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2024-03-29 15:47:48, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_144632               3588 bp    mRNA    linear   PRI 15-JUN-2013
DEFINITION  Homo sapiens transmembrane protein 182 (TMEM182), mRNA.
ACCESSION   NM_144632
VERSION     NM_144632.3  GI:188528657
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 3588)
  AUTHORS   Lauc,G., Huffman,J.E., Pucic,M., Zgaga,L., Adamczyk,B., Muzinic,A.,
            Novokmet,M., Polasek,O., Gornik,O., Kristic,J., Keser,T.,
            Vitart,V., Scheijen,B., Uh,H.W., Molokhia,M., Patrick,A.L.,
            McKeigue,P., Kolcic,I., Lukic,I.K., Swann,O., van Leeuwen,F.N.,
            Ruhaak,L.R., Houwing-Duistermaat,J.J., Slagboom,P.E., Beekman,M.,
            de Craen,A.J., Deelder,A.M., Zeng,Q., Wang,W., Hastie,N.D.,
            Gyllensten,U., Wilson,J.F., Wuhrer,M., Wright,A.F., Rudd,P.M.,
            Hayward,C., Aulchenko,Y., Campbell,H. and Rudan,I.
  TITLE     Loci associated with N-glycosylation of human immunoglobulin G show
            pleiotropy with autoimmune diseases and haematological cancers
  JOURNAL   PLoS Genet. 9 (1), E1003225 (2013)
   PUBMED   23382691
REFERENCE   2  (bases 1 to 3588)
  AUTHORS   Clark,H.F., Gurney,A.L., Abaya,E., Baker,K., Baldwin,D., Brush,J.,
            Chen,J., Chow,B., Chui,C., Crowley,C., Currell,B., Deuel,B.,
            Dowd,P., Eaton,D., Foster,J., Grimaldi,C., Gu,Q., Hass,P.E.,
            Heldens,S., Huang,A., Kim,H.S., Klimowski,L., Jin,Y., Johnson,S.,
            Lee,J., Lewis,L., Liao,D., Mark,M., Robbie,E., Sanchez,C.,
            Schoenfeld,J., Seshagiri,S., Simmons,L., Singh,J., Smith,V.,
            Stinson,J., Vagts,A., Vandlen,R., Watanabe,C., Wieand,D., Woods,K.,
            Xie,M.H., Yansura,D., Yi,S., Yu,G., Yuan,J., Zhang,M., Zhang,Z.,
            Goddard,A., Wood,W.I., Godowski,P. and Gray,A.
  TITLE     The secreted protein discovery initiative (SPDI), a large-scale
            effort to identify novel human secreted and transmembrane proteins:
            a bioinformatics assessment
  JOURNAL   Genome Res. 13 (10), 2265-2270 (2003)
   PUBMED   12975309
  REMARK    Erratum:[Genome Res. 2003 Dec;13(12):2759]
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            AY358262.1 and AC007251.4.
            On May 17, 2008 this sequence version replaced gi:40255064.
            
            Sequence Note: This RefSeq record was created from transcript and
            genomic sequence data because no single transcript was available
            for the full length of the gene. The extent of this transcript is
            supported by transcript alignments.
            
            ##Evidence-Data-START##
            Transcript exon combination :: CR936735.1, AK129862.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025083, ERS025084 [ECO:0000348]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-853               AY358262.1         99-951
            854-3588            AC007251.4         84870-87604
FEATURES             Location/Qualifiers
     source          1..3588
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="2"
                     /map="2q12.1"
     gene            1..3588
                     /gene="TMEM182"
                     /note="transmembrane protein 182"
                     /db_xref="GeneID:130827"
                     /db_xref="HGNC:26391"
     exon            1..319
                     /gene="TMEM182"
                     /inference="alignment:Splign:1.39.8"
     variation       10
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:118026982"
     variation       17
                     /gene="TMEM182"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:115087473"
     variation       18
                     /gene="TMEM182"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:111261034"
     STS             53..1165
                     /gene="TMEM182"
                     /db_xref="UniSTS:494500"
     variation       71
                     /gene="TMEM182"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:2732839"
     variation       93
                     /gene="TMEM182"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:5833037"
     variation       149
                     /gene="TMEM182"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:185595389"
     misc_feature    164..166
                     /gene="TMEM182"
                     /note="upstream in-frame stop codon"
     CDS             188..877
                     /gene="TMEM182"
                     /codon_start=1
                     /product="transmembrane protein 182 precursor"
                     /protein_id="NP_653233.3"
                     /db_xref="GI:188528658"
                     /db_xref="CCDS:CCDS2064.1"
                     /db_xref="GeneID:130827"
                     /db_xref="HGNC:26391"
                     /translation="
MRLNIAIFFGALFGALGVLLFLVAFGSDYWLLATEVGRCSGEKNIENVTFHHEGFFWRCWFNGIVEENDSNIWKFWYTNQPPSKNCTHAYLSPYPFMRGEHNSTSYDSAVIYRGFWAVLMLLGVVAVVIASFLIICAAPFASHFLYKAGGGSYIAAGILFSLVVMLYVIWVQAVADMESYRNMKMKDCLDFTPSVLYGWSFFLAPAGIFFSLLAGLLFLVVGWHIQIHH
"
     sig_peptide     188..265
                     /gene="TMEM182"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="Potential; propagated from UniProtKB/Swiss-Prot
                     (Q6ZP80.2)"
     mat_peptide     266..874
                     /gene="TMEM182"
                     /product="Transmembrane protein 182"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q6ZP80.2)"
     misc_feature    266..847
                     /gene="TMEM182"
                     /note="PMP-22/EMP/MP20/Claudin tight junction; Region:
                     Claudin_2; pfam13903"
                     /db_xref="CDD:206074"
     misc_feature    530..592
                     /gene="TMEM182"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q6ZP80.2);
                     transmembrane region"
     misc_feature    647..709
                     /gene="TMEM182"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q6ZP80.2);
                     transmembrane region"
     misc_feature    788..850
                     /gene="TMEM182"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q6ZP80.2);
                     transmembrane region"
     variation       203
                     /gene="TMEM182"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:145943993"
     variation       208
                     /gene="TMEM182"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:141575902"
     variation       241
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139384397"
     variation       256
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368685589"
     variation       268
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147702904"
     variation       278
                     /gene="TMEM182"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200405126"
     exon            320..419
                     /gene="TMEM182"
                     /inference="alignment:Splign:1.39.8"
     variation       329
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370445639"
     variation       332
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200283037"
     variation       363
                     /gene="TMEM182"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201534618"
     variation       368
                     /gene="TMEM182"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144693740"
     variation       418
                     /gene="TMEM182"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148918467"
     exon            420..518
                     /gene="TMEM182"
                     /inference="alignment:Splign:1.39.8"
     variation       432
                     /gene="TMEM182"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376506997"
     variation       433
                     /gene="TMEM182"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:369237390"
     variation       466
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:79354230"
     variation       485
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:137985902"
     variation       495
                     /gene="TMEM182"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377199521"
     exon            519..656
                     /gene="TMEM182"
                     /inference="alignment:Splign:1.39.8"
     variation       524
                     /gene="TMEM182"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199691513"
     variation       525
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376008407"
     variation       532
                     /gene="TMEM182"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369312176"
     variation       556
                     /gene="TMEM182"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:373489178"
     variation       575
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:114571302"
     variation       607
                     /gene="TMEM182"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140175654"
     variation       651
                     /gene="TMEM182"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:147305207"
     exon            657..3588
                     /gene="TMEM182"
                     /inference="alignment:Splign:1.39.8"
     variation       671
                     /gene="TMEM182"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:115991670"
     variation       683
                     /gene="TMEM182"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200341477"
     variation       703
                     /gene="TMEM182"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:189839305"
     variation       716
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374072656"
     variation       729
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199665908"
     variation       754
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369032228"
     variation       811
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144729903"
     variation       844
                     /gene="TMEM182"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:114369090"
     variation       854
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:887987"
     variation       925
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368028024"
     variation       964
                     /gene="TMEM182"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:112070535"
     variation       1033
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:113860378"
     variation       1055
                     /gene="TMEM182"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146311996"
     variation       1158
                     /gene="TMEM182"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:112432276"
     variation       1160
                     /gene="TMEM182"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:148527685"
     variation       1249..1250
                     /gene="TMEM182"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:377063389"
     variation       1377
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:79127541"
     variation       1453
                     /gene="TMEM182"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:142881486"
     variation       1516
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:151186061"
     variation       1582
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140305419"
     variation       1616
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370851484"
     variation       1663
                     /gene="TMEM182"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:187080616"
     variation       1664
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370654099"
     variation       1718
                     /gene="TMEM182"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:368850580"
     variation       1768
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:878802"
     variation       1787
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2732822"
     variation       1804
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145270982"
     variation       1813
                     /gene="TMEM182"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:189530221"
     variation       1859
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:111896953"
     variation       1882
                     /gene="TMEM182"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:112687821"
     variation       1948
                     /gene="TMEM182"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:180810596"
     variation       2076
                     /gene="TMEM182"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:185418708"
     variation       2100
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:367806688"
     variation       2175
                     /gene="TMEM182"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:10201334"
     variation       2237
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:4476374"
     variation       2259
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371556407"
     STS             2261..2372
                     /gene="TMEM182"
                     /standard_name="D2S1551E"
                     /db_xref="UniSTS:150636"
     variation       2367
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:190229516"
     variation       2381
                     /gene="TMEM182"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:147640501"
     variation       2390
                     /gene="TMEM182"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:181432006"
     variation       2393
                     /gene="TMEM182"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:186594943"
     variation       2419..2420
                     /gene="TMEM182"
                     /replace=""
                     /replace="aat"
                     /db_xref="dbSNP:367982014"
     variation       2420..2421
                     /gene="TMEM182"
                     /replace=""
                     /replace="aat"
                     /db_xref="dbSNP:72378965"
     variation       2422..2423
                     /gene="TMEM182"
                     /replace=""
                     /replace="taa"
                     /replace="taataa"
                     /db_xref="dbSNP:72301570"
     variation       2429..2430
                     /gene="TMEM182"
                     /replace=""
                     /replace="aataat"
                     /replace="ataata"
                     /db_xref="dbSNP:10661746"
     variation       2430..2431
                     /gene="TMEM182"
                     /replace=""
                     /replace="ataata"
                     /db_xref="dbSNP:34075213"
     variation       2449..2450
                     /gene="TMEM182"
                     /replace=""
                     /replace="taataa"
                     /db_xref="dbSNP:71989508"
     variation       2485
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:191382079"
     variation       2515
                     /gene="TMEM182"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:183748203"
     variation       2634
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142310271"
     variation       2652
                     /gene="TMEM182"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:113531244"
     variation       2742
                     /gene="TMEM182"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:6752950"
     variation       2783
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:79663120"
     variation       2793
                     /gene="TMEM182"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:111739828"
     variation       2847
                     /gene="TMEM182"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:188630784"
     variation       2965
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:191017848"
     variation       2968
                     /gene="TMEM182"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:10204500"
     variation       2984
                     /gene="TMEM182"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:111540340"
     STS             2986..3137
                     /gene="TMEM182"
                     /standard_name="RH94134"
                     /db_xref="UniSTS:91767"
     variation       3037
                     /gene="TMEM182"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367658201"
     variation       3074
                     /gene="TMEM182"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:2540321"
     variation       3329
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:116709911"
     variation       3436
                     /gene="TMEM182"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369173661"
     variation       3459
                     /gene="TMEM182"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:370136386"
ORIGIN      
gaatctgccggtggggcgtgagcgagaagccaccaaaacatgagctaggacagccttctcaagaagattctgccaactcaaaaatattattcttttttttttttttttgctgttgtttctgagaaactaggtgtcttaccattttaaaatttcatattttatttaaaaggaaaccagtgaattgaaaatgagactaaatatcgctatcttctttggagctctctttggtgctttgggggtgttactctttttggtggcttttggatcggattattggcttcttgcaactgaagtggggagatgttcaggtgaaaagaatatagagaacgtcacttttcaccatgaagggttcttctggaggtgttggtttaatgggattgtggaagagaatgactccaatatttggaagttctggtacaccaatcagccaccgtccaagaactgcacacatgcttacctgtctccgtaccccttcatgagaggcgagcacaactcgacctcctatgactctgcagttatttaccgtggtttctgggcagtcctgatgctcctgggggtagttgctgtagtcatcgcaagctttttgatcatctgtgcagcccccttcgccagccattttctctacaaagctgggggaggctcatatattgctgcaggcatcctattttcattggtggtgatgctgtatgtcatctgggtccaggcagtggctgacatggaaagctaccgaaacatgaaaatgaaggactgcctggatttcaccccttctgttctgtatggctggtcatttttcctggccccagctgggatatttttttctttgctagctggattactatttctggttgttggatggcatattcagatacatcactaaatcaactgttgccacaagtattttcttgagagattttaaaacaaggaatactttttttccattttgtttcattgatcccagcataaagttagtagatataactttttagttgctattcaaattaatcattttactaaaattttcttcagtaagaaggtcctagaatctctccagacaccagcaagcctctatcttgtctaagtgctgtcaaggacctagttctttagggaataggtaaacaggtctccctttcattgaacatgttagagttcatgcaggtcgcaaaggcctgataatagcttaataccatgacatggggaaaatctcgatagatttggcttaaagtctccttggcattcacttctgctaattaaaaaaaatccttgaagaataattaagaatgggcaaggttgtcagagaatttattttgtttcttgcccacacagataatatccacatacacattcactggctcttgtgagcaaatgaatttaaaaatagacagcagttgttctaattagtgggagccatgtactcaccagttaaaatgggccacaacaaacaagactgagagcatgtacttatcttgctttttcaccaacagtggtttggttacctagttttattcacttaattgtgcatgcttacataaactttaaactacatttaaaactagcaaatctgcataccaaattatgtataacgtagattgaatttttatgaacttaaagtgagttaattgtataatgtaatattgtttaaaatatgtaaaaaccaagcatttccgcttggtccataattctatttgatattttaaaattctcatttaaaaattatattgctatcattcagcatgtgaaaatttattgataaaatgtgattttaatattttttagatataaactttcaacgtacttccatatgaggattataatagccctgctttattaaagaccataaaatattaactttccccaagatgttatgggttccagttcttctgatcatttgattcctttaattactgtccctcaatttcttcatctttacaatagatatattaacatttacagatcgactatttcctttaacctcctagaagaaagtttttgtggggaaagatgattctgtattattcagtagcatagacattttgcatatcaaagatgttcatttggcactaatgttgattgaaatcaaatccatctgagatgcctagctcgtatttgcattctggaagcctccatcgcaggggagctcggcagggtatgtgagctttgttggaggtgcggtgtttcattctgcagctgttgtgaggacagagaggcatggcccacaggcaaaaaaagtcaccacccagaagatgctctgggatagaggaactgctccttttcatcagctcttccaatgccgtgggagaggtgatcccagtcttctctgtacatcttgtgcttttccattaagacttgttccagtgggaaggagctttggaaaaattgcaaaggtctgaatcttcagggcattttcatgacaggacttgccaataataataataataataataataataataataataaagctccagaggcctaactggtttctcaagtcatttcagtgatatcattgaaacgtttttgtggtacttccctttgtctttcactgtttcatttttatattgcttcatttacttctttgcttttggctttgttattagaaaaaataattatgaggtctgttgtgcatgttgactgtgatattaagttatggcatgccattaagttttccagacgatgttggatgtatctgattagttcatgtcatctgtaaatacaattcttttttgtagtactttggaatggagcctttttctggtgtactgtatgccatttaagtttcacatacaagctgctttcggcaaaggcttgaatatttataaatttcagatggttatcctcactttatagtacacttaagtggctaccatatattttttatatgacaattggctgaatagctgatgtgtatgacacttttacacagatttgcactttggaactattttatagttgtaatgcatcaatcaaatacatttcaagcacatttcttgatcaatttaccagcaaccctctgaaggaatgaaggagagttgtgattgctatgtcaatgagtgaaatatacttaaaaatggcagagttatatagtacattattgtagcaaccttatatctgatttgagatactgtgttgccaaatgtccatgttatgtttatttctctattggttgtatttattaatttttagaagcctttaaactgtgttagaatctttttgaaaaatgttgattttgcatcataaagtttcaatttatcaaggatatcttttcagttacacttttagaaagagtgaataaaaagggcagtgagttatgctcttggacttggtgaaagctatcatctctccatattgtatttgttcagctggtttaattcactcaggtggatgattgcacatacattggaattggctggagagactacacagagaagtttaatgatcgtgtacaatttgagggttgatggtagggctttctaaaaaaagtaatatcaagtgtgttgttagtattcatttagtcatttttattactaatctataaatatatttattaaatttgaagattaaatggaattataaaggaatatattggaggaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:130827 -> Cellular component: GO:0016021 [integral to membrane] evidence: IEA

by @meso_cacase at DBCLS
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