GGRNA | NM_015267.3

LOCUS       NM_015267               6855 bp    mRNA    linear   PRI 15-JUN-2013
DEFINITION  Homo sapiens cut-like homeobox 2 (CUX2), mRNA.
ACCESSION   NM_015267 XM_027045
VERSION     NM_015267.3  GI:291045458
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 6855)
  AUTHORS   Lee,J.Y., Lee,B.S., Shin,D.J., Woo Park,K., Shin,Y.A., Joong
            Kim,K., Heo,L., Young Lee,J., Kyoung Kim,Y., Jin Kim,Y., Bum
            Hong,C., Lee,S.H., Yoon,D., Jung Ku,H., Oh,I.Y., Kim,B.J., Lee,J.,
            Park,S.J., Kim,J., Kawk,H.K., Lee,J.E., Park,H.K., Lee,J.E.,
            Nam,H.Y., Park,H.Y., Shin,C., Yokota,M., Asano,H., Nakatochi,M.,
            Matsubara,T., Kitajima,H., Yamamoto,K., Kim,H.L., Han,B.G.,
            Cho,M.C., Jang,Y., Kim,H.S., Euy Park,J. and Lee,J.Y.
  TITLE     A genome-wide association study of a coronary artery disease risk
            variant
  JOURNAL   J. Hum. Genet. 58 (3), 120-126 (2013)
   PUBMED   23364394
REFERENCE   2  (bases 1 to 6855)
  AUTHORS   Huang,J., Ellinghaus,D., Franke,A., Howie,B. and Li,Y.
  TITLE     1000 Genomes-based imputation identifies novel and refined
            associations for the Wellcome Trust Case Control Consortium phase 1
            Data
  JOURNAL   Eur. J. Hum. Genet. 20 (7), 801-805 (2012)
   PUBMED   22293688
REFERENCE   3  (bases 1 to 6855)
  AUTHORS   Maestrini,E., Pagnamenta,A.T., Lamb,J.A., Bacchelli,E., Sykes,N.H.,
            Sousa,I., Toma,C., Barnby,G., Butler,H., Winchester,L.,
            Scerri,T.S., Minopoli,F., Reichert,J., Cai,G., Buxbaum,J.D.,
            Korvatska,O., Schellenberg,G.D., Dawson,G., de Bildt,A.,
            Minderaa,R.B., Mulder,E.J., Morris,A.P., Bailey,A.J. and
            Monaco,A.P.
  CONSRTM   IMGSAC
  TITLE     High-density SNP association study and copy number variation
            analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4
            gene region in autism susceptibility
  JOURNAL   Mol. Psychiatry 15 (9), 954-968 (2010)
   PUBMED   19401682
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   4  (bases 1 to 6855)
  AUTHORS   Jugessur,A., Shi,M., Gjessing,H.K., Lie,R.T., Wilcox,A.J.,
            Weinberg,C.R., Christensen,K., Boyles,A.L., Daack-Hirsch,S.,
            Nguyen,T.T., Christiansen,L., Lidral,A.C. and Murray,J.C.
  TITLE     Maternal genes and facial clefts in offspring: a comprehensive
            search for genetic associations in two population-based cleft
            studies from Scandinavia
  JOURNAL   PLoS ONE 5 (7), E11493 (2010)
   PUBMED   20634891
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
            Publication Status: Online-Only
REFERENCE   5  (bases 1 to 6855)
  AUTHORS   Yosifova,A., Mushiroda,T., Stoianov,D., Vazharova,R., Dimova,I.,
            Karachanak,S., Zaharieva,I., Milanova,V., Madjirova,N.,
            Gerdjikov,I., Tolev,T., Velkova,S., Kirov,G., Owen,M.J.,
            O'Donovan,M.C., Toncheva,D. and Nakamura,Y.
  TITLE     Case-control association study of 65 candidate genes revealed a
            possible association of a SNP of HTR5A to be a factor susceptible
            to bipolar disease in Bulgarian population
  JOURNAL   J Affect Disord 117 (1-2), 87-97 (2009)
   PUBMED   19328558
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   6  (bases 1 to 6855)
  AUTHORS   Gingras,H., Cases,O., Krasilnikova,M., Berube,G. and Nepveu,A.
  TITLE     Biochemical characterization of the mammalian Cux2 protein
  JOURNAL   Gene 344, 273-285 (2005)
   PUBMED   15656993
REFERENCE   7  (bases 1 to 6855)
  AUTHORS   Jacobsen,N.J., Elvidge,G., Franks,E.K., O'Donovan,M.C., Craddock,N.
            and Owen,M.J.
  TITLE     CUX2, a potential regulator of NCAM expression: genomic
            characterization and analysis as a positional candidate
            susceptibility gene for bipolar disorder
  JOURNAL   Am. J. Med. Genet. 105 (3), 295-300 (2001)
   PUBMED   11353453
REFERENCE   8  (bases 1 to 6855)
  AUTHORS   Coqueret,O., Martin,N., Berube,G., Rabbat,M., Litchfield,D.W. and
            Nepveu,A.
  TITLE     DNA binding by cut homeodomain proteins is down-modulated by casein
            kinase II
  JOURNAL   J. Biol. Chem. 273 (5), 2561-2566 (1998)
   PUBMED   9446557
REFERENCE   9  (bases 1 to 6855)
  AUTHORS   Ohara,O., Nagase,T., Ishikawa,K., Nakajima,D., Ohira,M., Seki,N.
            and Nomura,N.
  TITLE     Construction and characterization of human brain cDNA libraries
            suitable for analysis of cDNA clones encoding relatively large
            proteins
  JOURNAL   DNA Res. 4 (1), 53-59 (1997)
   PUBMED   9179496
REFERENCE   10 (bases 1 to 6855)
  AUTHORS   Quaggin,S.E., Heuvel,G.B., Golden,K., Bodmer,R. and Igarashi,P.
  TITLE     Primary structure, neural-specific expression, and chromosomal
            localization of Cux-2, a second murine homeobox gene related to
            Drosophila cut
  JOURNAL   J. Biol. Chem. 271 (37), 22624-22634 (1996)
   PUBMED   8798433
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from BC151245.1 and AC005805.12.
            This sequence is a reference standard in the RefSeqGene project.
            On Mar 13, 2010 this sequence version replaced gi:116517291.
            
            Summary: This gene encodes a protein which contains three CUT
            domains and a homeodomain; both domains are DNA-binding motifs. A
            similar gene, whose gene product possesses different DNA-binding
            activities, is located on chromosome on chromosome 7. Two
            pseudogenes of this gene have been identified on chromosomes 10 and
            4. [provided by RefSeq, Jan 2013].
            
            ##Evidence-Data-START##
            Transcript exon combination :: BC151245.1, AB006631.2 [ECO:0000332]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-4567              BC151245.1         11-4577
            4568-4568           AC005805.12        41462-41462
            4569-6855           BC151245.1         4579-6865
FEATURES             Location/Qualifiers
     source          1..6855
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="12"
                     /map="12q24.12"
     gene            1..6855
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /note="cut-like homeobox 2"
                     /db_xref="GeneID:23316"
                     /db_xref="HGNC:19347"
                     /db_xref="MIM:610648"
     exon            1..217
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /inference="alignment:Splign:1.39.8"
     misc_feature    95..97
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /note="upstream in-frame stop codon"
     variation       132
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201250355"
     CDS             155..4615
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /note="homeobox protein cux-2"
                     /codon_start=1
                     /product="homeobox protein cut-like 2"
                     /protein_id="NP_056082.2"
                     /db_xref="GI:116517292"
                     /db_xref="CCDS:CCDS41837.1"
                     /db_xref="GeneID:23316"
                     /db_xref="HGNC:19347"
                     /db_xref="MIM:610648"
                     /translation="

MAANVGSMFQYWKRFDLRRLQKELNSVASELSARQEESEHSHKHLIELRREFKKNVPEEIREMVAPVLKSFQAEVVALSKRSQEAEAAFLSVYKQLIEAPDPVPVFEAARSLDDRLQPPSFDPSGQPRRDLHTSWKRNPELLSPKEQREGTSPAGPTLTEGSRLPGIPGKALLTETLLQRNEAEKQKGLQEVQITLAARLGEAEEKIKVLHSALKATQAELLELRRKYDEEAASKADEVGLIMTNLEKANQRAEAAQREVESLREQLASVNSSIRLACCSPQGPSGDKVNFTLCSGPRLEAALASKDREILRLLKDVQHLQSSLQELEEASANQIADLERQLTAKSEAIEKLEEKLQAQSDYEEIKTELSILKAMKLASSTCSLPQGMAKPEDSLLIAKEAFFPTQKFLLEKPSLLASPEEDPSEDDSIKDSLGTEQSYPSPQQLPPPPGPEDPLSPSPGQPLLGPSLGPDGTRTFSLSPFPSLASGERLMMPPAAFKGEAGGLLVFPPAFYGAKPPTAPATPAPGPEPLGGPEPADGGGGGAAGPGAEEEQLDTAEIAFQVKEQLLKHNIGQRVFGHYVLGLSQGSVSEILARPKPWRKLTVKGKEPFIKMKQFLSDEQNVLALRTIQVRQRGSITPRIRTPETGSDDAIKSILEQAKKEIESQKGGEPKTSVAPLSIANGTTPASTSEDAIKSILEQARREMQAQQQALLEMEVAPRGRSVPPSPPERPSLATASQNGAPALVKQEEGSGGPAQAPLPVLSPAAFVQSIIRKVKSEIGDAGYFDHHWASDRGLLSRPYASVSPSLSSSSSSGYSGQPNGRAWPRGDEAPVPPEDEAAAGAEDEPPRTGELKAEGATAEAGARLPYYPAYVPRTLKPTVPPLTPEQYELYMYREVDTLELTRQVKEKLAKNGICQRIFGEKVLGLSQGSVSDMLSRPKPWSKLTQKGREPFIRMQLWLSDQLGQAVGQQPGASQASPTEPRSSPSPPPSPTEPEKSSQEPLSLSLESSKENQQPEGRSSSSLSGKMYSGSQAPGGIQEIVAMSPELDTYSITKRVKEVLTDNNLGQRLFGESILGLTQGSVSDLLSRPKPWHKLSLKGREPFVRMQLWLNDPHNVEKLRDMKKLEKKAYLKRRYGLISTGSDSESPATRSECPSPCLQPQDLSLLQIKKPRVVLAPEEKEALRKAYQLEPYPSQQTIELLSFQLNLKTNTVINWFHNYRSRMRREMLVEGTQDEPDLDPSGGPGILPPGHSHPDPTPQSPDSETEDQKPTVKELELQEGPEENSTPLTTQDKAQVRIKQEQMEEDAEEEAGSQPQDSGELDKGQGPPKEEHPDPPGNDGLPKVAPGPLLPGGSTPDCPSLHPQQESEAGERLHPDPLSFKSASESSRCSLEVSLNSPSAASSPGLMMSVSPVPSSSAPISPSPPGAPPAKVPSASPTADMAGALHPSAKVNPNLQRRHEKMANLNNIIYRVERAANREEALEWEF

"
     misc_feature    581..583
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (O14529.4); phosphorylation site"
     misc_feature    1808..2047
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /note="CUT domain; Region: CUT; pfam02376"
                     /db_xref="CDD:202226"
     misc_feature    2816..3037
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /note="CUT domain; Region: CUT; pfam02376"
                     /db_xref="CDD:202226"
     misc_feature    3272..3526
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /note="CUT domain; Region: CUT; pfam02376"
                     /db_xref="CDD:202226"
     misc_feature    3659..3835
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /note="Homeodomain;  DNA binding domains involved in the
                     transcriptional regulation of key eukaryotic developmental
                     processes; may bind to DNA as monomers or as homo- and/or
                     heterodimers, in a sequence-specific manner; Region:
                     homeodomain; cd00086"
                     /db_xref="CDD:28970"
     misc_feature    order(3659..3673,3677..3679,3728..3730,3746..3748,
                     3785..3787,3791..3796,3803..3808,3812..3820,3824..3829)
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /note="DNA binding site [nucleotide binding]"
                     /db_xref="CDD:28970"
     misc_feature    order(3665..3667,3674..3676,3794..3796,3803..3808,
                     3815..3817)
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /note="specific DNA base contacts [nucleotide binding];
                     other site"
                     /db_xref="CDD:28970"
     variation       167
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201720614"
     exon            218..328
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /inference="alignment:Splign:1.39.8"
     variation       233
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:200420920"
     variation       235
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:190091435"
     variation       236
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374906688"
     variation       254
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199531850"
     variation       291
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:371927310"
     variation       299
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201396910"
     exon            329..376
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /inference="alignment:Splign:1.39.8"
     exon            377..455
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /inference="alignment:Splign:1.39.8"
     variation       408
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376298955"
     variation       418
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:201675970"
     exon            456..590
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /inference="alignment:Splign:1.39.8"
     variation       460
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371918039"
     variation       477
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377178903"
     variation       478
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372659202"
     variation       494
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374932745"
     variation       508
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367783595"
     variation       511
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:372694667"
     variation       556
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376308961"
     variation       561
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372460519"
     variation       568
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:199677779"
     variation       571
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200963731"
     variation       572
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:202077929"
     variation       584
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200363695"
     variation       585
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200036593"
     exon            591..714
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /inference="alignment:Splign:1.39.8"
     variation       607
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374694155"
     variation       616
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369037997"
     variation       617
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144303972"
     variation       632
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199526069"
     variation       641
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202242120"
     exon            715..791
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /inference="alignment:Splign:1.39.8"
     variation       727
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:370570178"
     variation       745
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373930409"
     variation       754
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200159605"
     exon            792..858
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /inference="alignment:Splign:1.39.8"
     variation       793
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375250431"
     variation       796
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372596321"
     variation       805
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:116003760"
     variation       828
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371574153"
     variation       831
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375029073"
     variation       833
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:74641910"
     exon            859..907
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /inference="alignment:Splign:1.39.8"
     variation       874
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:375736198"
     variation       904
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:370133313"
     exon            908..1012
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /inference="alignment:Splign:1.39.8"
     variation       926
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:377564745"
     variation       927
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370159212"
     variation       1001
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374504502"
     variation       1003
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:373120851"
     exon            1013..1204
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /inference="alignment:Splign:1.39.8"
     variation       1039
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200854950"
     variation       1046
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199740303"
     variation       1047
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368309448"
     variation       1058
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199624287"
     variation       1060
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373879856"
     variation       1068
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200917097"
     variation       1089
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368058847"
     variation       1103
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369796774"
     variation       1160
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375793621"
     variation       1163
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201601231"
     variation       1173
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372765675"
     variation       1183
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199929446"
     variation       1184
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:184253691"
     variation       1191
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201856438"
     variation       1193
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376759807"
     exon            1205..1263
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /inference="alignment:Splign:1.39.8"
     variation       1222
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:369105020"
     variation       1255
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373896743"
     exon            1264..1312
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /inference="alignment:Splign:1.39.8"
     exon            1313..1412
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /inference="alignment:Splign:1.39.8"
     variation       1368
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375886505"
     variation       1369
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370694033"
     exon            1413..2054
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /inference="alignment:Splign:1.39.8"
     variation       1501
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371416832"
     variation       1531
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:3742007"
     variation       1567
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368575682"
     variation       1631
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:202129111"
     variation       1639
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:73418724"
     variation       1660
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:377024868"
     variation       1760
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200889290"
     variation       1762
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369149848"
     variation       1783
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200518721"
     variation       1785
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199576286"
     variation       1786
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372631563"
     variation       1819
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376365293"
     variation       1831
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199689266"
     variation       1846
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373544048"
     variation       1888
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376202322"
     variation       1921
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201284456"
     variation       1949
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200707164"
     variation       1950
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200610249"
     variation       1957
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370950366"
     variation       2005
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374551900"
     variation       2025
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376543487"
     exon            2055..2156
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /inference="alignment:Splign:1.39.8"
     variation       2076
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371998616"
     variation       2080
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201990238"
     variation       2098
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199957017"
     variation       2101
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369334691"
     variation       2112
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371230082"
     variation       2141
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374696777"
     variation       2155
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369060124"
     exon            2157..2920
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /inference="alignment:Splign:1.39.8"
     variation       2192
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200561197"
     variation       2376
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369648566"
     variation       2424
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:114719470"
     variation       2450
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199879473"
     variation       2454
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:111721455"
     variation       2456
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:202122088"
     variation       2497
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370447580"
     variation       2501
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:200046675"
     variation       2533
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:112401949"
     variation       2542
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:377379460"
     variation       2553
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370451307"
     variation       2611
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:201135503"
     variation       2758
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:183927879"
     variation       2763
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368685733"
     variation       2764
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:187693295"
     variation       2791
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371020289"
     variation       2797
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200061368"
     variation       2816
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:368608329"
     variation       2872
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:202035426"
     exon            2921..3080
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /inference="alignment:Splign:1.39.8"
     variation       2929
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:374013343"
     variation       2947
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:3742006"
     variation       3031
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200188128"
     variation       3044
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:369707993"
     exon            3081..3350
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /inference="alignment:Splign:1.39.8"
     variation       3095
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202210621"
     variation       3128
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371029227"
     variation       3157
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375629258"
     variation       3210
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:368356891"
     variation       3253
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:182436226"
     variation       3254
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370757379"
     variation       3290
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376357240"
     exon            3351..3539
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /inference="alignment:Splign:1.39.8"
     variation       3360..3361
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:370320416"
     variation       3362
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:183351547"
     variation       3412
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368083044"
     variation       3486
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201719553"
     variation       3499
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200333006"
     exon            3540..3813
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /inference="alignment:Splign:1.39.8"
     variation       3574
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376748122"
     variation       3575
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200121526"
     variation       3594
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373425760"
     variation       3596
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201245757"
     variation       3602
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201979932"
     variation       3603
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373295855"
     variation       3647
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377515407"
     variation       3704
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201155645"
     variation       3709
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200742986"
     variation       3736
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199568145"
     variation       3748
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:16941414"
     variation       3760
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199713824"
     exon            3814..6844
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /inference="alignment:Splign:1.39.8"
     variation       3849
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200760684"
     variation       3878
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201097767"
     variation       3887
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:199977880"
     variation       3898
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:372290639"
     variation       3927
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202163528"
     variation       3928
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200919469"
     variation       3966
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369695847"
     variation       3967
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201865813"
     variation       4001
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:61745424"
     variation       4006
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:368882902"
     variation       4014
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:375034259"
     variation       4028
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376380265"
     variation       4029
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369781381"
     variation       4062
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373549547"
     variation       4072
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:3803167"
     variation       4088
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371358726"
     variation       4096
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373830228"
     variation       4099
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:189935634"
     variation       4111
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370091064"
     variation       4125
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:374410985"
     variation       4151
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201289447"
     variation       4156
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367779122"
     variation       4161
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:372685449"
     variation       4164
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201485891"
     variation       4173
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:375555910"
     variation       4193
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368160942"
     variation       4224
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:372473676"
     variation       4231
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199885312"
     variation       4261
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138469924"
     variation       4262
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143575822"
     variation       4287
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200377020"
     variation       4289
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147019586"
     variation       4317
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371792382"
     variation       4344
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374715486"
     variation       4351
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199519872"
     variation       4354
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369066161"
     variation       4377
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373437895"
     variation       4401
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:147161135"
     variation       4402
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147713700"
     variation       4438
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:201395094"
     variation       4452
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200547493"
     variation       4494
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369462639"
     variation       4499
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373670237"
     variation       4523
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369537072"
     variation       4524
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201245096"
     variation       4568
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:6490073"
     variation       4598
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:377383876"
     variation       4626..4627
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:372425523"
     variation       4630
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370460243"
     variation       4651
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:375935204"
     variation       4666
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142069226"
     variation       4689
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:142641895"
     variation       4705
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:182832397"
     variation       4751
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:188205921"
     variation       5020
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:192763882"
     variation       5068
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:185266929"
     variation       5100
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:12298196"
     variation       5162
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:3742005"
     variation       5164
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:187509906"
     variation       5212
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:369988664"
     variation       5220..5221
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace=""
                     /replace="tg"
                     /db_xref="dbSNP:112005266"
     variation       5280
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:373875175"
     variation       5358
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:192335387"
     variation       5378
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:7398833"
     variation       5385
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184722668"
     STS             5480..5734
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /standard_name="A004C03"
                     /db_xref="UniSTS:3698"
     variation       5565
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:114903592"
     variation       5701
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:188029244"
     variation       5747
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373774988"
     variation       5753
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:201355972"
     variation       5786
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150711405"
     variation       5845
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:180957696"
     variation       5853
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:116655528"
     variation       5965
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:184480673"
     variation       6022
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139201571"
     variation       6057
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:189752698"
     variation       6150
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:181438521"
     variation       6155
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:36070546"
     variation       6167
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:185943876"
     variation       6194
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:201621322"
     variation       6249
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:189095594"
     variation       6268
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:76899457"
     variation       6448
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:146497939"
     variation       6510
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:181840805"
     variation       6631
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:186488047"
     variation       6654
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:76686788"
     variation       6655
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139916485"
     STS             6683..6832
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /standard_name="SGC32083"
                     /db_xref="UniSTS:68614"
     variation       6691
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:144322907"
     variation       6720
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:78091273"
     variation       6730..6731
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace=""
                     /replace="ac"
                     /db_xref="dbSNP:375852085"
     variation       6770
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:79804441"
     variation       6799
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371090826"
     polyA_site      6844
                     /gene="CUX2"
                     /gene_synonym="CDP2; CUTL2"
ORIGIN

ggccggagggcgcccgaggggccccgggccgcggcgctcagggcccgggcggccggcggcggccccggggctggggggagtccagcccggatattgagtgcagccattgagaaaagccaaactcttgtgtgtgcgcgtctcgatagcccccaagatggccgccaatgtgggatcgatgtttcaatattggaagcgatttgatctacggcgactccagaaggagcttaattccgtcgcttctgagctgtctgcacggcaggaggagagtgaacattctcataaacatttaattgaactccgccgggaatttaagaaaaatgtacctgaggaaatcagagagatggtggctcctgtattaaaaagcttccaagccgaggtggtggcccttagtaagagaagtcaggaggcggaggctgcttttctgagtgtttacaagcaattaattgaagcaccagaccccgtgcctgtgtttgaggcggcacgcagcctagacgacagactgcagccccccagctttgaccccagtgggcagccccggcgagacctccacacttcgtggaagaggaaccccgagctcctcagccccaaagagcagagagaggggacgtcgcctgccgggcccacgctgaccgagggaagccgcctcccaggcattcccgggaaagccctcctgacagaaaccttgctgcagagaaatgaggcggaaaaacaaaagggccttcaagaagtacagatcactttggcggccagactgggggaggcagaggagaaaatcaaagtcctacattcagcgctaaaggctacgcaggcagagctgctagagctgcggcggaagtacgacgaggaggcagcatccaaggcagatgaagtcggcctgatcatgaccaacctggagaaagctaatcagcgagctgaggctgcccagcgggaggtggaaagtctccgggaacagctggcctctgtcaacagctccatccgcctggcttgctgctctccccaggggcccagtggggataaggtgaacttcactctgtgctcgggccctcggctggaggccgcgctggcctccaaggacagggagatcctgcggctgctgaaggacgtgcagcacctccagagctcactgcaggagctggaggaggcatccgccaaccagatcgccgacctggagcggcagctcacggccaagtccgaggccatagaaaagctggaagagaagctccaggcccagtctgactatgaggaaattaaaacggagctgagcatcctgaaagccatgaagctggcctccagcacctgcagcctcccccagggcatggccaagcctgaagactcactgcttattgcaaaggaggccttcttccccacgcagaaattccttctggagaagcccagcctcctggccagccctgaggaagacccatcagaggacgattccatcaaggattcactgggcacggagcagtcctacccctcccctcagcagctcccacctccaccagggccagaagaccccctgtctcccagccccgggcagcccctgctgggccccagcttggggcctgacggcactcggactttctcgctgtcccccttccccagcctggcatcaggggagagactgatgatgcccccagccgccttcaagggagaggcgggcggcctgctggtgttccccccagccttctatggcgccaagccccccacagcccctgccaccccggcccctggccctgagccactgggcggtcctgagcccgcggatggtggtgggggcggagcggcggggcccggggcagaggaggagcagctggacacggcagagatcgccttccaggtgaaggagcagctgctgaaacacaacatcgggcagcgggtgtttgggcattacgtgctggggctgtcgcagggctcggtcagcgagatcctagcccggcccaagccctggcgcaagctcacggtgaagggcaaggagcccttcatcaagatgaagcagttcctgtcggatgagcagaatgtactggcgctcaggaccatccaagtgcggcagcgaggcagcatcaccccgagaatccgcacgcctgagacaggctcagacgacgccatcaagagcattctagagcaggccaagaaggagatcgagtcgcagaagggcggcgagcccaagacctcggtggccccgctgagcatcgccaacggcacgacccccgccagcacctcggaggacgccatcaagagcatcctggagcaggcacgccgtgagatgcaggcgcaacagcaggcgctgctggagatggaggtggcgcccaggggccgctcggtgcccccctcgcccccggagcggccatcactggccaccgcgagccagaacggggccccggccttggtgaagcaggaggagggcagcgggggccccgcgcaggcgccgctcccggtcctgtcccccgccgccttcgtgcagagcatcatccgcaaggtcaagtccgagatcggcgacgccggctacttcgaccaccactgggcctccgaccgcggcctgctcagccgcccctacgcctccgtgtcgccctcgctgtcctcctcctcctcctctggctactctggccagcccaacggccgcgcctggccccgcggggacgaggcccctgtgccccccgaggacgaggcggcggcaggggcggaggacgaaccccccaggacgggcgagctcaaggctgagggcgcgacggccgaggcgggcgcgcggctgccctactacccggcctacgtgccgcgcaccctgaagcccaccgtgccgccgctgacccccgagcagtacgagctgtacatgtaccgtgaggtagacacgctggagctcacccgccaggtcaaggagaagctggccaagaacggcatctgccagaggatcttcggggagaaggtgctgggcctgtcacagggcagcgtgagcgacatgctgtcccggccgaagccatggagcaagctgacgcagaaggggcgggagcccttcatccgcatgcagctgtggctctctgaccagctcggccaggcagtgggccagcagcctggtgcctcccaggccagtcccacagaaccaaggtcctcaccatccccaccccccagccccacagagcctgagaagagctcccaggagccgttgagcctgtccctggagagcagcaaggagaaccagcagccagagggccgctccagctcctcgttgagcgggaagatgtactcaggcagccaggccccagggggcatccaggagatcgtggccatgtcccccgagctggacacgtactccatcaccaagagggtgaaggaggtcctcacagacaacaatctagggcagcggctgtttggggaaagcatcctgggtctgacacagggctccgtgtctgacctgctgtcccggcccaaaccctggcacaagctgagcctgaaggggcgggagccttttgtccgcatgcagctgtggctcaatgacccccataacgtggagaagctgagggatatgaagaagctggagaagaaagcctacctgaaacgtcgctatggcctcatcagcaccggctcagacagtgagtccccggccacccgctcagagtgccccagcccctgcctgcagccccaggacctgagcctcctgcagatcaagaagccccgggtggtgctggcacccgaggagaaggaggcactgcggaaggcctatcagctggaaccctacccctcgcagcagaccatcgagctcctctccttccagctcaacctcaagaccaacaccgtcatcaactggttccacaactacaggtcccggatgcgccgggagatgttggtggaggggacccaggatgagccagaccttgatccaagcgggggtcctggaatcctaccgccaggccactcccacccagaccccaccccgcagagccctgactctgagactgaggaccagaagccaaccgtgaaggaactggagcttcaggagggccctgaggagaacagcacacccctgaccacccaggacaaggcccaagtgaggatcaagcaggaacagatggaggaggatgctgaggaagaggcaggcagccagccccaggactcaggggagctggacaaaggccaaggtccccccaaagaggagcatcccgaccctccgggtaatgatggactcccaaaagtggctcccgggcccctccttccaggtggatccaccccagactgtccctcacttcatccccaacaggagagtgaggccggggagcgacttcacccggaccctttaagttttaagtcagcctcagagtcctcacgctgcagcctggaggtgtcactgaactcgccctcggccgcctcctcaccaggcctcatgatgtctgtgtcacctgtcccctcctcctcagctcccatctccccatccccacctggcgccccccctgccaaagtgccgagtgccagccccactgctgacatggctggagccttgcaccccagtgccaaggtgaaccccaacttgcagcggcggcatgagaagatggccaatctgaacaacatcatttaccgagtagagcgggctgccaatcgggaggaggccctggagtgggagttctgaaggcagggtgagggggcaagggacataccctggtaactaccttccttctcgcacttactctcctcaacaggatggggtaagggagggaggaactcaaccatcaaaatgtggacagcaatgttatgccgtttacgttttttgttgtaatcctagttctatgaagctgtgtgagcaggtgggtcaaatgccattgcctccacttttctgcacccccctgctcctcttcaccctgacccctctgcaggaggcagaagcaaaatggcaccacatattcacctgaaaactccaaactcttttagaaaaataaataaatatttatagacctcttttagatattttaataaaggatcctttggaatttatcccagctgatgctgttttgatattacagagagttataaaatcaggatgctgtcacaactgttgcgaagtatacactgaagttgtgtcgtttttgccactagatgagattaaaagaagacaattattcaaagccatcacaaaacactataagactgaccaaaatttagataacctttgaaccacgatttttttccacatctgtctgtgagacacagcgcaatgctactgcccttccagaaactgtgctaaaaagagaaagtccaaaagactctaaacaaaaacctcgacgccgttgaggatgtgtttcattctggtggtctgttttgcaagcttgataacagaatgtccgtgccattgtaaatgttgtagagatgtgggccgtggcccaaccgtcctatatgagatgtagcatggtacagaacaaactgcttacacaggtctcactagttagaaacctgtgggccatggaggtcagacatccatcttgtccatctataggcaagaagtgtttccagatcctttggaaaggtgggcatggggcaggtgcttggagagtggcgtttgagccagagcgaccccatttcccgtgtgaaccataggcacaacccaggaagtttccccacttgtaggagtgtgggtattccagagcaagactgtggccaccatcttcccctcttggtgttttccgaaagtgacagtgttggtcatcccatgaccactgaagcttagtaaccagcgccaaaaagtagattcatcaaactagagaccccagctccccttctcgccatcttctttctcaagttgaccgtggtgctgtttctggaaggcatctgcaactccaagtccatgcagaactctggaaggccaagttcatcgcagcatgttcaccatatcccagcctccaaatctatcctcctaccttccaacgcatgacctgttggggagcagagacttaacccccaactcagaggaacccttcctccagcgtctttggcatggtttctagggtgagagttcccaatttggatagaacggccaccatattggttactgaatctctctcccttgtttttattacgtttcctttttcaaactgtccatgggaaggctgaattgagtgactccccagaatgaagatgagaaggtgaatataatcaatgccaatgtaatgccagcgggtgagatggccgatggaggtttcaaagatgtagctagcattttgaaaccatatgggcaaaacccggcaaccagaaggggacagataaggaccgttccagaaatcccaactctcacacccagcccaggctgcagtctccacaccaaacagtcaacaaaacacaaaccctgaaggaaaaccttttccatacacccaggctatgcattgaagagttttccactgtatacatttttatccagatgaaggtatttttatattttgacaataggaaacagtgaccattttcagagtaatcaaatctggaacaaatgaaacatcttttagccaccaccaccctgttgcaattaagacaaccgtgggggaacacaccactttttactgttgaaaccaacacaacgttgaaatccaggcttatacgcagactccgattcctagagaactaaatttggctttagtgtgacgggatttgattaagcacttagtatagtcttttgaacacggaaatcctgttgtacttaaagctagcggacccgtgaacaactttgtcaggttcacgtcctataacggttaaaaaacacacacacacatacacaaaccgtttctatgagagattgatgaactttgtttaaaattttaaaaaaaggaacacgttctgtaaacgagtcgctaaatacagaattgtataataaaaaaaaaaaaa

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