205
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="t"
/db_xref="dbSNP:189836593"
variation 5437
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="c"
/db_xref="dbSNP:149934062"
variation 5485
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:146483810"
variation 5610
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="g"
/replace="t"
/db_xref="dbSNP:183519969"
variation 5646
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:73614092"
variation 5865
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="t"
/db_xref="dbSNP:370253663"
variation 6002
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:193174908"
variation 6006
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:7887569"
STS 6031..6152
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/standard_name="RH66769"
/db_xref="UniSTS:63444"
variation 6104
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="c"
/db_xref="dbSNP:144651539"
variation 6262
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="c"
/db_xref="dbSNP:146685166"
variation 6339
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="t"
/db_xref="dbSNP:185031722"
variation 6457
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="g"
/db_xref="dbSNP:74842027"
variation 6723
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:148829584"
variation 6738
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:188291029"
variation 6921
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="t"
/db_xref="dbSNP:57460991"
variation 7172
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:191480494"
variation 7247
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="c"
/db_xref="dbSNP:183971008"
variation 7420
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="g"
/replace="t"
/db_xref="dbSNP:188324044"
variation 7645
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="t"
/db_xref="dbSNP:6540412"
variation 7771
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="t"
/db_xref="dbSNP:146861668"
variation 7835
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:6540413"
variation 8031
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:374709006"
variation 8099
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:73614095"
variation 8143
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="g"
/db_xref="dbSNP:191231389"
variation 8235
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="g"
/db_xref="dbSNP:41304960"
variation 8357
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="g"
/db_xref="dbSNP:73614097"
variation 8543
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:77735141"
variation 8655
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:185805080"
variation 8664..8665
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace=""
/replace="a"
/db_xref="dbSNP:35032574"
variation 8705
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="g"
/db_xref="dbSNP:190283117"
polyA_signal 8756..8761
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
polyA_site 8780
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
variation 8879
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:368052114"
variation 9130
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:182046461"
variation 9300
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="g"
/replace="t"
/db_xref="dbSNP:186583805"
variation 9384
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:12014237"
variation 9489
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="c"
/db_xref="dbSNP:189857586"
variation 9509
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:369931707"
variation 9751
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="g"
/db_xref="dbSNP:375981595"
variation 9808
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="c"
/db_xref="dbSNP:149563971"
variation 10096
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:200859798"
variation 10126
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="g"
/db_xref="dbSNP:181428846"
variation 10180
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:367789536"
variation 10262
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:185640541"
variation 10266
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:189959029"
variation 10338..10339
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace=""
/replace="acacacac"
/db_xref="dbSNP:372046631"
variation 10347..10348
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace=""
/replace="cacaca"
/db_xref="dbSNP:72232616"
variation 10353..10354
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace=""
/replace="ct"
/db_xref="dbSNP:201960244"
variation 10354
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="t"
/db_xref="dbSNP:58381608"
variation 10428..10429
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace=""
/replace="a"
/db_xref="dbSNP:200419224"
variation 10429..10430
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace=""
/replace="a"
/db_xref="dbSNP:376910951"
variation 10432..10433
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace=""
/replace="a"
/db_xref="dbSNP:372432066"
STS 10547..10879
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/standard_name="RH119837"
/db_xref="UniSTS:133582"
STS 10547..10818
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/standard_name="RH120439"
/db_xref="UniSTS:133434"
variation 10552
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="g"
/db_xref="dbSNP:72611275"
variation 10560
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:59400074"
variation 10688
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="g"
/db_xref="dbSNP:375161046"
variation 10759..10764
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace=""
/replace="ttacac"
/db_xref="dbSNP:201762227"
variation 10764
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace=""
/replace="ttacac"
/db_xref="dbSNP:146492736"
variation 10785
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:187462374"
variation 10790
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="g"
/db_xref="dbSNP:191815457"
variation 10880
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:148492729"
variation 10935
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:17318323"
variation 11047
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="g"
/db_xref="dbSNP:183687258"
STS 11075..11171
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/standard_name="SHGC-7435"
/db_xref="UniSTS:1300"
variation 11145..11146
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace=""
/replace="a"
/db_xref="dbSNP:199721412"
variation 11162
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="c"
/db_xref="dbSNP:16994920"
variation 11238
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="g"
/db_xref="dbSNP:139910801"
variation 11263
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="c"
/db_xref="dbSNP:58901446"
variation 11292
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:188550543"
variation 11323..11324
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace=""
/replace="tc"
/db_xref="dbSNP:201953511"
variation 11339
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace=""
/replace="g"
/db_xref="dbSNP:34561342"
variation 11400
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:16994922"
variation 11471
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:192044449"
variation 11514
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:140152199"
variation 11518
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="t"
/db_xref="dbSNP:372650180"
variation 11520
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="t"
/db_xref="dbSNP:182660223"
variation 11578
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:186936515"
variation 11606
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="g"
/replace="t"
/db_xref="dbSNP:191374718"
variation 11618
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:6641482"
variation 11808
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace=""
/replace="t"
/db_xref="dbSNP:200791203"
variation 11827
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:184174133"
variation 11854
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="g"
/db_xref="dbSNP:190676602"
variation 11858
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:193010493"
variation 11898..11899
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace=""
/replace="ga"
/db_xref="dbSNP:3831669"
variation 11908..11911
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace=""
/replace="tctc"
/db_xref="dbSNP:374459444"
variation 12138
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:185676537"
variation 12221
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:57522049"
variation 12247
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:189235006"
variation 12255
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:144890448"
variation 12258
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:181528352"
variation 12276
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:149225473"
variation 12317
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:146899103"
variation 12328
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="t"
/db_xref="dbSNP:41304958"
variation 12390
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:188535773"
variation 12402
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="g"
/replace="t"
/db_xref="dbSNP:371099570"
variation 12579
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:180936669"
variation 12583
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:185757853"
variation 12633..12634
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace=""
/replace="gt"
/db_xref="dbSNP:374190214"
variation 12641..12670
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace=""
/replace="gtgtgtgtgtgtgtgcgcgcacgcacgtgc"
/db_xref="dbSNP:66940095"
variation 12651..12680
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace=""
/replace="gtgtgcgcgcacacacgtgcgtgtgtgtgt"
/db_xref="dbSNP:371166069"
variation 12657
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:372884334"
variation 12659
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:191010209"
variation 12663
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:184050542"
variation 12673
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="g"
/replace="t"
/db_xref="dbSNP:75188108"
variation 12748
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="t"
/db_xref="dbSNP:187336298"
variation 12872
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:139310302"
variation 12873
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:190620184"
variation 12974
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:141776682"
variation 13014
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="g"
/replace="t"
/db_xref="dbSNP:73640620"
variation 13124
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:4844081"
variation 13132
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="c"
/db_xref="dbSNP:182791112"
variation 13185
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="g"
/db_xref="dbSNP:5980619"
variation 13217
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="g"
/db_xref="dbSNP:6641483"
variation 13241
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:41301301"
variation 13248
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="g"
/db_xref="dbSNP:41312787"
variation 13300
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:191519536"
variation 13384
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="g"
/db_xref="dbSNP:142697456"
STS 13421..13547
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/standard_name="RH18451"
/db_xref="UniSTS:76815"
variation 13467
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="a"
/replace="g"
/db_xref="dbSNP:182871110"
variation 13523
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="t"
/db_xref="dbSNP:41304956"
variation 13640
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
/replace="c"
/replace="g"
/db_xref="dbSNP:192692172"
polyA_signal 13693..13698
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
polyA_site 13716
/gene="AFF2"
/gene_synonym="FMR2; FMR2P; FRAXE; MRX2; OX19"
ORIGIN
cgccgcctgtgcagccgctgccgccgccgccgccgccgccgccgccgccgccgccgccgccgccgctgccgccccggctgccgcgccgcgccgctgcctctgccccggccgcccccgccgccgctgccgccgccggcccgcagccagccaggcgggcggcccagcccgcctgagcccgcagcggctgccgccgcagcgtcgggtcgctgggtgcgcgggctaccgcggaccgagcggacccgagtgggcgaccaggcgcttgcccgcccagtgccactgccgccgcttcctcgccggagcacaggaccagacacctccagcgcccgctgctgctgccgatgcggcccggacacttttagctgggcgggagggctggagagccgggggccgccgagaaccgccagcgagctgtgccgagagccgcgccgacccgctgcgatcagggacaggcgcccgcccgccgccgccgcctggccgctatggatctattcgactttttcagagactgggacttggagcagcagtgtcactatgaacaagaccgtagtgcacttaaaaaaagggaatgggagcggaggaatcaagaagtccagcaagaagacgatctcttttcttcaggctttgatctttttggggagccatacaagacaaacaaaggtgatgcacttgccaaccgagtccagaacacgcttggaaactatgatgaaatgaagaatttgctaactaaccattctaatcagaatcacctagtgggaattccaaagaattctgtgccccagaatcccaacaacaaaaatgaaccaagcttttttccagaacaaaagaacagaataattccacctcaccaggataatacccatccttcagcaccaatgcctccaccttctgttgtgatactgaattcaactctaatacacagcaacagaaaatcaaaacctgagtggtcacgtgatagtcataaccctagcactgtactggcaagccaggccagtggtcagccaaacaagatgcagactttgacacaggaccagtctcaagccaaactggaagacttctttgtctacccagctgaacagccccagattggagaagttgaagagtcaaacccatctgcaaaggaagacagtaaccctaattctagtggagaagatgctttcaaagaaatctttcaatccaattcaccggaagaatctgaattcgccgtgcaagcgcctgggtctcccctagtggcttcctctttattagctcctagcagtggcctttcagttcaaaacttcccaccagggctttactgcaaaacaagcatggggcagcaaaagccaactgcatacgtcagacccatggatggccaggaccaggcaccggacatctcaccaacactgaaaccttcaattgaatttgagaacagctttgggaatctgtcatttggaacactcttggatggaaaacccagtgcagccagttcaaagactaaactgccaaagttcaccatcctccaaacaagtgaagtaagccttcccagtgatccaagctgtgttgaagaaatcttgcgggagatgacccattcctggcctactcctctcacttccatgcatactgctggacactctgagcagagcaccttttccatcccaggacaggaatcgcagcatctgaccccaggattcaccttacaaaagtggaatgacccaaccaccagagcttctacaaagatgcttgaggatgacctgaagctgagcagtgatgaagatgaccttgagcctgtgaagaccttgaccactcagtgcactgccactgagctctaccaggctgttgaaaaggcaaaacctaggaataatcctgtgaacccacccttggccactccccagcccccacctgcagtgcaagccagcgggggttctggcagctccagcgaatcggagagcagctctgagtcggattcagacactgaaagtagcaccactgacagcgaatctaatgaggcacctcgtgtggcaactccagagcctgagccaccctcaaccaacaagtggcaactggataaatggcttaacaaagtgacatcccagaacaagtcttttatttgtggccaaaatgaaacacccatggagactatttctctgcctcctccaatcatccaaccaatggaagtccagatgaaagtgaagacgaatgccagtcaggtcccagctgaacccaaagaaaggcctctcctcagtctcattagggagaaagcccgtccacggcccactcagaaaattccagaaacaaaggctttgaagcataagttgtcaacaactagtgagacagtgtctcaaaggacaattgggaaaaaacagcccaaaaaagttgagaagaacaccagcactgacgagtttacctggcccaaaccaaatattaccagcagcactcccaaagaaaaagaaagtgtggagcttcatgacccaccaagaggccgcaacaaagccactgcccacaaaccagcccctaggaaagaaccaagacctaacatccctttggctcccgagaagaagaagtacagagggcctggcaagattgtgccaaagtctcgggaattcattgaaacagattcatctacatctgactccaacacagatcaggaagagaccctgcaaatcaaagtcctgcctccgtgcattatttctggaggtaatactgccaaatccaaggaaatctgtggtgccagcctgaccctcagcaccttaatgagtagcagtggcagcaacaacaacttatccatcagtaatgaagagccaacattttcacctattcctgtcatgcaaactgaaatcctgtcccctctgcgagatcatgagaacctgaaaaacctctgggtgaagattgaccttgacttactctctagagtacctggccacagctcactccatgcagcacctgccaagccagaccacaaggagactgccacaaaacccaagcgtcagacagctgtcacagctgtggagaaaccagcccctaagggcaaacgtaagcacaagccaatagaagttgcagagaagatccctgagaagaagcagcgcctggaggaggccacaactatctgcttgctccctccttgcatctcaccagccccaccccacaagcctcccaacactagagaaaataattcatccaggagagcaaatagaagaaaggaagaaaaactatttcctcctccactttccccactgccagaggaccctccacgccgcagaaatgtcagtggcaataatggtccctttggtcaagacaaaaacatcgccatgactggacaaatcacatctaccaaacctaagagaactgaaggcaaattctgtgctactttcaaagggatatcggtaaatgagggagacactccaaaaaaggcatcctctgccaccatcactgtcaccaatactgctattgccactgctactgtcactgctactgccattgtcaccaccactgtcacagctactgccaccgccacggccaccaccacaactactaccactaccatttccaccatcacctctaccatcactactggcctcatggatagcagtcacctggagatgacgtcctgggcggctctgccccttctatccagcagcagcactaatgtccggagacccaagctcacttttgatgactcggttcacaatgctgattattacatgcaagaagctaagaagctgaagcacaaagctgatgcactgttcgagaaatttggcaaagctgtgaattatgctgatgccgccctctccttcactgaatgtggcaatgccatggaacgcgaccctctggaagcaaagtccccatacaccatgtactctgagactgtggagctcctcaggtatgcaatgaggctgaagaactttgcaagtcccttggcttcggatggggacaaaaagctagcagtactatgctaccgatgtttatcactcctctatttgagaatgtttaagctgaagaaggaccatgctatgaagtactccagatcactgatggaatattttaagcaaaatgcttcaaaagtcgcacagataccctctccatgggtaagcaatggaaagaacactccatccccagtgtctctcaacaacgtctcccccatcaacgcaatggggaactgtaacaatggcccagtcaccattccccagcgcattcaccacatggctgccagccacgtcaacatcactagcaatgtgttacggggctatgaacactgggatatggccgacaaactgacaagagaaaacaaagaattctttggtgatctggacacgctgatggggcctctgacccagcacagcagcatgaccaatcttgtccgctacgttcgccaaggactgtgttggctgcgcatcgatgcccacttgttgtagtgggtgttctcagatctctagcatcacgacccatcactctacctctaccagcgcactgatggtcactggtggaactccactcactggggaacgttctctttggttatgtttgtttttatgcttcttttgttatctgtaaaaaacagaagtcattgtaagttgacactacaacttaagggcagtgtacgttttattacttagtcattttttttcttttagcatttgatatgcatttctcagattccaccatctttttgtgctttatggaatgacagtccctacaatattgttttaagcccacactacccaaaacaaagaatgggaagcacttgtgataaagacaggctcctgagaaatgcaacaagtggtcttacatatacatgagaacttagacacaagggaccatcccccaaactctactcttatacccagaaaagaacatatttcagaatctgtcaaacttttgtgtatcccacagattcaatcttcaggtgagaattttcattgtcaaaacccactggttagatgttgtagcaacatcataaaatcaagagtatcaagaaaataaatgagcatagcaatgctactcttaaaaagatgctatgccacacaaccagaggactttcttgttagcatccctttcctgattccctattttgttaattttaatgataagaagaaagggtgacatttattttgacaagttttaggcatcagctggcatcagtgtttttcaactccattatttgaagtgtaaatcctcacctggggttctctgtgtgcaaagctgtccttttgaagaacagtttggttgatgcatgccttagtagccaaaatgctacactctagacttacaagtgggagttaagagaggtctggaaagtgtccaacaaggaattcacacctctgcctcctttgcaacaacaacatttacacagttggtaagtgggtccataactggcaggatttttaaattgtattttgctcaaatctatgggaacaaaagtcaaggtatcactacctagaagtaatgatatacagttttcttcctagtggcttgaaaatctggacttcctcaattattattcacattttctctcttataggttttctgttttctactttcttttttctcttatctgtgtttccctttcctttgtttggctcattaacttttgactgaattacaattactccttttattaaagtccatattattgtgaatcatttccatgaaaatttctaagaaaactccaaactctctaaatagtagctaacttttatttttttaaaatgagtcgtggggtagtgcttcaccttgagatgctttgaaagagccctaaacattgggaaccattcacctaatttggagacatttctcactggttgtgactacccccttatgatccttcacattcattttatgtccctaaacatcacaatgtaaatatcatttttgatgttccagctcaccagaagattcttacacttggggtaaacactatccatgcattacttactggtaattacctgctggtatataattccatgtagcctttaatatgctgggttatcaaattctgttcactgagttatgaccagataaataatagatatgcacatgaaagatgcaaacttgtgtgattattaaagccagccatgcaggtccatgatagaaacagcaggtgatgactctgcactctcattgtcaaggttagatatatccccagttgcaaaacagccagacttgagctgtgctctggtcatctttgagtttaaggccttttgttgtataaggctgtggaagttgtactccaatggctgaagccatgttgttaatatggctgatgggagcatccctgcagctgaacccagcactttttatgctcccactgtggttgagctttatgtttacagtctcagcaacaacacttatgcatccaaacactcacaaatgaaacctgaaagaatcttttctgagcctcttaaaagaggaaaatgatgataacattaaagactctgaacacccaaggttggtgtcacatataaaaattaagctgatgactttgcagtgactcaagttgtctctttatcatggtttaccaggtagagtgcctggctattactatataatgaagcccactggcttgacttgtaagttcaacctaaaccacaatcctagaccatcatggatttaggagtagattcttcttgaaatcccacatccagaaactagacattagaatgttgaggcagtttcccagagaaacaagcatattgcctcatggatgaaagacttgtagttctagtttcagtgacttgttatatctacttacatacaacagggaggcaagaggattctctgtcatctctggtgactgagtgtaaaatatgtgccaagtctgcagcacagtgaccaaatctgacaatcgagctctggatcaccacttgattatgtagtagactcatttataaagcagcttaggaactaattaaacatggaggatgaattaccttcctatcccttgagataagacatctttcagtttcatgattaaggattgttgctgttttatagttactctgttcatcacagtgtaaatggtgatgcgtgtcgtaggtgtgcagctatttgagggactaagggatggagatattctgtcaaatgaatctcttcagtataccagtttgtgggagggatatgagacatgtggatggcagtgagagatcgtgcctctagatcttgatggaggcttggtgagacacacttaaataagcacgtggaggttagaatagagggcagagtaaaaggaagctccatctgagcaagtacaccaaatgatctcagccctgcaacttgacccaggtagggccaccactacgccttcacttgtcacccaagctccaaccacagagagtttgacaagtttgtgttatgatgttggcttggctttgtatttttaattaactttggatttttagtggttttgtcatataactgtctgagtttggtaggtaggattactttgaaaagggtttactagtgtggtcctccgggtagaatttagctgtaagcatgttgttagccagcctgtagactgttaattacttaataatctcattgggaaaatactagtagttttatatttggatgacataattggaaaagcagattagctgctactacttttaaaagacttaaggtcgggatgcctttttttccatgtaaggaaatgaaaagaccaaaatcttcaggcaaaaagcaagttgcaaaattagaaaccattggctaaaaatgtgttttgttgagtttccaaatggatgaattttcatttggacattacatcactaaattcattagattttgtctgcattggaaagatactcttctagcatatctttcccaaagatatctaatttggattctgtttcatgcaaatttgcatcccggaggttgaagttggagtttgaggttggaaaatatctttgaaggcagaatcagttgagttgtgagggtgaagcctcacatacttctcaacagacatgataaaattcacctgcatgagttggcaggtgggagaaccaaactggatcactgggtaagactactcagtaaagcaatgaactgcttgcttagagaagcatcactatccccattgagaaaaatgtgtggcaagatgatacagctacacagtatcaaatgaatgggtcaattcagcacccccaaatttaattctgtggggaaaaattattgagccagttgtcagtgttctgttacatgactggcagactaaattcttcatcgttgttgttattgttgttgttgtttctcattttcactcgcacggccttattctcataattaaaatctaattcattttctctttagtgttagtagactccaacaacagaagtggcatctgtgtattcataatcagcatttaccctggcaggagactaatcagataggccggtctcagacattaatcctaccatctgatatttttggtgaaggaaaaagtattaattctctttccatcctcctcctcagaaatatagaagccctctttaccaaaatcatcacattttactctgtaatctaccagctaaaagaaaattgcattgtggggagggcagaaagggggtgggggtgggggcgggggggtggggggtggggaagccccacaaagccagattgcagttcttgcccctttttgcgtctgacatgagatgttaaagaattattcatagtgctcacattgggttaggggacactgaactgctttttagatccatgatcagtcatcattcttctaagagattggagctttgctgtttcattaactgtgcagtgtagactaatggtgtttaataaaaatcattcaaaatttcaaactcttttgccagtgacctcaattttgttggctctgtgatttgtatcagactttgaggagggaagggggaagtgaaggaagcctacgtccaggcccctgacaggatgctgcagtagcaagctcaagctcgcctgcctgccagcagttgctggtgagcagcagcatgcagaccagctgtgggaagcctcctgaagaatgccccagctgatgctttcagctgggaatagtttgttcctattggggaactcattgttctccagtctctgcagcaggaagccagctgtcatattcggagggaatttcagatgctttacctttttggttttgtcctgcatcactcatgtggctacgaaagtgtctctgagaatagagcccaatgtggtgacaatgggtagtcaaatgcaccccagatgctcaagccctgttgtggttctgcagtgtttatgaaattgggaggaaggagaccctggacagtaagcaaaattggagacactccaacgaggctaagttaatgccgtgttgcccagaacaagatctagcttctcatttggtcagcctagcatgcaaccagtggtgtgctggtaaaatgtttaacaaccagctcgctgagaatagaaagcacctggtttgcaccatttgccaatttccatggcataaatactaccactttagatgattttaagctaccaactgtgatgtcactgaacacatggttggaaagagatgcacgcagttggctcttgcaagcctgggcaaaaatgcttcaacacgccactggatgcagccagtcagagggttcatatttaatatatgtgttcatgtggacacacacagacacacacacacaaactcacccttacacacacacttcgatgactaaaacaattacatagttttaagatatgaatcaatgtgtgaatgtagaaagcttatgataaggccctagaggtatgggttgccctggaagcctaggttttaagcaggagaatagctgagaagaatgaagccctcctgagctgaaaggagagatggatcaatggagatggttccatcatctccttccatatctcacaggtaaaatgggcactcagaaaaccctcacgattgattttttaaaaagataagtgagtgttttttattttattattattgtcatcattattttgatttacaaatgctatttgtaacttttacatgtaactaggataaagtatttacgggaactctatggagaatagcacaatccagaatttactgtgtttttcttttatgtgacgtggaaactcagtaattctcccaccttcacattgttgttcataagaattttactttagttattagggaatctaagttttttgttaacatttgtttttagttaaaagtatctacttactgttttagctctgaactcaaaccagaatatctctgtatcaattgcatgactattcagaaacaataatccaaaccaaaataattctttttccacccagtacgaagaaaactaagctcagtaacaagaaggcataaactaaagtatataatgaggctttcattaaatacacacacacacacactcacacacacacacatacactttttaaatttttaaattaggcctccacacataaatcattttgaaagtagaatagaaaatctcaaagaattcattctcctggtcctgtgcatcttctgcagttaataagaggtttgtatctggaaagatggaagaacttgttctaaaatcttatttttcaaaaaaaaatttccattttctctctgggcctgtatccatggttgaatgttagccctggaggagatccatgtcttactcgctctttctggcccttctgtcttttgcctctgcaattctttttgtagctggcacgatagcagggactgggggtctatcctttcatggtattgctacaatatttgtccttactggaaaatggtaacatccgggtctgatttaattggcattacacttacacagggactctgagcacccccgtcaccacaccagacagtggaccagttttcacagctacaaagagctagaaatgtgtttaacatcatccagtgcatcccctaattcaaaaccatcctcactaatcaatcatattcacccataaatattacaaatgagattgattccatctcaagacaatttgtcaaatacttaattttcttcctggatgattctacttactggatattttagaaagagaaatgtctgagataaaatccctcacatttactcaatataacaaattactgtttctactcctattctgagtagtgcttctgaagattgtttgctgtagtgttgtctttgataaaatgaatgtcagtagtgagccttttagagataccatgctcagaaatcctctttgggatcagaagatacctaaaattctccccttttgcccacttggttagatgagtgatatattctttggatcctgcaaagaagagattggtttattttcttttctggtggtggtagtggttgtatctgtggctgtgatggttgttgttacttgtctctctctctctctggctctggcttttgctttcctgctagtgttctttctctttccaaacaaatagttaaattaaatgtgagcttctgaattgtacttgttcatactttcaaaacataacagattaataaaaatagatgtgtcctgatttaaaacatgccccctggaaaggcatgctgtattatgaaatcgtgataatataactgcattattacatggcagtataaatattagtctgttgaattcatttgtccaattgtataactttgtggagcagtgttttgacctttgatacataattctggagcaagtggagtggttgcaggcagatgagacagtgttatatcaggatttttcaatcaactttagttggaggcctggcaattacaaacatcttcagatgtttctgtaaccattataaatatgaaaaaaacctcttcaaaaaatttcccatagtacttcagtcaagactttttaggtttatcttttttttttcatttctccttttccttttccattatttttcgatgggggggttgttatcattgactgaagaaatattttgattgcaatggtctctctctctctccccctctctctctctctcctctattctttcctccttccctctgtccatcacccctcattaaaatattgaaatctggagtctttgataaatctgcattagaccaggctatatgctaggaatgaaatctgggcaaatatcgatgggttttcaaagaatgctccatgttcattgggccctttcacaccccacagtgataaatgaaaaggatagaggtagttttttcaaaagagcactttaataatatcctctgagacctaatgcagtttaacaaatgactccacctatttttccagtaggtaaattgactgagacttgcaaaatacccctgagagttgtcaggggtgtcttctgcctggtctatagcgtgtgtgtttgctttgtatctaacaggcacattcacgtctcgtgtactcatatgaagtatttcctaacattcccattagcctgtatataagaatcagaaagataatcccaacatgttgtaaatgaagatgtgactctataacctttctcttcttcctggaaaaaaaaggacattttcatgcatattttaaacagaaattttgtatatttaagtgtcatagaaaatatttattgagtaactgggacacaaatgggaatttaattgtcatcatatgctttgtgtgtggggatgcttaccaacaccatgtcgctggaccattgtggcaagccataactgcacaaagagtacacatcgtcagtgtgtgtgtgtgtgtgtgtgtgcgcgcacacacgtgcgtgtgtgtgtccctgcatgtgcaacatgtctagcttgctgtccttcatgggattttagctttcccttcttgaaaaacattattttacagttccaggaggccctggttacattactatatgaaggcagtgatttgaaatgaaaattcctttcctcttggaagctttggtcataatatcatggttcaattaaacggattccaccggactttgtgatgaaaaaggctctgttaaaatccaattgagtttccaagaggaaattgtagtaggtcaagatgcatgagagggaagatggaggccacctcaactggagaacatgagctgagttgagccctcagtgttgaagttgacttgctccaagctgcagtctaaaaccctggggcccgtgcctggcctatgctccctcccaagtaagtagaggagcagaaccatcaggaacagcctgcctggctcctatgaagaaaacttcctgacgtcctgtccccaaaggaagaccctttccccaagggcaccccaggtggccattaaattgtgatgatcattcagaaagtgcccccttggctttatgagaatccaattagtcttctgaaccaccttttcttgggtgcagatttccaacattcatgctcattgcagatccaccaactgtcactgttcttaacaagcatgctcgtcttgtcagaatttcagtaagttccaatttcctgtacagaccagggtaaactgttctaaaatcaatcaattaatgaaatgttatctggtttttaaaagctggtttcatgtgctttatgtgtataaaactatatctgcctgtgtggctttgcatttcaaatgtgtggcgcacaagcgttttgttggtgctttgttctcagtacagtaactctgtgtacaaacattttaatgtggttttgttgttttccaacaagatgtctctgtaaaaatgatattggctgagctggtgcgttggtttctctcatagaggcattaactatactgccaatgcattgaattatttaaaaatgcaaaataaaatttttatgaaaatctca
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:2334 -> Molecular function: GO:0002151 [G-quadruplex RNA binding] evidence: ISS
GeneID:2334 -> Biological process: GO:0006397 [mRNA processing] evidence: IEA
GeneID:2334 -> Biological process: GO:0007420 [brain development] evidence: TAS
GeneID:2334 -> Biological process: GO:0007611 [learning or memory] evidence: IEA
GeneID:2334 -> Biological process: GO:0008380 [RNA splicing] evidence: IEA
GeneID:2334 -> Biological process: GO:0043484 [regulation of RNA splicing] evidence: IMP
GeneID:2334 -> Cellular component: GO:0016607 [nuclear speck] evidence: IDA
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