GGRNA Home | Help | Advanced search

2024-03-29 13:38:18, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_181531               3251 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens butyrophilin, subfamily 2, member A2 (BTN2A2),
            transcript variant 2, mRNA.
ACCESSION   NM_181531
VERSION     NM_181531.2  GI:308522744
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 3251)
  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 3251)
  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 3251)
  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 3251)
  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 3251)
  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 3251)
  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, AK289883.1 and
            BC013258.2.
            On Oct 14, 2010 this sequence version replaced gi:31881692.
            
            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 (2) lacks an in-frame exon in the
            5' region compared to variant 1, resulting in a shorter protein
            (isoform b), compared to isoform a.
            
            ##Evidence-Data-START##
            Transcript exon combination :: AK289883.1 [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
            1-12                DC388932.1         2-13
            13-1160             AK289883.1         1-1148
            1161-3251           BC013258.2         1081-3171
FEATURES             Location/Qualifiers
     source          1..3251
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="6"
                     /map="6p22.1"
     gene            1..3251
                     /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"
     STS             92..1696
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /db_xref="UniSTS:485838"
     CDS             112..1335
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /note="isoform b precursor is encoded by transcript
                     variant 2; butyrophilin 2"
                     /codon_start=1
                     /product="butyrophilin subfamily 2 member A2 isoform b
                     precursor"
                     /protein_id="NP_853509.1"
                     /db_xref="GI:31881693"
                     /db_xref="CCDS:CCDS4607.1"
                     /db_xref="GeneID:10385"
                     /db_xref="HGNC:1137"
                     /db_xref="MIM:613591"
                     /translation="
MEPAAALHFSLPASLLLLLLLLLLSLCALVSGLGSKPLIEIKAQEDGSIWLECISGGWYPEPLTVWRDPYGEVVPALKEVSIADADGLFMVTTAVIIRDKYVRNVSCSVNNTLLGQEKETVIFIPESFMPSASPWMVALAVILTASPWMVSMTVILAVFIIFMAVSICCIKKLQREKKILSGEKKVEQEEKEIAQQLQEELRWRRTFLHAADVVLDPDTAHPELFLSEDRRSVRRGPYRQRVPDNPERFDSQPCVLGWESFASGKHYWEVEVENVMVWTVGVCRHSVERKGEVLLIPQNGFWTLEMFGNQYRALSSPERILPLKESLCRVGVFLDYEAGDVSFYNMRDRSHIYTCPRSAFTVPVRPFFRLGSDDSPIFICPALTGASGVMVPEEGLKLHRVGTHQSL
"
     sig_peptide     112..207
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="COORDINATES: ab initio prediction:SignalP:4.0"
     mat_peptide     208..1332
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /product="butyrophilin subfamily 2 member A2 isoform b"
     misc_feature    217..465
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /note="Immunoglobulin domain; Region: Ig; cl11960"
                     /db_xref="CDD:213125"
     misc_feature    739..894
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /note="associated with SPRY domains; Region: PRY;
                     smart00589"
                     /db_xref="CDD:128857"
     misc_feature    898..1254
                     /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..487
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="alignment:Splign:1.39.8"
     variation       265
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:369291221"
     variation       279
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142411775"
     variation       318
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:76088803"
     variation       321
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:200834687"
     variation       337
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:144410497"
     variation       345
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372854548"
     variation       355
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200036284"
     variation       358
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201605260"
     variation       362
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139541725"
     variation       370
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:62617839"
     variation       390
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370196656"
     variation       428
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145439434"
     variation       447
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201008184"
     variation       451
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200096466"
     variation       454
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373346354"
     variation       485
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201995913"
     exon            488..694
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="alignment:Splign:1.39.8"
     variation       491
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:375385023"
     variation       550
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369920399"
     variation       562
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:113893469"
     variation       563
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373492069"
     variation       571
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:147003451"
     variation       694
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201972159"
     exon            695..715
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="alignment:Splign:1.39.8"
     exon            716..742
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="alignment:Splign:1.39.8"
     exon            743..3242
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="alignment:Splign:1.39.8"
     variation       743
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147646031"
     variation       747
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142151655"
     variation       753
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:368319822"
     variation       768
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148323426"
     variation       769
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142803339"
     variation       774
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:150431575"
     variation       777
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370826490"
     variation       778
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:138172438"
     variation       799
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374005579"
     variation       800
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200473019"
     variation       806
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112054667"
     variation       808
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372706575"
     variation       825
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368149710"
     variation       859
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200468059"
     variation       881
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200546581"
     variation       894
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375971811"
     variation       896
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374942833"
     variation       897
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200047445"
     variation       908
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:142785600"
     variation       913..914
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:34248025"
     variation       933
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146142561"
     variation       934
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:372254650"
     variation       939
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:140196606"
     variation       941
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:149403458"
     variation       954
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:181793664"
     variation       960
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202000782"
     variation       964
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:148562624"
     variation       1021
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369578278"
     variation       1045..1046
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:35755065"
     variation       1045
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:62617840"
     variation       1051
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:199832316"
     variation       1057
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:114760306"
     variation       1065
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:139419531"
     variation       1074
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2072802"
     variation       1097
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201353973"
     variation       1098
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372541099"
     variation       1103
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200888343"
     variation       1105
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376736237"
     variation       1124
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147634987"
     variation       1142
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:111615265"
     variation       1153
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375693447"
     variation       1161
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1614887"
     variation       1173
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369209046"
     variation       1180
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145542993"
     variation       1181
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200276371"
     variation       1198
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:16891646"
     variation       1230
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:376227483"
     variation       1271
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369257115"
     variation       1280
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143694906"
     variation       1288
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:114098566"
     variation       1301
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:73736249"
     variation       1310
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:199706137"
     variation       1344
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:377572514"
     variation       1363
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370709739"
     variation       1365
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201460456"
     variation       1377
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:190569086"
     variation       1385
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:370507187"
     variation       1440
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144477860"
     variation       1455
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:111432027"
     variation       1463
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:181721317"
     variation       1512
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372246478"
     variation       1532
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:186915774"
     variation       1627
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:3927423"
     variation       1774..1775
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace=""
                     /replace="ttc"
                     /db_xref="dbSNP:201274736"
     variation       1927
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:1804836"
     STS             1994..2106
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /standard_name="NIB885"
                     /db_xref="UniSTS:41935"
     variation       2069
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:75254848"
     variation       2071
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:191285742"
     variation       2091
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140325542"
     variation       2107
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:77055120"
     STS             2118..2326
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /standard_name="RH15843"
                     /db_xref="UniSTS:21190"
     variation       2120
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:182538207"
     variation       2215
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:75435297"
     variation       2299
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:7355"
     variation       2316..2317
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:138497943"
     variation       2460
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1131936"
     variation       2491
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149930183"
     variation       2502
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:55674248"
     variation       2505
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:61527210"
     variation       2646
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184920379"
     variation       2672
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:113353347"
     variation       2713
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:72500812"
     variation       2867
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:59001682"
     variation       2901
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:73387026"
     variation       3174
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:189684950"
     polyA_signal    3222..3227
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
     polyA_site      3242
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
ORIGIN      
aaatcttgggactttttggacacccagagaacaggtcccagataccgagtccgcaactccaaacatcgcgattaataggaggcctctggtctctgcctgccctgggtgctcatggaaccagctgctgctctgcacttctccctgccagcctccctcctcctcctcctgctcctcctccttctcagcctgtgtgcactggtctcaggccttgggtctaagcccctcattgaaatcaaggcccaagaggatgggagcatctggctggagtgcatatctggagggtggtacccagagcccctcacagtgtggagggacccctacggtgaggttgtgcccgccctgaaggaggtttccatcgctgatgctgacggcctcttcatggtcaccacagctgtgatcatcagagacaagtatgtgaggaatgtgtcctgctctgtcaacaacaccctgctcggccaggagaaggaaactgtcatttttattccagaatcctttatgcccagcgcatctccctggatggtggccctagctgtcatcctgaccgcatctccctggatggtgtccatgactgtcatcctggctgttttcatcatcttcatggctgtcagcatctgttgcatcaagaaacttcaaagggaaaaaaagattctgtcaggggaaaagaaagttgaacaagaggaaaaagaaattgcacagcaacttcaagaagaattgcgatggagaagaacattcttacatgctgctgatgtggtcctggatccagacaccgctcatcccgagctcttcctgtcagaggaccggagaagtgtgaggcggggcccctacaggcagagagtgcctgacaacccagagagattcgacagtcagccttgtgtcctgggatgggagagcttcgcctcagggaaacattactgggaggtggaggtggaaaacgtgatggtgtggactgtgggggtctgcagacacagtgttgagaggaaaggggaggtcctgctgattcctcagaatggcttctggaccctggagatgtttggaaaccaataccgggccctgtcctcccctgagaggattctccctttgaaggagtccctttgccgggtgggcgtcttcctggactatgaagctggagatgtctccttctacaacatgagggacagatcgcacatctacacatgtccccgttcagcctttactgtgcctgtgaggcccttcttcaggttagggtctgatgacagccccatcttcatctgccctgcactcacaggagccagtggggtcatggtgcctgaagagggcctgaaacttcacagagtggggacccaccagagcctatagaatcaattccttggactcacagccatgcagataagccctggccatctcagcagccaccgcacaacccccctaatgaaagacacgccctcctcccctctggtcacgtaagagaacatcttccagctgcctttttcacacccactccagccctctgccccagttttctcctcctcactagtctgtggctttagtagttcctttgcttgtaattatgggatgggatccaggcatagggaactagttgtttcatagctcccagtcaaaaagaaagtgagagaagctgttgggcagcgaacctactgtttaaaatcaggataaccacattaagcccaatatgccagttggcaccagatgctgtggacttggaatgaggccaacagggttcaccaggatgagagaggagagaggaatccacaggaccaccagaagggagagggaaccagatatgcagatcagagatagaggaagtggaaccagagagctgggagggaccaaggttgtaaggatggctaagtcccaccataagagctaaagggtcctgggagatgatggctcatttccacccaaccccaggatttccacagcacacacccacaggcctggacctgggatgaagatgaatgaagaacatggactcatgtggatgtggtttggctcagatgtccctgcaataaacaaggggtcagtacttagtccctgagtgtggttgaggtttgaggtcctggtcgagcagggcagtactggaccaggtctacgtcagcattcaggttcaatggggacaccagtggcttcaaacttcctgatctaattatgtttttagacacttagaagttattgaggactttaaagagcttttgtttatttgggttaatatttatgacatttgacattgaaacaaaaatttaaaatgttatcttttaatttatgttaaaatagcattaataaatcagttataggttaatgtagataggatgttttgtgaaaaagcaatctattgtgtccaaataaaaaaacaaaaagtgtgacactggttaactttttccagatctcatgtctggcttaataagagatatttgtattatcatatctgcctttgtattaaacctattggtatatcataggtcatgttagctcaaaaaaactttactgcacactactgagagaatgagatgaaaaacgattaatgtttcattattattattgtgaaaatattattaacactggggactccttaagagtacatcagagttctctctaggaatcccaaaaccacattttgaaactagaatagtggatcctggaagttaatccatgtgctggttaattttagatgtcaacctgactggattaaggaatacctagacagctggtacaacattatttctgggtgtgtctgtgagtgtgtttccagaagagattggcaagtgagtcagtgggaaattctctccttctgttggctgggtgcccaatacaacaaaaaggcagaggaaaggcaaattcttctctcctctggagctgagacactcttcttcttctgcccttggacatcagaactcctggctctccggcctttgaacttcaggacttgtaccaggaggccctgggttctcaggcctttggctttggactgagagttacacaatcagcttccctggttctgaggctttcagacttaaactgagccatgctaccagcatcccagggtctccagcctacagatgagctgttgtgcgatttcttagcctccataatcacatgagccaatctccttaataaatgcctgctcatagatctgtatctacatctatatctgtatgtgcatctatatctatgcctatatctatatctatatcatattgattttgtctctctggagaaccctgactaataaaatgaggcatctaaaaaaaaaaaaa
//

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
This page is licensed under a Creative Commons Attribution 2.1 Japan License.