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2024-03-29 15:07:04, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_001185073            3645 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens claudin 12 (CLDN12), transcript variant 2, mRNA.
ACCESSION   NM_001185073
VERSION     NM_001185073.2  GI:313760614
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 3645)
  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 3645)
  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 3645)
  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 3645)
  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 3645)
  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 3645)
  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 3645)
  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 3645)
  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 3645)
  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 3645)
  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, DB224591.1,
            AK312480.1, BC036754.2, BC068532.1 and AL136770.1.
            On Dec 9, 2010 this sequence version replaced gi:297374759.
            
            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 (2) uses an alternate splice site
            and lacks an exon in the 5' UTR, as compared to variant 1.
            
            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 :: BI523949.1, DR000767.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025082, ERS025083 [ECO:0000348]
            ##Evidence-Data-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-147               DB062973.1         1-147
            148-675             DB224591.1         34-561
            676-818             AK312480.1         600-742
            819-1656            BC036754.2         604-1441
            1657-2771           BC068532.1         1539-2653
            2772-3645           AL136770.1         2620-3493
FEATURES             Location/Qualifiers
     source          1..3645
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="7"
                     /map="7q21"
     gene            1..3645
                     /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..310
                     /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            311..3621
                     /gene="CLDN12"
                     /inference="alignment:Splign:1.39.8"
     misc_feature    317..319
                     /gene="CLDN12"
                     /note="upstream in-frame stop codon"
     CDS             344..1078
                     /gene="CLDN12"
                     /codon_start=1
                     /product="claudin-12"
                     /protein_id="NP_001172002.1"
                     /db_xref="GI:297374760"
                     /db_xref="CCDS:CCDS5618.1"
                     /db_xref="GeneID:9069"
                     /db_xref="HGNC:2034"
                     /db_xref="MIM:611232"
                     /translation="
MGCRDVHAATVLSFLCGIASVAGLFAGTLLPNWRKLRLITFNRNEKNLTVYTGLWVKCARYDGSSDCLMYDTTWYSSVDQLDLRVLQFALPLSMLIAMGALLLCLIGMCNTAFRSSVPNIKLAKCLVNSAGCHLVAGLLFFLAGTVSLSPSIWVIFYNIHLNKKFEPVFSFDYAVYVTIASAGGLFMTSLILFIWYCTCKSLPSPFWQPLYSHPPSMHTYSQPYSARSRLSAIEIDIPVVSHTT
"
     misc_feature    374..436
                     /gene="CLDN12"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (P56749.1);
                     transmembrane region"
     misc_feature    605..667
                     /gene="CLDN12"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (P56749.1);
                     transmembrane region"
     misc_feature    749..811
                     /gene="CLDN12"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (P56749.1);
                     transmembrane region"
     misc_feature    866..928
                     /gene="CLDN12"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (P56749.1);
                     transmembrane region"
     misc_feature    1034..1036
                     /gene="CLDN12"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (P56749.1); phosphorylation site"
     variation       354
                     /gene="CLDN12"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:200372770"
     variation       355
                     /gene="CLDN12"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:201163165"
     variation       397
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374340236"
     STS             432..676
                     /gene="CLDN12"
                     /standard_name="REN107123"
                     /db_xref="UniSTS:431920"
     variation       475
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140108357"
     variation       521
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367561054"
     variation       525
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371660301"
     variation       529
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:17862175"
     variation       530
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200164858"
     variation       553
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:185427290"
     variation       554
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368401578"
     variation       570
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372373015"
     variation       574
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200281270"
     variation       635
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:76988207"
     STS             656..892
                     /gene="CLDN12"
                     /standard_name="REN107124"
                     /db_xref="UniSTS:431921"
     variation       658
                     /gene="CLDN12"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:79632494"
     variation       691
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:34378679"
     variation       699
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370065476"
     variation       700
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373294317"
     variation       708
                     /gene="CLDN12"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:146056566"
     variation       816
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139669349"
     STS             836..1088
                     /gene="CLDN12"
                     /standard_name="REN107125"
                     /db_xref="UniSTS:431922"
     variation       896
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149798695"
     variation       937
                     /gene="CLDN12"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:148668482"
     variation       943
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142157384"
     STS             953..1853
                     /gene="CLDN12"
                     /standard_name="ECD00552"
                     /db_xref="UniSTS:281662"
     variation       990
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376598671"
     variation       1010
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:189780617"
     variation       1019
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147857522"
     variation       1022
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141430153"
     STS             1065..1308
                     /gene="CLDN12"
                     /standard_name="REN107126"
                     /db_xref="UniSTS:431923"
     variation       1086
                     /gene="CLDN12"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:374720515"
     variation       1101
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375989620"
     variation       1110
                     /gene="CLDN12"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:182726869"
     variation       1118
                     /gene="CLDN12"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:147269114"
     variation       1160
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140861444"
     variation       1210
                     /gene="CLDN12"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:3810874"
     variation       1217
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:187870115"
     STS             1272..1496
                     /gene="CLDN12"
                     /standard_name="REN107127"
                     /db_xref="UniSTS:431924"
     STS             1336..2385
                     /gene="CLDN12"
                     /standard_name="stSG614603"
                     /db_xref="UniSTS:450490"
     variation       1343
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:191882778"
     STS             1385..1639
                     /gene="CLDN12"
                     /standard_name="REN107128"
                     /db_xref="UniSTS:431925"
     variation       1449
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:183250663"
     variation       1455
                     /gene="CLDN12"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:17865130"
     variation       1535
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1017104"
     STS             1634..1867
                     /gene="CLDN12"
                     /standard_name="REN107129"
                     /db_xref="UniSTS:431926"
     variation       1657
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1017105"
     variation       1667
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1017106"
     variation       1737
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374000239"
     STS             1838..2088
                     /gene="CLDN12"
                     /standard_name="REN107130"
                     /db_xref="UniSTS:431927"
     STS             1890..2786
                     /gene="CLDN12"
                     /standard_name="ECD00648"
                     /db_xref="UniSTS:281757"
     variation       1894
                     /gene="CLDN12"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:376739855"
     variation       2005
                     /gene="CLDN12"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:140787647"
     variation       2030
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:193147106"
     STS             2080..2335
                     /gene="CLDN12"
                     /standard_name="REN107131"
                     /db_xref="UniSTS:431928"
     variation       2218
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142246998"
     variation       2222
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:11563542"
     STS             2321..2584
                     /gene="CLDN12"
                     /standard_name="REN107132"
                     /db_xref="UniSTS:431929"
     variation       2324
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:151249770"
     STS             2366..3487
                     /gene="CLDN12"
                     /standard_name="stSG614604"
                     /db_xref="UniSTS:450491"
     variation       2501
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:17861306"
     variation       2515
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:34833025"
     STS             2583..2852
                     /gene="CLDN12"
                     /standard_name="REN107133"
                     /db_xref="UniSTS:431930"
     variation       2676
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:17867644"
     STS             2827..3073
                     /gene="CLDN12"
                     /standard_name="REN107134"
                     /db_xref="UniSTS:431931"
     variation       2910..2911
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1048881"
     variation       2952
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:184613376"
     variation       2995
                     /gene="CLDN12"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:1048883"
     STS             3042..3314
                     /gene="CLDN12"
                     /standard_name="REN107135"
                     /db_xref="UniSTS:431932"
     STS             3114..3298
                     /gene="CLDN12"
                     /standard_name="RH65832"
                     /db_xref="UniSTS:43176"
     variation       3163
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:186714887"
     variation       3191
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:191175070"
     variation       3216
                     /gene="CLDN12"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:370567033"
     STS             3261..3488
                     /gene="CLDN12"
                     /standard_name="REN107136"
                     /db_xref="UniSTS:431933"
     variation       3298
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:9731"
     STS             3336..3487
                     /gene="CLDN12"
                     /standard_name="RH47948"
                     /db_xref="UniSTS:37396"
     variation       3453
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:17863096"
     variation       3580
                     /gene="CLDN12"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184005906"
     variation       3606
                     /gene="CLDN12"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:17866176"
ORIGIN      
aggatgttgcctgcggctggcggcccagtggattctgggaattgtagtcccagccatccagggcattgccgttcagggccacgggaaaacctgactgcgctcccagaagcctccggtgtacctcgctgggaacgcacttcctgggacgctgagagggagacgctccaagaggctcctcagtgtgggcgagtaaaatgccctgcgtgtgagaagcaggctcagattattgctactctgtattcagatcttcatgtgtctcttctaagctgaataaagctgttttggaactgtcaggtacctcaaagcgtaatctgactgacagtactccacaagcttgcctgccatgggctgtcgggatgtccacgcagccacagtcctttccttcctgtgtggaatcgcctcagtagcaggcctctttgcagggactctgcttcccaactggagaaaattacgattgatcacattcaacagaaacgagaagaacctgactgtttacacaggcctgtgggtgaaatgtgcccggtatgacgggagcagtgactgcctgatgtacgacactacttggtactcatcagttgaccagctggacctgcgtgtcctccagtttgccctacccctcagcatgctgatcgccatgggtgccctgctgctctgcctgattggaatgtgcaacactgccttcaggtcctcggtgcccaacatcaaactggccaagtgtctggtcaatagtgcaggttgccacctggtggctgggctgctatttttcctggcaggtactgtgagcctctccccatctatctgggtcatcttttataacatccatctgaacaagaagtttgagccagtcttttcatttgactatgcagtgtatgtcactattgctagtgctgggggcctgtttatgacttcccttatactatttatttggtattgtacatgcaaatctttgccttctcctttctggcaaccattgtactcccatccacccagtatgcatacttactcacagccctattcagcacgctctcgcctctctgccattgaaattgacattccagtagtttcacacaccacttaatggggaaatagttaattgttaaagaaaacttcttgtagcctcacattccccttgtgcaaagagctcttttggacctacatacattttcctttgtttttgaccaatcaatgaagccaaatttatatgtcctagtagaatgaagtgctgctagtttttatgagaagtatattatattaaatgtgaattttttaaattttgcttcttatactggaaggaattttagccttcatattgatatctaattaattatttaagtggaagaggcctgcatcacaattgaggtaatgtagagcaacatgttaaagaatgatggttagcagaagctgttgtatacaatcttcatgaaaatttcagtgtgtatttttctttttctataatacctttaactgcaaagaaaaggcagtttcaaatataagaaatttatttcaggtaagggtaatattttaatagtagtcaataatctagcttaaggctgtaactcttctatcggggctaattgtatgaataggtgtcagtatgttgaagattactttcttttgtgactttcttctacctcatgccactgtttaaaagtaaaacgtattttaatgatgttagaataagactaccattctaaatatcacctacttatgaataacatgtaataatttttaacattaatgattccataaattgtattattgggattagaatgtgctttatgacaggttagtgtttcctctgaggcagaaaactcttttttggagatatcttccatcaagcagtactcgtgcccatatacaatctcttagtggctaggagaaataaataaaagggccataatggtttgttctctttcagacataatttagtaggggacaagaagtctgttcttcagtgagtacactagagatttactctggtgactgccttttgagttatgggtgaagtaaggtatggctttaccataaccttgattcattcacccttgattcatttctcgcccccgtcactgattatttccttgagcatatatctctgcctaacactttagtaggtgctatagaggatacatgaaaagtatgagatctggttccatccagtaagacattttaatagagaagatcaaaatgttacctggcagttggggaataatctgacttcgttggcagttggccttaacttcttaatcattgatccaggaatatttcaaccagagacacaactttctggcagacagacaaattgtacaacaccaacaatatcctggaccttgaaattctgtttacttcagtccattgtatcctttaaggcacctgtgctagcctagattttgtaataacactgatttatgagaatggacaaaagtggtagggaaattgttccctctccacttctgaaagtatgatgatgtattaaggatggaggagttattaaaaatgtctcttctgatgaggtaacaattagatgaaaccatgttaaagctgagatgaacacttagaaattcagggatattgggtctttagccttatgaatttgagctgcttatttaattggtgtaatttactacatattagtactatattcgtaaggattttttattaaccattacagattttacaaacagctagttatatggtaaacagattattatgcctttttgcaattctgaatatgattctagtatttgtgtagatgtatttggtactttttcccctaattccaacactagtttatatatatagcgaataaatctagttgtataaatttttaaatgccgtcagtagaaagcacacaaggttatgatttttttaattactggcttctgatttctttcacttctgatccttttcctttttctcagatgtagctgagtcttgatcattttaagacaacgatgggtagaattttgagattaatgttaattttccctttttgttaatttcagtcccctctcactatgcttttgtccagaaggatcaagaattctaccatcccttgggtctttgtgtataaacaatgttaaataaaggtagactcagtctttaagatattagacagtttttttagtccatgggattgtaaatataaacattaactttcctataagaatattttggctttgtaatctatagcctcaaattggtatttattatggattcactagacaaacagctgtttccttattgtcttttttctttagtgtttctgatttgctatcagtagctgtttttaaagccgtccaaggaaaataattatttacagtttttgaagtcacttttgagccctcatcaagctctcattgtgatgggagggatacctttttgttgttaaaagcctattattgttaaaggccttttatggaaaccaacttggaaaacaaccttaaatgtggatgtatcagatttggtttatccagccatgggagagaaaacaaacctaagtttactttacttgtacatatacactacaatggatagtatatttgctgtaaactacaatgtaaaacctcaataaaagtgcgctgtacttcttaatgtttattaaaagatgtatttttacaaaaaaaaaaaaaaaaaaaaaaaaaa
//

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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