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2024-04-26 01:10:00, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_004271                895 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens lymphocyte antigen 86 (LY86), mRNA.
ACCESSION   NM_004271
VERSION     NM_004271.3  GI:55775471
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 895)
  AUTHORS   Ohto,U., Miyake,K. and Shimizu,T.
  TITLE     Crystal structures of mouse and human RP105/MD-1 complexes reveal
            unique dimer organization of the toll-like receptor family
  JOURNAL   J. Mol. Biol. 413 (4), 815-825 (2011)
   PUBMED   21959264
  REMARK    GeneRIF: Both mouse and human RP105/MD-1 exhibit dimerization of
            the 1:1 RP105/MD-1 complex, demonstrating a novel organization.
REFERENCE   2  (bases 1 to 895)
  AUTHORS   Mengwasser,K.E., Bryant,C.E., Gay,N.J. and Gangloff,M.
  TITLE     LPS ligand and culture additives improve production of monomeric
            MD-1 and 2 in Pichia pastoris by decreasing aggregation and
            intermolecular disulfide bonding
  JOURNAL   Protein Expr. Purif. 76 (2), 173-183 (2011)
   PUBMED   21130168
  REMARK    GeneRIF: In this study, we produced variants of MD-1 and MD-2 in
            Pichia pastoris. Contrary to previous reports, this study suggests
            that MD-1 can bind to LPS.
REFERENCE   3  (bases 1 to 895)
  AUTHORS   Tan,J.Y., Luo,Y.L., Huang,X., Shao,J.L., Lin,L. and Yang,X.X.
  TITLE     [Association of single nucleotide polymorphisms of MD-1 gene with
            asthma in adults of Han Nationality in Southern China]
  JOURNAL   Zhonghua Jie He He Hu Xi Za Zhi 34 (2), 104-108 (2011)
   PUBMED   21426727
  REMARK    GeneRIF: MD-1 may be a disease susceptibility gene for adult asthma
            in a Southern Han population in China.
REFERENCE   4  (bases 1 to 895)
  AUTHORS   Heid,I.M., Jackson,A.U., Randall,J.C., Winkler,T.W., Qi,L.,
            Steinthorsdottir,V., Thorleifsson,G., Zillikens,M.C.,
            Speliotes,E.K., Magi,R., Workalemahu,T., White,C.C.,
            Bouatia-Naji,N., Harris,T.B., Berndt,S.I., Ingelsson,E.,
            Willer,C.J., Weedon,M.N., Luan,J., Vedantam,S., Esko,T.,
            Kilpelainen,T.O., Kutalik,Z., Li,S., Monda,K.L., Dixon,A.L.,
            Holmes,C.C., Kaplan,L.M., Liang,L., Min,J.L., Moffatt,M.F.,
            Molony,C., Nicholson,G., Schadt,E.E., Zondervan,K.T., Feitosa,M.F.,
            Ferreira,T., Lango Allen,H., Weyant,R.J., Wheeler,E., Wood,A.R.,
            Estrada,K., Goddard,M.E., Lettre,G., Mangino,M., Nyholt,D.R.,
            Purcell,S., Smith,A.V., Visscher,P.M., Yang,J., McCarroll,S.A.,
            Nemesh,J., Voight,B.F., Absher,D., Amin,N., Aspelund,T., Coin,L.,
            Glazer,N.L., Hayward,C., Heard-Costa,N.L., Hottenga,J.J.,
            Johansson,A., Johnson,T., Kaakinen,M., Kapur,K., Ketkar,S.,
            Knowles,J.W., Kraft,P., Kraja,A.T., Lamina,C., Leitzmann,M.F.,
            McKnight,B., Morris,A.P., Ong,K.K., Perry,J.R., Peters,M.J.,
            Polasek,O., Prokopenko,I., Rayner,N.W., Ripatti,S., Rivadeneira,F.,
            Robertson,N.R., Sanna,S., Sovio,U., Surakka,I., Teumer,A., van
            Wingerden,S., Vitart,V., Zhao,J.H., Cavalcanti-Proenca,C.,
            Chines,P.S., Fisher,E., Kulzer,J.R., Lecoeur,C., Narisu,N.,
            Sandholt,C., Scott,L.J., Silander,K., Stark,K., Tammesoo,M.L.,
            Teslovich,T.M., Timpson,N.J., Watanabe,R.M., Welch,R.,
            Chasman,D.I., Cooper,M.N., Jansson,J.O., Kettunen,J.,
            Lawrence,R.W., Pellikka,N., Perola,M., Vandenput,L., Alavere,H.,
            Almgren,P., Atwood,L.D., Bennett,A.J., Biffar,R., Bonnycastle,L.L.,
            Bornstein,S.R., Buchanan,T.A., Campbell,H., Day,I.N., Dei,M.,
            Dorr,M., Elliott,P., Erdos,M.R., Eriksson,J.G., Freimer,N.B.,
            Fu,M., Gaget,S., Geus,E.J., Gjesing,A.P., Grallert,H., Grassler,J.,
            Groves,C.J., Guiducci,C., Hartikainen,A.L., Hassanali,N.,
            Havulinna,A.S., Herzig,K.H., Hicks,A.A., Hui,J., Igl,W.,
            Jousilahti,P., Jula,A., Kajantie,E., Kinnunen,L., Kolcic,I.,
            Koskinen,S., Kovacs,P., Kroemer,H.K., Krzelj,V., Kuusisto,J.,
            Kvaloy,K., Laitinen,J., Lantieri,O., Lathrop,G.M., Lokki,M.L.,
            Luben,R.N., Ludwig,B., McArdle,W.L., McCarthy,A., Morken,M.A.,
            Nelis,M., Neville,M.J., Pare,G., Parker,A.N., Peden,J.F.,
            Pichler,I., Pietilainen,K.H., Platou,C.G., Pouta,A.,
            Ridderstrale,M., Samani,N.J., Saramies,J., Sinisalo,J., Smit,J.H.,
            Strawbridge,R.J., Stringham,H.M., Swift,A.J., Teder-Laving,M.,
            Thomson,B., Usala,G., van Meurs,J.B., van Ommen,G.J., Vatin,V.,
            Volpato,C.B., Wallaschofski,H., Walters,G.B., Widen,E., Wild,S.H.,
            Willemsen,G., Witte,D.R., Zgaga,L., Zitting,P., Beilby,J.P.,
            James,A.L., Kahonen,M., Lehtimaki,T., Nieminen,M.S., Ohlsson,C.,
            Palmer,L.J., Raitakari,O., Ridker,P.M., Stumvoll,M., Tonjes,A.,
            Viikari,J., Balkau,B., Ben-Shlomo,Y., Bergman,R.N., Boeing,H.,
            Smith,G.D., Ebrahim,S., Froguel,P., Hansen,T., Hengstenberg,C.,
            Hveem,K., Isomaa,B., Jorgensen,T., Karpe,F., Khaw,K.T., Laakso,M.,
            Lawlor,D.A., Marre,M., Meitinger,T., Metspalu,A., Midthjell,K.,
            Pedersen,O., Salomaa,V., Schwarz,P.E., Tuomi,T., Tuomilehto,J.,
            Valle,T.T., Wareham,N.J., Arnold,A.M., Beckmann,J.S., Bergmann,S.,
            Boerwinkle,E., Boomsma,D.I., Caulfield,M.J., Collins,F.S.,
            Eiriksdottir,G., Gudnason,V., Gyllensten,U., Hamsten,A.,
            Hattersley,A.T., Hofman,A., Hu,F.B., Illig,T., Iribarren,C.,
            Jarvelin,M.R., Kao,W.H., Kaprio,J., Launer,L.J., Munroe,P.B.,
            Oostra,B., Penninx,B.W., Pramstaller,P.P., Psaty,B.M.,
            Quertermous,T., Rissanen,A., Rudan,I., Shuldiner,A.R., Soranzo,N.,
            Spector,T.D., Syvanen,A.C., Uda,M., Uitterlinden,A., Volzke,H.,
            Vollenweider,P., Wilson,J.F., Witteman,J.C., Wright,A.F.,
            Abecasis,G.R., Boehnke,M., Borecki,I.B., Deloukas,P.,
            Frayling,T.M., Groop,L.C., Haritunians,T., Hunter,D.J.,
            Kaplan,R.C., North,K.E., O'Connell,J.R., Peltonen,L.,
            Schlessinger,D., Strachan,D.P., Hirschhorn,J.N., Assimes,T.L.,
            Wichmann,H.E., Thorsteinsdottir,U., van Duijn,C.M., Stefansson,K.,
            Cupples,L.A., Loos,R.J., Barroso,I., McCarthy,M.I., Fox,C.S.,
            Mohlke,K.L. and Lindgren,C.M.
  CONSRTM   MAGIC
  TITLE     Meta-analysis identifies 13 new loci associated with waist-hip
            ratio and reveals sexual dimorphism in the genetic basis of fat
            distribution
  JOURNAL   Nat. Genet. 42 (11), 949-960 (2010)
   PUBMED   20935629
  REMARK    GeneRIF: Observational study and genome-wide association study of
            gene-disease association. (HuGE Navigator)
            Erratum:[Nat Genet. 2011 Nov;43(11):1164]
REFERENCE   5  (bases 1 to 895)
  AUTHORS   Davila,S., Froeling,F.E., Tan,A., Bonnard,C., Boland,G.J.,
            Snippe,H., Hibberd,M.L. and Seielstad,M.
  TITLE     New genetic associations detected in a host response study to
            hepatitis B vaccine
  JOURNAL   Genes Immun. 11 (3), 232-238 (2010)
   PUBMED   20237496
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   6  (bases 1 to 895)
  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
REFERENCE   7  (bases 1 to 895)
  AUTHORS   Ogata,H., Su,I., Miyake,K., Nagai,Y., Akashi,S., Mecklenbrauker,I.,
            Rajewsky,K., Kimoto,M. and Tarakhovsky,A.
  TITLE     The toll-like receptor protein RP105 regulates lipopolysaccharide
            signaling in B cells
  JOURNAL   J. Exp. Med. 192 (1), 23-29 (2000)
   PUBMED   10880523
REFERENCE   8  (bases 1 to 895)
  AUTHORS   Begum,N.A., Tsuji,S., Nomura,M., Shida,K., Azuma,I., Hayashi,A.,
            Matsumoto,M., Seya,T. and Toyoshima,K.
  TITLE     Human MD-1 homologue is a BCG-regulated gene product in monocytes:
            its identification by differential display
  JOURNAL   Biochem. Biophys. Res. Commun. 256 (2), 325-329 (1999)
   PUBMED   10079183
REFERENCE   9  (bases 1 to 895)
  AUTHORS   Miura,Y., Shimazu,R., Miyake,K., Akashi,S., Ogata,H., Yamashita,Y.,
            Narisawa,Y. and Kimoto,M.
  TITLE     RP105 is associated with MD-1 and transmits an activation signal in
            human B cells
  JOURNAL   Blood 92 (8), 2815-2822 (1998)
   PUBMED   9763566
REFERENCE   10 (bases 1 to 895)
  AUTHORS   Miyake,K., Shimazu,R., Kondo,J., Niki,T., Akashi,S., Ogata,H.,
            Yamashita,Y., Miura,Y. and Kimoto,M.
  TITLE     Mouse MD-1, a molecule that is physically associated with RP105 and
            positively regulates its expression
  JOURNAL   J. Immunol. 161 (3), 1348-1353 (1998)
   PUBMED   9686597
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            CD695164.1 and BC038846.1.
            On Nov 16, 2004 this sequence version replaced gi:52856401.
            
            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 :: BC038846.1, AF057178.2 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025084, ERS025088 [ECO:0000348]
            ##Evidence-Data-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-527               CD695164.1         65-591
            528-895             BC038846.1         538-905
FEATURES             Location/Qualifiers
     source          1..895
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="6"
                     /map="6p25.1"
     gene            1..895
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /note="lymphocyte antigen 86"
                     /db_xref="GeneID:9450"
                     /db_xref="HGNC:16837"
                     /db_xref="HPRD:05578"
                     /db_xref="MIM:605241"
     exon            1..170
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /inference="alignment:Splign:1.39.8"
     variation       3
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376619727"
     variation       31
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141209631"
     variation       33
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142081955"
     CDS             35..523
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /note="MD-1, RP105-associated; ly-86; protein MD-1"
                     /codon_start=1
                     /product="lymphocyte antigen 86 precursor"
                     /protein_id="NP_004262.1"
                     /db_xref="GI:4758708"
                     /db_xref="CCDS:CCDS4498.1"
                     /db_xref="GeneID:9450"
                     /db_xref="HGNC:16837"
                     /db_xref="HPRD:05578"
                     /db_xref="MIM:605241"
                     /translation="
MKGFTATLFLWTLIFPSCSGGGGGKAWPTHVVCSDSGLEVLYQSCDPLQDFGFSVEKCSKQLKSNINIRFGIILREDIKELFLDLALMSQGSSVLNFSYPICEAALPKFSFCGRRKGEQIYYAGPVNNPEFTIPQGEYQVLLELYTEKRSTVACANATIMCS
"
     sig_peptide     35..94
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /inference="COORDINATES: ab initio prediction:SignalP:4.0"
     mat_peptide     95..520
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /product="Lymphocyte antigen 86"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (O95711.1)"
     misc_feature    122..511
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /note="MD-1 and MD-2 are cofactors required for LPS
                     signaling through cell surface receptors. MD-2 and its
                     binding partner, Toll-like receptor 4 (TLR4), are
                     essential for the innate immune responses of mammalian
                     cells to bacterial lipopolysaccharide (LPS); MD-2...;
                     Region: MD-1_MD-2; cd00915"
                     /db_xref="CDD:29926"
     misc_feature    order(122..124,146..148,152..154,158..160,212..214,
                     230..232,236..238,242..244,281..283,287..289,293..295,
                     335..337,374..376,398..400,449..451,455..457,461..463,
                     467..469,488..490,497..499,503..505,509..511)
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /note="putative lipid binding cavity [chemical binding];
                     other site"
                     /db_xref="CDD:29926"
     variation       40
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:369059581"
     variation       47..48
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace=""
                     /replace="cccc"
                     /replace="ccccc"
                     /db_xref="dbSNP:145808577"
     variation       47
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:78057476"
     variation       64
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:74356155"
     variation       100
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139269722"
     variation       101
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376603538"
     variation       107
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:75006006"
     variation       109
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149989688"
     variation       111
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370576233"
     variation       136
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144373281"
     variation       137
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:377638373"
     variation       156
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199618297"
     variation       162
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374594594"
     variation       169
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201912095"
     exon            171..257
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /inference="alignment:Splign:1.39.8"
     variation       197
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148799324"
     variation       200..201
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:34247656"
     variation       208
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:201924366"
     variation       249
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:142377958"
     variation       252
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:200582242"
     exon            258..386
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /inference="alignment:Splign:1.39.8"
     variation       311
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:5743649"
     variation       331
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:371613117"
     exon            387..439
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /inference="alignment:Splign:1.39.8"
     variation       396
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:5743651"
     variation       399
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144342238"
     variation       400
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147765605"
     variation       428
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146986566"
     variation       434
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140062866"
     exon            440..879
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /inference="alignment:Splign:1.39.8"
     variation       480
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:76751952"
     variation       481
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:185732402"
     variation       493
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377039830"
     STS             499..869
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /standard_name="LY86__7346"
                     /db_xref="UniSTS:466288"
     variation       512
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1802323"
     variation       519
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:371434032"
     variation       537
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:201979655"
     variation       561
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:190409396"
     variation       562
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2233128"
     variation       565
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112322999"
     STS             714..840
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /standard_name="SHGC-33709"
                     /db_xref="UniSTS:12891"
     variation       793
                     /gene="LY86"
                     /gene_synonym="dJ80N2.1; MD-1; MMD-1; RP1-80N2.1"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:116693754"
ORIGIN      
ttatttttctgtgtgtcccatacaggcccccaccatgaagggtttcacagccactctcttcctctggactctgatttttcccagctgcagtggaggcggcggtgggaaagcctggcccacacacgtggtctgtagcgacagcggcttggaagtgctctaccagagttgcgatccattacaagattttggcttttctgttgaaaagtgttccaagcaattaaaatcaaatatcaacattagatttggaattattctgagagaggacatcaaagagctttttcttgacctagctctcatgtctcaaggctcatctgttttgaatttctcctatcccatctgtgaggcggctctgcccaagttttctttctgtggaagaaggaaaggagagcagatttactatgctgggcctgtcaataatcctgaatttactattcctcagggagaataccaggttttgctggaactgtacactgaaaaacggtccaccgtggcctgtgccaatgctactatcatgtgctcctgactgtggcctgtagcaaaaatcacagccagctgcatctcgtgggacctccaagctcctctgactgaacctactgtgggaggagaagcagctgatgacagagagaggctctacaaagaagcgcccccaaagagtgcagctgctaattttagtcccaggaccagacatccccagactccacagatgtaatgaagtccccgaatgtatctgtttctaaggagcctcttggcagtccttaagcagtcttgagggtccatcctttttctctaattggtcgcctcccaccagactcacctgcttttcaactttttaggagtgcttcctcacagttaccaagaataaagaaagctggccaccataaaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:9450 -> Biological process: GO:0006915 [apoptotic process] evidence: TAS
            GeneID:9450 -> Biological process: GO:0006954 [inflammatory response] evidence: IEA
            GeneID:9450 -> Biological process: GO:0006959 [humoral immune response] evidence: TAS
            GeneID:9450 -> Biological process: GO:0008283 [cell proliferation] evidence: TAS
            GeneID:9450 -> Biological process: GO:0031666 [positive regulation of lipopolysaccharide-mediated signaling pathway] evidence: IGI
            GeneID:9450 -> Biological process: GO:0045087 [innate immune response] evidence: IEA
            GeneID:9450 -> Cellular component: GO:0005615 [extracellular space] evidence: IEA
            GeneID:9450 -> Cellular component: GO:0005886 [plasma membrane] evidence: TAS

by @meso_cacase at DBCLS
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