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2019-03-25 14:29:57, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_006995               3602 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens butyrophilin, subfamily 2, member A2 (BTN2A2),
            transcript variant 1, mRNA.
ACCESSION   NM_006995
VERSION     NM_006995.4  GI:308522743
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 3602)
  AUTHORS   Shi,J., Levinson,D.F., Duan,J., Sanders,A.R., Zheng,Y., Pe'er,I.,
            Dudbridge,F., Holmans,P.A., Whittemore,A.S., Mowry,B.J., Olincy,A.,
            Amin,F., Cloninger,C.R., Silverman,J.M., Buccola,N.G.,
            Byerley,W.F., Black,D.W., Crowe,R.R., Oksenberg,J.R., Mirel,D.B.,
            Kendler,K.S., Freedman,R. and Gejman,P.V.
  TITLE     Common variants on chromosome 6p22.1 are associated with
            schizophrenia
  JOURNAL   Nature 460 (7256), 753-757 (2009)
   PUBMED   19571809
REFERENCE   2  (bases 1 to 3602)
  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   3  (bases 1 to 3602)
  AUTHORS   Cavaletto,M., Giuffrida,M.G., Fortunato,D., Gardano,L.,
            Dellavalle,G., Napolitano,L., Giunta,C., Bertino,E., Fabris,C. and
            Conti,A.
  TITLE     A proteomic approach to evaluate the butyrophilin gene family
            expression in human milk fat globule membrane
  JOURNAL   Proteomics 2 (7), 850-856 (2002)
   PUBMED   12124930
REFERENCE   4  (bases 1 to 3602)
  AUTHORS   Rhodes,D.A., Stammers,M., Malcherek,G., Beck,S. and Trowsdale,J.
  TITLE     The cluster of BTN genes in the extended major histocompatibility
            complex
  JOURNAL   Genomics 71 (3), 351-362 (2001)
   PUBMED   11170752
REFERENCE   5  (bases 1 to 3602)
  AUTHORS   Henry,J., Miller,M.M. and Pontarotti,P.
  TITLE     Structure and evolution of the extended B7 family
  JOURNAL   Immunol. Today 20 (6), 285-288 (1999)
   PUBMED   10354554
  REMARK    Review article
REFERENCE   6  (bases 1 to 3602)
  AUTHORS   Ruddy,D.A., Kronmal,G.S., Lee,V.K., Mintier,G.A., Quintana,L.,
            Domingo,R. Jr., Meyer,N.C., Irrinki,A., McClelland,E.E., Fullan,A.,
            Mapa,F.A., Moore,T., Thomas,W., Loeb,D.B., Harmon,C.,
            Tsuchihashi,Z., Wolff,R.K., Schatzman,R.C. and Feder,J.N.
  TITLE     A 1.1-Mb transcript map of the hereditary hemochromatosis locus
  JOURNAL   Genome Res. 7 (5), 441-456 (1997)
   PUBMED   9149941
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from DC388932.1, U90550.1 and
            BC014021.2.
            On Oct 14, 2010 this sequence version replaced gi:31881700.
            
            Summary: Butyrophilin is the major protein associated with fat
            droplets in the milk. This gene is a member of the BTN2 subfamily
            of genes, which encode proteins belonging to the butyrophilin
            protein family. The gene is located in a cluster on chromosome 6,
            consisting of seven genes belonging to the expanding
            B7/butyrophilin-like group, a subset of the immunoglobulin gene
            superfamily. The encoded protein is a type I receptor glycoprotein
            involved in lipid, fatty-acid and sterol metabolism. Several
            alternatively spliced transcript variants encoding different
            isoforms have been found for this gene. [provided by RefSeq, Oct
            2010].
            
            Transcript Variant: This variant (1) and variant 3 encode the
            longest isoform (a).
            
            ##Evidence-Data-START##
            Transcript exon combination :: U90550.1 [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
            1-58                DC388932.1         2-59
            59-1508             U90550.1           34-1483
            1509-2708           BC014021.2         1507-2706
            2709-3602           U90550.1           2685-3578
FEATURES             Location/Qualifiers
     source          1..3602
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="6"
                     /map="6p22.1"
     gene            1..3602
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /note="butyrophilin, subfamily 2, member A2"
                     /db_xref="GeneID:10385"
                     /db_xref="HGNC:1137"
                     /db_xref="HPRD:12545"
                     /db_xref="MIM:613591"
     exon            1..81
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="alignment:Splign:1.39.8"
     variation       58
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:9461249"
     misc_feature    76..78
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /note="upstream in-frame stop codon"
     exon            82..205
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="alignment:Splign:1.39.8"
     CDS             112..1683
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /note="isoform a precursor is encoded by transcript
                     variant 1; butyrophilin 2"
                     /codon_start=1
                     /product="butyrophilin subfamily 2 member A2 isoform a
                     precursor"
                     /protein_id="NP_008926.2"
                     /db_xref="GI:6453813"
                     /db_xref="CCDS:CCDS4606.1"
                     /db_xref="GeneID:10385"
                     /db_xref="HGNC:1137"
                     /db_xref="HPRD:12545"
                     /db_xref="MIM:613591"
                     /translation="
MEPAAALHFSLPASLLLLLLLLLLSLCALVSAQFTVVGPANPILAMVGENTTLRCHLSPEKNAEDMEVRWFRSQFSPAVFVYKGGRERTEEQMEEYRGRITFVSKDINRGSVALVIHNVTAQENGIYRCYFQEGRSYDEAILRLVVAGLGSKPLIEIKAQEDGSIWLECISGGWYPEPLTVWRDPYGEVVPALKEVSIADADGLFMVTTAVIIRDKYVRNVSCSVNNTLLGQEKETVIFIPESFMPSASPWMVALAVILTASPWMVSMTVILAVFIIFMAVSICCIKKLQREKKILSGEKKVEQEEKEIAQQLQEELRWRRTFLHAADVVLDPDTAHPELFLSEDRRSVRRGPYRQRVPDNPERFDSQPCVLGWESFASGKHYWEVEVENVMVWTVGVCRHSVERKGEVLLIPQNGFWTLEMFGNQYRALSSPERILPLKESLCRVGVFLDYEAGDVSFYNMRDRSHIYTCPRSAFTVPVRPFFRLGSDDSPIFICPALTGASGVMVPEEGLKLHRVGTHQSL
"
     sig_peptide     112..207
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="COORDINATES: ab initio prediction:SignalP:4.0"
     mat_peptide     208..1680
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /product="butyrophilin subfamily 2 member A2 isoform a"
     misc_feature    208..549
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /note="Immunoglobulin V-set domain; Region: V-set;
                     pfam07686"
                     /db_xref="CDD:203725"
     misc_feature    253..552
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /note="Immunoglobulin (Ig)-like domain of myelin
                     oligodendrocyte glycoprotein (MOG); Region: Ig_MOG_like;
                     cd05713"
                     /db_xref="CDD:143190"
     misc_feature    order(301..306,361..363,394..396,505..507,511..528)
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /note="antigen binding site; other site"
                     /db_xref="CDD:143190"
     misc_feature    565..813
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /note="Immunoglobulin domain; Region: Ig; cl11960"
                     /db_xref="CDD:213125"
     misc_feature    907..969
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q8WVV5.2);
                     transmembrane region"
     misc_feature    1087..1242
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /note="associated with SPRY domains; Region: PRY;
                     smart00589"
                     /db_xref="CDD:128857"
     misc_feature    1246..1602
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /note="Domain in SPla and the RYanodine Receptor; Region:
                     SPRY; smart00449"
                     /db_xref="CDD:128725"
     variation       117
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375369181"
     variation       119
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202213069"
     variation       122
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:73736234"
     variation       150
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:147636357"
     variation       168
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:115247877"
     exon            206..553
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="alignment:Splign:1.39.8"
     variation       219
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138070617"
     variation       220
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143653188"
     variation       226
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:57038103"
     variation       271
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370867259"
     variation       288
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150302333"
     variation       289
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:181037825"
     variation       316
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375285642"
     variation       317
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368009368"
     variation       352
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:372237219"
     variation       354
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376950043"
     variation       374
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376558792"
     variation       399
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:112257227"
     variation       400
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367692328"
     variation       401
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144702884"
     variation       437
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149453161"
     variation       438
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377645117"
     variation       465
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143017993"
     variation       523
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146154371"
     variation       539
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201687793"
     exon            554..835
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="alignment:Splign:1.39.8"
     variation       613
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:369291221"
     variation       627
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142411775"
     variation       666
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:76088803"
     variation       669
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:200834687"
     variation       685
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:144410497"
     variation       693
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372854548"
     variation       703
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200036284"
     variation       706
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201605260"
     variation       710
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139541725"
     variation       718
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:62617839"
     variation       738
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370196656"
     variation       776
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145439434"
     variation       795
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201008184"
     variation       799
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200096466"
     variation       802
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373346354"
     variation       833
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201995913"
     exon            836..1042
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="alignment:Splign:1.39.8"
     variation       839
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:375385023"
     variation       898
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369920399"
     variation       910
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:113893469"
     variation       911
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373492069"
     variation       919
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:147003451"
     variation       1042
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201972159"
     exon            1043..1063
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="alignment:Splign:1.39.8"
     exon            1064..1090
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="alignment:Splign:1.39.8"
     exon            1091..3590
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="alignment:Splign:1.39.8"
     variation       1091
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147646031"
     variation       1095
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142151655"
     variation       1101
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:368319822"
     variation       1116
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148323426"
     variation       1117
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142803339"
     variation       1122
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:150431575"
     variation       1125
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370826490"
     variation       1126
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:138172438"
     variation       1147
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374005579"
     variation       1148
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200473019"
     variation       1154
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112054667"
     variation       1156
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372706575"
     variation       1173
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368149710"
     variation       1207
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200468059"
     variation       1229
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200546581"
     variation       1242
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375971811"
     variation       1244
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374942833"
     variation       1245
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200047445"
     variation       1256
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:142785600"
     variation       1261..1262
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:34248025"
     variation       1281
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146142561"
     variation       1282
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:372254650"
     variation       1287
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:140196606"
     variation       1289
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:149403458"
     variation       1302
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:181793664"
     variation       1308
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202000782"
     variation       1312
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:148562624"
     variation       1369
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369578278"
     variation       1393..1394
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:35755065"
     variation       1393
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:62617840"
     variation       1399
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:199832316"
     variation       1405
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:114760306"
     variation       1413
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:139419531"
     variation       1422
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2072802"
     variation       1445
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201353973"
     variation       1446
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372541099"
     variation       1451
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200888343"
     variation       1453
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376736237"
     variation       1472
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147634987"
     variation       1490
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:111615265"
     variation       1501
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375693447"
     variation       1509
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1614887"
     variation       1521
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369209046"
     variation       1528
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145542993"
     variation       1529
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200276371"
     variation       1546
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:16891646"
     variation       1578
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:376227483"
     variation       1619
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369257115"
     variation       1628
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143694906"
     variation       1636
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:114098566"
     variation       1649
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:73736249"
     variation       1658
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:199706137"
     variation       1692
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:377572514"
     variation       1711
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370709739"
     variation       1713
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201460456"
     variation       1725
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:190569086"
     variation       1733
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:370507187"
     variation       1788
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144477860"
     variation       1803
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:111432027"
     variation       1811
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:181721317"
     variation       1860
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372246478"
     variation       1880
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:186915774"
     variation       1975
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:3927423"
     variation       2122..2123
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace=""
                     /replace="ttc"
                     /db_xref="dbSNP:201274736"
     variation       2275
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:1804836"
     STS             2342..2454
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /standard_name="NIB885"
                     /db_xref="UniSTS:41935"
     variation       2417
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:75254848"
     variation       2419
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:191285742"
     variation       2439
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140325542"
     variation       2455
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:77055120"
     STS             2466..2674
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /standard_name="RH15843"
                     /db_xref="UniSTS:21190"
     variation       2468
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:182538207"
     variation       2563
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:75435297"
     variation       2647
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:7355"
     variation       2664..2665
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:138497943"
     variation       2808
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1131936"
     variation       2839
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149930183"
     variation       2850
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:55674248"
     variation       2853
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:61527210"
     variation       2994
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184920379"
     variation       3020
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:113353347"
     variation       3061
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:72500812"
     variation       3215
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:59001682"
     variation       3249
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:73387026"
     variation       3522
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:189684950"
     polyA_signal    3570..3575
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
     polyA_site      3590
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
ORIGIN      
aaatcttgggactttttggacacccagagaacaggtcccagataccgagtccgcaactccaaacatcgcgattaataggaggcctctggtctctgcctgccctgggtgctcatggaaccagctgctgctctgcacttctccctgccagcctccctcctcctcctcctgctcctcctccttctcagcctgtgtgcactggtctcagcccagtttactgtcgtggggccagctaatcccatcctggccatggtgggagaaaacactacattacgctgccatctgtcacccgagaaaaatgctgaggacatggaggtgcggtggttccggtctcagttctcccccgcagtgtttgtgtataagggtgggagagagagaacagaggagcagatggaggagtaccggggaagaatcacctttgtgagcaaagacatcaacaggggcagcgtggccctggtcatacataacgtcacagcccaggagaatgggatctaccgctgttacttccaagaaggcaggtcctacgatgaggccatcctacgcctcgtggtggcaggccttgggtctaagcccctcattgaaatcaaggcccaagaggatgggagcatctggctggagtgcatatctggagggtggtacccagagcccctcacagtgtggagggacccctacggtgaggttgtgcccgccctgaaggaggtttccatcgctgatgctgacggcctcttcatggtcaccacagctgtgatcatcagagacaagtatgtgaggaatgtgtcctgctctgtcaacaacaccctgctcggccaggagaaggaaactgtcatttttattccagaatcctttatgcccagcgcatctccctggatggtggccctagctgtcatcctgaccgcatctccctggatggtgtccatgactgtcatcctggctgttttcatcatcttcatggctgtcagcatctgttgcatcaagaaacttcaaagggaaaaaaagattctgtcaggggaaaagaaagttgaacaagaggaaaaagaaattgcacagcaacttcaagaagaattgcgatggagaagaacattcttacatgctgctgatgtggtcctggatccagacaccgctcatcccgagctcttcctgtcagaggaccggagaagtgtgaggcggggcccctacaggcagagagtgcctgacaacccagagagattcgacagtcagccttgtgtcctgggatgggagagcttcgcctcagggaaacattactgggaggtggaggtggaaaacgtgatggtgtggactgtgggggtctgcagacacagtgttgagaggaaaggggaggtcctgctgattcctcagaatggcttctggaccctggagatgtttggaaaccaataccgggccctgtcctcccctgagaggattctccctttgaaggagtccctttgccgggtgggcgtcttcctggactatgaagctggagatgtctccttctacaacatgagggacagatcgcacatctacacatgtccccgttcagcctttactgtgcctgtgaggcccttcttcaggttagggtctgatgacagccccatcttcatctgccctgcactcacaggagccagtggggtcatggtgcctgaagagggcctgaaacttcacagagtggggacccaccagagcctatagaatcaattccttggactcacagccatgcagataagccctggccatctcagcagccaccgcacaacccccctaatgaaagacacgccctcctcccctctggtcacgtaagagaacatcttccagctgcctttttcacacccactccagccctctgccccagttttctcctcctcactagtctgtggctttagtagttcctttgcttgtaattatgggatgggatccaggcatagggaactagttgtttcatagctcccagtcaaaaagaaagtgagagaagctgttgggcagcgaacctactgtttaaaatcaggataaccacattaagcccaatatgccagttggcaccagatgctgtggacttggaatgaggccaacagggttcaccaggatgagagaggagagaggaatccacaggaccaccagaagggagagggaaccagatatgcagatcagagatagaggaagtggaaccagagagctgggagggaccaaggttgtaaggatggctaagtcccaccataagagctaaagggtcctgggagatgatggctcatttccacccaaccccaggatttccacagcacacacccacaggcctggacctgggatgaagatgaatgaagaacatggactcatgtggatgtggtttggctcagatgtccctgcaataaacaaggggtcagtacttagtccctgagtgtggttgaggtttgaggtcctggtcgagcagggcagtactggaccaggtctacgtcagcattcaggttcaatggggacaccagtggcttcaaacttcctgatctaattatgtttttagacacttagaagttattgaggactttaaagagcttttgtttatttgggttaatatttatgacatttgacattgaaacaaaaatttaaaatgttatcttttaatttatgttaaaatagcattaataaatcagttataggttaatgtagataggatgttttgtgaaaaagcaatctattgtgtccaaataaaaaaacaaaaagtgtgacactggttaactttttccagatctcatgtctggcttaataagagatatttgtattatcatatctgcctttgtattaaacctattggtatatcataggtcatgttagctcaaaaaaactttactgcacactactgagagaatgagatgaaaaacgattaatgtttcattattattattgtgaaaatattattaacactggggactccttaagagtacatcagagttctctctaggaatcccaaaaccacattttgaaactagaatagtggatcctggaagttaatccatgtgctggttaattttagatgtcaacctgactggattaaggaatacctagacagctggtacaacattatttctgggtgtgtctgtgagtgtgtttccagaagagattggcaagtgagtcagtgggaaattctctccttctgttggctgggtgcccaatacaacaaaaaggcagaggaaaggcaaattcttctctcctctggagctgagacactcttcttcttctgcccttggacatcagaactcctggctctccggcctttgaacttcaggacttgtaccaggaggccctgggttctcaggcctttggctttggactgagagttacacaatcagcttccctggttctgaggctttcagacttaaactgagccatgctaccagcatcccagggtctccagcctacagatgagctgttgtgcgatttcttagcctccataatcacatgagccaatctccttaataaatgcctgctcatagatctgtatctacatctatatctgtatgtgcatctatatctatgcctatatctatatctatatcatattgattttgtctctctggagaaccctgactaataaaatgaggcatctaaaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:10385 -> Biological process: GO:0031324 [negative regulation of cellular metabolic process] evidence: ISS
            GeneID:10385 -> Biological process: GO:0046007 [negative regulation of activated T cell proliferation] evidence: ISS
            GeneID:10385 -> Biological process: GO:0050710 [negative regulation of cytokine secretion] evidence: ISS
            GeneID:10385 -> Cellular component: GO:0016021 [integral to membrane] evidence: IEA

by @meso_cacase at DBCLS
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