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2025-05-09 18:58:31, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_020823 5397 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens transmembrane protein 181 (TMEM181), mRNA.
ACCESSION NM_020823 XM_376550 XM_941693
VERSION NM_020823.1 GI:153792041
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 5397)
AUTHORS Carette,J.E., Guimaraes,C.P., Varadarajan,M., Park,A.S.,
Wuethrich,I., Godarova,A., Kotecki,M., Cochran,B.H., Spooner,E.,
Ploegh,H.L. and Brummelkamp,T.R.
TITLE Haploid genetic screens in human cells identify host factors used
by pathogens
JOURNAL Science 326 (5957), 1231-1235 (2009)
PUBMED 19965467
REFERENCE 2 (bases 1 to 5397)
AUTHORS Wollscheid,B., Bausch-Fluck,D., Henderson,C., O'Brien,R., Bibel,M.,
Schiess,R., Aebersold,R. and Watts,J.D.
TITLE Mass-spectrometric identification and relative quantification of
N-linked cell surface glycoproteins
JOURNAL Nat. Biotechnol. 27 (4), 378-386 (2009)
PUBMED 19349973
REMARK Erratum:[Nat Biotechnol. 2009 Sep;27(9):864]
REFERENCE 3 (bases 1 to 5397)
AUTHORS Wistrand,M., Kall,L. and Sonnhammer,E.L.
TITLE A general model of G protein-coupled receptor sequences and its
application to detect remote homologs
JOURNAL Protein Sci. 15 (3), 509-521 (2006)
PUBMED 16452613
REFERENCE 4 (bases 1 to 5397)
AUTHORS Cheng,J., Kapranov,P., Drenkow,J., Dike,S., Brubaker,S., Patel,S.,
Long,J., Stern,D., Tammana,H., Helt,G., Sementchenko,V.,
Piccolboni,A., Bekiranov,S., Bailey,D.K., Ganesh,M., Ghosh,S.,
Bell,I., Gerhard,D.S. and Gingeras,T.R.
TITLE Transcriptional maps of 10 human chromosomes at 5-nucleotide
resolution
JOURNAL Science 308 (5725), 1149-1154 (2005)
PUBMED 15790807
REFERENCE 5 (bases 1 to 5397)
AUTHORS Mungall,A.J., Palmer,S.A., Sims,S.K., Edwards,C.A., Ashurst,J.L.,
Wilming,L., Jones,M.C., Horton,R., Hunt,S.E., Scott,C.E.,
Gilbert,J.G., Clamp,M.E., Bethel,G., Milne,S., Ainscough,R.,
Almeida,J.P., Ambrose,K.D., Andrews,T.D., Ashwell,R.I.,
Babbage,A.K., Bagguley,C.L., Bailey,J., Banerjee,R., Barker,D.J.,
Barlow,K.F., Bates,K., Beare,D.M., Beasley,H., Beasley,O.,
Bird,C.P., Blakey,S., Bray-Allen,S., Brook,J., Brown,A.J.,
Brown,J.Y., Burford,D.C., Burrill,W., Burton,J., Carder,C.,
Carter,N.P., Chapman,J.C., Clark,S.Y., Clark,G., Clee,C.M.,
Clegg,S., Cobley,V., Collier,R.E., Collins,J.E., Colman,L.K.,
Corby,N.R., Coville,G.J., Culley,K.M., Dhami,P., Davies,J.,
Dunn,M., Earthrowl,M.E., Ellington,A.E., Evans,K.A., Faulkner,L.,
Francis,M.D., Frankish,A., Frankland,J., French,L., Garner,P.,
Garnett,J., Ghori,M.J., Gilby,L.M., Gillson,C.J., Glithero,R.J.,
Grafham,D.V., Grant,M., Gribble,S., Griffiths,C., Griffiths,M.,
Hall,R., Halls,K.S., Hammond,S., Harley,J.L., Hart,E.A.,
Heath,P.D., Heathcott,R., Holmes,S.J., Howden,P.J., Howe,K.L.,
Howell,G.R., Huckle,E., Humphray,S.J., Humphries,M.D., Hunt,A.R.,
Johnson,C.M., Joy,A.A., Kay,M., Keenan,S.J., Kimberley,A.M.,
King,A., Laird,G.K., Langford,C., Lawlor,S., Leongamornlert,D.A.,
Leversha,M., Lloyd,C.R., Lloyd,D.M., Loveland,J.E., Lovell,J.,
Martin,S., Mashreghi-Mohammadi,M., Maslen,G.L., Matthews,L.,
McCann,O.T., McLaren,S.J., McLay,K., McMurray,A., Moore,M.J.,
Mullikin,J.C., Niblett,D., Nickerson,T., Novik,K.L., Oliver,K.,
Overton-Larty,E.K., Parker,A., Patel,R., Pearce,A.V., Peck,A.I.,
Phillimore,B., Phillips,S., Plumb,R.W., Porter,K.M., Ramsey,Y.,
Ranby,S.A., Rice,C.M., Ross,M.T., Searle,S.M., Sehra,H.K.,
Sheridan,E., Skuce,C.D., Smith,S., Smith,M., Spraggon,L.,
Squares,S.L., Steward,C.A., Sycamore,N., Tamlyn-Hall,G., Tester,J.,
Theaker,A.J., Thomas,D.W., Thorpe,A., Tracey,A., Tromans,A.,
Tubby,B., Wall,M., Wallis,J.M., West,A.P., White,S.S.,
Whitehead,S.L., Whittaker,H., Wild,A., Willey,D.J., Wilmer,T.E.,
Wood,J.M., Wray,P.W., Wyatt,J.C., Young,L., Younger,R.M.,
Bentley,D.R., Coulson,A., Durbin,R., Hubbard,T., Sulston,J.E.,
Dunham,I., Rogers,J. and Beck,S.
TITLE The DNA sequence and analysis of human chromosome 6
JOURNAL Nature 425 (6960), 805-811 (2003)
PUBMED 14574404
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
AB037844.1 and AL591025.8.
On or before Jul 26, 2007 this sequence version replaced
gi:113417757, gi:113418355.
Summary: The TMEM181 gene encodes a putative G protein-coupled
receptor expressed on the cell surface (Carette et al., 2009
[PubMed 19965467]; Wollscheid et al., 2009 [PubMed
19349973]).[supplied by OMIM, Jan 2010].
Sequence Note: This RefSeq record was created from transcript and
genomic sequence data because no single transcript matching the
reference genome 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 :: AB037844.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025081 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-2272 AB037844.1 3-2274
2273-5397 AL591025.8 108031-111155
FEATURES Location/Qualifiers
source 1..5397
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="6"
/map="6q25.3"
gene 1..5397
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/note="transmembrane protein 181"
/db_xref="GeneID:57583"
/db_xref="HGNC:20958"
/db_xref="MIM:613209"
exon 1..430
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/inference="alignment:Splign:1.39.8"
CDS 12..1850
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/note="G protein-coupled receptor 178"
/codon_start=1
/product="transmembrane protein 181"
/protein_id="NP_065874.1"
/db_xref="GI:153792042"
/db_xref="CCDS:CCDS43520.1"
/db_xref="GeneID:57583"
/db_xref="HGNC:20958"
/db_xref="MIM:613209"
/translation="
MGAAPSPTQASSRGGGPGPPAPTRAVSSSSRARGGALSALGPSPARPLTTSPAPAPPPRSRPARQQPDPQCWEKRGGAGGDTKGGAAGPGPGRLRGMDAEYPAFEPPLCSELKHLCRRLREAYRELKEDLTPFKDDRYYRLAPMRLYTLSKRHFVLVFVVFFICFGLTIFVGIRGPKVIQTSAANFSLNNSKKLKPIQILSNPLSTYNQQLWLTCVVELDQSKETSIKTSFPMTVKVDGVAQDGTTMYIHNKVHNRTRTLTCAGKCAEIIVAHLGYLNYTQYTVIVGFEHLKLPIKGMNFTWKTYNPAFSRLEIWFRFFFVVLTFIVTCLFAHSLRKFSMRDWGIEQKWMSVLLPLLLLYNDPFFPLSFLVNSWLPGMLDDLFQSMFLCALLLFWLCVYHGIRVQGERKCLTFYLPKFFIVGLLWLASVTLGIWQTVNELHDPMYQYRVDTGNFQGMKVFFMVVAAVYILYLLFLIVRACSELRHMPYVDLRLKFLTALTFVVLVISIAILYLRFGAQVLQDNFVAELSTHYQNSAEFLSFYGLLNFYLYTLAFVYSPSKNALYESQLKDNPAFSMLNDSDDDVIYGSDYEEMPLQNGQAIRAKYKEESDSD
"
misc_feature 468..530
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q9P2C4.2);
transmembrane region"
misc_feature 801..1694
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/note="Wnt-binding factor required for Wnt secretion;
Region: MIG-14_Wnt-bd; pfam06664"
/db_xref="CDD:191577"
misc_feature 813..875
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q9P2C4.2);
transmembrane region"
misc_feature 945..1007
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q9P2C4.2);
transmembrane region"
misc_feature 1062..1124
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q9P2C4.2);
transmembrane region"
misc_feature 1155..1217
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q9P2C4.2);
transmembrane region"
misc_feature 1248..1310
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q9P2C4.2);
transmembrane region"
misc_feature 1380..1442
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q9P2C4.2);
transmembrane region"
misc_feature 1488..1550
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q9P2C4.2);
transmembrane region"
misc_feature 1623..1685
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q9P2C4.2);
transmembrane region"
misc_feature 1749..1751
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(Q9P2C4.2); phosphorylation site"
variation 75
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:189350156"
variation 96
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:373189136"
variation 100
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="c"
/db_xref="dbSNP:113634273"
variation 189
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:377412402"
variation 246
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:199707996"
variation 297
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:200591589"
variation 306
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:375585407"
variation 315
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="c"
/db_xref="dbSNP:201958009"
exon 431..534
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/inference="alignment:Splign:1.39.8"
variation 432
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="g"
/db_xref="dbSNP:368007038"
variation 436
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:371659971"
variation 464
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:149757220"
variation 479
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:367777102"
variation 486
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:146748290"
variation 492
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="g"
/replace="t"
/db_xref="dbSNP:201003165"
variation 497
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:140357617"
variation 515
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="c"
/db_xref="dbSNP:6926561"
exon 535..590
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/inference="alignment:Splign:1.39.8"
variation 538
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:35044164"
variation 559
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:146210447"
variation 566
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:137908897"
exon 591..681
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/inference="alignment:Splign:1.39.8"
variation 594
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:376234781"
variation 656
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:370374691"
exon 682..803
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/inference="alignment:Splign:1.39.8"
variation 685
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="c"
/db_xref="dbSNP:372779214"
variation 719
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="c"
/db_xref="dbSNP:41266341"
variation 732
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="g"
/db_xref="dbSNP:369652765"
variation 744
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:371922418"
variation 745
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="g"
/db_xref="dbSNP:199898880"
variation 749
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:376062690"
variation 777
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:145714004"
variation 794
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:202188884"
exon 804..914
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/inference="alignment:Splign:1.39.8"
variation 805
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="c"
/db_xref="dbSNP:370699533"
variation 812
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:143737957"
variation 848
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:373212277"
variation 857
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:201786380"
variation 888
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:377172594"
exon 915..995
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/inference="alignment:Splign:1.39.8"
variation 922
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:199963911"
variation 943
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:200307986"
variation 995
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:16900870"
exon 996..1095
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/inference="alignment:Splign:1.39.8"
variation 1017
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:199672326"
exon 1096..1226
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/inference="alignment:Splign:1.39.8"
variation 1155
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:375780117"
variation 1179
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:368999298"
variation 1188
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:372625737"
variation 1211
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:375358191"
variation 1218
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:117665206"
variation 1219
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:201228986"
variation 1222
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:373615885"
exon 1227..1318
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/inference="alignment:Splign:1.39.8"
variation 1234
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="g"
/replace="t"
/db_xref="dbSNP:139585306"
variation 1270
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:202196627"
exon 1319..1376
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/inference="alignment:Splign:1.39.8"
variation 1325
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:371995265"
variation 1354
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:375221837"
variation 1357
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:368115901"
variation 1363
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:371313932"
variation 1365
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:188259608"
variation 1368
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="t"
/db_xref="dbSNP:374825278"
exon 1377..1479
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/inference="alignment:Splign:1.39.8"
variation 1389
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="g"
/replace="t"
/db_xref="dbSNP:201875244"
variation 1408
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:369643226"
variation 1421
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:373726849"
variation 1448
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:189597784"
exon 1480..1531
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/inference="alignment:Splign:1.39.8"
variation 1514
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:377410212"
variation 1515
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:371179534"
exon 1532..1614
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/inference="alignment:Splign:1.39.8"
variation 1535
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:187514314"
variation 1536
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:372660843"
variation 1541
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:200561894"
variation 1561
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:375809123"
variation 1562
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:370162407"
variation 1607
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:371977391"
exon 1615..1704
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/inference="alignment:Splign:1.39.8"
variation 1616
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:199504572"
variation 1641
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="c"
/db_xref="dbSNP:371624907"
variation 1654
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:200662769"
variation 1663
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:374166832"
variation 1666
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:376231183"
variation 1683
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:370364023"
variation 1685
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:145210472"
exon 1705..1771
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/inference="alignment:Splign:1.39.8"
variation 1750
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="c"
/db_xref="dbSNP:201415597"
variation 1758
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:200013277"
exon 1772..5397
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/inference="alignment:Splign:1.39.8"
variation 1777
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="c"
/db_xref="dbSNP:201627006"
variation 1792
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:185734564"
variation 1793
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:374121310"
variation 1816
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:190592782"
variation 1822
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="c"
/db_xref="dbSNP:201122405"
variation 1832
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:113530638"
variation 1855
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="g"
/db_xref="dbSNP:189102191"
variation 1868
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:200433730"
variation 1873
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:376138263"
variation 1897
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:370691973"
variation 2105
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:144567368"
variation 2273
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:3734472"
variation 2396
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:34023783"
variation 2412
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:148450060"
variation 2499
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace=""
/replace="g"
/db_xref="dbSNP:368992499"
variation 2507
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:193145058"
variation 2602
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="c"
/db_xref="dbSNP:370770310"
variation 2646
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:182733607"
variation 2699
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:186918241"
variation 2700
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:142895749"
STS 2810..2838
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/standard_name="D3S1674"
/db_xref="UniSTS:148451"
variation 2864
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="g"
/replace="t"
/db_xref="dbSNP:375394154"
variation 2926
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:373271706"
variation 3057
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:73016232"
variation 3105
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace=""
/replace="a"
/db_xref="dbSNP:142870502"
variation 3191
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:75508037"
variation 3240
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:191658026"
variation 3297
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:140774869"
variation 3307
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:144620981"
variation 3331
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:184254063"
variation 3350
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:111558708"
variation 3357
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:11543368"
variation 3375
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:188882238"
variation 3416
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="c"
/db_xref="dbSNP:147869095"
variation 3438
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:75157333"
variation 3449
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="g"
/db_xref="dbSNP:192190578"
variation 3464
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:374887737"
variation 3470
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:367785548"
variation 3547
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:185330620"
variation 3561..3562
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace=""
/replace="gt"
/db_xref="dbSNP:60360053"
variation 3562..3563
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace=""
/replace="gt"
/db_xref="dbSNP:376707444"
variation 3673
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:55748809"
variation 3701
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:190626470"
variation 3702
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="t"
/db_xref="dbSNP:182230045"
variation 3720
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:114916045"
variation 3752
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:3199558"
variation 3764
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace=""
/replace="g"
/db_xref="dbSNP:200651708"
variation 3791..3793
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace=""
/replace="aat"
/db_xref="dbSNP:371183793"
variation 3822
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:77608006"
variation 3833
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:150478439"
variation 3857
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="t"
/db_xref="dbSNP:184413954"
variation 4004
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:145366725"
variation 4008
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="t"
/db_xref="dbSNP:11543927"
variation 4049
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="c"
/db_xref="dbSNP:188222183"
variation 4079
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:376943436"
variation 4124..4125
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace=""
/replace="agtt"
/db_xref="dbSNP:66520149"
variation 4125
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace=""
/replace="gtt"
/db_xref="dbSNP:375778443"
variation 4130
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace=""
/replace="ctaa"
/db_xref="dbSNP:67738343"
variation 4190
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="g"
/replace="t"
/db_xref="dbSNP:1136284"
variation 4212
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:3199561"
variation 4269
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:181098822"
variation 4299
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:185490085"
variation 4334
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:190350171"
variation 4353
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="c"
/db_xref="dbSNP:143517935"
variation 4388..4389
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace=""
/replace="tt"
/db_xref="dbSNP:368761683"
variation 4445
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:372409002"
STS 4469..4597
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/standard_name="RH46845"
/db_xref="UniSTS:62402"
STS 4469..4592
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/standard_name="G59555"
/db_xref="UniSTS:136859"
variation 4489
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:137939476"
variation 4531
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="g"
/replace="t"
/db_xref="dbSNP:142429743"
variation 4571
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:1842"
variation 4733
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:373996388"
variation 4815
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:181819178"
variation 4860
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:14759"
variation 4884
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:41267047"
variation 4913
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="c"
/db_xref="dbSNP:113987879"
variation 4962
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:192211409"
variation 4967
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:8036"
variation 4978
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="g"
/replace="t"
/db_xref="dbSNP:144614116"
variation 4991
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:78044784"
variation 5071
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="g"
/replace="t"
/db_xref="dbSNP:183935134"
variation 5134
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="c"
/replace="t"
/db_xref="dbSNP:375982260"
STS 5202..5364
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/standard_name="HUM000S407"
/db_xref="UniSTS:76397"
STS 5205..5335
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/standard_name="RH12655"
/db_xref="UniSTS:67349"
variation 5217
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:370670348"
variation 5221
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="g"
/replace="t"
/db_xref="dbSNP:186672191"
STS 5269..5375
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/standard_name="SHGC-31686"
/db_xref="UniSTS:20442"
variation 5334
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
/replace="a"
/replace="g"
/db_xref="dbSNP:138521207"
polyA_signal 5373..5378
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
polyA_site 5391
/gene="TMEM181"
/gene_synonym="GPR178; KIAA1423"
ORIGIN
cgcggaggcggatgggcgcggctccctcccccactcaggcctcttcacggggcggggggccgggtcccccagcccccacccgcgccgtgtccagctcctcgcgtgctcgcggcggagccctgagcgcactgggtccgagtcctgcgcgccccctcaccacctcccccgcacctgctcctcctcctcggtcccgcccagcgcgccagcagcccgatccccagtgctgggagaagagagggggcgcaggcggcgacacaaagggtggagcggcgggaccgggacccgggaggctgcgcggcatggacgccgagtaccctgcctttgagcccccgctctgcagcgagctcaagcacctgtgccggcggctgcgggaagcgtaccgcgagctcaaggaggacctcacgcccttcaaggatgaccgctactacaggctggcgcccatgcggctctacacgctctccaagcgccactttgtcctcgtgtttgtcgtcttcttcatctgctttggcctgaccatcttcgttgggatcagaggacctaaagtgatccagacttctgcggctaatttttcactaaataatagcaaaaagctaaagccaattcaaatactttcaaatccactgtctacatacaatcagcaactatggctgacatgtgttgttgagttggatcaatcaaaagaaacttctattaagacaagctttcccatgactgttaaagtcgatggtgtagctcaagatggaaccacgatgtacattcataacaaagttcacaaccggacaaggaccctcacatgtgcagggaaatgtgcggagattattgtggctcaccttggctacctgaactacactcagtatacagtgatagtgggatttgaacacctgaagctccccatcaagggaatgaacttcacatggaagacttataaccctgccttctcccggttggaaatctggttccggtttttctttgtggtgctcaccttcatcgtcacttgcctgtttgcgcattccctccggaaattttccatgagagactggggcatcgagcagaagtggatgtctgttctcctgcctctgctgctactttacaatgatccgttcttccccctctccttcctggtcaacagctggctcccagggatgctggatgacctctttcagtccatgttcctgtgcgccctgctgctcttctggctgtgcgtgtaccacgggattcgtgtccagggagaaagaaagtgtttaactttctatttgcctaaattcttcattgttggactattgtggttggcttctgttacgctaggaatatggcaaacagttaacgaattacatgatccaatgtaccagtatcgagttgataccggaaattttcagggaatgaaggtcttcttcatggtggtggcagcggtgtacattctgtacctcttgttcttgatagtgcgggcgtgttccgagctacgtcacatgccttatgtggatctcaggttgaaatttttgactgcattgactttcgtagtacttgtcattagcatcgccatcctttatttgagatttggggcgcaagtactacaagacaattttgtagcagagctgtcaactcactaccagaattcagccgagttcttatctttctatggcctgttgaacttctatctctacaccttggcctttgtatattctccatcgaagaatgccctctatgagtcccagctgaaagacaatcctgccttctccatgctgaatgactcggatgatgatgtgatttatgggagtgactatgaggaaatgccgctgcagaacggccaggccatccgggccaagtacaaggaggagtcagatagtgactgagccccggccagcccagcgaggcgacaagatgcctggatgctttccccggtgaccgtctgctgaccttcccctgttatattcagatttttcttacaagcagagatttcctgttcatttgtttacatatttttttaaaggaaaaccaaaactgagggtaaatttaaatgtttagccaaatttattgtcatggtggctacgagaagaggcattgataacaagtttcaacagccaaatccttttttacagagatttcagatgagcgtgttttcagtgatgaggaaatttcacgtttttagtacagtgaattatgtacttttttttcctgtaatcattcactgattccaagttcacgggcagcctgtgactaggtcctcagcgtgacagcatcaccctctttcttcccttttccatggtactgttttgtgaccctttaaactcaaagggaagccttatctgtggctgcttcagggcagtccttcctcgttgagtggccagtgccctgggtaaccaggtggctgaagtgattggtcagttatgtggactgcgttttgtgcagtgtgtgagttatgactcatcgggaatgggagatgctggggttccaacccttcacgtcaccaaaggggaagtaatagtgtggagttctgaggagggtttgataagttgaataaggaaaggctaagataatttacaggttaccaactcatgtggggaaggtcttactgccatggtgcttttcaggggcctgtgtgtacacacatgattaaatggatttgcctgtgggaggtatgggcaggagaggaacccttaccattccagtaaatagcagtttctgcaattctgttgaatatgaaatgccatagagctttatttatttatgtaagtaaaagctaaatgaggggccaggtgcagtggctcacatctgtaatctcaacactttgggaggccaaggtgggaggatcacttgagcccaggagtttgagaccagcctgggcaacacagggagaccccgtctctataaaacatttagaaagttggctgggcatgctggggcatgcccatagtcccagctactcaggaggctgaggtgggaggattgcttgagccctggaggtcaaggctgcagtgagccatgattgcaccactgcactccagcctgggtgtcagagcgagaacccgtgtcataaataaataaagctacatgaaagattgatagaatattttagattatttattggccaaaagtttttaaaactcatatttggaagcaaaatgaaaagcaagtaaaatgttttaaatggttcatggaaaacgtatttgggtagaaggcaactcgtgcttccggaaggggttccctgtcctccatgtgtccacatggcggtcaggtagggacgacctgttctgtaaagtccttggcactgctgaatctgtggcatcatagaaggccctggagcttccccgttcctttcagtcagggactccatatagagtctcatgtggacgtctcccgtgctttcctcttgacctctacagtcacacttctgttaacatctggtaactgtgggcaacctgactgatgccgtcttggcaattgaggtccagaagatgatagttccgcaacgcaagcagtacctactttttttcttcatctatgcattgactctcagattaccatgcagagcttcacgttatcatccacgttaagtagtgctaggtaggaccttagagatgttcatgagaaactatttgttatgactttcctttgtatctttccttttaatttaaactttaatgataatgtacttttaatatggattctattcacatttgttttaaaaaccttgtaaatatgaatgtttaagacaacttactgcaagggtaattcaagtttacatgatttttaaatttgcaatgatgttttttttattctgtgtattgaaaaaaattttctgttaccaaattttacaacttctaataagactactataactttatgtaaactgatgaagatgtgctgattaacatattctgtgatatggtttacaacttttaatcataattgtccatgattttggaatgctgttatttatcagtaaatgtaaaatatttgaggcatttagccatacacacactagaactttttaaaactttgtcctatagtgtaattataaactgatgactattatcttcatacattgagtcttcatgcatcaatgaaatgaaaaatataggattatttatttactttttgtaactaagtgggaaataagaaaaaaagttagaaagtacttaaggggaaaatcgttcttactaagtcatgtattttcaacttgtcttccctggtatatcataaataccgacatattacataccccatgtaaaattttgcttaaactctctagcacttggcatgtagaatatgtaccataggtatcaggttaaaacactaaagtctgccagaaacttttgacagtagcaagaaaattgttgaagaaaaaataaattatttactgagggtagttatgttaaagttttgcgaacttaaagggctgactttagttccttcatggtaatggcttgagtaacatcatctttgggattttttaaatactggtccagtctaggagaacctggaagatgaccagaggtatttcagtttccctagggagagcttcgttatccatgtggatgataagtctgcttgatttattattaaatcattatagcagtgaagtggtgccattttctctctcttaagccccatttgaaaggctagagaaggggatatatatactatgttcaaggtttgtaaggttgttaatgtacataattgcagattgcaataaaagcttagatacattttgtaaacccaacccactaaatgagcaggttacaagacaaatgtcaccagcctcaagtattttatgaactatttactgagggtagttatgttaaatagattataatgtggtaaattatttcctgaatcctttatcacaggaaaaacacagaccctcataaaagggataattaaaacggatgtgtctgaacatttagtgaagatgagacttaaaacatgaaagtgtatttgtgtattttgagggttttagaaaccggttgccttagaggttagacttttgaagaaaaaaaaaaaaagatacagatcttttcccctggccaaagggaagttgtattagtctgtgacatcttgtgatgctgtttatcttggtttgacattggagatacgctagtaactgtgataccatactataaaacagaagaattttctgctactaaaaactgcctttttacaaaatgactgtaaatatttgtaaaataaaataacactaaactttaagcccaaaaggagagatagagccatgtgttcagttgtggacctgtccgtggggcacagtgccaccccatcacagtgttgctgtcatcaggcaaaagtgaatgtttgtttatggcaaattcgtcttttgcgaatggcttaattctgacactacctttctgggaaatgttaataaatttttaatattcacttcta
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:57583 -> Molecular function: GO:0015643 [toxic substance binding] evidence: IDA
GeneID:57583 -> Biological process: GO:0009405 [pathogenesis] evidence: IMP
GeneID:57583 -> Cellular component: GO:0016021 [integral to membrane] evidence: IEA
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