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2025-05-09 18:33:15, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001197240 3470 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens butyrophilin, subfamily 2, member A2 (BTN2A2),
transcript variant 6, mRNA.
ACCESSION NM_001197240
VERSION NM_001197240.1 GI:308522751
KEYWORDS RefSeq.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
REFERENCE 1 (bases 1 to 3470)
AUTHORS Shi,J., Levinson,D.F., Duan,J., Sanders,A.R., Zheng,Y., Pe'er,I.,
Dudbridge,F., Holmans,P.A., Whittemore,A.S., Mowry,B.J., Olincy,A.,
Amin,F., Cloninger,C.R., Silverman,J.M., Buccola,N.G.,
Byerley,W.F., Black,D.W., Crowe,R.R., Oksenberg,J.R., Mirel,D.B.,
Kendler,K.S., Freedman,R. and Gejman,P.V.
TITLE Common variants on chromosome 6p22.1 are associated with
schizophrenia
JOURNAL Nature 460 (7256), 753-757 (2009)
PUBMED 19571809
REFERENCE 2 (bases 1 to 3470)
AUTHORS Mungall,A.J., Palmer,S.A., Sims,S.K., Edwards,C.A., Ashurst,J.L.,
Wilming,L., Jones,M.C., Horton,R., Hunt,S.E., Scott,C.E.,
Gilbert,J.G., Clamp,M.E., Bethel,G., Milne,S., Ainscough,R.,
Almeida,J.P., Ambrose,K.D., Andrews,T.D., Ashwell,R.I.,
Babbage,A.K., Bagguley,C.L., Bailey,J., Banerjee,R., Barker,D.J.,
Barlow,K.F., Bates,K., Beare,D.M., Beasley,H., Beasley,O.,
Bird,C.P., Blakey,S., Bray-Allen,S., Brook,J., Brown,A.J.,
Brown,J.Y., Burford,D.C., Burrill,W., Burton,J., Carder,C.,
Carter,N.P., Chapman,J.C., Clark,S.Y., Clark,G., Clee,C.M.,
Clegg,S., Cobley,V., Collier,R.E., Collins,J.E., Colman,L.K.,
Corby,N.R., Coville,G.J., Culley,K.M., Dhami,P., Davies,J.,
Dunn,M., Earthrowl,M.E., Ellington,A.E., Evans,K.A., Faulkner,L.,
Francis,M.D., Frankish,A., Frankland,J., French,L., Garner,P.,
Garnett,J., Ghori,M.J., Gilby,L.M., Gillson,C.J., Glithero,R.J.,
Grafham,D.V., Grant,M., Gribble,S., Griffiths,C., Griffiths,M.,
Hall,R., Halls,K.S., Hammond,S., Harley,J.L., Hart,E.A.,
Heath,P.D., Heathcott,R., Holmes,S.J., Howden,P.J., Howe,K.L.,
Howell,G.R., Huckle,E., Humphray,S.J., Humphries,M.D., Hunt,A.R.,
Johnson,C.M., Joy,A.A., Kay,M., Keenan,S.J., Kimberley,A.M.,
King,A., Laird,G.K., Langford,C., Lawlor,S., Leongamornlert,D.A.,
Leversha,M., Lloyd,C.R., Lloyd,D.M., Loveland,J.E., Lovell,J.,
Martin,S., Mashreghi-Mohammadi,M., Maslen,G.L., Matthews,L.,
McCann,O.T., McLaren,S.J., McLay,K., McMurray,A., Moore,M.J.,
Mullikin,J.C., Niblett,D., Nickerson,T., Novik,K.L., Oliver,K.,
Overton-Larty,E.K., Parker,A., Patel,R., Pearce,A.V., Peck,A.I.,
Phillimore,B., Phillips,S., Plumb,R.W., Porter,K.M., Ramsey,Y.,
Ranby,S.A., Rice,C.M., Ross,M.T., Searle,S.M., Sehra,H.K.,
Sheridan,E., Skuce,C.D., Smith,S., Smith,M., Spraggon,L.,
Squares,S.L., Steward,C.A., Sycamore,N., Tamlyn-Hall,G., Tester,J.,
Theaker,A.J., Thomas,D.W., Thorpe,A., Tracey,A., Tromans,A.,
Tubby,B., Wall,M., Wallis,J.M., West,A.P., White,S.S.,
Whitehead,S.L., Whittaker,H., Wild,A., Willey,D.J., Wilmer,T.E.,
Wood,J.M., Wray,P.W., Wyatt,J.C., Young,L., Younger,R.M.,
Bentley,D.R., Coulson,A., Durbin,R., Hubbard,T., Sulston,J.E.,
Dunham,I., Rogers,J. and Beck,S.
TITLE The DNA sequence and analysis of human chromosome 6
JOURNAL Nature 425 (6960), 805-811 (2003)
PUBMED 14574404
REFERENCE 3 (bases 1 to 3470)
AUTHORS Cavaletto,M., Giuffrida,M.G., Fortunato,D., Gardano,L.,
Dellavalle,G., Napolitano,L., Giunta,C., Bertino,E., Fabris,C. and
Conti,A.
TITLE A proteomic approach to evaluate the butyrophilin gene family
expression in human milk fat globule membrane
JOURNAL Proteomics 2 (7), 850-856 (2002)
PUBMED 12124930
REFERENCE 4 (bases 1 to 3470)
AUTHORS Rhodes,D.A., Stammers,M., Malcherek,G., Beck,S. and Trowsdale,J.
TITLE The cluster of BTN genes in the extended major histocompatibility
complex
JOURNAL Genomics 71 (3), 351-362 (2001)
PUBMED 11170752
REFERENCE 5 (bases 1 to 3470)
AUTHORS Henry,J., Miller,M.M. and Pontarotti,P.
TITLE Structure and evolution of the extended B7 family
JOURNAL Immunol. Today 20 (6), 285-288 (1999)
PUBMED 10354554
REMARK Review article
REFERENCE 6 (bases 1 to 3470)
AUTHORS Ruddy,D.A., Kronmal,G.S., Lee,V.K., Mintier,G.A., Quintana,L.,
Domingo,R. Jr., Meyer,N.C., Irrinki,A., McClelland,E.E., Fullan,A.,
Mapa,F.A., Moore,T., Thomas,W., Loeb,D.B., Harmon,C.,
Tsuchihashi,Z., Wolff,R.K., Schatzman,R.C. and Feder,J.N.
TITLE A 1.1-Mb transcript map of the hereditary hemochromatosis locus
JOURNAL Genome Res. 7 (5), 441-456 (1997)
PUBMED 9149941
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from DC388932.1, AK298570.1 and
BC013258.2.
Summary: Butyrophilin is the major protein associated with fat
droplets in the milk. This gene is a member of the BTN2 subfamily
of genes, which encode proteins belonging to the butyrophilin
protein family. The gene is located in a cluster on chromosome 6,
consisting of seven genes belonging to the expanding
B7/butyrophilin-like group, a subset of the immunoglobulin gene
superfamily. The encoded protein is a type I receptor glycoprotein
involved in lipid, fatty-acid and sterol metabolism. Several
alternatively spliced transcript variants encoding different
isoforms have been found for this gene. [provided by RefSeq, Oct
2010].
Transcript Variant: This variant (6) lacks an in-frame exon in the
5' region and has an additional segment in the 3' region, compared
to variant 1. The resulting isoform (b) lacks an internal segment
and has a shorter and distinct C-terminus, compared to isoform a.
##Evidence-Data-START##
Transcript exon combination :: AK298570.1 [ECO:0000332]
RNAseq introns :: mixed/partial sample support
ERS025082, ERS025084 [ECO:0000350]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-58 DC388932.1 2-59
59-1045 AK298570.1 34-1020
1046-3470 BC013258.2 747-3171
FEATURES Location/Qualifiers
source 1..3470
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="6"
/map="6p22.1"
gene 1..3470
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/note="butyrophilin, subfamily 2, member A2"
/db_xref="GeneID:10385"
/db_xref="HGNC:1137"
/db_xref="MIM:613591"
exon 1..81
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/inference="alignment:Splign:1.39.8"
variation 58
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:9461249"
misc_feature 76..78
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/note="upstream in-frame stop codon"
exon 82..205
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/inference="alignment:Splign:1.39.8"
CDS 112..882
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/note="isoform e precursor is encoded by transcript
variant 6; butyrophilin 2"
/codon_start=1
/product="butyrophilin subfamily 2 member A2 isoform e
precursor"
/protein_id="NP_001184169.1"
/db_xref="GI:308522752"
/db_xref="CCDS:CCDS56402.1"
/db_xref="GeneID:10385"
/db_xref="HGNC:1137"
/db_xref="MIM:613591"
/translation="
MEPAAALHFSLPASLLLLLLLLLLSLCALVSAQFTVVGPANPILAMVGENTTLRCHLSPEKNAEDMEVRWFRSQFSPAVFVYKGGRERTEEQMEEYRGRITFVSKDINRGSVALVIHNVTAQENGIYRCYFQEGRSYDEAILRLVVAESFMPSASPWMVALAVILTASPWMVSMTVILAVFIIFMAVSICCIKKLQREKKILSGEKKVEQEEKEIAQQLQEELRWRRTFLHAGYELPGIRGPSWKRPLHGEPPSAF
"
sig_peptide 112..207
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/inference="COORDINATES: ab initio prediction:SignalP:4.0"
mat_peptide 208..879
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/product="butyrophilin subfamily 2 member A2 isoform e"
misc_feature 208..549
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/note="Immunoglobulin V-set domain; Region: V-set;
pfam07686"
/db_xref="CDD:203725"
misc_feature 253..552
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/note="Immunoglobulin (Ig)-like domain of myelin
oligodendrocyte glycoprotein (MOG); Region: Ig_MOG_like;
cd05713"
/db_xref="CDD:143190"
misc_feature order(301..306,361..363,394..396,505..507,511..528)
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/note="antigen binding site; other site"
/db_xref="CDD:143190"
variation 117
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:375369181"
variation 119
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:202213069"
variation 122
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:73736234"
variation 150
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="c"
/db_xref="dbSNP:147636357"
variation 168
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:115247877"
exon 206..553
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/inference="alignment:Splign:1.39.8"
variation 219
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:138070617"
variation 220
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:143653188"
variation 226
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="g"
/db_xref="dbSNP:57038103"
variation 271
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:370867259"
variation 288
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:150302333"
variation 289
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:181037825"
variation 316
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:375285642"
variation 317
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:368009368"
variation 352
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="g"
/replace="t"
/db_xref="dbSNP:372237219"
variation 354
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:376950043"
variation 374
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:376558792"
variation 399
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:112257227"
variation 400
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:367692328"
variation 401
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:144702884"
variation 437
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:149453161"
variation 438
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:377645117"
variation 465
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:143017993"
variation 523
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:146154371"
variation 539
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:201687793"
exon 554..760
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/inference="alignment:Splign:1.39.8"
variation 557
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="c"
/db_xref="dbSNP:375385023"
variation 616
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:369920399"
variation 628
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="g"
/replace="t"
/db_xref="dbSNP:113893469"
variation 629
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:373492069"
variation 637
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="g"
/db_xref="dbSNP:147003451"
variation 760
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="g"
/db_xref="dbSNP:201972159"
exon 761..781
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/inference="alignment:Splign:1.39.8"
exon 782..808
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/inference="alignment:Splign:1.39.8"
exon 809..3461
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/inference="alignment:Splign:1.39.8"
variation 847
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:114402470"
variation 848
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:191843070"
variation 874
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2072803"
variation 921
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:183676835"
variation 962
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:147646031"
variation 966
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:142151655"
variation 972
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="c"
/db_xref="dbSNP:368319822"
variation 987
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:148323426"
variation 988
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:142803339"
variation 993
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="t"
/db_xref="dbSNP:150431575"
variation 996
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:370826490"
variation 997
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:138172438"
variation 1018
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:374005579"
variation 1019
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200473019"
variation 1025
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:112054667"
variation 1027
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:372706575"
variation 1044
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:368149710"
variation 1078
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200468059"
variation 1100
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="g"
/db_xref="dbSNP:200546581"
variation 1113
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:375971811"
variation 1115
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:374942833"
variation 1116
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:200047445"
variation 1127
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="t"
/db_xref="dbSNP:142785600"
variation 1132..1133
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace=""
/replace="g"
/db_xref="dbSNP:34248025"
variation 1152
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:146142561"
variation 1153
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="g"
/db_xref="dbSNP:372254650"
variation 1158
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="g"
/replace="t"
/db_xref="dbSNP:140196606"
variation 1160
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="t"
/db_xref="dbSNP:149403458"
variation 1173
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="g"
/replace="t"
/db_xref="dbSNP:181793664"
variation 1179
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:202000782"
variation 1183
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="g"
/db_xref="dbSNP:148562624"
variation 1240
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:369578278"
variation 1264..1265
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace=""
/replace="g"
/db_xref="dbSNP:35755065"
variation 1264
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:62617840"
variation 1270
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="g"
/db_xref="dbSNP:199832316"
variation 1276
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="t"
/db_xref="dbSNP:114760306"
variation 1284
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:139419531"
variation 1293
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2072802"
variation 1316
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:201353973"
variation 1317
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:372541099"
variation 1322
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="g"
/db_xref="dbSNP:200888343"
variation 1324
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:376736237"
variation 1343
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:147634987"
variation 1361
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:111615265"
variation 1372
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:375693447"
variation 1380
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1614887"
variation 1392
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:369209046"
variation 1399
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:145542993"
variation 1400
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200276371"
variation 1417
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:16891646"
variation 1449
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="g"
/replace="t"
/db_xref="dbSNP:376227483"
variation 1490
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:369257115"
variation 1499
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:143694906"
variation 1507
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:114098566"
variation 1520
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="c"
/db_xref="dbSNP:73736249"
variation 1529
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="g"
/db_xref="dbSNP:199706137"
variation 1563
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="c"
/db_xref="dbSNP:377572514"
variation 1582
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:370709739"
variation 1584
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="g"
/db_xref="dbSNP:201460456"
variation 1596
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:190569086"
variation 1604
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="g"
/replace="t"
/db_xref="dbSNP:370507187"
variation 1659
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:144477860"
variation 1674
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:111432027"
variation 1682
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:181721317"
variation 1731
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:372246478"
variation 1751
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:186915774"
variation 1846
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:3927423"
variation 1993..1994
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace=""
/replace="ttc"
/db_xref="dbSNP:201274736"
variation 2146
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1804836"
STS 2213..2325
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/standard_name="NIB885"
/db_xref="UniSTS:41935"
variation 2288
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:75254848"
variation 2290
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="c"
/db_xref="dbSNP:191285742"
variation 2310
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:140325542"
variation 2326
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="c"
/db_xref="dbSNP:77055120"
STS 2337..2545
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/standard_name="RH15843"
/db_xref="UniSTS:21190"
variation 2339
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="g"
/replace="t"
/db_xref="dbSNP:182538207"
variation 2434
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:75435297"
variation 2518
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="t"
/db_xref="dbSNP:7355"
variation 2535..2536
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace=""
/replace="a"
/db_xref="dbSNP:138497943"
variation 2679
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1131936"
variation 2710
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:149930183"
variation 2721
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="g"
/replace="t"
/db_xref="dbSNP:55674248"
variation 2724
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:61527210"
variation 2865
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:184920379"
variation 2891
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="t"
/db_xref="dbSNP:113353347"
variation 2932
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:72500812"
variation 3086
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:59001682"
variation 3120
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="c"
/replace="t"
/db_xref="dbSNP:73387026"
variation 3393
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
/replace="a"
/replace="g"
/db_xref="dbSNP:189684950"
polyA_signal 3441..3446
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
polyA_site 3461
/gene="BTN2A2"
/gene_synonym="BT2.2; BTF2"
ORIGIN
aaatcttgggactttttggacacccagagaacaggtcccagataccgagtccgcaactccaaacatcgcgattaataggaggcctctggtctctgcctgccctgggtgctcatggaaccagctgctgctctgcacttctccctgccagcctccctcctcctcctcctgctcctcctccttctcagcctgtgtgcactggtctcagcccagtttactgtcgtggggccagctaatcccatcctggccatggtgggagaaaacactacattacgctgccatctgtcacccgagaaaaatgctgaggacatggaggtgcggtggttccggtctcagttctcccccgcagtgtttgtgtataagggtgggagagagagaacagaggagcagatggaggagtaccggggaagaatcacctttgtgagcaaagacatcaacaggggcagcgtggccctggtcatacataacgtcacagcccaggagaatgggatctaccgctgttacttccaagaaggcaggtcctacgatgaggccatcctacgcctcgtggtggcagaatcctttatgcccagcgcatctccctggatggtggccctagctgtcatcctgaccgcatctccctggatggtgtccatgactgtcatcctggctgttttcatcatcttcatggctgtcagcatctgttgcatcaagaaacttcaaagggaaaaaaagattctgtcaggggaaaagaaagttgaacaagaggaaaaagaaattgcacagcaacttcaagaagaattgcgatggagaagaacattcttacatgctgggtatgagctgcctgggatcaggggaccttcatggaaacggccactacatggggaacccccttcagctttctgagacttctctggggaccaggaaccacacaatccccagggttcctgagaccccaggcataaacctgagacttcctctgcagctgatgtggtcctggatccagacaccgctcatcccgagctcttcctgtcagaggaccggagaagtgtgaggcggggcccctacaggcagagagtgcctgacaacccagagagattcgacagtcagccttgtgtcctgggatgggagagcttcgcctcagggaaacattactgggaggtggaggtggaaaacgtgatggtgtggactgtgggggtctgcagacacagtgttgagaggaaaggggaggtcctgctgattcctcagaatggcttctggaccctggagatgtttggaaaccaataccgggccctgtcctcccctgagaggattctccctttgaaggagtccctttgccgggtgggcgtcttcctggactatgaagctggagatgtctccttctacaacatgagggacagatcgcacatctacacatgtccccgttcagcctttactgtgcctgtgaggcccttcttcaggttagggtctgatgacagccccatcttcatctgccctgcactcacaggagccagtggggtcatggtgcctgaagagggcctgaaacttcacagagtggggacccaccagagcctatagaatcaattccttggactcacagccatgcagataagccctggccatctcagcagccaccgcacaacccccctaatgaaagacacgccctcctcccctctggtcacgtaagagaacatcttccagctgcctttttcacacccactccagccctctgccccagttttctcctcctcactagtctgtggctttagtagttcctttgcttgtaattatgggatgggatccaggcatagggaactagttgtttcatagctcccagtcaaaaagaaagtgagagaagctgttgggcagcgaacctactgtttaaaatcaggataaccacattaagcccaatatgccagttggcaccagatgctgtggacttggaatgaggccaacagggttcaccaggatgagagaggagagaggaatccacaggaccaccagaagggagagggaaccagatatgcagatcagagatagaggaagtggaaccagagagctgggagggaccaaggttgtaaggatggctaagtcccaccataagagctaaagggtcctgggagatgatggctcatttccacccaaccccaggatttccacagcacacacccacaggcctggacctgggatgaagatgaatgaagaacatggactcatgtggatgtggtttggctcagatgtccctgcaataaacaaggggtcagtacttagtccctgagtgtggttgaggtttgaggtcctggtcgagcagggcagtactggaccaggtctacgtcagcattcaggttcaatggggacaccagtggcttcaaacttcctgatctaattatgtttttagacacttagaagttattgaggactttaaagagcttttgtttatttgggttaatatttatgacatttgacattgaaacaaaaatttaaaatgttatcttttaatttatgttaaaatagcattaataaatcagttataggttaatgtagataggatgttttgtgaaaaagcaatctattgtgtccaaataaaaaaacaaaaagtgtgacactggttaactttttccagatctcatgtctggcttaataagagatatttgtattatcatatctgcctttgtattaaacctattggtatatcataggtcatgttagctcaaaaaaactttactgcacactactgagagaatgagatgaaaaacgattaatgtttcattattattattgtgaaaatattattaacactggggactccttaagagtacatcagagttctctctaggaatcccaaaaccacattttgaaactagaatagtggatcctggaagttaatccatgtgctggttaattttagatgtcaacctgactggattaaggaatacctagacagctggtacaacattatttctgggtgtgtctgtgagtgtgtttccagaagagattggcaagtgagtcagtgggaaattctctccttctgttggctgggtgcccaatacaacaaaaaggcagaggaaaggcaaattcttctctcctctggagctgagacactcttcttcttctgcccttggacatcagaactcctggctctccggcctttgaacttcaggacttgtaccaggaggccctgggttctcaggcctttggctttggactgagagttacacaatcagcttccctggttctgaggctttcagacttaaactgagccatgctaccagcatcccagggtctccagcctacagatgagctgttgtgcgatttcttagcctccataatcacatgagccaatctccttaataaatgcctgctcatagatctgtatctacatctatatctgtatgtgcatctatatctatgcctatatctatatctatatcatattgattttgtctctctggagaaccctgactaataaaatgaggcatctaaaaaaaaaaaaa
//
ANNOTATIONS 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
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@meso_cacase at
DBCLS
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