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2025-05-09 16:31:20, 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 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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