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2024-04-23 19:25:05, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001017967 2273 bp mRNA linear PRI 22-JUN-2013
DEFINITION Homo sapiens MARVEL domain containing 3 (MARVELD3), transcript
variant 1, mRNA.
ACCESSION NM_001017967
VERSION NM_001017967.3 GI:404501494
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 2273)
AUTHORS Cording,J., Berg,J., Kading,N., Bellmann,C., Tscheik,C.,
Westphal,J.K., Milatz,S., Gunzel,D., Wolburg,H., Piontek,J.,
Huber,O. and Blasig,I.E.
TITLE In tight junctions, claudins regulate the interactions between
occludin, tricellulin and marvelD3, which, inversely, modulate
claudin oligomerization
JOURNAL J. Cell. Sci. 126 (PT 2), 554-564 (2013)
PUBMED 23203797
REFERENCE 2 (bases 1 to 2273)
AUTHORS Timmann,C., Thye,T., Vens,M., Evans,J., May,J., Ehmen,C.,
Sievertsen,J., Muntau,B., Ruge,G., Loag,W., Ansong,D., Antwi,S.,
Asafo-Adjei,E., Nguah,S.B., Kwakye,K.O., Akoto,A.O., Sylverken,J.,
Brendel,M., Schuldt,K., Loley,C., Franke,A., Meyer,C.G.,
Agbenyega,T., Ziegler,A. and Horstmann,R.D.
TITLE Genome-wide association study indicates two novel resistance loci
for severe malaria
JOURNAL Nature 489 (7416), 443-446 (2012)
PUBMED 22895189
REFERENCE 3 (bases 1 to 2273)
AUTHORS Kojima,T., Takasawa,A., Kyuno,D., Ito,T., Yamaguchi,H., Hirata,K.,
Tsujiwaki,M., Murata,M., Tanaka,S. and Sawada,N.
TITLE Downregulation of tight junction-associated MARVEL protein marvelD3
during epithelial-mesenchymal transition in human pancreatic cancer
cells
JOURNAL Exp. Cell Res. 317 (16), 2288-2298 (2011)
PUBMED 21763689
REMARK GeneRIF: MarvelD3 is transcriptionally downregulated in
Snail-induced epithelial-mesenchymal transition during the
progression for the pancreatic cancer.
REFERENCE 4 (bases 1 to 2273)
AUTHORS Raleigh,D.R., Marchiando,A.M., Zhang,Y., Shen,L., Sasaki,H.,
Wang,Y., Long,M. and Turner,J.R.
TITLE Tight junction-associated MARVEL proteins marveld3, tricellulin,
and occludin have distinct but overlapping functions
JOURNAL Mol. Biol. Cell 21 (7), 1200-1213 (2010)
PUBMED 20164257
REMARK GeneRIF: marvelD3, occludin, and tricellulin define the tight
junction-associated MARVEL protein family
REFERENCE 5 (bases 1 to 2273)
AUTHORS Steed,E., Rodrigues,N.T., Balda,M.S. and Matter,K.
TITLE Identification of MarvelD3 as a tight junction-associated
transmembrane protein of the occludin family
JOURNAL BMC Cell Biol. 10, 95 (2009)
PUBMED 20028514
REMARK GeneRIF: MarvelD3 co-localises with occludin at tight junctions in
intestinal and corneal epithelial cells.
Publication Status: Online-Only
REFERENCE 6 (bases 1 to 2273)
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 7 (bases 1 to 2273)
AUTHORS Oh,J.H., Yang,J.O., Hahn,Y., Kim,M.R., Byun,S.S., Jeon,Y.J.,
Kim,J.M., Song,K.S., Noh,S.M., Kim,S., Yoo,H.S., Kim,Y.S. and
Kim,N.S.
TITLE Transcriptome analysis of human gastric cancer
JOURNAL Mamm. Genome 16 (12), 942-954 (2005)
PUBMED 16341674
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
BP320419.1, AK292185.1, AC009097.9 and AA568498.1.
On Sep 15, 2012 this sequence version replaced gi:65301121.
Transcript Variant: This variant (1) represents the longer
transcript and encodes the longest isoform (1).
##Evidence-Data-START##
Transcript exon combination :: AK056842.1, AK292185.1 [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
1-34 BP320419.1 2-35
35-1632 AK292185.1 1-1598
1633-2068 AC009097.9 102131-102566
2069-2273 AA568498.1 1-205 c
FEATURES Location/Qualifiers
source 1..2273
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="16"
/map="16q22.2"
gene 1..2273
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/note="MARVEL domain containing 3"
/db_xref="GeneID:91862"
/db_xref="HGNC:30525"
/db_xref="HPRD:14365"
/db_xref="MIM:614094"
exon 1..544
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/inference="alignment:Splign:1.39.8"
variation 29
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="t"
/db_xref="dbSNP:199550688"
variation 60
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="g"
/db_xref="dbSNP:4788820"
CDS 78..1310
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/note="isoform 1 is encoded by transcript variant 1;
MARVEL (membrane-associating) domain containing 3; MARVEL
domain-containing protein 3"
/codon_start=1
/product="MARVEL domain-containing protein 3 isoform 1"
/protein_id="NP_001017967.2"
/db_xref="GI:65301122"
/db_xref="CCDS:CCDS32478.1"
/db_xref="GeneID:91862"
/db_xref="HGNC:30525"
/db_xref="HPRD:14365"
/db_xref="MIM:614094"
/translation="
MEDPSGAREPRARPRERDPGRRPHPDQGRTHDRPRDRPGDPRRKRSSDGNRRRDGDRDPERDQERDGNRDRNRDRERERERERDPDRGPRRDTHRDAGPRAGEHGVWEKPRQSRTRDGARGLTWDAAAPPGPAPWEAPEPPQPQRKGDPGRRRPESEPPSERYLPSTPRPGREEVEYYQSEAEGLLECHKCKYLCTGRGVVQIVEVVLNGMVLICIVASYFVLAGFSASFSSGGGFGNNYYSPFEGTELEQVRQLDQQYTILRSPLIYGGVAVSLGLGVLTMGVLLQGAKSRTMLSGKWLLTEAAFSLLAAVGYCTGIGVYLHVALQINSTDTCKTRERLYARKGLTWMDCQLAGTDGAAATFACLLVIMYGASVVLALRSYREQKRYKGSREQPGSYSDAPEYLWSGTL
"
variation 184
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="t"
/db_xref="dbSNP:376285378"
variation 187
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="g"
/db_xref="dbSNP:370821754"
variation 201
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="c"
/db_xref="dbSNP:373036309"
variation 228
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="t"
/db_xref="dbSNP:370366568"
variation 230
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="g"
/db_xref="dbSNP:374529307"
variation 255
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="g"
/db_xref="dbSNP:4788821"
variation 293
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="g"
/db_xref="dbSNP:76434914"
variation 305
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="g"
/db_xref="dbSNP:376026417"
variation 330
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="c"
/db_xref="dbSNP:201459139"
variation 339
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="g"
/db_xref="dbSNP:372441129"
variation 346
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="g"
/replace="t"
/db_xref="dbSNP:201434319"
variation 349
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="g"
/db_xref="dbSNP:61753635"
variation 384
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace=""
/replace="g"
/db_xref="dbSNP:35117580"
variation 435
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="t"
/db_xref="dbSNP:368013418"
variation 470
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="c"
/db_xref="dbSNP:11555794"
variation 490
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="g"
/db_xref="dbSNP:201373593"
exon 545..672
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/inference="alignment:Splign:1.39.8"
variation 545
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="t"
/db_xref="dbSNP:202067406"
variation 557
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="g"
/db_xref="dbSNP:149016402"
variation 565
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="g"
/db_xref="dbSNP:373378287"
variation 575
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:200818950"
variation 577
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="t"
/db_xref="dbSNP:146045891"
variation 625
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="g"
/db_xref="dbSNP:375223782"
variation 664
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="t"
/db_xref="dbSNP:199614023"
variation 669
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="t"
/db_xref="dbSNP:143759600"
exon 673..2248
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/inference="alignment:Splign:1.39.8"
variation 692
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="g"
/db_xref="dbSNP:375705658"
variation 700
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="t"
/db_xref="dbSNP:139665459"
variation 725
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="t"
/db_xref="dbSNP:117388624"
variation 749
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="t"
/db_xref="dbSNP:147595258"
variation 750
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="g"
/db_xref="dbSNP:369841189"
variation 773
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="t"
/db_xref="dbSNP:372495610"
variation 774
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="g"
/db_xref="dbSNP:111585833"
variation 777
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201509244"
variation 785
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="t"
/db_xref="dbSNP:72799852"
variation 796
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="g"
/db_xref="dbSNP:142054045"
variation 805
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="t"
/db_xref="dbSNP:376389459"
variation 809
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="t"
/db_xref="dbSNP:367694179"
variation 810
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200541338"
variation 834
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="g"
/db_xref="dbSNP:140602857"
variation 835
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:201544903"
variation 856
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="t"
/db_xref="dbSNP:371950282"
variation 887
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="t"
/db_xref="dbSNP:199750986"
variation 952
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="g"
/db_xref="dbSNP:199684141"
variation 990
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="g"
/db_xref="dbSNP:145897917"
variation 1046
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200660505"
variation 1070
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="c"
/db_xref="dbSNP:373575019"
variation 1087
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200552224"
variation 1088
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="g"
/db_xref="dbSNP:370061470"
variation 1112
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="t"
/db_xref="dbSNP:146595006"
variation 1146
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="g"
/db_xref="dbSNP:74425399"
variation 1178
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="g"
/db_xref="dbSNP:375582710"
variation 1179
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="g"
/db_xref="dbSNP:368492439"
variation 1191
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="g"
/db_xref="dbSNP:141358444"
variation 1224
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="t"
/db_xref="dbSNP:138854747"
variation 1227
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201839766"
variation 1256
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="g"
/db_xref="dbSNP:367583136"
variation 1261
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200621755"
variation 1262
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="g"
/db_xref="dbSNP:2303225"
variation 1286
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="g"
/db_xref="dbSNP:112608295"
variation 1294
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="g"
/replace="t"
/db_xref="dbSNP:371616837"
variation 1306
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="g"
/replace="t"
/db_xref="dbSNP:200707122"
variation 1319
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="g"
/replace="t"
/db_xref="dbSNP:79422919"
variation 1323
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="c"
/db_xref="dbSNP:200159769"
variation 1335
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="t"
/db_xref="dbSNP:13337162"
variation 1340
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="g"
/db_xref="dbSNP:74027272"
variation 1345
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="t"
/db_xref="dbSNP:193188432"
variation 1359
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="t"
/db_xref="dbSNP:372021599"
variation 1516
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="g"
/db_xref="dbSNP:8058188"
variation 1526
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="g"
/db_xref="dbSNP:182960094"
STS 1562..1785
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/standard_name="D8S2279"
/db_xref="UniSTS:473907"
variation 1593
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="g"
/db_xref="dbSNP:377086815"
variation 1610
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="c"
/db_xref="dbSNP:12927320"
STS 1697..1785
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/standard_name="D8S2279"
/db_xref="UniSTS:473907"
STS 1716..1826
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/standard_name="D10S275"
/db_xref="UniSTS:147992"
variation 1731
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="t"
/db_xref="dbSNP:111371379"
variation 1732
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="g"
/db_xref="dbSNP:139582245"
variation 1759
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="g"
/replace="t"
/db_xref="dbSNP:372937295"
variation 1820
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="g"
/db_xref="dbSNP:8058297"
variation 1865
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="t"
/db_xref="dbSNP:187330674"
variation 1904
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="t"
/db_xref="dbSNP:370661203"
variation 1931
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="t"
/db_xref="dbSNP:191783584"
variation 2003
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="t"
/db_xref="dbSNP:183625027"
variation 2024
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="t"
/db_xref="dbSNP:11555792"
variation 2027
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="a"
/replace="g"
/db_xref="dbSNP:186844947"
variation 2041
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="g"
/replace="t"
/db_xref="dbSNP:11555793"
variation 2237
/gene="MARVELD3"
/gene_synonym="MARVD3; MRVLDC3"
/replace="c"
/replace="t"
/db_xref="dbSNP:145662115"
ORIGIN
gggcttggccacctgcccaagaaacttgttggttgttgccctcaggtcgctcccgggcgcggacacggaacccggccatggaagatccgtcgggggctcgcgagccccgggcccggccgagagagcgggacccgggacggcgcccccacccagaccaaggccgcacccacgatcgaccgcgggaccgacccggggacccgcgcaggaagcgaagcagcgacgggaaccggcgaagggacggggaccgggacccggagagagaccaggagagggacgggaaccgcgaccggaaccgggaccgggagagggagagagagagggaaagagacccggaccgaggcccccgccgggacacacacagggacgcgggccctcgcgcaggtgaacacggagtttgggaaaaaccgcgccaaagccggacgcgggacggagcccggggactgacctgggacgcagccgcgcctcctgggcccgcgccctgggaagccccggagccgccgcagccgcagaggaagggagaccccgggcgccgcagacccgaaagtgaacccccttcggagagatatctgccctcgacccccaggcctggacgagaggaggtggaatattaccagtcagaggcggaaggactcctggaatgccacaaatgcaaatacttgtgcactgggagaggtgtggtgcagatagtggaggtggtcttgaatgggatggttctcatatgcatcgtggcctcctactttgtccttgccggattcagtgccagcttttccagcggcggtggctttgggaacaactactactcaccgttcgagggcactgagctagagcaggttcggcagctggaccagcagtacacgatcctccgctcgcccctgatatacggtggcgtggctgtttctctgggtctgggggtcctcaccatgggtgttttactccaaggagccaagagtcgaacaatgttgtcagggaagtggctcctcacggaggccgccttcagcctcctagcggcagtgggctactgcacaggcattggtgtttacctccacgtggctctgcagatcaatagcaccgacacttgcaaaacaagagagaggctctatgcccgcaagggtctcacctggatggactgccagctggcaggcaccgacggagcagcagccacctttgcttgtcttctcgtgatcatgtacggcgccagcgtggtgctggccctgcgtagctaccgagaacagaagcgctacaaaggcagccgagaacagcccggaagttacagtgatgcaccggaatatctgtggtctggaactctttgagatcttccggaacctaaatgtgaacgcacattgtttctctcaaaaagacaggtcttttaaaactccgcattagacaactatggttttcacacacttgactttataaatgctctctttggactgaggcaaagttaaagaattgaggacgggcatggtggctcatgcctgtaatcccagcactttgggaggctgaggtgggcggatcgcttgaggtcagcagattgagtccagcctggctcacatagcgaaaccctgtctctactaaaaatacaaaaaatcgccgggcatggtggctcacgcctgtaatcccagcactttaggaggccaaggcaggcagatcacctgaggtcaggtgtttgaaaccagtctggcaaacatggtgaaaccccatctctactaaaaatacaaaaattagctgggcgtggtggcaggcacctgtaattccagctactctggaggctgaggcaggagaatctcttaaacccgggaggcagaggttgcagtgagccaagaccattgcactccagcctgggcaacaagagcgagactccgtctcaaaaaaatacaaaaaatcatctgggcttggtggtgaacgcctgtaatcccagttactcaggaggctaaaccacaagaatcacttgaacctgggaggcagaggttgcagtgagcaaactccactccacgtcactgcactccagcctgggtaacagagcgaggctctgtctcaaaaacaacaactacaacaaaaaagataggacagtagattttattagaccctgaagcatactggaggctttttcatttctgcattccctgacagtgctccatagagtaggtcttcaaaggtagatagtaatctcattaccctggactgttctcataatgtaacagatcactaacactgaatcttaaaaataaagttcttttagtaattttaaaaaaaaaaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:91862 -> Biological process: GO:0045216 [cell-cell junction organization] evidence: IMP
GeneID:91862 -> Cellular component: GO:0005923 [tight junction] evidence: IDA
GeneID:91862 -> Cellular component: GO:0016021 [integral to membrane] evidence: IEA
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