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2019-03-25 14:31:54, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_030583               4065 bp    mRNA    linear   PRI 11-MAY-2013
DEFINITION  Homo sapiens matrilin 2 (MATN2), transcript variant 2, mRNA.
ACCESSION   NM_030583
VERSION     NM_030583.2  GI:62548861
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 4065)
  AUTHORS   Bailey,S.D., Xie,C., Do,R., Montpetit,A., Diaz,R., Mohan,V.,
            Keavney,B., Yusuf,S., Gerstein,H.C., Engert,J.C. and Anand,S.
  CONSRTM   DREAM investigators
  TITLE     Variation at the NFATC2 locus increases the risk of
            thiazolidinedione-induced edema in the Diabetes REduction
            Assessment with ramipril and rosiglitazone Medication (DREAM) study
  JOURNAL   Diabetes Care 33 (10), 2250-2253 (2010)
   PUBMED   20628086
  REMARK    GeneRIF: Observational study of gene-disease association,
            gene-environment interaction, and pharmacogenomic / toxicogenomic.
            (HuGE Navigator)
REFERENCE   2  (bases 1 to 4065)
  AUTHORS   Talmud,P.J., Drenos,F., Shah,S., Shah,T., Palmen,J., Verzilli,C.,
            Gaunt,T.R., Pallas,J., Lovering,R., Li,K., Casas,J.P., Sofat,R.,
            Kumari,M., Rodriguez,S., Johnson,T., Newhouse,S.J., Dominiczak,A.,
            Samani,N.J., Caulfield,M., Sever,P., Stanton,A., Shields,D.C.,
            Padmanabhan,S., Melander,O., Hastie,C., Delles,C., Ebrahim,S.,
            Marmot,M.G., Smith,G.D., Lawlor,D.A., Munroe,P.B., Day,I.N.,
            Kivimaki,M., Whittaker,J., Humphries,S.E. and Hingorani,A.D.
  CONSRTM   ASCOT investigators; NORDIL investigators; BRIGHT Consortium
  TITLE     Gene-centric association signals for lipids and apolipoproteins
            identified via the HumanCVD BeadChip
  JOURNAL   Am. J. Hum. Genet. 85 (5), 628-642 (2009)
   PUBMED   19913121
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   3  (bases 1 to 4065)
  AUTHORS   Wheeler,H.E., Metter,E.J., Tanaka,T., Absher,D., Higgins,J.,
            Zahn,J.M., Wilhelmy,J., Davis,R.W., Singleton,A., Myers,R.M.,
            Ferrucci,L. and Kim,S.K.
  TITLE     Sequential use of transcriptional profiling, expression
            quantitative trait mapping, and gene association implicates MMP20
            in human kidney aging
  JOURNAL   PLoS Genet. 5 (10), E1000685 (2009)
   PUBMED   19834535
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   4  (bases 1 to 4065)
  AUTHORS   Landa,I., Ruiz-Llorente,S., Montero-Conde,C., Inglada-Perez,L.,
            Schiavi,F., Leskela,S., Pita,G., Milne,R., Maravall,J., Ramos,I.,
            Andia,V., Rodriguez-Poyo,P., Jara-Albarran,A., Meoro,A., del
            Peso,C., Arribas,L., Iglesias,P., Caballero,J., Serrano,J.,
            Pico,A., Pomares,F., Gimenez,G., Lopez-Mondejar,P., Castello,R.,
            Merante-Boschin,I., Pelizzo,M.R., Mauricio,D., Opocher,G.,
            Rodriguez-Antona,C., Gonzalez-Neira,A., Matias-Guiu,X.,
            Santisteban,P. and Robledo,M.
  TITLE     The variant rs1867277 in FOXE1 gene confers thyroid cancer
            susceptibility through the recruitment of USF1/USF2 transcription
            factors
  JOURNAL   PLoS Genet. 5 (9), E1000637 (2009)
   PUBMED   19730683
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   5  (bases 1 to 4065)
  AUTHORS   Szabo,E., Korpos,E., Batmunkh,E., Lotz,G., Holczbauer,A.,
            Kovalszky,I., Deak,F., Kiss,I., Schaff,Z. and Kiss,A.
  TITLE     Expression of matrilin-2 in liver cirrhosis and hepatocellular
            carcinoma
  JOURNAL   Pathol. Oncol. Res. 14 (1), 15-22 (2008)
   PUBMED   18386166
  REMARK    GeneRIF: data indicate matrilin-2 is a novel basement membrane
            component in the liver, synthesized during sinusoidal
            'capillarization' in cirrhosis & in hepatocellular carcinoma
REFERENCE   6  (bases 1 to 4065)
  AUTHORS   Piecha,D., Hartmann,K., Kobbe,B., Haase,I., Mauch,C., Krieg,T. and
            Paulsson,M.
  TITLE     Expression of matrilin-2 in human skin
  JOURNAL   J. Invest. Dermatol. 119 (1), 38-43 (2002)
   PUBMED   12164922
  REMARK    GeneRIF: matrilin-2 is expressed in normal skin by keratinocytes
            and fibroblasts and may thus contribute to cutaneous homeostasis.
REFERENCE   7  (bases 1 to 4065)
  AUTHORS   Frank,S., Schulthess,T., Landwehr,R., Lustig,A., Mini,T., Jeno,P.,
            Engel,J. and Kammerer,R.A.
  TITLE     Characterization of the matrilin coiled-coil domains reveals seven
            novel isoforms
  JOURNAL   J. Biol. Chem. 277 (21), 19071-19079 (2002)
   PUBMED   11896063
REFERENCE   8  (bases 1 to 4065)
  AUTHORS   Mates,L., Korpos,E., Deak,F., Liu,Z., Beier,D.R., Aszodi,A. and
            Kiss,I.
  TITLE     Comparative analysis of the mouse and human genes (Matn2 and MATN2)
            for matrilin-2, a filament-forming protein widely distributed in
            extracellular matrices
  JOURNAL   Matrix Biol. 21 (2), 163-174 (2002)
   PUBMED   11852232
  REMARK    GeneRIF: matrilin-2, a filament-forming protein widely distributed
            in extracellular matrices.
REFERENCE   9  (bases 1 to 4065)
  AUTHORS   Muratoglu,S., Krysan,K., Balazs,M., Sheng,H., Zakany,R., Modis,L.,
            Kiss,I. and Deak,F.
  TITLE     Primary structure of human matrilin-2, chromosome location of the
            MATN2 gene and conservation of an AT-AC intron in matrilin genes
  JOURNAL   Cytogenet. Cell Genet. 90 (3-4), 323-327 (2000)
   PUBMED   11124542
REFERENCE   10 (bases 1 to 4065)
  AUTHORS   Deak,F., Piecha,D., Bachrati,C., Paulsson,M. and Kiss,I.
  TITLE     Primary structure and expression of matrilin-2, the closest
            relative of cartilage matrix protein within the von Willebrand
            factor type A-like module superfamily
  JOURNAL   J. Biol. Chem. 272 (14), 9268-9274 (1997)
   PUBMED   9083061
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from CB988661.1, AY358895.1,
            AK075489.1, BX649093.1, BC010444.1, AL833931.1 and AI434413.1.
            On Apr 14, 2005 this sequence version replaced gi:13518038.
            
            Summary: This gene encodes a member of the von Willebrand factor A
            domain containing protein family. This family of proteins is
            thought to be involved in the formation of filamentous networks in
            the extracellular matrices of various tissues. This protein
            contains five von Willebrand factor A domains. The specific
            function of this gene has not yet been determined. Two transcript
            variants encoding different isoforms have been found for this gene.
            [provided by RefSeq, Jul 2008].
            
            Transcript Variant: This variant (2) uses an alternate in-frame
            splice site compared to variant 1. The resulting isoform (b) has
            the same N- and C-termini but is shorter compared to isoform a.
            
            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 :: BC010444.1, AK289721.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025081, ERS025082 [ECO:0000348]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-638               CB988661.1         29-666
            639-1296            AY358895.1         611-1268
            1297-1558           AK075489.1         1267-1528
            1559-1985           AY358895.1         1408-1834
            1986-2812           BX649093.1         1102-1928
            2813-3153           BC010444.1         2804-3144
            3154-3547           AL833931.1         3161-3554
            3548-4065           AI434413.1         1-518               c
FEATURES             Location/Qualifiers
     source          1..4065
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="8"
                     /map="8q22"
     gene            1..4065
                     /gene="MATN2"
                     /note="matrilin 2"
                     /db_xref="GeneID:4147"
                     /db_xref="HGNC:6908"
                     /db_xref="HPRD:03660"
                     /db_xref="MIM:602108"
     exon            1..205
                     /gene="MATN2"
                     /inference="alignment:Splign:1.39.8"
     variation       135
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375817069"
     exon            206..373
                     /gene="MATN2"
                     /inference="alignment:Splign:1.39.8"
     variation       227
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367644090"
     variation       231
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:11559203"
     CDS             232..3045
                     /gene="MATN2"
                     /note="isoform b precursor is encoded by transcript
                     variant 2; matrilin-2"
                     /codon_start=1
                     /product="matrilin-2 isoform b precursor"
                     /protein_id="NP_085072.2"
                     /db_xref="GI:62548862"
                     /db_xref="CCDS:CCDS55265.1"
                     /db_xref="GeneID:4147"
                     /db_xref="HGNC:6908"
                     /db_xref="HPRD:03660"
                     /db_xref="MIM:602108"
                     /translation="
MEKMLAGCFLLILGQIVLLPAEARERSRGRSISRGRHARTHPQTALLESSCENKRADLVFIIDSSRSVNTHDYAKVKEFIVDILQFLDIGPDVTRVGLLQYGSTVKNEFSLKTFKRKSEVERAVKRMRHLSTGTMTGLAIQYALNIAFSEAEGARPLRENVPRVIMIVTDGRPQDSVAEVAAKARDTGILIFAIGVGQVDFNTLKSIGSEPHEDHVFLVANFSQIETLTSVFQKKLCTAHMCSTLEHNCAHFCINIPGSYVCRCKQGYILNSDQTTCRIQDLCAMEDHNCEQLCVNVPGSFVCQCYSGYALAEDGKRCVAVDYCASENHGCEHECVNADGSYLCQCHEGFALNPDKKTCTKIDYCASSNHGCQHECVNTDDSYSCHCLKGFTLNPDKKTCRRINYCALNKPGCEHECVNMEESYYCRCHRGYTLDPNGKTCSRVDHCAQQDHGCEQLCLNTEDSFVCQCSEGFLINEDLKTCSRVDYCLLSDHGCEYSCVNMDRSFACQCPEGHVLRSDGKTCAKLDSCALGDHGCEHSCVSSEDSFVCQCFEGYILREDGKTCRRKDVCQAIDHGCEHICVNSDDSYTCECLEGFRLAEDGKRCRRKDVCKSTHHGCEHICVNNGNSYICKCSEGFVLAEDGRRCKKCTEGPIDLVFVIDGSKSLGEENFEVVKQFVTGIIDSLTISPKAARVGLLQYSTQVHTEFTLRNFNSAKDMKKAVAHMKYMGKGSMTGLALKHMFERSFTQGEGARPLSTRVPRAAIVFTDGRAQDDVSEWASKAKANGITMYAVGVGKAIEEELQEIASEPTNKHLFYAEDFSTMDEISEKLKKGICEALEDSDGRQDSPAGELPKTVQQPTVQHRYLFEEDNLLRSTQKLSHSTKPSGSPLEEKHDQCKCENLIMFQNLANEEVRKLTQRLEEMTQRMEALENRLRYR
"
     sig_peptide     232..300
                     /gene="MATN2"
                     /inference="COORDINATES: ab initio prediction:SignalP:4.0"
     mat_peptide     301..3042
                     /gene="MATN2"
                     /product="matrilin-2 isoform b"
     misc_feature    391..1059
                     /gene="MATN2"
                     /note="VWA_Matrilin: In cartilaginous plate, extracellular
                     matrix molecules mediate cell-matrix and matrix-matrix
                     interactions thereby providing tissue integrity. Some
                     members of the matrilin family are expressed specifically
                     in developing cartilage rudiments; Region: vWA_Matrilin;
                     cd01475"
                     /db_xref="CDD:29248"
     misc_feature    order(418..420,424..426,430..432,631..633,739..741)
                     /gene="MATN2"
                     /note="metal ion-dependent adhesion site (MIDAS); other
                     site"
                     /db_xref="CDD:29248"
     misc_feature    1129..1197
                     /gene="MATN2"
                     /note="Complement Clr-like EGF-like; Region: cEGF;
                     pfam12662"
                     /db_xref="CDD:205000"
     misc_feature    <1174..1305
                     /gene="MATN2"
                     /note="Von Willebrand factor type A (vWA) domain was
                     originally found in the blood coagulation protein von
                     Willebrand factor (vWF). Typically, the vWA domain is made
                     up of approximately 200 amino acid residues folded into a
                     classic a/b para-rossmann type of...; Region: vWFA;
                     cl00057"
                     /db_xref="CDD:206808"
     misc_feature    <1273..1428
                     /gene="MATN2"
                     /note="Von Willebrand factor type A (vWA) domain was
                     originally found in the blood coagulation protein von
                     Willebrand factor (vWF). Typically, the vWA domain is made
                     up of approximately 200 amino acid residues folded into a
                     classic a/b para-rossmann type of...; Region: vWFA;
                     cl00057"
                     /db_xref="CDD:206808"
     misc_feature    1498..1566
                     /gene="MATN2"
                     /note="Complement Clr-like EGF-like; Region: cEGF;
                     pfam12662"
                     /db_xref="CDD:205000"
     misc_feature    <1543..1674
                     /gene="MATN2"
                     /note="Von Willebrand factor type A (vWA) domain was
                     originally found in the blood coagulation protein von
                     Willebrand factor (vWF). Typically, the vWA domain is made
                     up of approximately 200 amino acid residues folded into a
                     classic a/b para-rossmann type of...; Region: vWFA;
                     cl00057"
                     /db_xref="CDD:206808"
     misc_feature    <1669..1797
                     /gene="MATN2"
                     /note="Von Willebrand factor type A (vWA) domain was
                     originally found in the blood coagulation protein von
                     Willebrand factor (vWF). Typically, the vWA domain is made
                     up of approximately 200 amino acid residues folded into a
                     classic a/b para-rossmann type of...; Region: vWFA;
                     cl00057"
                     /db_xref="CDD:206808"
     misc_feature    <1789..1920
                     /gene="MATN2"
                     /note="Von Willebrand factor type A (vWA) domain was
                     originally found in the blood coagulation protein von
                     Willebrand factor (vWF). Typically, the vWA domain is made
                     up of approximately 200 amino acid residues folded into a
                     classic a/b para-rossmann type of...; Region: vWFA;
                     cl00057"
                     /db_xref="CDD:206808"
     misc_feature    <1912..2040
                     /gene="MATN2"
                     /note="Von Willebrand factor type A (vWA) domain was
                     originally found in the blood coagulation protein von
                     Willebrand factor (vWF). Typically, the vWA domain is made
                     up of approximately 200 amino acid residues folded into a
                     classic a/b para-rossmann type of...; Region: vWFA;
                     cl00057"
                     /db_xref="CDD:206808"
     misc_feature    <2035..2163
                     /gene="MATN2"
                     /note="Von Willebrand factor type A (vWA) domain was
                     originally found in the blood coagulation protein von
                     Willebrand factor (vWF). Typically, the vWA domain is made
                     up of approximately 200 amino acid residues folded into a
                     classic a/b para-rossmann type of...; Region: vWFA;
                     cl00057"
                     /db_xref="CDD:206808"
     misc_feature    2185..2850
                     /gene="MATN2"
                     /note="VWA_Matrilin: In cartilaginous plate, extracellular
                     matrix molecules mediate cell-matrix and matrix-matrix
                     interactions thereby providing tissue integrity. Some
                     members of the matrilin family are expressed specifically
                     in developing cartilage rudiments; Region: vWA_Matrilin;
                     cd01475"
                     /db_xref="CDD:29248"
     misc_feature    order(2212..2214,2218..2220,2224..2226,2425..2427,
                     2533..2535)
                     /gene="MATN2"
                     /note="metal ion-dependent adhesion site (MIDAS); other
                     site"
                     /db_xref="CDD:29248"
     misc_feature    2854..2856
                     /gene="MATN2"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="phosphorylation site"
     misc_feature    2857..2859
                     /gene="MATN2"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="phosphorylation site"
     misc_feature    2908..3036
                     /gene="MATN2"
                     /note="Trimeric coiled-coil oligomerisation domain of
                     matrilin; Region: Matrilin_ccoil; pfam10393"
                     /db_xref="CDD:204471"
     variation       270
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376715058"
     variation       272
                     /gene="MATN2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:35804177"
     variation       279
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:186093758"
     variation       303
                     /gene="MATN2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:373506520"
     variation       308
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201879642"
     variation       313
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200041053"
     variation       334
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200952405"
     variation       342
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372776833"
     variation       351
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375784459"
     exon            374..943
                     /gene="MATN2"
                     /inference="alignment:Splign:1.39.8"
     variation       384
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368301779"
     variation       394
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199853259"
     variation       398
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138635803"
     variation       406
                     /gene="MATN2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:375231141"
     variation       453
                     /gene="MATN2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:367834031"
     variation       462
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:34316794"
     variation       471
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375876006"
     variation       472
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368734164"
     variation       514
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372069733"
     variation       515
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377512829"
     variation       534
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376568364"
     variation       537
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369492139"
     variation       555
                     /gene="MATN2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200323821"
     variation       585
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200280956"
     variation       586
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374944195"
     variation       595
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368952003"
     variation       599
                     /gene="MATN2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:372409910"
     variation       613
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377009254"
     variation       615
                     /gene="MATN2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:371585254"
     variation       627
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373379380"
     variation       634
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377400284"
     variation       639
                     /gene="MATN2"
                     /replace="c"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:2290470"
     variation       669
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375276855"
     variation       692
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201589846"
     variation       719
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370342485"
     variation       723
                     /gene="MATN2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:374221169"
     variation       733
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:367650776"
     variation       738
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2290471"
     variation       763
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:34354598"
     variation       785
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200270504"
     variation       791
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:2290472"
     variation       798
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374969831"
     variation       817
                     /gene="MATN2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:369127604"
     variation       851
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374817323"
     variation       858
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:187552048"
     variation       930
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368966602"
     variation       937
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374084643"
     exon            944..1066
                     /gene="MATN2"
                     /inference="alignment:Splign:1.39.8"
     variation       944
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199768448"
     variation       951
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:2513845"
     variation       958
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200822499"
     variation       1012
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377586756"
     variation       1019
                     /gene="MATN2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:139657774"
     variation       1047
                     /gene="MATN2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:35407519"
     exon            1067..1189
                     /gene="MATN2"
                     /inference="alignment:Splign:1.39.8"
     variation       1079
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370199325"
     variation       1084
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375539224"
     variation       1085
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201458081"
     variation       1127
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199611870"
     variation       1134
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374362031"
     variation       1155
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:112626438"
     variation       1158
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372237220"
     exon            1190..1312
                     /gene="MATN2"
                     /inference="alignment:Splign:1.39.8"
     variation       1205
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146982976"
     variation       1218
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369817801"
     variation       1219
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374391695"
     variation       1234
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184482356"
     variation       1244
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138153044"
     variation       1266
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375963488"
     variation       1286
                     /gene="MATN2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:373486105"
     variation       1297
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1869609"
     variation       1299
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1869608"
     variation       1304
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372424373"
     variation       1305
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376481997"
     variation       1311
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371119965"
     exon            1313..1435
                     /gene="MATN2"
                     /inference="alignment:Splign:1.39.8"
     variation       1329
                     /gene="MATN2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:12234986"
     variation       1341
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:11559202"
     variation       1353
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:11559201"
     variation       1363
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376658286"
     variation       1381
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:77491480"
     variation       1392
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:16896514"
     variation       1394
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200521380"
     exon            1436..1558
                     /gene="MATN2"
                     /inference="alignment:Splign:1.39.8"
     variation       1464
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369211555"
     variation       1483
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:78489540"
     variation       1490
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375793969"
     variation       1505
                     /gene="MATN2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:199538521"
     variation       1520
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199953090"
     variation       1537
                     /gene="MATN2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:371094213"
     variation       1541
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373444732"
     exon            1559..1681
                     /gene="MATN2"
                     /inference="alignment:Splign:1.39.8"
     variation       1568
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375245334"
     variation       1613
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367846991"
     variation       1626
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371466690"
     variation       1627
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377254481"
     variation       1645
                     /gene="MATN2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:74893724"
     variation       1659
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201014732"
     variation       1672
                     /gene="MATN2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:372520103"
     exon            1682..1804
                     /gene="MATN2"
                     /inference="alignment:Splign:1.39.8"
     variation       1727
                     /gene="MATN2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:377530523"
     variation       1733
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199931655"
     variation       1765
                     /gene="MATN2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:369974305"
     variation       1774
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372608950"
     variation       1780
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373873113"
     variation       1781
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201090956"
     variation       1785
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370974462"
     variation       1794
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201718231"
     exon            1805..1927
                     /gene="MATN2"
                     /inference="alignment:Splign:1.39.8"
     variation       1811
                     /gene="MATN2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:202116053"
     variation       1833
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199532725"
     variation       1836
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374977318"
     variation       1848
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:79255841"
     variation       1869
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371554342"
     variation       1875
                     /gene="MATN2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:192237299"
     variation       1881
                     /gene="MATN2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:369131291"
     variation       1886
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144603993"
     variation       1896
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377427173"
     variation       1900
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369620547"
     variation       1904
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374039867"
     exon            1928..2050
                     /gene="MATN2"
                     /inference="alignment:Splign:1.39.8"
     variation       1953
                     /gene="MATN2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:192151558"
     variation       1973
                     /gene="MATN2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:376327150"
     variation       1977
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370242394"
     variation       1986
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:2248014"
     variation       1987
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:75614624"
     variation       1998
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371980475"
     variation       2001
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374356192"
     variation       2026
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:35120814"
     variation       2028
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371829719"
     variation       2039
                     /gene="MATN2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:376127621"
     variation       2041
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367737640"
     variation       2042
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371684809"
     variation       2048
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201583801"
     exon            2051..2173
                     /gene="MATN2"
                     /inference="alignment:Splign:1.39.8"
     variation       2059
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:61729731"
     variation       2067
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140221245"
     variation       2130
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370250391"
     variation       2164
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200356542"
     variation       2165
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375640185"
     exon            2174..2587
                     /gene="MATN2"
                     /inference="alignment:Splign:1.39.8"
     variation       2176
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368472674"
     variation       2222
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:11559204"
     variation       2236
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370962170"
     variation       2288
                     /gene="MATN2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:74661302"
     variation       2294
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374024071"
     variation       2304
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:2290466"
     variation       2305
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139198886"
     variation       2345
                     /gene="MATN2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:371472415"
     variation       2348
                     /gene="MATN2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:201479365"
     variation       2355
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:17850662"
     variation       2356
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:183598203"
     variation       2394
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376653466"
     variation       2395
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:367650132"
     variation       2403
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372927139"
     variation       2535
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377164086"
     variation       2553
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369605561"
     variation       2576
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373541180"
     exon            2588..2740
                     /gene="MATN2"
                     /inference="alignment:Splign:1.39.8"
     variation       2613
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375792756"
     variation       2620
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370142554"
     variation       2704
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200768007"
     variation       2719
                     /gene="MATN2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:138475492"
     exon            2741..2812
                     /gene="MATN2"
                     /inference="alignment:Splign:1.39.8"
     variation       2748..2749
                     /gene="MATN2"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:56823249"
     variation       2752
                     /gene="MATN2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:375073171"
     variation       2789
                     /gene="MATN2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:202178487"
     variation       2795
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2255317"
     variation       2796
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199863822"
     exon            2813..2890
                     /gene="MATN2"
                     /inference="alignment:Splign:1.39.8"
     variation       2814
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:367696106"
     variation       2830
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149724220"
     variation       2835
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376180527"
     variation       2851
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145754758"
     variation       2852
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199687930"
     variation       2859
                     /gene="MATN2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:372223458"
     exon            2891..2989
                     /gene="MATN2"
                     /inference="alignment:Splign:1.39.8"
     variation       2894
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:78719741"
     variation       2968
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:17831160"
     variation       2985
                     /gene="MATN2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:181639683"
     variation       2989
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374854256"
     exon            2990..4053
                     /gene="MATN2"
                     /inference="alignment:Splign:1.39.8"
     variation       2998
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:191138606"
     variation       2999
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:151208737"
     STS             3038..3571
                     /gene="MATN2"
                     /standard_name="MATN2__7381"
                     /db_xref="UniSTS:466303"
     variation       3058
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376487178"
     variation       3060
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370172576"
     variation       3067
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373385394"
     variation       3078
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374486028"
     variation       3085
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370794970"
     variation       3098
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375294399"
     variation       3114
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112570015"
     variation       3132
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377765681"
     variation       3154
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:3088121"
     variation       3166
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:182693939"
     variation       3260
                     /gene="MATN2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:139149764"
     STS             3313..3521
                     /gene="MATN2"
                     /standard_name="HSCZPH042"
                     /db_xref="UniSTS:74693"
     STS             3316..3422
                     /gene="MATN2"
                     /standard_name="G59494"
                     /db_xref="UniSTS:136658"
     variation       3348
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:113398442"
     variation       3357
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146582723"
     STS             3385..3497
                     /gene="MATN2"
                     /standard_name="A006G02"
                     /db_xref="UniSTS:7196"
     STS             3385..3497
                     /gene="MATN2"
                     /standard_name="G20777"
                     /db_xref="UniSTS:7195"
     variation       3393
                     /gene="MATN2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:187288490"
     STS             3398..3522
                     /gene="MATN2"
                     /standard_name="SHGC-36779"
                     /db_xref="UniSTS:80543"
     variation       3421
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371021657"
     variation       3434
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2615"
     variation       3472
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141191569"
     variation       3520
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145016770"
     polyA_signal    3524..3529
                     /gene="MATN2"
     polyA_site      3547
                     /gene="MATN2"
                     /experiment="experimental evidence, no additional details
                     recorded"
     polyA_site      3552
                     /gene="MATN2"
                     /experiment="experimental evidence, no additional details
                     recorded"
     variation       3578
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:192228074"
     variation       3713
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:55643500"
     variation       3727
                     /gene="MATN2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:115856396"
     variation       3770..3779
                     /gene="MATN2"
                     /replace=""
                     /replace="gcaaatggca"
                     /db_xref="dbSNP:139522061"
     variation       3772..3779
                     /gene="MATN2"
                     /replace=""
                     /replace="aaatggca"
                     /db_xref="dbSNP:202201727"
     STS             3824..3962
                     /gene="MATN2"
                     /standard_name="RH66182"
                     /db_xref="UniSTS:27244"
     variation       3836
                     /gene="MATN2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:145858235"
     variation       3860
                     /gene="MATN2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:55698709"
     variation       3872
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:111317182"
     variation       3897
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:77361665"
     variation       3908
                     /gene="MATN2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:60891161"
     variation       3980
                     /gene="MATN2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:183104114"
     variation       4012
                     /gene="MATN2"
                     /replace="a"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:149017371"
     polyA_signal    4033..4038
                     /gene="MATN2"
     polyA_site      4053
                     /gene="MATN2"
ORIGIN      
gcgagcgaagggagcgctctgggatgggacttggagcaagcggcggcggcggagacagaggcagaggcagaagctggggctccgtcctcgcctcccacgagcgatccccgaggagagccgcggccctcggcgaggcgaagaggccgacgaggaagacccgggtggctgcgcccctgcctcgcttcccaggcgccggcggctgcagccttgcccctcttgctcgccttgaaaatggaaaagatgctcgcaggctgctttctgctgatcctcggacagatcgtcctcctccctgccgaggccagggagcggtcacgtgggaggtccatctctaggggcagacacgctcggacccacccgcagacggcccttctggagagttcctgtgagaacaagcgggcagacctggttttcatcattgacagctctcgcagtgtcaacacccatgactatgcaaaggtcaaggagttcatcgtggacatcttgcaattcttggacattggtcctgatgtcacccgagtgggcctgctccaatatggcagcactgtcaagaatgagttctccctcaagaccttcaagaggaagtccgaggtggagcgtgctgtcaagaggatgcggcatctgtccacgggcaccatgactgggctggccatccagtatgccctgaacatcgcattctcagaagcagagggggcccggcccctgagggagaatgtgccacgggtcataatgatcgtgacagatgggagacctcaggactccgtggccgaggtggctgctaaggcacgggacacgggcatcctaatctttgccattggtgtgggccaggtagacttcaacaccttgaagtccattgggagtgagccccatgaggaccatgtcttccttgtggccaatttcagccagattgagacgctgacctccgtgttccagaagaagttgtgcacggcccacatgtgcagcaccctggagcataactgtgcccacttctgcatcaacatccctggctcatacgtctgcaggtgcaaacaaggctacattctcaactcggatcagacgacttgcagaatccaggatctgtgtgccatggaggaccacaactgtgagcagctctgtgtgaatgtgccgggctccttcgtctgccagtgctacagtggctacgccctggctgaggatgggaagaggtgtgtggctgtggactactgtgcctcagaaaaccacggatgtgaacatgagtgtgtaaatgctgatggctcctacctttgccagtgccatgaaggatttgctcttaacccagataaaaaaacgtgcacaaagatagactactgtgcctcatctaatcacggatgtcagcacgagtgtgttaacacagatgattcctattcctgccactgcctgaaaggctttaccctgaatccagataagaaaacctgcagaaggatcaactactgtgcactgaacaaaccgggctgtgagcatgagtgcgtcaacatggaggagagctactactgccgctgccaccgtggctacactctggaccccaatggcaaaacctgcagccgagtggaccactgtgcacagcaggaccatggctgtgagcagctgtgtctgaacacggaggattccttcgtctgccagtgctcagaaggcttcctcatcaacgaggacctcaagacctgctcccgggtggattactgcctgctgagtgaccatggttgtgaatactcctgtgtcaacatggacagatcctttgcctgtcagtgtcctgagggacacgtgctccgcagcgatgggaagacgtgtgcaaaattggactcttgtgctctgggggaccacggttgtgaacattcgtgtgtaagcagtgaagattcgtttgtgtgccagtgctttgaaggttatatactccgtgaagatggaaaaacctgcagaaggaaagatgtctgccaagctatagaccatggctgtgaacacatttgtgtgaacagtgatgactcatacacgtgcgagtgcttggagggattccggctcgctgaggatgggaaacgctgccgaaggaaggatgtctgcaaatcaacccaccatggctgcgaacacatttgtgttaataatgggaattcctacatctgcaaatgctcagagggatttgttctagctgaggacggaagacggtgcaagaaatgcactgaaggcccaattgacctggtctttgtgatcgatggatccaagagtcttggagaagagaattttgaggtcgtgaagcagtttgtcactggaattatagattccttgacaatttcccccaaagccgctcgagtggggctgctccagtattccacacaggtccacacagagttcactctgagaaacttcaactcagccaaagacatgaaaaaagccgtggcccacatgaaatacatgggaaagggctctatgactgggctggccctgaaacacatgtttgagagaagttttacccaaggagaaggggccaggcccctttccacaagggtgcccagagcagccattgtgttcaccgacggacgggctcaggatgacgtctccgagtgggccagtaaagccaaggccaatggtatcactatgtatgctgttggggtaggaaaagccattgaggaggaactacaagagattgcctctgagcccacaaacaagcatctcttctatgccgaagacttcagcacaatggatgagataagtgaaaaactcaagaaaggcatctgtgaagctctagaagactccgatggaagacaggactctccagcaggggaactgccaaaaacggtccaacagccaacagtgcaacacagatatctgtttgaagaagacaatcttttacggtctacacaaaagctttcccattcaacaaaaccttcaggaagccctttggaagaaaaacacgatcaatgcaaatgtgaaaaccttataatgttccagaaccttgcaaacgaagaagtaagaaaattaacacagcgcttagaagaaatgacacagagaatggaagccctggaaaatcgcctgagatacagatgaagattagaaatcgcgacacatttgtagtcattgtatcacggattacaatgaacgcagtgcagagccccaaagctcaggctattgttaaatcaataatgttgtgaagtaaaacaatcagtactgagaaacctggtttgccacagaacaaagacaagaagtatacactaacttgtataaatttatctaggaaaaaaatccttcagaattctaagatgaatttaccaggtgagaatgaataagctatgcaaggtattttgtaatatactgtggacacaacttgcttctgcctcatcctgccttagtgtgcaatctcatttgactatacgataaagtttgcacagtcttacttctgtagaacactggccataggaaatgctgtttttttgtactggactttaccttgatatatgtatatggatgtatgcataaaatcataggacatatgtacttgtggaacaagttggattttttatacaatattaaaattcaccacttcagagaatggtattcagtgcaaaaattcttagtttaactttaaatggaagatatgtatgtatgagaaatggccaacatgcctatgaaaaaaatgctgaatctcatcagtaatcaggaaaatgcaggttaaaacaataccatttttcacccatcagcttagcaaaaatgagtatattttttaacaagtgttggtaaggatgtggaaatgtgaggttcttgtagtaagaatgcaaatggcactctttgtagagtaagtctgttgacatctcataaaactgaaaatgcacacaaccctgtaaatctagcaactgcactcagttgatttcagcccatacatacaaagagacctgcataagaatgttactaggctttgtaaaagcaaaaaataaggaacaacttaaacatcatcagaaggggaactgataaactctggtgtaatccataccacagaaatacaacaccgcatgtacaggaatgtgctacatctatacaaataaatggtcaaactcaaaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:4147 -> Molecular function: GO:0003674 [molecular_function] evidence: ND
            GeneID:4147 -> Molecular function: GO:0005509 [calcium ion binding] evidence: IEA
            GeneID:4147 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
            GeneID:4147 -> Biological process: GO:0001764 [neuron migration] evidence: IEA
            GeneID:4147 -> Biological process: GO:0007411 [axon guidance] evidence: IEA
            GeneID:4147 -> Biological process: GO:0008150 [biological_process] evidence: ND
            GeneID:4147 -> Biological process: GO:0008347 [glial cell migration] evidence: IEA
            GeneID:4147 -> Biological process: GO:0031104 [dendrite regeneration] evidence: IEA
            GeneID:4147 -> Biological process: GO:0048678 [response to axon injury] evidence: IEA
            GeneID:4147 -> Cellular component: GO:0005578 [proteinaceous extracellular matrix] evidence: NAS
            GeneID:4147 -> Cellular component: GO:0005604 [basement membrane] evidence: IEA
            GeneID:4147 -> Cellular component: GO:0031012 [extracellular matrix] evidence: IDA
            GeneID:4147 -> Cellular component: GO:0031012 [extracellular matrix] evidence: ISS

by @meso_cacase at DBCLS
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