GGRNA Home | Help | Advanced search

2024-03-28 20:02:31, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_001197238            1820 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens butyrophilin, subfamily 2, member A2 (BTN2A2),
            transcript variant 4, mRNA.
ACCESSION   NM_001197238
VERSION     NM_001197238.1  GI:308522747
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 1820)
  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 1820)
  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 1820)
  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 1820)
  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 1820)
  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 1820)
  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 BP234194.1, BC017497.1 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 (4) lacks an alternate segment in
            the 3' region compared to variant 1, resulting in a shorter isoform
            (c) with distinct C-terminus, compared to isoform a.
            
            ##Evidence-Data-START##
            Transcript exon combination :: BC017497.1 [ECO:0000332]
            RNAseq introns              :: mixed/partial sample support
                                           ERS025084, ERS025088 [ECO:0000350]
            ##Evidence-Data-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-108               BP234194.1         1-108
            109-1355            BC017497.1         1-1247
            1356-1356           BC013258.2         2728-2728
            1357-1820           BC017497.1         1249-1712
FEATURES             Location/Qualifiers
     source          1..1820
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="6"
                     /map="6p22.1"
     gene            1..1820
                     /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..204
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="alignment:Splign:1.39.8"
     variation       63
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:9461249"
     variation       136
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:9467741"
     misc_feature    151..153
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /note="upstream in-frame stop codon"
     variation       200
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:375893732"
     variation       201..202
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace=""
                     /replace="ag"
                     /db_xref="dbSNP:3832422"
     exon            205..328
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="alignment:Splign:1.39.8"
     CDS             235..1245
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /note="isoform c precursor is encoded by transcript
                     variant 4; butyrophilin 2"
                     /codon_start=1
                     /product="butyrophilin subfamily 2 member A2 isoform c
                     precursor"
                     /protein_id="NP_001184167.1"
                     /db_xref="GI:308522748"
                     /db_xref="CCDS:CCDS56401.1"
                     /db_xref="GeneID:10385"
                     /db_xref="HGNC:1137"
                     /db_xref="MIM:613591"
                     /translation="
MEPAAALHFSLPASLLLLLLLLLLSLCALVSAQFTVVGPANPILAMVGENTTLRCHLSPEKNAEDMEVRWFRSQFSPAVFVYKGGRERTEEQMEEYRGRITFVSKDINRGSVALVIHNVTAQENGIYRCYFQEGRSYDEAILRLVVAGLGSKPLIEIKAQEDGSIWLECISGGWYPEPLTVWRDPYGEVVPALKEVSIADADGLFMVTTAVIIRDKYVRNVSCSVNNTLLGQEKETVIFIPESFMPSASPWMVALAVILTASPWMVSMTVILAVFIIFMAVSICCIKKLQREKKILSGEKKVEQEEKEIAQQLQEELRWRRTFLHADVNLTGLRNT
"
     sig_peptide     235..330
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="COORDINATES: ab initio prediction:SignalP:4.0"
     mat_peptide     331..1242
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /product="butyrophilin subfamily 2 member A2 isoform c"
     misc_feature    331..672
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /note="Immunoglobulin V-set domain; Region: V-set;
                     pfam07686"
                     /db_xref="CDD:203725"
     misc_feature    376..675
                     /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(424..429,484..486,517..519,628..630,634..651)
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /note="antigen binding site; other site"
                     /db_xref="CDD:143190"
     misc_feature    688..936
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /note="Immunoglobulin domain; Region: Ig; cl11960"
                     /db_xref="CDD:213125"
     misc_feature    1030..1092
                     /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"
     variation       240
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375369181"
     variation       242
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202213069"
     variation       245
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:73736234"
     variation       273
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:147636357"
     variation       291
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:115247877"
     exon            329..676
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="alignment:Splign:1.39.8"
     variation       342
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138070617"
     variation       343
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143653188"
     variation       349
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:57038103"
     variation       394
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370867259"
     variation       411
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150302333"
     variation       412
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:181037825"
     variation       439
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375285642"
     variation       440
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368009368"
     variation       475
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:372237219"
     variation       477
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376950043"
     variation       497
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376558792"
     variation       522
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:112257227"
     variation       523
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367692328"
     variation       524
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144702884"
     variation       560
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149453161"
     variation       561
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377645117"
     variation       588
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143017993"
     variation       646
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146154371"
     variation       662
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201687793"
     exon            677..958
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="alignment:Splign:1.39.8"
     variation       736
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:369291221"
     variation       750
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142411775"
     variation       789
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:76088803"
     variation       792
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:200834687"
     variation       808
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:144410497"
     variation       816
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372854548"
     variation       826
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200036284"
     variation       829
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201605260"
     variation       833
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139541725"
     variation       841
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:62617839"
     variation       861
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370196656"
     variation       899
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145439434"
     variation       918
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201008184"
     variation       922
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200096466"
     variation       925
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373346354"
     variation       956
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201995913"
     exon            959..1165
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="alignment:Splign:1.39.8"
     variation       962
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:375385023"
     variation       1021
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369920399"
     variation       1033
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:113893469"
     variation       1034
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373492069"
     variation       1042
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:147003451"
     variation       1165
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201972159"
     exon            1166..1186
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="alignment:Splign:1.39.8"
     exon            1187..1213
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="alignment:Splign:1.39.8"
     exon            1214..1790
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /inference="alignment:Splign:1.39.8"
     variation       1220
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:113353347"
     variation       1261
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:72500812"
     variation       1415
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:59001682"
     variation       1449
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:73387026"
     variation       1722
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:189684950"
     polyA_signal    1770..1775
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
     polyA_site      1790
                     /gene="BTN2A2"
                     /gene_synonym="BT2.2; BTF2"
ORIGIN      
agtggaaatcttgggactttttggacacccagagaacaggtcccagataccgagtccgcaactccaaacatcgcgattaataggaggtgaacacagcttttctcttctctttgggatgctttgttgtctggtggtgactgtgcccatgggtgagttgtatcggaaaatcgtcatgtgaggatcagaggggaaaagaaaacagaggcctctggtctctgcctgccctgggtgctcatggaaccagctgctgctctgcacttctccctgccagcctccctcctcctcctcctgctcctcctccttctcagcctgtgtgcactggtctcagcccagtttactgtcgtggggccagctaatcccatcctggccatggtgggagaaaacactacattacgctgccatctgtcacccgagaaaaatgctgaggacatggaggtgcggtggttccggtctcagttctcccccgcagtgtttgtgtataagggtgggagagagagaacagaggagcagatggaggagtaccggggaagaatcacctttgtgagcaaagacatcaacaggggcagcgtggccctggtcatacataacgtcacagcccaggagaatgggatctaccgctgttacttccaagaaggcaggtcctacgatgaggccatcctacgcctcgtggtggcaggccttgggtctaagcccctcattgaaatcaaggcccaagaggatgggagcatctggctggagtgcatatctggagggtggtacccagagcccctcacagtgtggagggacccctacggtgaggttgtgcccgccctgaaggaggtttccatcgctgatgctgacggcctcttcatggtcaccacagctgtgatcatcagagacaagtatgtgaggaatgtgtcctgctctgtcaacaacaccctgctcggccaggagaaggaaactgtcatttttattccagaatcctttatgcccagcgcatctccctggatggtggccctagctgtcatcctgaccgcatctccctggatggtgtccatgactgtcatcctggctgttttcatcatcttcatggctgtcagcatctgttgcatcaagaaacttcaaagggaaaaaaagattctgtcaggggaaaagaaagttgaacaagaggaaaaagaaattgcacagcaacttcaagaagaattgcgatggagaagaacattcttacatgctgatgtcaacctgactggattaaggaatacctagacagctggtacaacattatttctgggtgtgtctgtgagtgtgtttccagaagagattggcaagtgagtcagtgggaaattctctccttctgttggctgggtgcccaatacaacaaaaaggcagaggaaaggcaaattcttctctcctctggagctgagacactcttcttcttctgcccttggacatcagaactcctggctctccggcctttgaacttcaggacttgtaccaggaggccctgggttctcaggcctttggctttggactgagagttacacaatcagcttccctggttctgaggctttcagacttaaactgagccatgctaccagcatcccagggtctccagcctacagatgagctgttgtgcgatttcttagcctccataatcacatgagccaatctccttaataaatgcctgctcatagatctgtatctacatctatatctgtatgtgcatctatatctatgcctatatctatatctatatcatattgattttgtctctctggagaaccctgactaataaaatgaggcatctaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:10385 -> Biological process: GO:0031324 [negative regulation of cellular metabolic process] evidence: ISS
            GeneID:10385 -> Biological process: GO:0046007 [negative regulation of activated T cell proliferation] evidence: ISS
            GeneID:10385 -> Biological process: GO:0050710 [negative regulation of cytokine secretion] evidence: ISS
            GeneID:10385 -> Cellular component: GO:0016021 [integral to membrane] evidence: IEA

by @meso_cacase at DBCLS
This page is licensed under a Creative Commons Attribution 2.1 Japan License.