Home |
Help |
Advanced search
2025-05-09 18:30:43, 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 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.