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2024-03-30 00:51:51, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_001271329            2110 bp    mRNA    linear   PRI 22-JUN-2013
DEFINITION  Homo sapiens MARVEL domain containing 3 (MARVELD3), transcript
            variant 3, mRNA.
ACCESSION   NM_001271329
VERSION     NM_001271329.1  GI:404501497
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 2110)
  AUTHORS   Cording,J., Berg,J., Kading,N., Bellmann,C., Tscheik,C.,
            Westphal,J.K., Milatz,S., Gunzel,D., Wolburg,H., Piontek,J.,
            Huber,O. and Blasig,I.E.
  TITLE     In tight junctions, claudins regulate the interactions between
            occludin, tricellulin and marvelD3, which, inversely, modulate
            claudin oligomerization
  JOURNAL   J. Cell. Sci. 126 (PT 2), 554-564 (2013)
   PUBMED   23203797
REFERENCE   2  (bases 1 to 2110)
  AUTHORS   Timmann,C., Thye,T., Vens,M., Evans,J., May,J., Ehmen,C.,
            Sievertsen,J., Muntau,B., Ruge,G., Loag,W., Ansong,D., Antwi,S.,
            Asafo-Adjei,E., Nguah,S.B., Kwakye,K.O., Akoto,A.O., Sylverken,J.,
            Brendel,M., Schuldt,K., Loley,C., Franke,A., Meyer,C.G.,
            Agbenyega,T., Ziegler,A. and Horstmann,R.D.
  TITLE     Genome-wide association study indicates two novel resistance loci
            for severe malaria
  JOURNAL   Nature 489 (7416), 443-446 (2012)
   PUBMED   22895189
REFERENCE   3  (bases 1 to 2110)
  AUTHORS   Kojima,T., Takasawa,A., Kyuno,D., Ito,T., Yamaguchi,H., Hirata,K.,
            Tsujiwaki,M., Murata,M., Tanaka,S. and Sawada,N.
  TITLE     Downregulation of tight junction-associated MARVEL protein marvelD3
            during epithelial-mesenchymal transition in human pancreatic cancer
            cells
  JOURNAL   Exp. Cell Res. 317 (16), 2288-2298 (2011)
   PUBMED   21763689
  REMARK    GeneRIF: MarvelD3 is transcriptionally downregulated in
            Snail-induced epithelial-mesenchymal transition during the
            progression for the pancreatic cancer.
REFERENCE   4  (bases 1 to 2110)
  AUTHORS   Raleigh,D.R., Marchiando,A.M., Zhang,Y., Shen,L., Sasaki,H.,
            Wang,Y., Long,M. and Turner,J.R.
  TITLE     Tight junction-associated MARVEL proteins marveld3, tricellulin,
            and occludin have distinct but overlapping functions
  JOURNAL   Mol. Biol. Cell 21 (7), 1200-1213 (2010)
   PUBMED   20164257
  REMARK    GeneRIF: marvelD3, occludin, and tricellulin define the tight
            junction-associated MARVEL protein family
REFERENCE   5  (bases 1 to 2110)
  AUTHORS   Steed,E., Rodrigues,N.T., Balda,M.S. and Matter,K.
  TITLE     Identification of MarvelD3 as a tight junction-associated
            transmembrane protein of the occludin family
  JOURNAL   BMC Cell Biol. 10, 95 (2009)
   PUBMED   20028514
  REMARK    GeneRIF: MarvelD3 co-localises with occludin at tight junctions in
            intestinal and corneal epithelial cells.
            Publication Status: Online-Only
REFERENCE   6  (bases 1 to 2110)
  AUTHORS   Lamesch,P., Li,N., Milstein,S., Fan,C., Hao,T., Szabo,G., Hu,Z.,
            Venkatesan,K., Bethel,G., Martin,P., Rogers,J., Lawlor,S.,
            McLaren,S., Dricot,A., Borick,H., Cusick,M.E., Vandenhaute,J.,
            Dunham,I., Hill,D.E. and Vidal,M.
  TITLE     hORFeome v3.1: a resource of human open reading frames representing
            over 10,000 human genes
  JOURNAL   Genomics 89 (3), 307-315 (2007)
   PUBMED   17207965
REFERENCE   7  (bases 1 to 2110)
  AUTHORS   Oh,J.H., Yang,J.O., Hahn,Y., Kim,M.R., Byun,S.S., Jeon,Y.J.,
            Kim,J.M., Song,K.S., Noh,S.M., Kim,S., Yoo,H.S., Kim,Y.S. and
            Kim,N.S.
  TITLE     Transcriptome analysis of human gastric cancer
  JOURNAL   Mamm. Genome 16 (12), 942-954 (2005)
   PUBMED   16341674
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            BP320419.1, AK307585.1, AC009097.9 and AA568498.1.
            
            Transcript Variant: This variant (3) uses an alternate splice site
            in the 5' coding region which results in a frameshift compared to
            variant 1. The resulting protein (isoform 3) is shorter and has a
            distinct C-terminus compared to isoform 1. There is no support for
            the protein predicted to be encoded by this variant.
            
            ##Evidence-Data-START##
            Transcript exon combination :: AK307585.1 [ECO:0000332]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-31                BP320419.1         2-32
            32-1382             AK307585.1         1-1351
            1383-1905           AC009097.9         102044-102566
            1906-2110           AA568498.1         1-205               c
FEATURES             Location/Qualifiers
     source          1..2110
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="16"
                     /map="16q22.2"
     gene            1..2110
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /note="MARVEL domain containing 3"
                     /db_xref="GeneID:91862"
                     /db_xref="HGNC:30525"
                     /db_xref="MIM:614094"
     exon            1..381
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /inference="alignment:Splign:1.39.8"
     variation       29
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199550688"
     variation       60
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:4788820"
     CDS             78..524
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /note="isoform 3 is encoded by transcript variant 3;
                     MARVEL (membrane-associating) domain containing 3; MARVEL
                     domain-containing protein 3"
                     /codon_start=1
                     /product="MARVEL domain-containing protein 3 isoform 3"
                     /protein_id="NP_001258258.1"
                     /db_xref="GI:404501498"
                     /db_xref="CCDS:CCDS59270.1"
                     /db_xref="GeneID:91862"
                     /db_xref="HGNC:30525"
                     /db_xref="MIM:614094"
                     /translation="
MEDPSGAREPRARPRERDPGRRPHPDQGRTHDRPRDRPGDPRRKRSSDGNRRRDGDRDPERDQERDGNRDRNRDRERERERERDPDRGPRRDTHRDAGPRAVNPLRRDICPRPPGLDERRWNITSQRRKDSWNATNANTCALGEVWCR
"
     variation       184
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:376285378"
     variation       187
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370821754"
     variation       201
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:373036309"
     variation       228
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370366568"
     variation       230
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374529307"
     variation       255
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:4788821"
     variation       293
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:76434914"
     variation       305
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:376026417"
     variation       330
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:201459139"
     variation       339
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372441129"
     variation       346
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:201434319"
     variation       349
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:61753635"
     exon            382..509
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /inference="alignment:Splign:1.39.8"
     variation       382
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202067406"
     variation       394
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:149016402"
     variation       402
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373378287"
     variation       412
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:200818950"
     variation       414
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146045891"
     variation       462
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375223782"
     variation       501
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199614023"
     variation       506
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:143759600"
     exon            510..2085
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /inference="alignment:Splign:1.39.8"
     variation       529
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375705658"
     variation       537
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139665459"
     variation       562
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:117388624"
     variation       586
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147595258"
     variation       587
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369841189"
     variation       610
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372495610"
     variation       611
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:111585833"
     variation       614
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201509244"
     variation       622
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:72799852"
     variation       633
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142054045"
     variation       642
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376389459"
     variation       646
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367694179"
     variation       647
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200541338"
     variation       671
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:140602857"
     variation       672
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201544903"
     variation       693
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371950282"
     variation       724
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199750986"
     variation       789
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199684141"
     variation       827
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145897917"
     variation       883
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200660505"
     variation       907
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:373575019"
     variation       924
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200552224"
     variation       925
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370061470"
     variation       949
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146595006"
     variation       983
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:74425399"
     variation       1015
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:375582710"
     variation       1016
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:368492439"
     variation       1028
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:141358444"
     variation       1061
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138854747"
     variation       1064
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201839766"
     variation       1093
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:367583136"
     variation       1098
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200621755"
     variation       1099
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:2303225"
     variation       1123
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112608295"
     variation       1131
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:371616837"
     variation       1143
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:200707122"
     variation       1156
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:79422919"
     variation       1160
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:200159769"
     variation       1172
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:13337162"
     variation       1177
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:74027272"
     variation       1182
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:193188432"
     variation       1196
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372021599"
     variation       1353
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:8058188"
     variation       1363
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:182960094"
     STS             1399..1622
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /standard_name="D8S2279"
                     /db_xref="UniSTS:473907"
     variation       1430
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377086815"
     variation       1447
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:12927320"
     STS             1534..1622
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /standard_name="D8S2279"
                     /db_xref="UniSTS:473907"
     STS             1553..1663
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /standard_name="D10S275"
                     /db_xref="UniSTS:147992"
     variation       1568
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:111371379"
     variation       1569
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139582245"
     variation       1596
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:372937295"
     variation       1657
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:8058297"
     variation       1702
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:187330674"
     variation       1741
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370661203"
     variation       1768
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:191783584"
     variation       1840
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:183625027"
     variation       1861
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:11555792"
     variation       1864
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:186844947"
     variation       1878
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:11555793"
     variation       2074
                     /gene="MARVELD3"
                     /gene_synonym="MARVD3; MRVLDC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145662115"
ORIGIN      
gggcttggccacctgcccaagaaacttgttggttgttgccctcaggtcgctcccgggcgcggacacggaacccggccatggaagatccgtcgggggctcgcgagccccgggcccggccgagagagcgggacccgggacggcgcccccacccagaccaaggccgcacccacgatcgaccgcgggaccgacccggggacccgcgcaggaagcgaagcagcgacgggaaccggcgaagggacggggaccgggacccggagagagaccaggagagggacgggaaccgcgaccggaaccgggaccgggagagggagagagagagggaaagagacccggaccgaggcccccgccgggacacacacagggacgcgggccctcgcgcagtgaacccccttcggagagatatctgccctcgacccccaggcctggacgagaggaggtggaatattaccagtcagaggcggaaggactcctggaatgccacaaatgcaaatacttgtgcactgggagaggtgtggtgcagatagtggaggtggtcttgaatgggatggttctcatatgcatcgtggcctcctactttgtccttgccggattcagtgccagcttttccagcggcggtggctttgggaacaactactactcaccgttcgagggcactgagctagagcaggttcggcagctggaccagcagtacacgatcctccgctcgcccctgatatacggtggcgtggctgtttctctgggtctgggggtcctcaccatgggtgttttactccaaggagccaagagtcgaacaatgttgtcagggaagtggctcctcacggaggccgccttcagcctcctagcggcagtgggctactgcacaggcattggtgtttacctccacgtggctctgcagatcaatagcaccgacacttgcaaaacaagagagaggctctatgcccgcaagggtctcacctggatggactgccagctggcaggcaccgacggagcagcagccacctttgcttgtcttctcgtgatcatgtacggcgccagcgtggtgctggccctgcgtagctaccgagaacagaagcgctacaaaggcagccgagaacagcccggaagttacagtgatgcaccggaatatctgtggtctggaactctttgagatcttccggaacctaaatgtgaacgcacattgtttctctcaaaaagacaggtcttttaaaactccgcattagacaactatggttttcacacacttgactttataaatgctctctttggactgaggcaaagttaaagaattgaggacgggcatggtggctcatgcctgtaatcccagcactttgggaggctgaggtgggcggatcgcttgaggtcagcagattgagtccagcctggctcacatagcgaaaccctgtctctactaaaaatacaaaaaatcgccgggcatggtggctcacgcctgtaatcccagcactttaggaggccaaggcaggcagatcacctgaggtcaggtgtttgaaaccagtctggcaaacatggtgaaaccccatctctactaaaaatacaaaaattagctgggcgtggtggcaggcacctgtaattccagctactctggaggctgaggcaggagaatctcttaaacccgggaggcagaggttgcagtgagccaagaccattgcactccagcctgggcaacaagagcgagactccgtctcaaaaaaatacaaaaaatcatctgggcttggtggtgaacgcctgtaatcccagttactcaggaggctaaaccacaagaatcacttgaacctgggaggcagaggttgcagtgagcaaactccactccacgtcactgcactccagcctgggtaacagagcgaggctctgtctcaaaaacaacaactacaacaaaaaagataggacagtagattttattagaccctgaagcatactggaggctttttcatttctgcattccctgacagtgctccatagagtaggtcttcaaaggtagatagtaatctcattaccctggactgttctcataatgtaacagatcactaacactgaatcttaaaaataaagttcttttagtaattttaaaaaaaaaaaaaaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:91862 -> Biological process: GO:0045216 [cell-cell junction organization] evidence: IMP
            GeneID:91862 -> Cellular component: GO:0005923 [tight junction] evidence: IDA
            GeneID:91862 -> Cellular component: GO:0016021 [integral to membrane] evidence: IEA

by @meso_cacase at DBCLS
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