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2024-03-29 21:48:04, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_001197240            3470 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens butyrophilin, subfamily 2, member A2 (BTN2A2),
            transcript variant 6, mRNA.
ACCESSION   NM_001197240
VERSION     NM_001197240.1  GI:308522751
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 3470)
  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 3470)
  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 3470)
  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 3470)
  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 3470)
  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 3470)
  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, AK298570.1 and
            BC013258.2.
            
            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 (6) lacks an in-frame exon in the
            5' region and has an additional segment in the 3' region, compared
            to variant 1. The resulting isoform (b) lacks an internal segment
            and has a shorter and distinct C-terminus, compared to isoform a.
            
            ##Evidence-Data-START##
            Transcript exon combination :: AK298570.1 [ECO:0000332]
            RNAseq introns              :: mixed/partial sample support
                                           ERS025082, ERS025084 [ECO:0000350]
            ##Evidence-Data-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-58                DC388932.1         2-59
            59-1045             AK298570.1         34-1020
            1046-3470           BC013258.2         747-3171
FEATURES             Location/Qualifiers
     source          1..3470
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="6"
                     /map="6p22.1"
     gene            1..3470
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /note="butyrophilin, subfamily 2, member A2"
                     /db_xref="GeneID:10385"
                     /db_xref="HGNC:1137"
                     /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..882
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /note="isoform e precursor is encoded by transcript
                     variant 6; butyrophilin 2"
                     /codon_start=1
                     /product="butyrophilin subfamily 2 member A2 isoform e
                     precursor"
                     /protein_id="NP_001184169.1"
                     /db_xref="GI:308522752"
                     /db_xref="CCDS:CCDS56402.1"
                     /db_xref="GeneID:10385"
                     /db_xref="HGNC:1137"
                     /db_xref="MIM:613591"
                     /translation="
MEPAAALHFSLPASLLLLLLLLLLSLCALVSAQFTVVGPANPILAMVGENTTLRCHLSPEKNAEDMEVRWFRSQFSPAVFVYKGGRERTEEQMEEYRGRITFVSKDINRGSVALVIHNVTAQENGIYRCYFQEGRSYDEAILRLVVAESFMPSASPWMVALAVILTASPWMVSMTVILAVFIIFMAVSICCIKKLQREKKILSGEKKVEQEEKEIAQQLQEELRWRRTFLHAGYELPGIRGPSWKRPLHGEPPSAF
"
     sig_peptide     112..207
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="COORDINATES: ab initio prediction:SignalP:4.0"
     mat_peptide     208..879
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /product="butyrophilin subfamily 2 member A2 isoform e"
     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"
     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..760
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="alignment:Splign:1.39.8"
     variation       557
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:375385023"
     variation       616
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369920399"
     variation       628
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:113893469"
     variation       629
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373492069"
     variation       637
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:147003451"
     variation       760
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201972159"
     exon            761..781
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="alignment:Splign:1.39.8"
     exon            782..808
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="alignment:Splign:1.39.8"
     exon            809..3461
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="alignment:Splign:1.39.8"
     variation       847
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:114402470"
     variation       848
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:191843070"
     variation       874
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:2072803"
     variation       921
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:183676835"
     variation       962
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147646031"
     variation       966
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142151655"
     variation       972
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:368319822"
     variation       987
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148323426"
     variation       988
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142803339"
     variation       993
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:150431575"
     variation       996
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370826490"
     variation       997
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:138172438"
     variation       1018
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374005579"
     variation       1019
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200473019"
     variation       1025
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112054667"
     variation       1027
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372706575"
     variation       1044
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368149710"
     variation       1078
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200468059"
     variation       1100
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200546581"
     variation       1113
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375971811"
     variation       1115
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374942833"
     variation       1116
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200047445"
     variation       1127
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:142785600"
     variation       1132..1133
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:34248025"
     variation       1152
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146142561"
     variation       1153
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:372254650"
     variation       1158
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:140196606"
     variation       1160
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:149403458"
     variation       1173
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:181793664"
     variation       1179
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202000782"
     variation       1183
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:148562624"
     variation       1240
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369578278"
     variation       1264..1265
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:35755065"
     variation       1264
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:62617840"
     variation       1270
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:199832316"
     variation       1276
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:114760306"
     variation       1284
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:139419531"
     variation       1293
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2072802"
     variation       1316
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201353973"
     variation       1317
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372541099"
     variation       1322
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200888343"
     variation       1324
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376736237"
     variation       1343
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147634987"
     variation       1361
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:111615265"
     variation       1372
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375693447"
     variation       1380
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1614887"
     variation       1392
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369209046"
     variation       1399
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145542993"
     variation       1400
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200276371"
     variation       1417
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:16891646"
     variation       1449
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:376227483"
     variation       1490
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369257115"
     variation       1499
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143694906"
     variation       1507
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:114098566"
     variation       1520
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:73736249"
     variation       1529
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:199706137"
     variation       1563
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:377572514"
     variation       1582
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370709739"
     variation       1584
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201460456"
     variation       1596
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:190569086"
     variation       1604
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:370507187"
     variation       1659
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144477860"
     variation       1674
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:111432027"
     variation       1682
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:181721317"
     variation       1731
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372246478"
     variation       1751
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:186915774"
     variation       1846
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:3927423"
     variation       1993..1994
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace=""
                     /replace="ttc"
                     /db_xref="dbSNP:201274736"
     variation       2146
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:1804836"
     STS             2213..2325
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /standard_name="NIB885"
                     /db_xref="UniSTS:41935"
     variation       2288
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:75254848"
     variation       2290
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:191285742"
     variation       2310
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140325542"
     variation       2326
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:77055120"
     STS             2337..2545
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /standard_name="RH15843"
                     /db_xref="UniSTS:21190"
     variation       2339
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:182538207"
     variation       2434
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:75435297"
     variation       2518
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:7355"
     variation       2535..2536
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:138497943"
     variation       2679
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1131936"
     variation       2710
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149930183"
     variation       2721
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:55674248"
     variation       2724
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:61527210"
     variation       2865
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184920379"
     variation       2891
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:113353347"
     variation       2932
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:72500812"
     variation       3086
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:59001682"
     variation       3120
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:73387026"
     variation       3393
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:189684950"
     polyA_signal    3441..3446
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
     polyA_site      3461
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
ORIGIN      
aaatcttgggactttttggacacccagagaacaggtcccagataccgagtccgcaactccaaacatcgcgattaataggaggcctctggtctctgcctgccctgggtgctcatggaaccagctgctgctctgcacttctccctgccagcctccctcctcctcctcctgctcctcctccttctcagcctgtgtgcactggtctcagcccagtttactgtcgtggggccagctaatcccatcctggccatggtgggagaaaacactacattacgctgccatctgtcacccgagaaaaatgctgaggacatggaggtgcggtggttccggtctcagttctcccccgcagtgtttgtgtataagggtgggagagagagaacagaggagcagatggaggagtaccggggaagaatcacctttgtgagcaaagacatcaacaggggcagcgtggccctggtcatacataacgtcacagcccaggagaatgggatctaccgctgttacttccaagaaggcaggtcctacgatgaggccatcctacgcctcgtggtggcagaatcctttatgcccagcgcatctccctggatggtggccctagctgtcatcctgaccgcatctccctggatggtgtccatgactgtcatcctggctgttttcatcatcttcatggctgtcagcatctgttgcatcaagaaacttcaaagggaaaaaaagattctgtcaggggaaaagaaagttgaacaagaggaaaaagaaattgcacagcaacttcaagaagaattgcgatggagaagaacattcttacatgctgggtatgagctgcctgggatcaggggaccttcatggaaacggccactacatggggaacccccttcagctttctgagacttctctggggaccaggaaccacacaatccccagggttcctgagaccccaggcataaacctgagacttcctctgcagctgatgtggtcctggatccagacaccgctcatcccgagctcttcctgtcagaggaccggagaagtgtgaggcggggcccctacaggcagagagtgcctgacaacccagagagattcgacagtcagccttgtgtcctgggatgggagagcttcgcctcagggaaacattactgggaggtggaggtggaaaacgtgatggtgtggactgtgggggtctgcagacacagtgttgagaggaaaggggaggtcctgctgattcctcagaatggcttctggaccctggagatgtttggaaaccaataccgggccctgtcctcccctgagaggattctccctttgaaggagtccctttgccgggtgggcgtcttcctggactatgaagctggagatgtctccttctacaacatgagggacagatcgcacatctacacatgtccccgttcagcctttactgtgcctgtgaggcccttcttcaggttagggtctgatgacagccccatcttcatctgccctgcactcacaggagccagtggggtcatggtgcctgaagagggcctgaaacttcacagagtggggacccaccagagcctatagaatcaattccttggactcacagccatgcagataagccctggccatctcagcagccaccgcacaacccccctaatgaaagacacgccctcctcccctctggtcacgtaagagaacatcttccagctgcctttttcacacccactccagccctctgccccagttttctcctcctcactagtctgtggctttagtagttcctttgcttgtaattatgggatgggatccaggcatagggaactagttgtttcatagctcccagtcaaaaagaaagtgagagaagctgttgggcagcgaacctactgtttaaaatcaggataaccacattaagcccaatatgccagttggcaccagatgctgtggacttggaatgaggccaacagggttcaccaggatgagagaggagagaggaatccacaggaccaccagaagggagagggaaccagatatgcagatcagagatagaggaagtggaaccagagagctgggagggaccaaggttgtaaggatggctaagtcccaccataagagctaaagggtcctgggagatgatggctcatttccacccaaccccaggatttccacagcacacacccacaggcctggacctgggatgaagatgaatgaagaacatggactcatgtggatgtggtttggctcagatgtccctgcaataaacaaggggtcagtacttagtccctgagtgtggttgaggtttgaggtcctggtcgagcagggcagtactggaccaggtctacgtcagcattcaggttcaatggggacaccagtggcttcaaacttcctgatctaattatgtttttagacacttagaagttattgaggactttaaagagcttttgtttatttgggttaatatttatgacatttgacattgaaacaaaaatttaaaatgttatcttttaatttatgttaaaatagcattaataaatcagttataggttaatgtagataggatgttttgtgaaaaagcaatctattgtgtccaaataaaaaaacaaaaagtgtgacactggttaactttttccagatctcatgtctggcttaataagagatatttgtattatcatatctgcctttgtattaaacctattggtatatcataggtcatgttagctcaaaaaaactttactgcacactactgagagaatgagatgaaaaacgattaatgtttcattattattattgtgaaaatattattaacactggggactccttaagagtacatcagagttctctctaggaatcccaaaaccacattttgaaactagaatagtggatcctggaagttaatccatgtgctggttaattttagatgtcaacctgactggattaaggaatacctagacagctggtacaacattatttctgggtgtgtctgtgagtgtgtttccagaagagattggcaagtgagtcagtgggaaattctctccttctgttggctgggtgcccaatacaacaaaaaggcagaggaaaggcaaattcttctctcctctggagctgagacactcttcttcttctgcccttggacatcagaactcctggctctccggcctttgaacttcaggacttgtaccaggaggccctgggttctcaggcctttggctttggactgagagttacacaatcagcttccctggttctgaggctttcagacttaaactgagccatgctaccagcatcccagggtctccagcctacagatgagctgttgtgcgatttcttagcctccataatcacatgagccaatctccttaataaatgcctgctcatagatctgtatctacatctatatctgtatgtgcatctatatctatgcctatatctatatctatatcatattgattttgtctctctggagaaccctgactaataaaatgaggcatctaaaaaaaaaaaaa
//

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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