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2024-03-28 17:18:24, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_001197239            2969 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens butyrophilin, subfamily 2, member A2 (BTN2A2),
            transcript variant 5, mRNA.
ACCESSION   NM_001197239
VERSION     NM_001197239.1  GI:308522749
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 2969)
  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 2969)
  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 2969)
  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 2969)
  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 2969)
  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 2969)
  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, AK293526.1 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 (5) lacks two consecutive in-frame
            exons in the 5' region compared to variant 1, resulting in a
            shorter protein (isoform d), compared to isoform a.
            
            ##Evidence-Data-START##
            Transcript exon combination :: AK293526.1, BI754184.1 [ECO:0000332]
            RNAseq introns              :: mixed/partial sample support
                                           ERS025081, ERS025082 [ECO:0000350]
            ##Evidence-Data-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-189               DC388932.1         2-190
            190-207             AK293526.1         165-182
            208-2969            BC013258.2         410-3171
FEATURES             Location/Qualifiers
     source          1..2969
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="6"
                     /map="6p22.1"
     gene            1..2969
                     /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..1414
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /db_xref="UniSTS:485838"
     CDS             112..1053
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /note="isoform d precursor is encoded by transcript
                     variant 5; butyrophilin 2"
                     /codon_start=1
                     /product="butyrophilin subfamily 2 member A2 isoform d
                     precursor"
                     /protein_id="NP_001184168.1"
                     /db_xref="GI:308522750"
                     /db_xref="CCDS:CCDS56403.1"
                     /db_xref="GeneID:10385"
                     /db_xref="HGNC:1137"
                     /db_xref="MIM:613591"
                     /translation="
MEPAAALHFSLPASLLLLLLLLLLSLCALVSESFMPSASPWMVALAVILTASPWMVSMTVILAVFIIFMAVSICCIKKLQREKKILSGEKKVEQEEKEIAQQLQEELRWRRTFLHAADVVLDPDTAHPELFLSEDRRSVRRGPYRQRVPDNPERFDSQPCVLGWESFASGKHYWEVEVENVMVWTVGVCRHSVERKGEVLLIPQNGFWTLEMFGNQYRALSSPERILPLKESLCRVGVFLDYEAGDVSFYNMRDRSHIYTCPRSAFTVPVRPFFRLGSDDSPIFICPALTGASGVMVPEEGLKLHRVGTHQSL
"
     sig_peptide     112..204
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
     mat_peptide     205..1050
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /product="butyrophilin subfamily 2 member A2 isoform d"
     misc_feature    457..612
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /note="associated with SPRY domains; Region: PRY;
                     smart00589"
                     /db_xref="CDD:128857"
     misc_feature    616..972
                     /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..412
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="alignment:Splign:1.39.8"
     variation       209
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:375385023"
     variation       268
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369920399"
     variation       280
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:113893469"
     variation       281
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373492069"
     variation       289
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:147003451"
     variation       412
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201972159"
     exon            413..433
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="alignment:Splign:1.39.8"
     exon            434..460
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="alignment:Splign:1.39.8"
     exon            461..2960
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="alignment:Splign:1.39.8"
     variation       461
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147646031"
     variation       465
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142151655"
     variation       471
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:368319822"
     variation       486
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148323426"
     variation       487
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142803339"
     variation       492
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:150431575"
     variation       495
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370826490"
     variation       496
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:138172438"
     variation       517
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374005579"
     variation       518
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200473019"
     variation       524
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112054667"
     variation       526
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372706575"
     variation       543
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368149710"
     variation       577
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200468059"
     variation       599
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200546581"
     variation       612
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375971811"
     variation       614
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374942833"
     variation       615
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200047445"
     variation       626
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:142785600"
     variation       631..632
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:34248025"
     variation       651
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146142561"
     variation       652
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:372254650"
     variation       657
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:140196606"
     variation       659
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:149403458"
     variation       672
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:181793664"
     variation       678
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202000782"
     variation       682
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:148562624"
     variation       739
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369578278"
     variation       763..764
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:35755065"
     variation       763
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:62617840"
     variation       769
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:199832316"
     variation       775
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:114760306"
     variation       783
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:139419531"
     variation       792
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2072802"
     variation       815
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201353973"
     variation       816
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372541099"
     variation       821
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200888343"
     variation       823
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376736237"
     variation       842
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147634987"
     variation       860
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:111615265"
     variation       871
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375693447"
     variation       879
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1614887"
     variation       891
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369209046"
     variation       898
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145542993"
     variation       899
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200276371"
     variation       916
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:16891646"
     variation       948
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:376227483"
     variation       989
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369257115"
     variation       998
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143694906"
     variation       1006
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:114098566"
     variation       1019
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:73736249"
     variation       1028
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:199706137"
     variation       1062
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:377572514"
     variation       1081
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370709739"
     variation       1083
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201460456"
     variation       1095
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:190569086"
     variation       1103
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:370507187"
     variation       1158
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144477860"
     variation       1173
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:111432027"
     variation       1181
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:181721317"
     variation       1230
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372246478"
     variation       1250
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:186915774"
     variation       1345
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:3927423"
     variation       1492..1493
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace=""
                     /replace="ttc"
                     /db_xref="dbSNP:201274736"
     variation       1645
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:1804836"
     STS             1712..1824
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /standard_name="NIB885"
                     /db_xref="UniSTS:41935"
     variation       1787
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:75254848"
     variation       1789
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:191285742"
     variation       1809
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140325542"
     variation       1825
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:77055120"
     STS             1836..2044
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /standard_name="RH15843"
                     /db_xref="UniSTS:21190"
     variation       1838
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:182538207"
     variation       1933
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:75435297"
     variation       2017
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:7355"
     variation       2034..2035
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:138497943"
     variation       2178
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1131936"
     variation       2209
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149930183"
     variation       2220
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:55674248"
     variation       2223
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:61527210"
     variation       2364
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184920379"
     variation       2390
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:113353347"
     variation       2431
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:72500812"
     variation       2585
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:59001682"
     variation       2619
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:73387026"
     variation       2892
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:189684950"
     polyA_signal    2940..2945
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
     polyA_site      2960
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
ORIGIN      
aaatcttgggactttttggacacccagagaacaggtcccagataccgagtccgcaactccaaacatcgcgattaataggaggcctctggtctctgcctgccctgggtgctcatggaaccagctgctgctctgcacttctccctgccagcctccctcctcctcctcctgctcctcctccttctcagcctgtgtgcactggtctcagaatcctttatgcccagcgcatctccctggatggtggccctagctgtcatcctgaccgcatctccctggatggtgtccatgactgtcatcctggctgttttcatcatcttcatggctgtcagcatctgttgcatcaagaaacttcaaagggaaaaaaagattctgtcaggggaaaagaaagttgaacaagaggaaaaagaaattgcacagcaacttcaagaagaattgcgatggagaagaacattcttacatgctgctgatgtggtcctggatccagacaccgctcatcccgagctcttcctgtcagaggaccggagaagtgtgaggcggggcccctacaggcagagagtgcctgacaacccagagagattcgacagtcagccttgtgtcctgggatgggagagcttcgcctcagggaaacattactgggaggtggaggtggaaaacgtgatggtgtggactgtgggggtctgcagacacagtgttgagaggaaaggggaggtcctgctgattcctcagaatggcttctggaccctggagatgtttggaaaccaataccgggccctgtcctcccctgagaggattctccctttgaaggagtccctttgccgggtgggcgtcttcctggactatgaagctggagatgtctccttctacaacatgagggacagatcgcacatctacacatgtccccgttcagcctttactgtgcctgtgaggcccttcttcaggttagggtctgatgacagccccatcttcatctgccctgcactcacaggagccagtggggtcatggtgcctgaagagggcctgaaacttcacagagtggggacccaccagagcctatagaatcaattccttggactcacagccatgcagataagccctggccatctcagcagccaccgcacaacccccctaatgaaagacacgccctcctcccctctggtcacgtaagagaacatcttccagctgcctttttcacacccactccagccctctgccccagttttctcctcctcactagtctgtggctttagtagttcctttgcttgtaattatgggatgggatccaggcatagggaactagttgtttcatagctcccagtcaaaaagaaagtgagagaagctgttgggcagcgaacctactgtttaaaatcaggataaccacattaagcccaatatgccagttggcaccagatgctgtggacttggaatgaggccaacagggttcaccaggatgagagaggagagaggaatccacaggaccaccagaagggagagggaaccagatatgcagatcagagatagaggaagtggaaccagagagctgggagggaccaaggttgtaaggatggctaagtcccaccataagagctaaagggtcctgggagatgatggctcatttccacccaaccccaggatttccacagcacacacccacaggcctggacctgggatgaagatgaatgaagaacatggactcatgtggatgtggtttggctcagatgtccctgcaataaacaaggggtcagtacttagtccctgagtgtggttgaggtttgaggtcctggtcgagcagggcagtactggaccaggtctacgtcagcattcaggttcaatggggacaccagtggcttcaaacttcctgatctaattatgtttttagacacttagaagttattgaggactttaaagagcttttgtttatttgggttaatatttatgacatttgacattgaaacaaaaatttaaaatgttatcttttaatttatgttaaaatagcattaataaatcagttataggttaatgtagataggatgttttgtgaaaaagcaatctattgtgtccaaataaaaaaacaaaaagtgtgacactggttaactttttccagatctcatgtctggcttaataagagatatttgtattatcatatctgcctttgtattaaacctattggtatatcataggtcatgttagctcaaaaaaactttactgcacactactgagagaatgagatgaaaaacgattaatgtttcattattattattgtgaaaatattattaacactggggactccttaagagtacatcagagttctctctaggaatcccaaaaccacattttgaaactagaatagtggatcctggaagttaatccatgtgctggttaattttagatgtcaacctgactggattaaggaatacctagacagctggtacaacattatttctgggtgtgtctgtgagtgtgtttccagaagagattggcaagtgagtcagtgggaaattctctccttctgttggctgggtgcccaatacaacaaaaaggcagaggaaaggcaaattcttctctcctctggagctgagacactcttcttcttctgcccttggacatcagaactcctggctctccggcctttgaacttcaggacttgtaccaggaggccctgggttctcaggcctttggctttggactgagagttacacaatcagcttccctggttctgaggctttcagacttaaactgagccatgctaccagcatcccagggtctccagcctacagatgagctgttgtgcgatttcttagcctccataatcacatgagccaatctccttaataaatgcctgctcatagatctgtatctacatctatatctgtatgtgcatctatatctatgcctatatctatatctatatcatattgattttgtctctctggagaaccctgactaataaaatgaggcatctaaaaaaaaaaaaa
//

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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