2024-03-29 11:02:25, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_005602 2761 bp mRNA linear PRI 17-APR-2013 DEFINITION Homo sapiens claudin 11 (CLDN11), transcript variant 1, mRNA. ACCESSION NM_005602 VERSION NM_005602.5 GI:195947370 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 2761) AUTHORS Chiba,K., Yamaguchi,K., Ando,M., Miyake,H. and Fujisawa,M. TITLE Expression pattern of testicular claudin-11 in infertile men JOURNAL Urology 80 (5), 1161 (2012) PUBMED 22951003 REMARK GeneRIF: disorganization of claudin-11 expression in Sertoli cells might be one of the factors involved in the impairment of spermatogenesis. REFERENCE 2 (bases 1 to 2761) AUTHORS Katsushima,K., Shinjo,K., Natsume,A., Ohka,F., Fujii,M., Osada,H., Sekido,Y. and Kondo,Y. TITLE Contribution of microRNA-1275 to Claudin11 protein suppression via a polycomb-mediated silencing mechanism in human glioma stem-like cells JOURNAL J. Biol. Chem. 287 (33), 27396-27406 (2012) PUBMED 22736761 REMARK GeneRIF: Treatment with 3-deazaneplanocin A, an inhibitor of H3K27 methyltransferase, attenuated CLDN11 induction by serum stimulation in parallel with sustained miR-1275 expression REFERENCE 3 (bases 1 to 2761) AUTHORS Kote-Jarai,Z., Olama,A.A., Giles,G.G., Severi,G., Schleutker,J., Weischer,M., Campa,D., Riboli,E., Key,T., Gronberg,H., Hunter,D.J., Kraft,P., Thun,M.J., Ingles,S., Chanock,S., Albanes,D., Hayes,R.B., Neal,D.E., Hamdy,F.C., Donovan,J.L., Pharoah,P., Schumacher,F., Henderson,B.E., Stanford,J.L., Ostrander,E.A., Sorensen,K.D., Dork,T., Andriole,G., Dickinson,J.L., Cybulski,C., Lubinski,J., Spurdle,A., Clements,J.A., Chambers,S., Aitken,J., Gardiner,R.A., Thibodeau,S.N., Schaid,D., John,E.M., Maier,C., Vogel,W., Cooney,K.A., Park,J.Y., Cannon-Albright,L., Brenner,H., Habuchi,T., Zhang,H.W., Lu,Y.J., Kaneva,R., Muir,K., Benlloch,S., Leongamornlert,D.A., Saunders,E.J., Tymrakiewicz,M., Mahmud,N., Guy,M., O'Brien,L.T., Wilkinson,R.A., Hall,A.L., Sawyer,E.J., Dadaev,T., Morrison,J., Dearnaley,D.P., Horwich,A., Huddart,R.A., Khoo,V.S., Parker,C.C., Van As,N., Woodhouse,C.J., Thompson,A., Christmas,T., Ogden,C., Cooper,C.S., Lophatonanon,A., Southey,M.C., Hopper,J.L., English,D.R., Wahlfors,T., Tammela,T.L., Klarskov,P., Nordestgaard,B.G., Roder,M.A., Tybjaerg-Hansen,A., Bojesen,S.E., Travis,R., Canzian,F., Kaaks,R., Wiklund,F., Aly,M., Lindstrom,S., Diver,W.R., Gapstur,S., Stern,M.C., Corral,R., Virtamo,J., Cox,A., Haiman,C.A., Le Marchand,L., Fitzgerald,L., Kolb,S., Kwon,E.M., Karyadi,D.M., Orntoft,T.F., Borre,M., Meyer,A., Serth,J., Yeager,M., Berndt,S.I., Marthick,J.R., Patterson,B., Wokolorczyk,D., Batra,J., Lose,F., McDonnell,S.K., Joshi,A.D., Shahabi,A., Rinckleb,A.E., Ray,A., Sellers,T.A., Lin,H.Y., Stephenson,R.A., Farnham,J., Muller,H., Rothenbacher,D., Tsuchiya,N., Narita,S., Cao,G.W., Slavov,C., Mitev,V., Easton,D.F. and Eeles,R.A. CONSRTM UK Genetic Prostate Cancer Study Collaborators/British Association of Urological Surgeons' Section of Oncology; UK ProtecT Study Collaborators, The Australian Prostate Cancer BioResource; PRACTICAL Consortium TITLE Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study JOURNAL Nat. Genet. 43 (8), 785-791 (2011) PUBMED 21743467 REMARK Publication Status: Online-Only REFERENCE 4 (bases 1 to 2761) AUTHORS Awsare,N.S., Martin,T.A., Haynes,M.D., Matthews,P.N. and Jiang,W.G. TITLE Claudin-11 decreases the invasiveness of bladder cancer cells JOURNAL Oncol. Rep. 25 (6), 1503-1509 (2011) PUBMED 21468549 REMARK GeneRIF: claudin-11 may have a role in preventing cancer progression and may serve as a therapeutic target in reducing metastasis REFERENCE 5 (bases 1 to 2761) AUTHORS Nah,W.H., Lee,J.E., Park,H.J., Park,N.C. and Gye,M.C. TITLE Claudin-11 expression increased in spermatogenic defect in human testes JOURNAL Fertil. Steril. 95 (1), 385-388 (2011) PUBMED 20850723 REMARK GeneRIF: late spermatogenic wave may negatively regulate claudin-11 gene activation and the subcellular localization of claudin-11 in Sertoli cells, thus altering the blood testis barrier in the human testis REFERENCE 6 (bases 1 to 2761) 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 REFERENCE 7 (bases 1 to 2761) AUTHORS Gow,A., Southwood,C.M., Li,J.S., Pariali,M., Riordan,G.P., Brodie,S.E., Danias,J., Bronstein,J.M., Kachar,B. and Lazzarini,R.A. TITLE CNS myelin and sertoli cell tight junction strands are absent in Osp/claudin-11 null mice JOURNAL Cell 99 (6), 649-659 (1999) PUBMED 10612400 REFERENCE 8 (bases 1 to 2761) AUTHORS Shafit-Zagardo,B., Kress,Y., Zhao,M.L. and Lee,S.C. TITLE A novel microtubule-associated protein-2 expressed in oligodendrocytes in multiple sclerosis lesions JOURNAL J. Neurochem. 73 (6), 2531-2537 (1999) PUBMED 10582615 REFERENCE 9 (bases 1 to 2761) AUTHORS Bronstein,J.M., Popper,P., Micevych,P.E. and Farber,D.B. TITLE Isolation and characterization of a novel oligodendrocyte-specific protein JOURNAL Neurology 47 (3), 772-778 (1996) PUBMED 8797478 REFERENCE 10 (bases 1 to 2761) AUTHORS Bronstein,J.M., Kozak,C.A., Chen,X.N., Wu,S., Danciger,M., Korenberg,J.R. and Farber,D.B. TITLE Chromosomal localization of murine and human oligodendrocyte-specific protein genes JOURNAL Genomics 34 (2), 255-257 (1996) PUBMED 8661061 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from DC328248.1, BC013577.1 and AC008041.5. On Aug 7, 2008 this sequence version replaced gi:33598917. 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. The protein encoded by this gene is a major component of central nervous system (CNS) myelin and plays an important role in regulating proliferation and migration of oligodendrocytes. Mouse studies showed that the gene deficiency results in deafness and loss of the Sertoli cell epithelial phenotype in the testis. This protein is a tight junction protein at the human blood-testis barrier (BTB), and the BTB disruption is related to a dysfunction of this gene. Alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Aug 2010]. Transcript Variant: This variant (1) is the longer transcript and encodes the longer isoform (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 :: BC013577.1, BI824787.1 [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 1-12 DC328248.1 1-12 13-1093 BC013577.1 1-1081 1094-2761 AC008041.5 17342-19009 FEATURES Location/Qualifiers source 1..2761 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="3" /map="3q26.2-q26.3" gene 1..2761 /gene="CLDN11" /gene_synonym="OSP; OTM" /note="claudin 11" /db_xref="GeneID:5010" /db_xref="HGNC:8514" /db_xref="HPRD:03207" /db_xref="MIM:601326" exon 1..428 /gene="CLDN11" /gene_synonym="OSP; OTM" /inference="alignment:Splign:1.39.8" variation 73 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="a" /replace="c" /db_xref="dbSNP:370409883" misc_feature 167..169 /gene="CLDN11" /gene_synonym="OSP; OTM" /note="upstream in-frame stop codon" variation 186 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="a" /replace="g" /db_xref="dbSNP:8192636" CDS 203..826 /gene="CLDN11" /gene_synonym="OSP; OTM" /note="isoform 1 is encoded by transcript variant 1; oligodendrocyte transmembrane protein; claudin-11; oligodendrocyte-specific protein" /codon_start=1 /product="claudin-11 isoform 1" /protein_id="NP_005593.2" /db_xref="GI:10938016" /db_xref="CCDS:CCDS3213.1" /db_xref="GeneID:5010" /db_xref="HGNC:8514" /db_xref="HPRD:03207" /db_xref="MIM:601326" /translation="
MVATCLQVVGFVTSFVGWIGVIVTTSTNDWVVTCGYTIPTCRKLDELGSKGLWADCVMATGLYHCKPLVDILILPGYVQACRALMIAASVLGLPAILLLLTVLPCIRMGQEPGVAKYRRAQLAGVLLILLALCALVATIWFPVCAHRETTIVSFGYSLYAGWIGAVLCLVGGCVILCCAGDAQAFGENRFYYTAGSSSPTHAKSAHV
" misc_feature 206..268 /gene="CLDN11" /gene_synonym="OSP; OTM" /inference="non-experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (O75508.2); transmembrane region" misc_feature 218..>547 /gene="CLDN11" /gene_synonym="OSP; OTM" /note="PMP-22/EMP/MP20/Claudin family; Region: PMP22_Claudin; cl15797" /db_xref="CDD:210197" misc_feature 449..511 /gene="CLDN11" /gene_synonym="OSP; OTM" /inference="non-experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (O75508.2); transmembrane region" misc_feature 569..631 /gene="CLDN11" /gene_synonym="OSP; OTM" /inference="non-experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (O75508.2); transmembrane region" misc_feature 674..736 /gene="CLDN11" /gene_synonym="OSP; OTM" /inference="non-experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (O75508.2); transmembrane region" variation 268 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="c" /replace="t" /db_xref="dbSNP:145075208" variation 320 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="a" /replace="c" /db_xref="dbSNP:201720518" variation 331 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="c" /replace="g" /db_xref="dbSNP:376285070" variation 340 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="a" /replace="g" /db_xref="dbSNP:376171338" variation 418 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="c" /replace="t" /db_xref="dbSNP:370405833" exon 429..593 /gene="CLDN11" /gene_synonym="OSP; OTM" /inference="alignment:Splign:1.39.8" variation 433 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="c" /replace="t" /db_xref="dbSNP:367974397" variation 450 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="c" /replace="t" /db_xref="dbSNP:148297542" variation 484 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="g" /replace="t" /db_xref="dbSNP:141421186" variation 538 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="c" /replace="t" /db_xref="dbSNP:150789369" variation 590 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="c" /replace="t" /db_xref="dbSNP:371649486" exon 594..2761 /gene="CLDN11" /gene_synonym="OSP; OTM" /inference="alignment:Splign:1.39.8" variation 601 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="c" /replace="t" /db_xref="dbSNP:138100932" variation 602 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="a" /replace="g" /db_xref="dbSNP:143763226" variation 624..625 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="" /replace="a" /db_xref="dbSNP:34124448" variation 642 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="a" /replace="g" /db_xref="dbSNP:146493095" variation 656 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="a" /replace="g" /db_xref="dbSNP:377105856" variation 715 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="c" /replace="t" /db_xref="dbSNP:375051671" variation 784 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="a" /replace="g" /db_xref="dbSNP:369096350" variation 788 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="c" /replace="t" /db_xref="dbSNP:372554090" variation 797 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="a" /replace="c" /db_xref="dbSNP:144303681" variation 807 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="c" /replace="t" /db_xref="dbSNP:375624085" variation 808 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="a" /replace="g" /db_xref="dbSNP:140975891" variation 820 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="c" /replace="t" /db_xref="dbSNP:200665065" variation 837 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="c" /replace="t" /db_xref="dbSNP:369963006" variation 838 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="a" /replace="g" /db_xref="dbSNP:374008151" variation 850 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="a" /replace="t" /db_xref="dbSNP:373002112" variation 916 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="c" /replace="g" /db_xref="dbSNP:192477349" variation 967..968 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="" /replace="ttt" /db_xref="dbSNP:10620799" variation 1060 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="g" /replace="t" /db_xref="dbSNP:60306951" variation 1094 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="c" /replace="t" /db_xref="dbSNP:6770844" variation 1178 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="g" /replace="t" /db_xref="dbSNP:369372951" variation 1193 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="a" /replace="c" /db_xref="dbSNP:374137538" variation 1201 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="" /replace="t" /replace="ttt" /db_xref="dbSNP:11322219" variation 1447 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="a" /replace="g" /db_xref="dbSNP:144763446" variation 1506 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:75747180" variation 1603 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="a" /replace="g" /db_xref="dbSNP:71306669" variation 1616 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="c" /replace="t" /db_xref="dbSNP:146584959" variation 1632 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="c" /replace="g" /db_xref="dbSNP:77614151" variation 1740 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="a" /replace="g" /db_xref="dbSNP:116573207" variation 1764 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="a" /replace="g" /db_xref="dbSNP:114923460" variation 1790 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="a" /replace="t" /db_xref="dbSNP:184479005" variation 1830 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="a" /replace="c" /db_xref="dbSNP:76935838" variation 1956 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="g" /replace="t" /db_xref="dbSNP:141295233" variation 1973 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="c" /replace="t" /db_xref="dbSNP:13973" STS 2024..2151 /gene="CLDN11" /gene_synonym="OSP; OTM" /standard_name="SHGC-77525" /db_xref="UniSTS:21761" variation 2027 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="a" /replace="g" /db_xref="dbSNP:143257986" variation 2057 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="c" /replace="t" /db_xref="dbSNP:79247818" polyA_signal 2144..2149 /gene="CLDN11" /gene_synonym="OSP; OTM" variation 2156 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="a" /replace="g" /db_xref="dbSNP:188703062" polyA_site 2169 /gene="CLDN11" /gene_synonym="OSP; OTM" variation 2223 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="" /replace="t" /db_xref="dbSNP:199859109" polyA_signal 2302..2307 /gene="CLDN11" /gene_synonym="OSP; OTM" polyA_site 2320 /gene="CLDN11" /gene_synonym="OSP; OTM" variation 2325 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="c" /replace="t" /db_xref="dbSNP:192810780" variation 2326 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="a" /replace="g" /db_xref="dbSNP:74578076" variation 2327 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="a" /replace="g" /db_xref="dbSNP:184973915" variation 2340 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="a" /replace="g" /db_xref="dbSNP:189444465" variation 2413 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="a" /replace="g" /db_xref="dbSNP:77575392" variation 2418 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="c" /replace="t" /db_xref="dbSNP:141576986" variation 2469 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="a" /replace="g" /db_xref="dbSNP:191573902" variation 2490 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="c" /replace="g" /db_xref="dbSNP:150475064" variation 2654 /gene="CLDN11" /gene_synonym="OSP; OTM" /replace="c" /replace="t" /db_xref="dbSNP:138487700" ORIGIN
agcagcgctgctgtccccgccgtgcgcccttcgccgctgagctcgcagcctccggcgcccacctccacctccagtgtcccgcctcgggccgtcgccctccagcggctcgcgagcgtgggagacgtacctgggcaggcactgtccagcccaggcccaggcacagccgtgaggggcgaggcacggggacatcctggcggccaccatggtggccacgtgcctgcaggtggtgggcttcgtcacgagcttcgtgggctggatcggggtcatcgtgaccacctccaccaatgactgggtggtgacctgcggctacaccatccccacctgccgcaagctggatgagctgggctccaaggggctgtgggccgactgcgtcatggccacggggctgtaccactgcaagcccctggtggacatcctcatcctgccgggctacgtgcaggcctgccgcgccctgatgattgctgcctcggtcctgggtctgccggccattttactgctgctgactgttcttccctgcatccggatgggccaggagcccggtgtggctaagtacaggcgggcccagctggctggtgttttgctcattctgctggctctctgcgcccttgttgccaccatctggttccctgtgtgcgcccaccgtgagaccaccatcgtgagctttggctactccctgtatgcaggctggattggtgctgtgctgtgcctcgtgggtggctgtgtcatcctctgctgcgctggagatgcccaggcctttggtgaaaaccgtttctactacactgcgggctctagctccccgactcatgcgaagagtgcccacgtataagagggctgcccggctgcccacagaggtgctgtagatgctgggcccagggccctaggtttgctcgtcacagtgtggggaagcccattcctctgccaggctctaaagccaaaggtctagaaaagcatcctgtctggcattttgtagtcttaacttctccccatttcccccatcttttggttgccttaaaagaaatctctagctcagataatgcccagacatttttttcccttggtgttgcccctattagctcttttcttgggcattcttttgctgtttattaaaaatatattatatatattttgtttctttaaatttcaaatgttttgcaaacatcactgagttaggtgggggtggggaagagaaatacaagatacttttttttttttttttttttttttttttttaaatagggcctcactctgttgctcaggctggagtgcggtggtgtgatctcggctcatgtagcctcaacctccccggctcaagtgatcctcctgcctcagcctcccaagtagctgggactacaggcgttcactactacacccagctaatttttaagttttttatagagatgagggctccctatgttgcccaggttggtctcgaactcctggactcaaagtatcctcccgcctcggcctcccaaagtgttgggattataggagtgagccaccacaccggccaagatgcttttcaaactgatacagatgacaatgggagcctcataaagatggcttttgtttcttcccttcaaggtcatttacttgtacgagacagaaaaagatagcattggggacatgggatgggggagggagggcaatagtggaacgaactttccatgggaaactttcccttttgtaagttgagggccaggggtagggatattttttagtttgtgattttacatttatctgtacatactttttcaagattgatcatttttataaccatggttttcctgaaatcctcaattcatcaatatgaaggaaatgaaccacatagactttatgcaataaataacagtgcaagtgagtataactctaactgatgttccacaaaacatttttgatttcaggtttgtatgatgtagtttttaatcgtacattttcatatgcttcaaactaacacatttttaaagctttcccccacttttctctctatttgtattgttagccatcttgaagtgatgttgtttaacataaattgtactgttgaatttggctttacgggtgtaaacactgatggtatatcagtatctgagaccccaaactctccaaatactgatggtgcattttattcttgaagtgaaatctgtgcaataaaataacagactgtctgcaaaactggccttcaatcttctgttgtatccagaggtatcattattgatttaaaaaaatctcattaatctctactggtaatttatagggaatctgatcagtgattcaagaacaagtaattctgcattgccttgaataattaaaaagttatattttattcacggtattgcagtggtaatttgtggtcatgaaagcataacctcagtgctctctaggtttcttaagtggggtgactttatggcatctttaatcatcgatcaatgggcagcaatcagaaacaaagttctcagcattatgcagttaatgtccttcatctacttctaacacttagtaaaggaattgattggctaggtataaaaagagaattaacgaaacctattttattggatctttaagtaataatatctaaatacatttcgttcaaacatacatatgtagctgtttggacattttggacaaagacacattgagttgatttttatttgtttttctgttccagaaacttcatcaagttacgggcctggtctaagaaaacacattgcaatctattttggcagacttctttcaaataaaatactaatttcattagctgatagta
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ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:5010 -> Molecular function: GO:0005198 [structural molecule activity] evidence: IEA GeneID:5010 -> Molecular function: GO:0042802 [identical protein binding] evidence: ISS GeneID:5010 -> Biological process: GO:0007283 [spermatogenesis] evidence: IEA GeneID:5010 -> Biological process: GO:0008366 [axon ensheathment] evidence: IEA GeneID:5010 -> Biological process: GO:0016338 [calcium-independent cell-cell adhesion] evidence: ISS GeneID:5010 -> Cellular component: GO:0005886 [plasma membrane] evidence: IEA GeneID:5010 -> Cellular component: GO:0005923 [tight junction] evidence: ISS GeneID:5010 -> Cellular component: GO:0016021 [integral to membrane] evidence: IEA
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