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2024-03-29 18:37:22, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_001185072            3684 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens claudin 12 (CLDN12), transcript variant 1, mRNA.
ACCESSION   NM_001185072
VERSION     NM_001185072.2  GI:313760613
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 3684)
  AUTHORS   Ouban,A. and Ahmed,A.A.
  TITLE     Claudins in human cancer: a review
  JOURNAL   Histol. Histopathol. 25 (1), 83-90 (2010)
   PUBMED   19924644
  REMARK    Review article
REFERENCE   2  (bases 1 to 3684)
  AUTHORS   Lal-Nag,M. and Morin,P.J.
  TITLE     The claudins
  JOURNAL   Genome Biol. 10 (8), 235 (2009)
   PUBMED   19706201
  REMARK    Review article
REFERENCE   3  (bases 1 to 3684)
  AUTHORS   Fujita,H., Sugimoto,K., Inatomi,S., Maeda,T., Osanai,M.,
            Uchiyama,Y., Yamamoto,Y., Wada,T., Kojima,T., Yokozaki,H.,
            Yamashita,T., Kato,S., Sawada,N. and Chiba,H.
  TITLE     Tight junction proteins claudin-2 and -12 are critical for vitamin
            D-dependent Ca2+ absorption between enterocytes
  JOURNAL   Mol. Biol. Cell 19 (5), 1912-1921 (2008)
   PUBMED   18287530
  REMARK    GeneRIF: These findings strongly suggest that claudin-2- and/or
            claudin-12-based tight junctions form paracellular Ca(2+) channels
            in intestinal epithelia, and they highlight a novel mechanism
            behind vitamin D-dependent calcium homeostasis.
REFERENCE   4  (bases 1 to 3684)
  AUTHORS   Krause,G., Winkler,L., Mueller,S.L., Haseloff,R.F., Piontek,J. and
            Blasig,I.E.
  TITLE     Structure and function of claudins
  JOURNAL   Biochim. Biophys. Acta 1778 (3), 631-645 (2008)
   PUBMED   18036336
  REMARK    Review article
REFERENCE   5  (bases 1 to 3684)
  AUTHORS   Denoeud,F., Kapranov,P., Ucla,C., Frankish,A., Castelo,R.,
            Drenkow,J., Lagarde,J., Alioto,T., Manzano,C., Chrast,J., Dike,S.,
            Wyss,C., Henrichsen,C.N., Holroyd,N., Dickson,M.C., Taylor,R.,
            Hance,Z., Foissac,S., Myers,R.M., Rogers,J., Hubbard,T., Harrow,J.,
            Guigo,R., Gingeras,T.R., Antonarakis,S.E. and Reymond,A.
  TITLE     Prominent use of distal 5' transcription start sites and discovery
            of a large number of additional exons in ENCODE regions
  JOURNAL   Genome Res. 17 (6), 746-759 (2007)
   PUBMED   17567994
REFERENCE   6  (bases 1 to 3684)
  AUTHORS   Kiuchi-Saishin,Y., Gotoh,S., Furuse,M., Takasuga,A., Tano,Y. and
            Tsukita,S.
  TITLE     Differential expression patterns of claudins, tight junction
            membrane proteins, in mouse nephron segments
  JOURNAL   J. Am. Soc. Nephrol. 13 (4), 875-886 (2002)
   PUBMED   11912246
REFERENCE   7  (bases 1 to 3684)
  AUTHORS   Niimi,T., Nagashima,K., Ward,J.M., Minoo,P., Zimonjic,D.B.,
            Popescu,N.C. and Kimura,S.
  TITLE     claudin-18, a novel downstream target gene for the T/EBP/NKX2.1
            homeodomain transcription factor, encodes lung- and
            stomach-specific isoforms through alternative splicing
  JOURNAL   Mol. Cell. Biol. 21 (21), 7380-7390 (2001)
   PUBMED   11585919
REFERENCE   8  (bases 1 to 3684)
  AUTHORS   Tsukita,S., Furuse,M. and Itoh,M.
  TITLE     Multifunctional strands in tight junctions
  JOURNAL   Nat. Rev. Mol. Cell Biol. 2 (4), 285-293 (2001)
   PUBMED   11283726
  REMARK    Review article
REFERENCE   9  (bases 1 to 3684)
  AUTHORS   Heiskala,M., Peterson,P.A. and Yang,Y.
  TITLE     The roles of claudin superfamily proteins in paracellular transport
  JOURNAL   Traffic 2 (2), 93-98 (2001)
   PUBMED   11247307
  REMARK    Review article
REFERENCE   10 (bases 1 to 3684)
  AUTHORS   Kniesel,U. and Wolburg,H.
  TITLE     Tight junctions of the blood-brain barrier
  JOURNAL   Cell. Mol. Neurobiol. 20 (1), 57-76 (2000)
   PUBMED   10690502
  REMARK    Review article
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from DB062973.1, AK312480.1,
            BC036754.2, BC068532.1 and AL136770.1.
            On Dec 9, 2010 this sequence version replaced gi:297374757.
            
            Summary: This gene encodes a member of the claudin family. Claudins
            are integral membrane proteins and components of tight junction
            strands. Tight junction strands serve as a physical barrier to
            prevent solutes and water from passing freely through the
            paracellular space between epithelial or endothelial cell sheets,
            and also play critical roles in maintaining cell polarity and
            signal transductions. This gene is expressed in the inner ear and
            bladder epithelium, and it is over-expressed in colorectal
            carcinomas. This protein and claudin 2 are critical for vitamin
            D-dependent Ca2+ absorption between enterocytes. Multiple
            alternatively spliced transcript variants encoding the same protein
            have been found.[provided by RefSeq, Sep 2011].
            
            Transcript Variant: This variant (1) is the longest transcript.
            Variants 1-3 encode the same protein.
            
            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 :: AK312480.1, DA224259.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025084, ERS025088 [ECO:0000348]
            ##Evidence-Data-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-115               DB062973.1         1-115
            116-857             AK312480.1         1-742
            858-1695            BC036754.2         604-1441
            1696-2810           BC068532.1         1539-2653
            2811-3684           AL136770.1         2620-3493
FEATURES             Location/Qualifiers
     source          1..3684
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="7"
                     /map="7q21"
     gene            1..3684
                     /gene="CLDN12"
                     /note="claudin 12"
                     /db_xref="GeneID:9069"
                     /db_xref="HGNC:2034"
                     /db_xref="MIM:611232"
     exon            1..216
                     /gene="CLDN12"
                     /inference="alignment:Splign:1.39.8"
     variation       26
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:28947516"
     variation       81
                     /gene="CLDN12"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:138201646"
     variation       144
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370765493"
     variation       161
                     /gene="CLDN12"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:143733597"
     exon            217..306
                     /gene="CLDN12"
                     /inference="alignment:Splign:1.39.8"
     variation       233
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:116804658"
     variation       301
                     /gene="CLDN12"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:185475099"
     exon            307..349
                     /gene="CLDN12"
                     /inference="alignment:Splign:1.39.8"
     exon            350..3660
                     /gene="CLDN12"
                     /inference="alignment:Splign:1.39.8"
     misc_feature    356..358
                     /gene="CLDN12"
                     /note="upstream in-frame stop codon"
     CDS             383..1117
                     /gene="CLDN12"
                     /codon_start=1
                     /product="claudin-12"
                     /protein_id="NP_001172001.1"
                     /db_xref="GI:297374758"
                     /db_xref="CCDS:CCDS5618.1"
                     /db_xref="GeneID:9069"
                     /db_xref="HGNC:2034"
                     /db_xref="MIM:611232"
                     /translation="
MGCRDVHAATVLSFLCGIASVAGLFAGTLLPNWRKLRLITFNRNEKNLTVYTGLWVKCARYDGSSDCLMYDTTWYSSVDQLDLRVLQFALPLSMLIAMGALLLCLIGMCNTAFRSSVPNIKLAKCLVNSAGCHLVAGLLFFLAGTVSLSPSIWVIFYNIHLNKKFEPVFSFDYAVYVTIASAGGLFMTSLILFIWYCTCKSLPSPFWQPLYSHPPSMHTYSQPYSARSRLSAIEIDIPVVSHTT
"
     misc_feature    413..475
                     /gene="CLDN12"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (P56749.1);
                     transmembrane region"
     misc_feature    644..706
                     /gene="CLDN12"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (P56749.1);
                     transmembrane region"
     misc_feature    788..850
                     /gene="CLDN12"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (P56749.1);
                     transmembrane region"
     misc_feature    905..967
                     /gene="CLDN12"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (P56749.1);
                     transmembrane region"
     misc_feature    1073..1075
                     /gene="CLDN12"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (P56749.1); phosphorylation site"
     variation       393
                     /gene="CLDN12"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:200372770"
     variation       394
                     /gene="CLDN12"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:201163165"
     variation       436
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374340236"
     STS             471..715
                     /gene="CLDN12"
                     /standard_name="REN107123"
                     /db_xref="UniSTS:431920"
     variation       514
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140108357"
     variation       560
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367561054"
     variation       564
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371660301"
     variation       568
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:17862175"
     variation       569
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200164858"
     variation       592
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:185427290"
     variation       593
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368401578"
     variation       609
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372373015"
     variation       613
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200281270"
     variation       674
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:76988207"
     STS             695..931
                     /gene="CLDN12"
                     /standard_name="REN107124"
                     /db_xref="UniSTS:431921"
     variation       697
                     /gene="CLDN12"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:79632494"
     variation       730
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:34378679"
     variation       738
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370065476"
     variation       739
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373294317"
     variation       747
                     /gene="CLDN12"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:146056566"
     variation       855
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139669349"
     STS             875..1127
                     /gene="CLDN12"
                     /standard_name="REN107125"
                     /db_xref="UniSTS:431922"
     variation       935
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149798695"
     variation       976
                     /gene="CLDN12"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:148668482"
     variation       982
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142157384"
     STS             992..1892
                     /gene="CLDN12"
                     /standard_name="ECD00552"
                     /db_xref="UniSTS:281662"
     variation       1029
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376598671"
     variation       1049
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:189780617"
     variation       1058
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147857522"
     variation       1061
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141430153"
     STS             1104..1347
                     /gene="CLDN12"
                     /standard_name="REN107126"
                     /db_xref="UniSTS:431923"
     variation       1125
                     /gene="CLDN12"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:374720515"
     variation       1140
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375989620"
     variation       1149
                     /gene="CLDN12"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:182726869"
     variation       1157
                     /gene="CLDN12"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:147269114"
     variation       1199
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140861444"
     variation       1249
                     /gene="CLDN12"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:3810874"
     variation       1256
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:187870115"
     STS             1311..1535
                     /gene="CLDN12"
                     /standard_name="REN107127"
                     /db_xref="UniSTS:431924"
     STS             1375..2424
                     /gene="CLDN12"
                     /standard_name="stSG614603"
                     /db_xref="UniSTS:450490"
     variation       1382
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:191882778"
     STS             1424..1678
                     /gene="CLDN12"
                     /standard_name="REN107128"
                     /db_xref="UniSTS:431925"
     variation       1488
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:183250663"
     variation       1494
                     /gene="CLDN12"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:17865130"
     variation       1574
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1017104"
     STS             1673..1906
                     /gene="CLDN12"
                     /standard_name="REN107129"
                     /db_xref="UniSTS:431926"
     variation       1696
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1017105"
     variation       1706
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1017106"
     variation       1776
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374000239"
     STS             1877..2127
                     /gene="CLDN12"
                     /standard_name="REN107130"
                     /db_xref="UniSTS:431927"
     STS             1929..2825
                     /gene="CLDN12"
                     /standard_name="ECD00648"
                     /db_xref="UniSTS:281757"
     variation       1933
                     /gene="CLDN12"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:376739855"
     variation       2044
                     /gene="CLDN12"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:140787647"
     variation       2069
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:193147106"
     STS             2119..2374
                     /gene="CLDN12"
                     /standard_name="REN107131"
                     /db_xref="UniSTS:431928"
     variation       2257
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142246998"
     variation       2261
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:11563542"
     STS             2360..2623
                     /gene="CLDN12"
                     /standard_name="REN107132"
                     /db_xref="UniSTS:431929"
     variation       2363
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:151249770"
     STS             2405..3526
                     /gene="CLDN12"
                     /standard_name="stSG614604"
                     /db_xref="UniSTS:450491"
     variation       2540
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:17861306"
     variation       2554
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:34833025"
     STS             2622..2891
                     /gene="CLDN12"
                     /standard_name="REN107133"
                     /db_xref="UniSTS:431930"
     variation       2715
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:17867644"
     STS             2866..3112
                     /gene="CLDN12"
                     /standard_name="REN107134"
                     /db_xref="UniSTS:431931"
     variation       2949..2950
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1048881"
     variation       2991
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:184613376"
     variation       3034
                     /gene="CLDN12"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:1048883"
     STS             3081..3353
                     /gene="CLDN12"
                     /standard_name="REN107135"
                     /db_xref="UniSTS:431932"
     STS             3153..3337
                     /gene="CLDN12"
                     /standard_name="RH65832"
                     /db_xref="UniSTS:43176"
     variation       3202
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:186714887"
     variation       3230
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:191175070"
     variation       3255
                     /gene="CLDN12"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:370567033"
     STS             3300..3527
                     /gene="CLDN12"
                     /standard_name="REN107136"
                     /db_xref="UniSTS:431933"
     variation       3337
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:9731"
     STS             3375..3526
                     /gene="CLDN12"
                     /standard_name="RH47948"
                     /db_xref="UniSTS:37396"
     variation       3492
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:17863096"
     variation       3619
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184005906"
     variation       3645
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:17866176"
ORIGIN      
aggatgttgcctgcggctggcggcccagtggattctgggaattgtagtcccagccatccagggcattgccgttcagggccacgggaaaacctgactgcgctcccagaagcctccggtgtacctcgctgggaacgcacttcctgggacgctgagagggagacgctccaagaggctcctcagtgtgggcgagtaaaatgccctgcgtgtgagaagcaggctcagattattgctactctgtattcagatcttcatgtgtctcttctaagctgaataaagctgttttggaactgtcaggtacctcaaagcatgaagaaaacgaggcacagggaagttctgaatctggcccaagtctgactgacagtactccacaagcttgcctgccatgggctgtcgggatgtccacgcagccacagtcctttccttcctgtgtggaatcgcctcagtagcaggcctctttgcagggactctgcttcccaactggagaaaattacgattgatcacattcaacagaaacgagaagaacctgactgtttacacaggcctgtgggtgaaatgtgcccggtatgacgggagcagtgactgcctgatgtacgacactacttggtactcatcagttgaccagctggacctgcgtgtcctccagtttgccctacccctcagcatgctgatcgccatgggtgccctgctgctctgcctgattggaatgtgcaacactgccttcaggtcctcggtgcccaacatcaaactggccaagtgtctggtcaatagtgcaggttgccacctggtggctgggctgctatttttcctggcaggtactgtgagcctctccccatctatctgggtcatcttttataacatccatctgaacaagaagtttgagccagtcttttcatttgactatgcagtgtatgtcactattgctagtgctgggggcctgtttatgacttcccttatactatttatttggtattgtacatgcaaatctttgccttctcctttctggcaaccattgtactcccatccacccagtatgcatacttactcacagccctattcagcacgctctcgcctctctgccattgaaattgacattccagtagtttcacacaccacttaatggggaaatagttaattgttaaagaaaacttcttgtagcctcacattccccttgtgcaaagagctcttttggacctacatacattttcctttgtttttgaccaatcaatgaagccaaatttatatgtcctagtagaatgaagtgctgctagtttttatgagaagtatattatattaaatgtgaattttttaaattttgcttcttatactggaaggaattttagccttcatattgatatctaattaattatttaagtggaagaggcctgcatcacaattgaggtaatgtagagcaacatgttaaagaatgatggttagcagaagctgttgtatacaatcttcatgaaaatttcagtgtgtatttttctttttctataatacctttaactgcaaagaaaaggcagtttcaaatataagaaatttatttcaggtaagggtaatattttaatagtagtcaataatctagcttaaggctgtaactcttctatcggggctaattgtatgaataggtgtcagtatgttgaagattactttcttttgtgactttcttctacctcatgccactgtttaaaagtaaaacgtattttaatgatgttagaataagactaccattctaaatatcacctacttatgaataacatgtaataatttttaacattaatgattccataaattgtattattgggattagaatgtgctttatgacaggttagtgtttcctctgaggcagaaaactcttttttggagatatcttccatcaagcagtactcgtgcccatatacaatctcttagtggctaggagaaataaataaaagggccataatggtttgttctctttcagacataatttagtaggggacaagaagtctgttcttcagtgagtacactagagatttactctggtgactgccttttgagttatgggtgaagtaaggtatggctttaccataaccttgattcattcacccttgattcatttctcgcccccgtcactgattatttccttgagcatatatctctgcctaacactttagtaggtgctatagaggatacatgaaaagtatgagatctggttccatccagtaagacattttaatagagaagatcaaaatgttacctggcagttggggaataatctgacttcgttggcagttggccttaacttcttaatcattgatccaggaatatttcaaccagagacacaactttctggcagacagacaaattgtacaacaccaacaatatcctggaccttgaaattctgtttacttcagtccattgtatcctttaaggcacctgtgctagcctagattttgtaataacactgatttatgagaatggacaaaagtggtagggaaattgttccctctccacttctgaaagtatgatgatgtattaaggatggaggagttattaaaaatgtctcttctgatgaggtaacaattagatgaaaccatgttaaagctgagatgaacacttagaaattcagggatattgggtctttagccttatgaatttgagctgcttatttaattggtgtaatttactacatattagtactatattcgtaaggattttttattaaccattacagattttacaaacagctagttatatggtaaacagattattatgcctttttgcaattctgaatatgattctagtatttgtgtagatgtatttggtactttttcccctaattccaacactagtttatatatatagcgaataaatctagttgtataaatttttaaatgccgtcagtagaaagcacacaaggttatgatttttttaattactggcttctgatttctttcacttctgatccttttcctttttctcagatgtagctgagtcttgatcattttaagacaacgatgggtagaattttgagattaatgttaattttccctttttgttaatttcagtcccctctcactatgcttttgtccagaaggatcaagaattctaccatcccttgggtctttgtgtataaacaatgttaaataaaggtagactcagtctttaagatattagacagtttttttagtccatgggattgtaaatataaacattaactttcctataagaatattttggctttgtaatctatagcctcaaattggtatttattatggattcactagacaaacagctgtttccttattgtcttttttctttagtgtttctgatttgctatcagtagctgtttttaaagccgtccaaggaaaataattatttacagtttttgaagtcacttttgagccctcatcaagctctcattgtgatgggagggatacctttttgttgttaaaagcctattattgttaaaggccttttatggaaaccaacttggaaaacaaccttaaatgtggatgtatcagatttggtttatccagccatgggagagaaaacaaacctaagtttactttacttgtacatatacactacaatggatagtatatttgctgtaaactacaatgtaaaacctcaataaaagtgcgctgtacttcttaatgtttattaaaagatgtatttttacaaaaaaaaaaaaaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:9069 -> Molecular function: GO:0005198 [structural molecule activity] evidence: IEA
            GeneID:9069 -> Molecular function: GO:0042802 [identical protein binding] evidence: ISS
            GeneID:9069 -> Biological process: GO:0016338 [calcium-independent cell-cell adhesion] evidence: ISS
            GeneID:9069 -> Biological process: GO:0034329 [cell junction assembly] evidence: TAS
            GeneID:9069 -> Biological process: GO:0045216 [cell-cell junction organization] evidence: TAS
            GeneID:9069 -> Biological process: GO:0070830 [tight junction assembly] evidence: TAS
            GeneID:9069 -> Cellular component: GO:0005886 [plasma membrane] evidence: IEA
            GeneID:9069 -> Cellular component: GO:0005923 [tight junction] evidence: ISS
            GeneID:9069 -> Cellular component: GO:0016021 [integral to membrane] evidence: IEA

by @meso_cacase at DBCLS
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