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2025-05-09 18:29:51, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_006995 3602 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens butyrophilin, subfamily 2, member A2 (BTN2A2),
transcript variant 1, mRNA.
ACCESSION NM_006995
VERSION NM_006995.4 GI:308522743
KEYWORDS RefSeq.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
REFERENCE 1 (bases 1 to 3602)
AUTHORS Shi,J., Levinson,D.F., Duan,J., Sanders,A.R., Zheng,Y., Pe'er,I.,
Dudbridge,F., Holmans,P.A., Whittemore,A.S., Mowry,B.J., Olincy,A.,
Amin,F., Cloninger,C.R., Silverman,J.M., Buccola,N.G.,
Byerley,W.F., Black,D.W., Crowe,R.R., Oksenberg,J.R., Mirel,D.B.,
Kendler,K.S., Freedman,R. and Gejman,P.V.
TITLE Common variants on chromosome 6p22.1 are associated with
schizophrenia
JOURNAL Nature 460 (7256), 753-757 (2009)
PUBMED 19571809
REFERENCE 2 (bases 1 to 3602)
AUTHORS Mungall,A.J., Palmer,S.A., Sims,S.K., Edwards,C.A., Ashurst,J.L.,
Wilming,L., Jones,M.C., Horton,R., Hunt,S.E., Scott,C.E.,
Gilbert,J.G., Clamp,M.E., Bethel,G., Milne,S., Ainscough,R.,
Almeida,J.P., Ambrose,K.D., Andrews,T.D., Ashwell,R.I.,
Babbage,A.K., Bagguley,C.L., Bailey,J., Banerjee,R., Barker,D.J.,
Barlow,K.F., Bates,K., Beare,D.M., Beasley,H., Beasley,O.,
Bird,C.P., Blakey,S., Bray-Allen,S., Brook,J., Brown,A.J.,
Brown,J.Y., Burford,D.C., Burrill,W., Burton,J., Carder,C.,
Carter,N.P., Chapman,J.C., Clark,S.Y., Clark,G., Clee,C.M.,
Clegg,S., Cobley,V., Collier,R.E., Collins,J.E., Colman,L.K.,
Corby,N.R., Coville,G.J., Culley,K.M., Dhami,P., Davies,J.,
Dunn,M., Earthrowl,M.E., Ellington,A.E., Evans,K.A., Faulkner,L.,
Francis,M.D., Frankish,A., Frankland,J., French,L., Garner,P.,
Garnett,J., Ghori,M.J., Gilby,L.M., Gillson,C.J., Glithero,R.J.,
Grafham,D.V., Grant,M., Gribble,S., Griffiths,C., Griffiths,M.,
Hall,R., Halls,K.S., Hammond,S., Harley,J.L., Hart,E.A.,
Heath,P.D., Heathcott,R., Holmes,S.J., Howden,P.J., Howe,K.L.,
Howell,G.R., Huckle,E., Humphray,S.J., Humphries,M.D., Hunt,A.R.,
Johnson,C.M., Joy,A.A., Kay,M., Keenan,S.J., Kimberley,A.M.,
King,A., Laird,G.K., Langford,C., Lawlor,S., Leongamornlert,D.A.,
Leversha,M., Lloyd,C.R., Lloyd,D.M., Loveland,J.E., Lovell,J.,
Martin,S., Mashreghi-Mohammadi,M., Maslen,G.L., Matthews,L.,
McCann,O.T., McLaren,S.J., McLay,K., McMurray,A., Moore,M.J.,
Mullikin,J.C., Niblett,D., Nickerson,T., Novik,K.L., Oliver,K.,
Overton-Larty,E.K., Parker,A., Patel,R., Pearce,A.V., Peck,A.I.,
Phillimore,B., Phillips,S., Plumb,R.W., Porter,K.M., Ramsey,Y.,
Ranby,S.A., Rice,C.M., Ross,M.T., Searle,S.M., Sehra,H.K.,
Sheridan,E., Skuce,C.D., Smith,S., Smith,M., Spraggon,L.,
Squares,S.L., Steward,C.A., Sycamore,N., Tamlyn-Hall,G., Tester,J.,
Theaker,A.J., Thomas,D.W., Thorpe,A., Tracey,A., Tromans,A.,
Tubby,B., Wall,M., Wallis,J.M., West,A.P., White,S.S.,
Whitehead,S.L., Whittaker,H., Wild,A., Willey,D.J., Wilmer,T.E.,
Wood,J.M., Wray,P.W., Wyatt,J.C., Young,L., Younger,R.M.,
Bentley,D.R., Coulson,A., Durbin,R., Hubbard,T., Sulston,J.E.,
Dunham,I., Rogers,J. and Beck,S.
TITLE The DNA sequence and analysis of human chromosome 6
JOURNAL Nature 425 (6960), 805-811 (2003)
PUBMED 14574404
REFERENCE 3 (bases 1 to 3602)
AUTHORS Cavaletto,M., Giuffrida,M.G., Fortunato,D., Gardano,L.,
Dellavalle,G., Napolitano,L., Giunta,C., Bertino,E., Fabris,C. and
Conti,A.
TITLE A proteomic approach to evaluate the butyrophilin gene family
expression in human milk fat globule membrane
JOURNAL Proteomics 2 (7), 850-856 (2002)
PUBMED 12124930
REFERENCE 4 (bases 1 to 3602)
AUTHORS Rhodes,D.A., Stammers,M., Malcherek,G., Beck,S. and Trowsdale,J.
TITLE The cluster of BTN genes in the extended major histocompatibility
complex
JOURNAL Genomics 71 (3), 351-362 (2001)
PUBMED 11170752
REFERENCE 5 (bases 1 to 3602)
AUTHORS Henry,J., Miller,M.M. and Pontarotti,P.
TITLE Structure and evolution of the extended B7 family
JOURNAL Immunol. Today 20 (6), 285-288 (1999)
PUBMED 10354554
REMARK Review article
REFERENCE 6 (bases 1 to 3602)
AUTHORS Ruddy,D.A., Kronmal,G.S., Lee,V.K., Mintier,G.A., Quintana,L.,
Domingo,R. Jr., Meyer,N.C., Irrinki,A., McClelland,E.E., Fullan,A.,
Mapa,F.A., Moore,T., Thomas,W., Loeb,D.B., Harmon,C.,
Tsuchihashi,Z., Wolff,R.K., Schatzman,R.C. and Feder,J.N.
TITLE A 1.1-Mb transcript map of the hereditary hemochromatosis locus
JOURNAL Genome Res. 7 (5), 441-456 (1997)
PUBMED 9149941
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from DC388932.1, U90550.1 and
BC014021.2.
On Oct 14, 2010 this sequence version replaced gi:31881700.
Summary: Butyrophilin is the major protein associated with fat
droplets in the milk. This gene is a member of the BTN2 subfamily
of genes, which encode proteins belonging to the butyrophilin
protein family. The gene is located in a cluster on chromosome 6,
consisting of seven genes belonging to the expanding
B7/butyrophilin-like group, a subset of the immunoglobulin gene
superfamily. The encoded protein is a type I receptor glycoprotein
involved in lipid, fatty-acid and sterol metabolism. Several
alternatively spliced transcript variants encoding different
isoforms have been found for this gene. [provided by RefSeq, Oct
2010].
Transcript Variant: This variant (1) and variant 3 encode the
longest isoform (a).
##Evidence-Data-START##
Transcript exon combination :: U90550.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025084, ERS025088 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-58 DC388932.1 2-59
59-1508 U90550.1 34-1483
1509-2708 BC014021.2 1507-2706
2709-3602 U90550.1 2685-3578
FEATURES Location/Qualifiers
source 1..3602
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="6"
/map="6p22.1"
gene 1..3602
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/note="butyrophilin, subfamily 2, member A2"
/db_xref="GeneID:10385"
/db_xref="HGNC:1137"
/db_xref="HPRD:12545"
/db_xref="MIM:613591"
exon 1..81
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/inference="alignment:Splign:1.39.8"
variation 58
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:9461249"
misc_feature 76..78
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/note="upstream in-frame stop codon"
exon 82..205
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/inference="alignment:Splign:1.39.8"
CDS 112..1683
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/note="isoform a precursor is encoded by transcript
variant 1; butyrophilin 2"
/codon_start=1
/product="butyrophilin subfamily 2 member A2 isoform a
precursor"
/protein_id="NP_008926.2"
/db_xref="GI:6453813"
/db_xref="CCDS:CCDS4606.1"
/db_xref="GeneID:10385"
/db_xref="HGNC:1137"
/db_xref="HPRD:12545"
/db_xref="MIM:613591"
/translation="
MEPAAALHFSLPASLLLLLLLLLLSLCALVSAQFTVVGPANPILAMVGENTTLRCHLSPEKNAEDMEVRWFRSQFSPAVFVYKGGRERTEEQMEEYRGRITFVSKDINRGSVALVIHNVTAQENGIYRCYFQEGRSYDEAILRLVVAGLGSKPLIEIKAQEDGSIWLECISGGWYPEPLTVWRDPYGEVVPALKEVSIADADGLFMVTTAVIIRDKYVRNVSCSVNNTLLGQEKETVIFIPESFMPSASPWMVALAVILTASPWMVSMTVILAVFIIFMAVSICCIKKLQREKKILSGEKKVEQEEKEIAQQLQEELRWRRTFLHAADVVLDPDTAHPELFLSEDRRSVRRGPYRQRVPDNPERFDSQPCVLGWESFASGKHYWEVEVENVMVWTVGVCRHSVERKGEVLLIPQNGFWTLEMFGNQYRALSSPERILPLKESLCRVGVFLDYEAGDVSFYNMRDRSHIYTCPRSAFTVPVRPFFRLGSDDSPIFICPALTGASGVMVPEEGLKLHRVGTHQSL
"
sig_peptide 112..207
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/inference="COORDINATES: ab initio prediction:SignalP:4.0"
mat_peptide 208..1680
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/product="butyrophilin subfamily 2 member A2 isoform a"
misc_feature 208..549
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/note="Immunoglobulin V-set domain; Region: V-set;
pfam07686"
/db_xref="CDD:203725"
misc_feature 253..552
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/note="Immunoglobulin (Ig)-like domain of myelin
oligodendrocyte glycoprotein (MOG); Region: Ig_MOG_like;
cd05713"
/db_xref="CDD:143190"
misc_feature order(301..306,361..363,394..396,505..507,511..528)
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/note="antigen binding site; other site"
/db_xref="CDD:143190"
misc_feature 565..813
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/note="Immunoglobulin domain; Region: Ig; cl11960"
/db_xref="CDD:213125"
misc_feature 907..969
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q8WVV5.2);
transmembrane region"
misc_feature 1087..1242
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/note="associated with SPRY domains; Region: PRY;
smart00589"
/db_xref="CDD:128857"
misc_feature 1246..1602
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/note="Domain in SPla and the RYanodine Receptor; Region:
SPRY; smart00449"
/db_xref="CDD:128725"
variation 117
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:375369181"
variation 119
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:202213069"
variation 122
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:73736234"
variation 150
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="c"
/db_xref="dbSNP:147636357"
variation 168
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:115247877"
exon 206..553
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/inference="alignment:Splign:1.39.8"
variation 219
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:138070617"
variation 220
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:143653188"
variation 226
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="g"
/db_xref="dbSNP:57038103"
variation 271
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:370867259"
variation 288
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:150302333"
variation 289
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:181037825"
variation 316
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:375285642"
variation 317
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:368009368"
variation 352
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="g"
/replace="t"
/db_xref="dbSNP:372237219"
variation 354
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:376950043"
variation 374
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:376558792"
variation 399
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:112257227"
variation 400
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:367692328"
variation 401
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:144702884"
variation 437
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:149453161"
variation 438
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:377645117"
variation 465
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:143017993"
variation 523
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:146154371"
variation 539
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:201687793"
exon 554..835
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/inference="alignment:Splign:1.39.8"
variation 613
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="g"
/db_xref="dbSNP:369291221"
variation 627
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:142411775"
variation 666
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="g"
/db_xref="dbSNP:76088803"
variation 669
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="c"
/db_xref="dbSNP:200834687"
variation 685
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:144410497"
variation 693
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:372854548"
variation 703
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200036284"
variation 706
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:201605260"
variation 710
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:139541725"
variation 718
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:62617839"
variation 738
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:370196656"
variation 776
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:145439434"
variation 795
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:201008184"
variation 799
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:200096466"
variation 802
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:373346354"
variation 833
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:201995913"
exon 836..1042
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/inference="alignment:Splign:1.39.8"
variation 839
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="c"
/db_xref="dbSNP:375385023"
variation 898
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:369920399"
variation 910
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="g"
/replace="t"
/db_xref="dbSNP:113893469"
variation 911
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:373492069"
variation 919
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="g"
/db_xref="dbSNP:147003451"
variation 1042
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="g"
/db_xref="dbSNP:201972159"
exon 1043..1063
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/inference="alignment:Splign:1.39.8"
exon 1064..1090
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/inference="alignment:Splign:1.39.8"
exon 1091..3590
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/inference="alignment:Splign:1.39.8"
variation 1091
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:147646031"
variation 1095
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:142151655"
variation 1101
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="c"
/db_xref="dbSNP:368319822"
variation 1116
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:148323426"
variation 1117
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:142803339"
variation 1122
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="t"
/db_xref="dbSNP:150431575"
variation 1125
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:370826490"
variation 1126
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:138172438"
variation 1147
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:374005579"
variation 1148
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200473019"
variation 1154
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:112054667"
variation 1156
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:372706575"
variation 1173
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:368149710"
variation 1207
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200468059"
variation 1229
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="g"
/db_xref="dbSNP:200546581"
variation 1242
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:375971811"
variation 1244
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:374942833"
variation 1245
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:200047445"
variation 1256
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="t"
/db_xref="dbSNP:142785600"
variation 1261..1262
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace=""
/replace="g"
/db_xref="dbSNP:34248025"
variation 1281
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:146142561"
variation 1282
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="g"
/db_xref="dbSNP:372254650"
variation 1287
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="g"
/replace="t"
/db_xref="dbSNP:140196606"
variation 1289
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="t"
/db_xref="dbSNP:149403458"
variation 1302
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="g"
/replace="t"
/db_xref="dbSNP:181793664"
variation 1308
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:202000782"
variation 1312
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="g"
/db_xref="dbSNP:148562624"
variation 1369
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:369578278"
variation 1393..1394
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace=""
/replace="g"
/db_xref="dbSNP:35755065"
variation 1393
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:62617840"
variation 1399
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="g"
/db_xref="dbSNP:199832316"
variation 1405
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="t"
/db_xref="dbSNP:114760306"
variation 1413
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:139419531"
variation 1422
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2072802"
variation 1445
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:201353973"
variation 1446
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:372541099"
variation 1451
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="g"
/db_xref="dbSNP:200888343"
variation 1453
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:376736237"
variation 1472
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:147634987"
variation 1490
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:111615265"
variation 1501
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:375693447"
variation 1509
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1614887"
variation 1521
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:369209046"
variation 1528
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:145542993"
variation 1529
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200276371"
variation 1546
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:16891646"
variation 1578
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="g"
/replace="t"
/db_xref="dbSNP:376227483"
variation 1619
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:369257115"
variation 1628
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:143694906"
variation 1636
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:114098566"
variation 1649
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="c"
/db_xref="dbSNP:73736249"
variation 1658
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="g"
/db_xref="dbSNP:199706137"
variation 1692
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="c"
/db_xref="dbSNP:377572514"
variation 1711
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:370709739"
variation 1713
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="g"
/db_xref="dbSNP:201460456"
variation 1725
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:190569086"
variation 1733
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="g"
/replace="t"
/db_xref="dbSNP:370507187"
variation 1788
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:144477860"
variation 1803
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:111432027"
variation 1811
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:181721317"
variation 1860
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:372246478"
variation 1880
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:186915774"
variation 1975
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:3927423"
variation 2122..2123
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace=""
/replace="ttc"
/db_xref="dbSNP:201274736"
variation 2275
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1804836"
STS 2342..2454
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/standard_name="NIB885"
/db_xref="UniSTS:41935"
variation 2417
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:75254848"
variation 2419
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="c"
/db_xref="dbSNP:191285742"
variation 2439
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:140325542"
variation 2455
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="c"
/db_xref="dbSNP:77055120"
STS 2466..2674
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/standard_name="RH15843"
/db_xref="UniSTS:21190"
variation 2468
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="g"
/replace="t"
/db_xref="dbSNP:182538207"
variation 2563
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:75435297"
variation 2647
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="t"
/db_xref="dbSNP:7355"
variation 2664..2665
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace=""
/replace="a"
/db_xref="dbSNP:138497943"
variation 2808
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1131936"
variation 2839
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:149930183"
variation 2850
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="g"
/replace="t"
/db_xref="dbSNP:55674248"
variation 2853
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:61527210"
variation 2994
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:184920379"
variation 3020
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="t"
/db_xref="dbSNP:113353347"
variation 3061
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:72500812"
variation 3215
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:59001682"
variation 3249
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:73387026"
variation 3522
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:189684950"
polyA_signal 3570..3575
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
polyA_site 3590
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
ORIGIN
aaatcttgggactttttggacacccagagaacaggtcccagataccgagtccgcaactccaaacatcgcgattaataggaggcctctggtctctgcctgccctgggtgctcatggaaccagctgctgctctgcacttctccctgccagcctccctcctcctcctcctgctcctcctccttctcagcctgtgtgcactggtctcagcccagtttactgtcgtggggccagctaatcccatcctggccatggtgggagaaaacactacattacgctgccatctgtcacccgagaaaaatgctgaggacatggaggtgcggtggttccggtctcagttctcccccgcagtgtttgtgtataagggtgggagagagagaacagaggagcagatggaggagtaccggggaagaatcacctttgtgagcaaagacatcaacaggggcagcgtggccctggtcatacataacgtcacagcccaggagaatgggatctaccgctgttacttccaagaaggcaggtcctacgatgaggccatcctacgcctcgtggtggcaggccttgggtctaagcccctcattgaaatcaaggcccaagaggatgggagcatctggctggagtgcatatctggagggtggtacccagagcccctcacagtgtggagggacccctacggtgaggttgtgcccgccctgaaggaggtttccatcgctgatgctgacggcctcttcatggtcaccacagctgtgatcatcagagacaagtatgtgaggaatgtgtcctgctctgtcaacaacaccctgctcggccaggagaaggaaactgtcatttttattccagaatcctttatgcccagcgcatctccctggatggtggccctagctgtcatcctgaccgcatctccctggatggtgtccatgactgtcatcctggctgttttcatcatcttcatggctgtcagcatctgttgcatcaagaaacttcaaagggaaaaaaagattctgtcaggggaaaagaaagttgaacaagaggaaaaagaaattgcacagcaacttcaagaagaattgcgatggagaagaacattcttacatgctgctgatgtggtcctggatccagacaccgctcatcccgagctcttcctgtcagaggaccggagaagtgtgaggcggggcccctacaggcagagagtgcctgacaacccagagagattcgacagtcagccttgtgtcctgggatgggagagcttcgcctcagggaaacattactgggaggtggaggtggaaaacgtgatggtgtggactgtgggggtctgcagacacagtgttgagaggaaaggggaggtcctgctgattcctcagaatggcttctggaccctggagatgtttggaaaccaataccgggccctgtcctcccctgagaggattctccctttgaaggagtccctttgccgggtgggcgtcttcctggactatgaagctggagatgtctccttctacaacatgagggacagatcgcacatctacacatgtccccgttcagcctttactgtgcctgtgaggcccttcttcaggttagggtctgatgacagccccatcttcatctgccctgcactcacaggagccagtggggtcatggtgcctgaagagggcctgaaacttcacagagtggggacccaccagagcctatagaatcaattccttggactcacagccatgcagataagccctggccatctcagcagccaccgcacaacccccctaatgaaagacacgccctcctcccctctggtcacgtaagagaacatcttccagctgcctttttcacacccactccagccctctgccccagttttctcctcctcactagtctgtggctttagtagttcctttgcttgtaattatgggatgggatccaggcatagggaactagttgtttcatagctcccagtcaaaaagaaagtgagagaagctgttgggcagcgaacctactgtttaaaatcaggataaccacattaagcccaatatgccagttggcaccagatgctgtggacttggaatgaggccaacagggttcaccaggatgagagaggagagaggaatccacaggaccaccagaagggagagggaaccagatatgcagatcagagatagaggaagtggaaccagagagctgggagggaccaaggttgtaaggatggctaagtcccaccataagagctaaagggtcctgggagatgatggctcatttccacccaaccccaggatttccacagcacacacccacaggcctggacctgggatgaagatgaatgaagaacatggactcatgtggatgtggtttggctcagatgtccctgcaataaacaaggggtcagtacttagtccctgagtgtggttgaggtttgaggtcctggtcgagcagggcagtactggaccaggtctacgtcagcattcaggttcaatggggacaccagtggcttcaaacttcctgatctaattatgtttttagacacttagaagttattgaggactttaaagagcttttgtttatttgggttaatatttatgacatttgacattgaaacaaaaatttaaaatgttatcttttaatttatgttaaaatagcattaataaatcagttataggttaatgtagataggatgttttgtgaaaaagcaatctattgtgtccaaataaaaaaacaaaaagtgtgacactggttaactttttccagatctcatgtctggcttaataagagatatttgtattatcatatctgcctttgtattaaacctattggtatatcataggtcatgttagctcaaaaaaactttactgcacactactgagagaatgagatgaaaaacgattaatgtttcattattattattgtgaaaatattattaacactggggactccttaagagtacatcagagttctctctaggaatcccaaaaccacattttgaaactagaatagtggatcctggaagttaatccatgtgctggttaattttagatgtcaacctgactggattaaggaatacctagacagctggtacaacattatttctgggtgtgtctgtgagtgtgtttccagaagagattggcaagtgagtcagtgggaaattctctccttctgttggctgggtgcccaatacaacaaaaaggcagaggaaaggcaaattcttctctcctctggagctgagacactcttcttcttctgcccttggacatcagaactcctggctctccggcctttgaacttcaggacttgtaccaggaggccctgggttctcaggcctttggctttggactgagagttacacaatcagcttccctggttctgaggctttcagacttaaactgagccatgctaccagcatcccagggtctccagcctacagatgagctgttgtgcgatttcttagcctccataatcacatgagccaatctccttaataaatgcctgctcatagatctgtatctacatctatatctgtatgtgcatctatatctatgcctatatctatatctatatcatattgattttgtctctctggagaaccctgactaataaaatgaggcatctaaaaaaaaaaaaaaaa
//
ANNOTATIONS 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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