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2019-03-23 03:23:02, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_032521               4625 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens par-6 partitioning defective 6 homolog beta (C.
            elegans) (PARD6B), mRNA.
ACCESSION   NM_032521 XM_030559
VERSION     NM_032521.2  GI:82659099
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 4625)
  AUTHORS   Yosifova,A., Mushiroda,T., Kubo,M., Takahashi,A., Kamatani,Y.,
            Kamatani,N., Stoianov,D., Vazharova,R., Karachanak,S.,
            Zaharieva,I., Dimova,I., Hadjidekova,S., Milanova,V., Madjirova,N.,
            Gerdjikov,I., Tolev,T., Poryazova,N., O'Donovan,M.C., Owen,M.J.,
            Kirov,G., Toncheva,D. and Nakamura,Y.
  TITLE     Genome-wide association study on bipolar disorder in the Bulgarian
            population
  JOURNAL   Genes Brain Behav. 10 (7), 789-797 (2011)
   PUBMED   21771265
REFERENCE   2  (bases 1 to 4625)
  AUTHORS   Durgan,J., Kaji,N., Jin,D. and Hall,A.
  TITLE     Par6B and atypical PKC regulate mitotic spindle orientation during
            epithelial morphogenesis
  JOURNAL   J. Biol. Chem. 286 (14), 12461-12474 (2011)
   PUBMED   21300793
  REMARK    GeneRIF: Data conclude that Par6B and aPKC control mitotic spindle
            orientation in polarized epithelia and, furthermore, that aPKC
            coordinately regulates multiple processes to promote morphogenesis.
REFERENCE   3  (bases 1 to 4625)
  AUTHORS   Wallace,S.W., Durgan,J., Jin,D. and Hall,A.
  TITLE     Cdc42 regulates apical junction formation in human bronchial
            epithelial cells through PAK4 and Par6B
  JOURNAL   Mol. Biol. Cell 21 (17), 2996-3006 (2010)
   PUBMED   20631255
  REMARK    GeneRIF: This study demonstrates that controlled regulation of PAK4
            is required for apical junction formation in lung epithelial cells
            and highlights potential cross-talk between two Cdc42 targets, PAK4
            and Par6B.
REFERENCE   4  (bases 1 to 4625)
  AUTHORS   Horikoshi,Y., Suzuki,A., Yamanaka,T., Sasaki,K., Mizuno,K.,
            Sawada,H., Yonemura,S. and Ohno,S.
  TITLE     Interaction between PAR-3 and the aPKC-PAR-6 complex is
            indispensable for apical domain development of epithelial cells
  JOURNAL   J. Cell. Sci. 122 (PT 10), 1595-1606 (2009)
   PUBMED   19401335
  REMARK    GeneRIF: Interaction between PAR-3 and the aPKC-PAR-6 complex is
            indispensable for apical domain development of epithelial cells.
REFERENCE   5  (bases 1 to 4625)
  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   6  (bases 1 to 4625)
  AUTHORS   Kohjima,M., Noda,Y., Takeya,R., Saito,N., Takeuchi,K. and
            Sumimoto,H.
  TITLE     PAR3beta, a novel homologue of the cell polarity protein PAR3,
            localizes to tight junctions
  JOURNAL   Biochem. Biophys. Res. Commun. 299 (4), 641-646 (2002)
   PUBMED   12459187
REFERENCE   7  (bases 1 to 4625)
  AUTHORS   Gao,L., Macara,I.G. and Joberty,G.
  TITLE     Multiple splice variants of Par3 and of a novel related gene,
            Par3L, produce proteins with different binding properties
  JOURNAL   Gene 294 (1-2), 99-107 (2002)
   PUBMED   12234671
REFERENCE   8  (bases 1 to 4625)
  AUTHORS   Deloukas,P., Matthews,L.H., Ashurst,J., Burton,J., Gilbert,J.G.,
            Jones,M., Stavrides,G., Almeida,J.P., Babbage,A.K., Bagguley,C.L.,
            Bailey,J., Barlow,K.F., Bates,K.N., Beard,L.M., Beare,D.M.,
            Beasley,O.P., Bird,C.P., Blakey,S.E., Bridgeman,A.M., Brown,A.J.,
            Buck,D., Burrill,W., Butler,A.P., Carder,C., Carter,N.P.,
            Chapman,J.C., Clamp,M., Clark,G., Clark,L.N., Clark,S.Y.,
            Clee,C.M., Clegg,S., Cobley,V.E., Collier,R.E., Connor,R.,
            Corby,N.R., Coulson,A., Coville,G.J., Deadman,R., Dhami,P.,
            Dunn,M., Ellington,A.G., Frankland,J.A., Fraser,A., French,L.,
            Garner,P., Grafham,D.V., Griffiths,C., Griffiths,M.N., Gwilliam,R.,
            Hall,R.E., Hammond,S., Harley,J.L., Heath,P.D., Ho,S., Holden,J.L.,
            Howden,P.J., Huckle,E., Hunt,A.R., Hunt,S.E., Jekosch,K.,
            Johnson,C.M., Johnson,D., Kay,M.P., Kimberley,A.M., King,A.,
            Knights,A., Laird,G.K., Lawlor,S., Lehvaslaiho,M.H., Leversha,M.,
            Lloyd,C., Lloyd,D.M., Lovell,J.D., Marsh,V.L., Martin,S.L.,
            McConnachie,L.J., McLay,K., McMurray,A.A., Milne,S., Mistry,D.,
            Moore,M.J., Mullikin,J.C., Nickerson,T., Oliver,K., Parker,A.,
            Patel,R., Pearce,T.A., Peck,A.I., Phillimore,B.J.,
            Prathalingam,S.R., Plumb,R.W., Ramsay,H., Rice,C.M., Ross,M.T.,
            Scott,C.E., Sehra,H.K., Shownkeen,R., Sims,S., Skuce,C.D.,
            Smith,M.L., Soderlund,C., Steward,C.A., Sulston,J.E., Swann,M.,
            Sycamore,N., Taylor,R., Tee,L., Thomas,D.W., Thorpe,A., Tracey,A.,
            Tromans,A.C., Vaudin,M., Wall,M., Wallis,J.M., Whitehead,S.L.,
            Whittaker,P., Willey,D.L., Williams,L., Williams,S.A., Wilming,L.,
            Wray,P.W., Hubbard,T., Durbin,R.M., Bentley,D.R., Beck,S. and
            Rogers,J.
  TITLE     The DNA sequence and comparative analysis of human chromosome 20
  JOURNAL   Nature 414 (6866), 865-871 (2001)
   PUBMED   11780052
REFERENCE   9  (bases 1 to 4625)
  AUTHORS   Noda,Y., Takeya,R., Ohno,S., Naito,S., Ito,T. and Sumimoto,H.
  TITLE     Human homologues of the Caenorhabditis elegans cell polarity
            protein PAR6 as an adaptor that links the small GTPases Rac and
            Cdc42 to atypical protein kinase C
  JOURNAL   Genes Cells 6 (2), 107-119 (2001)
   PUBMED   11260256
REFERENCE   10 (bases 1 to 4625)
  AUTHORS   Joberty,G., Petersen,C., Gao,L. and Macara,I.G.
  TITLE     The cell-polarity protein Par6 links Par3 and atypical protein
            kinase C to Cdc42
  JOURNAL   Nat. Cell Biol. 2 (8), 531-539 (2000)
   PUBMED   10934474
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from BC060847.1, AB044555.1,
            AL031680.20 and CA435324.1.
            On Nov 25, 2005 this sequence version replaced gi:62955041.
            
            Summary: This gene is a member of the PAR6 family and encodes a
            protein with a PSD95/Discs-large/ZO1 (PDZ) domain, an OPR domain
            and a semi-Cdc42/Rac interactive binding (CRIB) domain. This
            cytoplasmic protein is involved in asymmetrical cell division and
            cell polarization processes as a member of a multi-protein complex.
            [provided by RefSeq, Jul 2008].
            
            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 :: BC060847.1, AB044555.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025084, ERS025088 [ECO:0000348]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-1215              BC060847.1         1-1215
            1216-1362           AB044555.1         973-1119
            1363-1573           BC060847.1         1363-1573
            1574-3985           AL031680.20        32662-35073
            3986-4625           CA435324.1         8-647               c
FEATURES             Location/Qualifiers
     source          1..4625
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="20"
                     /map="20q13.13"
     gene            1..4625
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /note="par-6 partitioning defective 6 homolog beta (C.
                     elegans)"
                     /db_xref="GeneID:84612"
                     /db_xref="HGNC:16245"
                     /db_xref="HPRD:18703"
                     /db_xref="MIM:608975"
     exon            1..309
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /inference="alignment:Splign:1.39.8"
     misc_feature    61..63
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /note="upstream in-frame stop codon"
     variation       131
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143376336"
     variation       194
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:6020716"
     CDS             244..1362
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /note="PAR-6 beta"
                     /codon_start=1
                     /product="partitioning defective 6 homolog beta"
                     /protein_id="NP_115910.1"
                     /db_xref="GI:62955042"
                     /db_xref="CCDS:CCDS33485.1"
                     /db_xref="GeneID:84612"
                     /db_xref="HGNC:16245"
                     /db_xref="HPRD:18703"
                     /db_xref="MIM:608975"
                     /translation="
MNRSHRHGAGSGCLGTMEVKSKFGAEFRRFSLERSKPGKFEEFYGLLQHVHKIPNVDVLVGYADIHGDLLPINNDDNYHKAVSTANPLLRIFIQKKEEADYSAFGTDTLIKKKNVLTNVLRPDNHRKKPHIVISMPQDFRPVSSIIDVDILPETHRRVRLYKYGTEKPLGFYIRDGSSVRVTPHGLEKVPGIFISRLVPGGLAQSTGLLAVNDEVLEVNGIEVSGKSLDQVTDMMIANSRNLIITVRPANQRNNVVRNSRTSGSSGQSTDNSLLGYPQQIEPSFEPEDEDSEEDDIIIEDNGVPQQIPKAVPNTESLESLTQIELSFESGQNGFIPSNEVSLAAIASSSNTEFETHAPDQKLLEEDGTIITL
"
     misc_feature    274..276
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (Q9BYG5.1); phosphorylation site"
     misc_feature    292..531
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /note="The PB1 domain is an essential part of Par6 protein
                     which in complex with Par3 and aPKC proteins is crucial
                     for establishment of apical-basal polarity of animal
                     cells. The PB1 domain is a modular domain mediating
                     specific protein-protein interactions...; Region:
                     PB1_Par6; cd06403"
                     /db_xref="CDD:99724"
     misc_feature    order(295..297,301..303,322..330,334..336,379..381,
                     391..393,511..513)
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /note="PB1 interaction surface [polypeptide binding];
                     other site"
                     /db_xref="CDD:99724"
     misc_feature    619..1002
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q9BYG5.1);
                     Region: Interaction with PARD3 and CDC42 (By similarity)"
     misc_feature    709..984
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /note="PDZ domain found in a variety of Eumetazoan
                     signaling molecules, often in tandem arrangements. May be
                     responsible for specific protein-protein interactions, as
                     most PDZ domains bind C-terminal polypeptides, and binding
                     to internal (non-C-terminal)...; Region: PDZ_signaling;
                     cd00992"
                     /db_xref="CDD:29049"
     misc_feature    order(745..756,760..762,934..939,946..951)
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /note="protein binding site [polypeptide binding]; other
                     site"
                     /db_xref="CDD:29049"
     exon            310..532
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /inference="alignment:Splign:1.39.8"
     variation       336
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:75953522"
     variation       400
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:138305853"
     variation       415
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142377445"
     variation       514
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142921418"
     exon            533..4615
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /inference="alignment:Splign:1.39.8"
     variation       566
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:61730982"
     STS             577..1429
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /standard_name="PARD6B_3691"
                     /db_xref="UniSTS:463270"
     variation       583
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:368916816"
     variation       685
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377211034"
     variation       705
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:141238890"
     variation       732
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:193145616"
     variation       733
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150776987"
     variation       737
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:367776100"
     variation       825
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:371618647"
     variation       828
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:61730981"
     variation       913
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:183958932"
     variation       931
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:76004231"
     variation       953
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:77747604"
     variation       961
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142463339"
     variation       973
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145980829"
     variation       1004
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368938462"
     variation       1010
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373485771"
     variation       1021
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:139812474"
     variation       1022
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143199204"
     variation       1028
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201967571"
     variation       1052
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:3810537"
     variation       1080
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:41283604"
     variation       1082
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148801972"
     variation       1084
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142389338"
     variation       1134
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:151301407"
     variation       1135
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368236261"
     variation       1145
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:111978462"
     variation       1149
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:372319099"
     variation       1182
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144796992"
     variation       1190
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:375415967"
     variation       1216
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:41283606"
     variation       1220
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139111657"
     variation       1291
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147700888"
     variation       1293
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:369290378"
     variation       1295
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142333280"
     variation       1315
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146391972"
     variation       1340
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:41283608"
     variation       1351
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:184193885"
     variation       1376
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:55948332"
     variation       1395
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201932178"
     variation       1410
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:188527390"
     variation       1413
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:6020721"
     variation       1434
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149899269"
     variation       1470
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144921171"
     variation       1494
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:370336354"
     variation       1573
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:143588050"
     variation       1573
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:79199393"
     variation       1574
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201394798"
     variation       1592
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149031514"
     variation       1608
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:376192736"
     variation       1619
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:192900373"
     variation       1679
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144895071"
     variation       1746
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:6091206"
     variation       1772
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:80287642"
     variation       1777
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:146742474"
     variation       1794
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:6091207"
     variation       1803
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:6091208"
     variation       1811
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:368499557"
     variation       1823
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:13042106"
     variation       1839
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace=""
                     /replace="tt"
                     /replace="ttttt"
                     /replace="tttttttt"
                     /db_xref="dbSNP:67916693"
     variation       1851..1852
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:11482729"
     variation       1860
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace=""
                     /replace="tt"
                     /replace="ttttttt"
                     /db_xref="dbSNP:57688441"
     variation       1862
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:76966666"
     variation       1905
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201112385"
     variation       1945
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:138005847"
     variation       1977
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376404812"
     variation       2057
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:6096079"
     variation       2154..2155
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:34538740"
     variation       2154
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:113583294"
     variation       2182
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:184537114"
     variation       2196
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150428245"
     variation       2213..2214
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:11484334"
     variation       2220
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201491403"
     variation       2225..2228
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace=""
                     /replace="tttt"
                     /db_xref="dbSNP:144055406"
     variation       2225
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace=""
                     /replace="t"
                     /replace="tt"
                     /replace="tttt"
                     /db_xref="dbSNP:11467364"
     variation       2239
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace=""
                     /replace="t"
                     /replace="tttt"
                     /db_xref="dbSNP:11478799"
     variation       2244..2245
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace=""
                     /replace="t"
                     /replace="tttt"
                     /db_xref="dbSNP:10597372"
     variation       2261
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:189370998"
     variation       2266
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:182257849"
     STS             2278..2367
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /standard_name="PMC156606P1"
                     /db_xref="UniSTS:271408"
     STS             2293..2501
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /standard_name="L18426"
                     /db_xref="UniSTS:34648"
     STS             2293..2375
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /standard_name="L18426"
                     /db_xref="UniSTS:34648"
     variation       2304
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:187247389"
     STS             2325..2418
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /standard_name="D8S2278"
                     /db_xref="UniSTS:473906"
     STS             2333..2769
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /standard_name="D8S2279"
                     /db_xref="UniSTS:473907"
     variation       2360
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:7273801"
     variation       2389
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:6013008"
     STS             2395..2497
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /standard_name="D11S3114"
                     /db_xref="UniSTS:152207"
     variation       2419
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370377076"
     variation       2456
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202064492"
     variation       2463
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374753508"
     variation       2466
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:8126455"
     variation       2469
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:189017935"
     STS             2473..2643
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /standard_name="L17705"
                     /db_xref="UniSTS:66091"
     STS             2476..2699
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /standard_name="GDB:434012"
                     /db_xref="UniSTS:157204"
     STS             2490..2643
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /standard_name="L17877"
                     /db_xref="UniSTS:61334"
     variation       2510
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:75343091"
     variation       2528
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375977861"
     variation       2590
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:7260805"
     variation       2614..2615
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace=""
                     /replace="ttt"
                     /db_xref="dbSNP:10686919"
     variation       2615..2616
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace=""
                     /replace="ttt"
                     /db_xref="dbSNP:377386931"
     variation       2648
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140988923"
     variation       2668
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369591808"
     STS             2679..2769
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /standard_name="D8S2279"
                     /db_xref="UniSTS:473907"
     variation       2680
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:181369950"
     variation       2820
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:185504621"
     variation       2863
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:7268617"
     variation       2868
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143302333"
     variation       2883
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:59057701"
     variation       2886
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:373025799"
     variation       2892
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148559733"
     variation       2947
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:7268691"
     variation       2953..2956
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace=""
                     /replace="aatt"
                     /db_xref="dbSNP:377231688"
     variation       2963
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142586330"
     variation       3018..3019
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:35346940"
     variation       3048
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:76228262"
     variation       3075
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:6091209"
     variation       3125
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150947689"
     variation       3199
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:45624032"
     variation       3206
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:5841810"
     variation       3206
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:200256456"
     variation       3219
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace=""
                     /replace="a"
                     /replace="aaa"
                     /db_xref="dbSNP:35818153"
     variation       3219
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:62202831"
     STS             3222..3361
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /standard_name="RH65940"
                     /db_xref="UniSTS:80811"
     variation       3230
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:6096080"
     variation       3256
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:6096081"
     variation       3287
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:6091210"
     STS             3322..3446
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /standard_name="SHGC-37653"
                     /db_xref="UniSTS:44733"
     variation       3343
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1054185"
     variation       3369
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139465911"
     variation       3412..3413
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace=""
                     /replace="gt"
                     /db_xref="dbSNP:11469424"
     variation       3413..3414
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace=""
                     /replace="tg"
                     /db_xref="dbSNP:11469337"
     variation       3536
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373191418"
     variation       3584
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:190264843"
     variation       3585
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112854632"
     variation       3593
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:6096082"
     variation       3599
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:372831252"
     variation       3632
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:73276585"
     variation       3666
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:183253488"
     variation       3670
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:186056261"
     variation       3672
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:117000341"
     variation       3698
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371683106"
     variation       3704
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:190963477"
     variation       3712
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:111984714"
     variation       3784
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:6096083"
     variation       3803
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376436316"
     variation       3828
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:6126089"
     variation       3858
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:183937302"
     variation       3942..3943
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace=""
                     /replace="ct"
                     /db_xref="dbSNP:143762554"
     variation       3943..3944
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace=""
                     /replace="ct"
                     /db_xref="dbSNP:11469346"
     variation       3949
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:201988460"
     variation       3949
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201229227"
     variation       3951
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:6096084"
     variation       3961
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:187709109"
     variation       3962
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:200895732"
     variation       3998
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:374046264"
     variation       4055
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:192202037"
     variation       4118
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:80162740"
     variation       4126
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:115752561"
     variation       4145
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:78735395"
     variation       4161
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:78174724"
     variation       4174
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:183186349"
     variation       4178
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371080969"
     variation       4232
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146760168"
     variation       4258
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:187516081"
     STS             4315..4421
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /standard_name="G42347"
                     /db_xref="UniSTS:94206"
     variation       4409
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375583186"
     polyA_signal    4424..4429
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
     polyA_site      4449
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /experiment="experimental evidence, no additional details
                     recorded"
     variation       4483
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:192761698"
     variation       4587
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:74274301"
     polyA_signal    4589..4594
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
     polyA_site      4615
                     /gene="PARD6B"
                     /gene_synonym="PAR6B"
ORIGIN      
gagggagggagctgcttccccgcctgccgcgccaccagtccgaccctcggtcccgccgtgtgagcagctggtggagtggagctcagcgcggacgccggagctgcggccgccccctctgcaggtgcctgtgaggaggcgcccgggccgcaaccgctttccgagatccccagtcgcgcactcgctccccgcgctcctgaggggccgcccggccggaggaggccgtcgcggggctcggcgttcagcatgaaccgcagccaccggcacggggcgggcagcggctgcctgggcactatggaggtgaagagcaagtttggagctgaatttcgtcggttttcgctggaaagatcaaaacctggaaaatttgaggagttttatggattactacaacatgttcataagatccccaatgttgacgttttggtaggctatgcagacatccatggagacttactacctataaataatgatgataattatcacaaagctgtttcaacggccaatccactgcttaggatatttatacaaaagaaggaagaagcagactacagtgcctttggtacagacacgctaataaagaagaagaatgttttaaccaacgtattgcgtcctgacaaccatagaaaaaagccacatatagtcattagtatgccccaagactttagacctgtgtcttctattatagacgtggatattctcccagaaacgcatcgtagggtacgtctttacaaatacggcacggagaaacccctaggattctacatccgggatggctccagtgtcagggtaacaccacatggcttagaaaaggttccagggatctttatatccaggcttgtcccaggaggtctggctcaaagtacaggactattagctgttaatgatgaagttttagaagttaatggcatagaagtttcagggaagagccttgatcaagtaacagacatgatgattgcaaatagccgtaacctcatcataacagtgagaccggcaaaccagaggaataatgttgtgaggaacagtcggacttctggcagttccggtcagtctactgataacagccttcttggctacccacagcagattgaaccaagctttgagccagaggatgaagacagcgaagaagatgacattatcattgaagacaatggagtgccacagcagattccaaaagctgttcctaatactgagagcctggagtcattaacacagatagagctaagctttgagtctggacagaatggctttattccctctaatgaagtgagcttagcagccatagcaagcagctcaaacacggaatttgaaacacatgctccagatcaaaaactcttagaagaagatggaacaatcataacattatgaaaccgtggtttgaatgttttcagagtgaggatgccatgaggacttgtacatttggctagtttaaaagcatatatacctctgaccagtgacgtggaataggcatgagacgagtaacgttgcaagcttacaatattattaaagtagtagtttgataattgttaatataaactttggtggatcagaggtgaatttaagtccaaaacaaaggggcctttgctgatgaagttacgtgcttttgctgttttgtctgtggagaatcagatgttaaagcacattcttggaactatgtgagaagactagatcatttctgttggaagtggttgcatatttaacctgctgtgcagagcccagttaatttttcctttaactgtatttttaaaattctaatgtgaagtctgattctctcttgtggtacattggggacctcagctcttaaaggtctcatgttcccaatattttattttgattttttttttttttttttttttttttttttttagtgactgggtctcactctgttgcccacactggaatgcagtggcatgatcacagctctctgcagcctcaatcccctgggctcaagcagtcctcccacctcagcctcctgagtagctgggaccataggcacataccaccacatctgtctactttttgtattttttgtagagacagggtttcgccatgttgcccaagttggtcttgaactcctgggcttaagcagtcctgcctcggcttcccaaaatgctaggattagagccaccatgcccagcctattttgatttttgtttttttatgttcctttctaataaattgtaacaaatgatgttctcaagtacatttccagtttcttttcttttctttctttttttttttttttttttttttgagatggagtctcgctctatcgcccaggctggagtgcagtggcgcgatcttggctcactgcaagctctacctcctgggttcacaccattctcctgcctcagcctcccaagtagctgggactacaggcgcctgccaccatgcctggctaatttttagtagagacggggtttcgcagtgttagccaggaaggtctcaatctcctgacctcctgatccgcccgcctcggcctcccaaagtgctgggattacaggcgtgagccaccgcgcccagttgtgcatttctggtttctaagaatcaaaccacttggctgtttttaggagttacttcccatgttataaagctgaggaagctttttttttttttttttgagacagagtctctgtcacccaggctggagtgcagtggtgcaatctcagctcccgggttcaagcaattctcctgcctcagccttctgagtagctaagattacaggtgtgcgccaacacgtctggcttatttttttgtatttttagtagagatggagtttcaccatgttggtcaggtgggtctcaaactcctgacctcaagtgatccgcccatctcctcccaaagtgctggattgcaggcatgagcgcctagccaggaagctatcttttcttgagttatgaaactttgcaacagttgttcaaattggtgtttgtccttcctatagctttcatattttcaaattaattctgtatggctatataatttatgttttaaaaggcaattctcttgactttggaaatatggaagtctctcctttaacctattcttgttcccattcccagtctcatttgaaatcattccttttattgttagtgtgtgtatttttgttggtgtgcttttaatgcatccaagtatgcatcattttggataaaaaatacatccaaattaagatgttttaacacataggacaaacttgtgcactttttatgccaaaaaaaaaaaaaattgggttttccttcatgggatttctagaaacactgcctacactttatgaaaactacatagtattcacctgtgacaggtagagtttatcactattaattttatgaggctatttattactttccaatgcatccacttagaacaagctaagagtaaggctgctaactttaattccttgcctgattttattgtacagtgtgcacaagcacaatggtatgcttgtatatagaaactaaaaatactatgaagtacataagttccctatggcttatggagagttatttattaattaactttatggtagggctagtatgaatacctttttaacaattgtgtgctattacaacaatgaagattcaaatgactccgctttgaaggatgttttctctatatggtaaaatatatatgaagaagtcttgattacgtgaagatcacttgactcagaatacttcaatgtattttgttcacattaccactaagcatattatcagtaaactattaactgactgcacattatgtaatacgttgtactttttgttgaattcaccgaagttcttccatttatatgctatttttaatggcattccggctttaacattctgtgagtcttacaaatttgactcttgaatggcaaaataatgttagtatgtagaaggttaactttcatttataatataagtggtgcaggggttcaacattttaagtaaaaatatttttacacactacctctctctttttttttttaaagttttaacatcagaacttttgggggaaaaactacttcagggcttgactttttgtacaaattttaactgtaaaatacagatttatcttgtacgcattcatggaaatggaaatcaaagctgctattgctttttattttaattatcctgttaagggtatctatcaatggtattttcaagtagatctctgtttcttaaattattggtgaaataattgattactagatatattgtaaaaccaatagatcctggttatacgataaaatatcagctcattggtaggctgaatcaattatttcaagtgcaccttattaacaaaagtatcagtggatccaacataaaattttatagtactaaatgtcaagcctaactgtgaattttgttctgtatcttaagtaaatttatgataatgttctcgagctatcaacaaaatatatgtacttttgtgagctatgaattttctaattaaattttacatgctataacatgatttttacatgaatgatactttgtttataactatcaaatgtcagtattttactacaattttattataaagtgtacattatcactaaatgaacttcgattttaaaaatcaaattagctttagttgtatattattttttacaaataaagatagacttgtataaaggctaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:84612 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
            GeneID:84612 -> Biological process: GO:0006461 [protein complex assembly] evidence: IDA
            GeneID:84612 -> Biological process: GO:0007043 [cell-cell junction assembly] evidence: TAS
            GeneID:84612 -> Biological process: GO:0007049 [cell cycle] evidence: IEA
            GeneID:84612 -> Biological process: GO:0007163 [establishment or maintenance of cell polarity] evidence: TAS
            GeneID:84612 -> Biological process: GO:0007409 [axonogenesis] evidence: TAS
            GeneID:84612 -> Biological process: GO:0030334 [regulation of cell migration] evidence: TAS
            GeneID:84612 -> Biological process: GO:0034329 [cell junction assembly] evidence: TAS
            GeneID:84612 -> Biological process: GO:0045216 [cell-cell junction organization] evidence: TAS
            GeneID:84612 -> Biological process: GO:0051301 [cell division] evidence: IEA
            GeneID:84612 -> Biological process: GO:0070830 [tight junction assembly] evidence: TAS
            GeneID:84612 -> Cellular component: GO:0005634 [nucleus] evidence: IEA
            GeneID:84612 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA
            GeneID:84612 -> Cellular component: GO:0005829 [cytosol] evidence: TAS
            GeneID:84612 -> Cellular component: GO:0005886 [plasma membrane] evidence: IDA
            GeneID:84612 -> Cellular component: GO:0005886 [plasma membrane] evidence: TAS
            GeneID:84612 -> Cellular component: GO:0005923 [tight junction] evidence: IDA
            GeneID:84612 -> Cellular component: GO:0005938 [cell cortex] evidence: IEA
            GeneID:84612 -> Cellular component: GO:0043234 [protein complex] evidence: IEA
            GeneID:84612 -> Cellular component: GO:0045177 [apical part of cell] evidence: IEA

by @meso_cacase at DBCLS
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