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2024-04-26 20:54:05, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001008405 5788 bp mRNA linear PRI 07-JUL-2013
DEFINITION Homo sapiens B-cell receptor-associated protein 29 (BCAP29),
transcript variant 1, mRNA.
ACCESSION NM_001008405
VERSION NM_001008405.2 GI:240255594
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 5788)
CONSRTM Coronary Artery Disease (C4D) Genetics Consortium
TITLE A genome-wide association study in Europeans and South Asians
identifies five new loci for coronary artery disease
JOURNAL Nat. Genet. 43 (4), 339-344 (2011)
PUBMED 21378988
REMARK Publication Status: Online-Only
REFERENCE 2 (bases 1 to 5788)
AUTHORS Evangelou E, Valdes AM, Kerkhof HJ, Styrkarsdottir U, Zhu Y,
Meulenbelt I, Lories RJ, Karassa FB, Tylzanowski P, Bos SD, Akune
T, Arden NK, Carr A, Chapman K, Cupples LA, Dai J, Deloukas P,
Doherty M, Doherty S, Engstrom G, Gonzalez A, Halldorsson BV,
Hammond CL, Hart DJ, Helgadottir H, Hofman A, Ikegawa S, Ingvarsson
T, Jiang Q, Jonsson H, Kaprio J, Kawaguchi H, Kisand K, Kloppenburg
M, Kujala UM, Lohmander LS, Loughlin J, Luyten FP, Mabuchi A,
McCaskie A, Nakajima M, Nilsson PM, Nishida N, Ollier WE,
Panoutsopoulou K, van de Putte T, Ralston SH, Rivadeneira F,
Saarela J, Schulte-Merker S, Shi D, Slagboom PE, Sudo A, Tamm A,
Tamm A, Thorleifsson G, Thorsteinsdottir U, Tsezou A, Wallis GA,
Wilkinson JM, Yoshimura N, Zeggini E, Zhai G, Zhang F, Jonsdottir
I, Uitterlinden AG, Felson DT, van Meurs JB, Stefansson K,
Ioannidis JP and Spector TD.
CONSRTM arcOGEN Consortium; Translation Research in Europe Applied
Technologies for Osteoarthritis (TreatOA)
TITLE Meta-analysis of genome-wide association studies confirms a
susceptibility locus for knee osteoarthritis on chromosome 7q22
JOURNAL Ann. Rheum. Dis. 70 (2), 349-355 (2011)
PUBMED 21068099
REMARK GeneRIF: Meta-analysis and genome-wide association study of
gene-disease association. (HuGE Navigator)
REFERENCE 3 (bases 1 to 5788)
AUTHORS Shimada,M., Miyagawa,T., Kawashima,M., Tanaka,S., Honda,Y.,
Honda,M. and Tokunaga,K.
TITLE An approach based on a genome-wide association study reveals
candidate loci for narcolepsy
JOURNAL Hum. Genet. 128 (4), 433-441 (2010)
PUBMED 20677014
REMARK GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
REFERENCE 4 (bases 1 to 5788)
AUTHORS Davila,S., Froeling,F.E., Tan,A., Bonnard,C., Boland,G.J.,
Snippe,H., Hibberd,M.L. and Seielstad,M.
TITLE New genetic associations detected in a host response study to
hepatitis B vaccine
JOURNAL Genes Immun. 11 (3), 232-238 (2010)
PUBMED 20237496
REMARK GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
REFERENCE 5 (bases 1 to 5788)
AUTHORS Rao,P.S., Bickel,U., Srivenugopal,K.S. and Rao,U.S.
TITLE Bap29varP, a variant of Bap29, influences the cell surface
expression of the human P-glycoprotein
JOURNAL Int. J. Oncol. 32 (1), 135-144 (2008)
PUBMED 18097552
REMARK GeneRIF: Bap29varP acts as an essential chaperone, influencing the
processing and trafficking of Pgp to the cell surface.
REFERENCE 6 (bases 1 to 5788)
AUTHORS Schamel,W.W., Kuppig,S., Becker,B., Gimborn,K., Hauri,H.P. and
Reth,M.
TITLE A high-molecular-weight complex of membrane proteins BAP29/BAP31 is
involved in the retention of membrane-bound IgD in the endoplasmic
reticulum
JOURNAL Proc. Natl. Acad. Sci. U.S.A. 100 (17), 9861-9866 (2003)
PUBMED 12886015
REFERENCE 7 (bases 1 to 5788)
AUTHORS Suzuki,H., Fukunishi,Y., Kagawa,I., Saito,R., Oda,H., Endo,T.,
Kondo,S., Bono,H., Okazaki,Y. and Hayashizaki,Y.
TITLE Protein-protein interaction panel using mouse full-length cDNAs
JOURNAL Genome Res. 11 (10), 1758-1765 (2001)
PUBMED 11591653
REFERENCE 8 (bases 1 to 5788)
AUTHORS Hu,R.M., Han,Z.G., Song,H.D., Peng,Y.D., Huang,Q.H., Ren,S.X.,
Gu,Y.J., Huang,C.H., Li,Y.B., Jiang,C.L., Fu,G., Zhang,Q.H.,
Gu,B.W., Dai,M., Mao,Y.F., Gao,G.F., Rong,R., Ye,M., Zhou,J.,
Xu,S.H., Gu,J., Shi,J.X., Jin,W.R., Zhang,C.K., Wu,T.M.,
Huang,G.Y., Chen,Z., Chen,M.D. and Chen,J.L.
TITLE Gene expression profiling in the human
hypothalamus-pituitary-adrenal axis and full-length cDNA cloning
JOURNAL Proc. Natl. Acad. Sci. U.S.A. 97 (17), 9543-9548 (2000)
PUBMED 10931946
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
AK289401.1, BP261060.1, BX647653.1, AK000878.1, BF434482.1,
DA569360.1, EB388415.1, BE006248.1, AW994087.1, H40966.1,
BM931263.1, AI684765.1 and BX101190.1.
On Jun 19, 2009 this sequence version replaced gi:56549092.
Transcript Variant: This variant (1) represents the shortest
transcript but encodes the longer isoform (a).
##Evidence-Data-START##
Transcript exon combination :: BI520365.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025081, ERS025082 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-336 AK289401.1 83-418
337-910 BP261060.1 1-574
911-2073 BX647653.1 867-2029
2074-2788 AK000878.1 503-1217
2789-2934 BF434482.1 6-151 c
2935-2972 AK000878.1 1364-1401
2973-3678 DA569360.1 22-727
3679-4326 EB388415.1 42-689
4327-4427 BE006248.1 335-435 c
4428-4927 AW994087.1 58-557
4928-4986 H40966.1 167-225
4987-5343 BM931263.1 18-374
5344-5768 AI684765.1 3-427 c
5769-5788 BX101190.1 653-672
FEATURES Location/Qualifiers
source 1..5788
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="7"
/map="7q22.3"
gene 1..5788
/gene="BCAP29"
/gene_synonym="BAP29"
/note="B-cell receptor-associated protein 29"
/db_xref="GeneID:55973"
/db_xref="HGNC:24131"
/db_xref="HPRD:16541"
exon 1..106
/gene="BCAP29"
/gene_synonym="BAP29"
/inference="alignment:Splign:1.39.8"
variation 1
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:199849251"
CDS 15..1061
/gene="BCAP29"
/gene_synonym="BAP29"
/note="isoform a is encoded by transcript variant 1;
BCR-associated protein 29"
/codon_start=1
/product="B-cell receptor-associated protein 29 isoform a"
/protein_id="NP_001008405.1"
/db_xref="GI:56549093"
/db_xref="CCDS:CCDS34730.1"
/db_xref="GeneID:55973"
/db_xref="HGNC:24131"
/db_xref="HPRD:16541"
/translation="
MTLQWAAVATFLYAEIGLILIFCLPFIPPQRWQKIFSFNVWGKIATFWNKAFLTIIILLIVLFLDAVREVRKYSSVHTIEKSSTSRPDAYEHTQMKLFRSQRNLYISGFSLFFWLVLRRLVTLITQLAKELSNKGVLKTQAENTNKAAKKFMEENEKLKRILKSHGKDEECVLEAENKKLVEDQEKLKTELRKTSDALSKAQNDVMEMKMQSERLSKEYDQLLKEHSELQHSSFGEFLSKRSHKNGSIGKQTGSRKGSFRKRQQEKTVNFIKDTCNILCQNDNFVMLASRKFKFRKMHYDRFVIFLMPHIGCIVMALSKYLMMFQIYCKVCIPALKKNISMLNTIFTY
"
misc_feature 15..674
/gene="BCAP29"
/gene_synonym="BAP29"
/note="B-cell receptor-associated protein 31-like; Region:
Bap31; pfam05529"
/db_xref="CDD:203268"
misc_feature 33..95
/gene="BCAP29"
/gene_synonym="BAP29"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q9UHQ4.2);
transmembrane region"
misc_feature 144..206
/gene="BCAP29"
/gene_synonym="BAP29"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q9UHQ4.2);
transmembrane region"
misc_feature 324..386
/gene="BCAP29"
/gene_synonym="BAP29"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q9UHQ4.2);
transmembrane region"
variation 20
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:147480624"
variation 26
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:79851050"
variation 31
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="g"
/db_xref="dbSNP:373953226"
variation 55
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:377691627"
variation 60
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:199610383"
variation 98
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:112014287"
variation 104
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:371256945"
exon 107..207
/gene="BCAP29"
/gene_synonym="BAP29"
/inference="alignment:Splign:1.39.8"
variation 110
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="g"
/db_xref="dbSNP:139985744"
variation 114
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:115265641"
variation 116
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:145323623"
variation 127
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="t"
/db_xref="dbSNP:377633207"
variation 183
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:11538934"
variation 194
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="g"
/replace="t"
/db_xref="dbSNP:147672425"
exon 208..358
/gene="BCAP29"
/gene_synonym="BAP29"
/inference="alignment:Splign:1.39.8"
variation 220
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="t"
/db_xref="dbSNP:201232183"
variation 300
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="t"
/db_xref="dbSNP:139180117"
variation 321
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="c"
/db_xref="dbSNP:371275655"
exon 359..494
/gene="BCAP29"
/gene_synonym="BAP29"
/inference="alignment:Splign:1.39.8"
variation 370
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:115169101"
variation 379
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:145143247"
variation 382
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:372162991"
variation 414
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:202114958"
variation 430
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="g"
/db_xref="dbSNP:201575711"
variation 474
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:149083912"
variation 480
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:200507390"
exon 495..603
/gene="BCAP29"
/gene_synonym="BAP29"
/inference="alignment:Splign:1.39.8"
variation 508
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:369170874"
variation 509
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:377378599"
variation 518
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:143137459"
variation 542
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="c"
/db_xref="dbSNP:370040223"
variation 551
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="c"
/db_xref="dbSNP:374387001"
variation 554
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:146681774"
variation 570
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:140300975"
exon 604..704
/gene="BCAP29"
/gene_synonym="BAP29"
/inference="alignment:Splign:1.39.8"
variation 665
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:374377179"
variation 690
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:377663210"
exon 705..783
/gene="BCAP29"
/gene_synonym="BAP29"
/inference="alignment:Splign:1.39.8"
variation 731
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="c"
/db_xref="dbSNP:77410087"
variation 736
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:200184386"
variation 772
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="g"
/db_xref="dbSNP:200602346"
exon 784..5773
/gene="BCAP29"
/gene_synonym="BAP29"
/inference="alignment:Splign:1.39.8"
variation 839
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="g"
/db_xref="dbSNP:374467600"
variation 840
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:202191845"
variation 854
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:115835071"
variation 859
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:141644610"
variation 867
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:10262001"
variation 907
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:138972250"
variation 915
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:146893215"
variation 918
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:6958094"
variation 921
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:201233658"
variation 942
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="t"
/db_xref="dbSNP:139945433"
variation 944
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:371866792"
variation 946
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="g"
/replace="t"
/db_xref="dbSNP:143920431"
variation 962
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:375907489"
variation 996
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:199509606"
variation 1194
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:115864140"
variation 1298
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:118011218"
STS 1355..1545
/gene="BCAP29"
/gene_synonym="BAP29"
/standard_name="GDB:1318014"
/db_xref="UniSTS:16776"
variation 1732
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:68170813"
variation 1742
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:147958146"
STS 1787..1881
/gene="BCAP29"
/gene_synonym="BAP29"
/standard_name="SHGC-56363"
/db_xref="UniSTS:55878"
variation 1905
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:191943063"
variation 2031
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:183323764"
variation 2088..2089
/gene="BCAP29"
/gene_synonym="BAP29"
/replace=""
/replace="g"
/db_xref="dbSNP:35850975"
variation 2189
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="c"
/db_xref="dbSNP:73189586"
variation 2237
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="g"
/replace="t"
/db_xref="dbSNP:188276191"
variation 2261
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:192562234"
variation 2295
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:370655627"
variation 2351
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:79352300"
variation 2371
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:371509524"
variation 2404
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="g"
/replace="t"
/db_xref="dbSNP:79568400"
variation 2516
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="g"
/db_xref="dbSNP:115358300"
variation 2625
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:182351772"
variation 2691
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="g"
/db_xref="dbSNP:148109169"
variation 2707
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="c"
/db_xref="dbSNP:186580286"
STS 2715..2895
/gene="BCAP29"
/gene_synonym="BAP29"
/standard_name="D7S2317"
/db_xref="UniSTS:72190"
STS 2724..2829
/gene="BCAP29"
/gene_synonym="BAP29"
/standard_name="D7S2087E"
/db_xref="UniSTS:73734"
variation 2751
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:368214337"
variation 2789
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:2807"
variation 2793
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:376330557"
variation 2867
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:2808"
variation 2957
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:141906379"
variation 3022
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:114911391"
variation 3324
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:192636539"
variation 3326
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="c"
/db_xref="dbSNP:184760147"
variation 3349
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:145449126"
variation 3385
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:190265502"
variation 3500
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="g"
/db_xref="dbSNP:138067581"
variation 3567
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:10274041"
variation 3587
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:114397560"
variation 3588
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:73421411"
variation 3709
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="g"
/db_xref="dbSNP:142568228"
variation 3711
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:116989627"
variation 3747
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="c"
/db_xref="dbSNP:374497980"
variation 3778
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:146015616"
variation 4053
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="g"
/replace="t"
/db_xref="dbSNP:369775506"
variation 4061
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:374055501"
variation 4071
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="g"
/replace="t"
/db_xref="dbSNP:375535508"
variation 4104
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="g"
/db_xref="dbSNP:147280763"
variation 4162
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:148717090"
STS 4185..4312
/gene="BCAP29"
/gene_synonym="BAP29"
/standard_name="SGC30522"
/db_xref="UniSTS:2297"
variation 4262
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:139636749"
variation 4263
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="t"
/db_xref="dbSNP:369614689"
variation 4286
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:2518"
variation 4294
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:376481325"
variation 4338
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:193156110"
variation 4382..4383
/gene="BCAP29"
/gene_synonym="BAP29"
/replace=""
/replace="g"
/db_xref="dbSNP:34205693"
variation 4403
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:142296035"
variation 4420
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="g"
/db_xref="dbSNP:149241331"
variation 4448
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:371995630"
variation 4453
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:200826621"
variation 4529
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:61743132"
variation 4558
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:377003341"
variation 4569
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="t"
/db_xref="dbSNP:2894475"
variation 4589..4590
/gene="BCAP29"
/gene_synonym="BAP29"
/replace=""
/replace="a"
/db_xref="dbSNP:376161660"
variation 4617
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="g"
/db_xref="dbSNP:144458228"
variation 4619
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="g"
/db_xref="dbSNP:111437695"
variation 4623
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:75316272"
variation 4637
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="g"
/replace="t"
/db_xref="dbSNP:375227036"
variation 4684..4685
/gene="BCAP29"
/gene_synonym="BAP29"
/replace=""
/replace="a"
/db_xref="dbSNP:199722961"
variation 4693
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="c"
/db_xref="dbSNP:74364257"
variation 4694
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:148429040"
variation 4725
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:115631817"
variation 4735
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:373068762"
variation 4781
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:17154251"
variation 4819
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:113098309"
variation 4889
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:145176882"
variation 4937
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:78581752"
variation 5148
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="t"
/db_xref="dbSNP:184999321"
variation 5172
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:189996300"
variation 5206
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:73724554"
variation 5268
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:140873571"
variation 5336
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="c"
/db_xref="dbSNP:181278738"
variation 5344
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="c"
/db_xref="dbSNP:9691194"
variation 5428
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:114064780"
variation 5457
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:185436022"
variation 5503
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:73724555"
variation 5513
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="c"
/db_xref="dbSNP:78850321"
variation 5593
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:188232319"
STS 5595..5744
/gene="BCAP29"
/gene_synonym="BAP29"
/standard_name="WI-15161"
/db_xref="UniSTS:18528"
variation 5620
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:115944436"
variation 5629
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:151316901"
variation 5635
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:140636962"
variation 5651
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:113818720"
variation 5677
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="c"
/db_xref="dbSNP:118044052"
variation 5714
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:180746547"
variation 5729
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="c"
/db_xref="dbSNP:187568187"
ORIGIN
gtgtgaagaaaaaaatgacactccaatgggctgcagtggcaacctttctttatgccgaaataggactcattttaatcttctgcctaccttttattcctcctcagagatggcagaagattttttcatttaatgtctggggtaaaattgcaactttttggaacaaggctttccttaccattatcatcctattgattgttctatttctagatgctgtgagagaagtaaggaaatattcctcagttcataccattgagaagagctccaccagcagacctgatgcctatgaacacacacagatgaaactttttaggtctcaaagaaatctttacatttctggattttccctatttttttggctagttttgagacgtctggttacgcttattactcaactggcaaaagaactgtcaaacaaaggtgtacttaaaactcaagcagaaaatactaacaaggctgccaaaaaatttatggaagaaaacgaaaaactaaaaaggattttgaaaagccatggtaaagatgaagaatgtgttttggaagcagaaaataaaaaactagtagaagaccaggagaaactgaaaactgaattaaggaagacttcagatgccctttctaaggcacaaaatgatgtgatggaaatgaagatgcagtcagagagactttcgaaagaatatgatcaactcctgaaagaacactctgaacttcagcattccagttttggtgaatttttaagcaaaagaagccacaaaaatggcagcattggaaaacagactggttctagaaaaggatcgtttagaaagaggcaacaagaaaagactgtgaactttataaaagacacttgcaatatactgtgtcaaaatgataattttgttatgttagcctctagaaaatttaagttcagaaaaatgcactatgaccggttcgtaatttttttaatgccacacataggttgtattgtaatggcattatcaaaatatttgatgatgtttcagatatattgcaaagtctgtattccagctcttaagaaaaatataagcatgttaaataccatatttacatattgataatgtcattggtatatggtggctgtttaccaataaaaggaaaaaattcattaaccggttgcttccaaaattagaagttttaagttgcatgaaaccattaatagccttgaaagctttgataagttttcagtaataataacctatttaatcagatgatgatgtgtttgaaaatagtgttcaatatcagcaaatttgtacacagggaatgtaaataaggataactgatcagagttatccactgtatttataaggaagagtcggaaaaaacaatgaccttagttttttttaagcctgatgatactatggtttactctaataagatagctatattgataattatatttttgttactgtgcccttgcacattttggtctttttgttaatatttttattaataacacataattagtaaccactctactgtttcaagttaatctagtaatagagcttacatatatttgtataactgctataccactgaactgaatttattttacaacagtgtagaattcttgaaaagttaacgtagaaaatatccaaaaagcagtatttctagaaagtgtccaaaaagcagtatttctttcccttggttgtgagagtaactaattatataaatattacctcaaaaatacatacactggtatcacacagtctttctacaatgtttctgtattctgaaagctaaatattaagtactatttttccattcaaatattcatttagaatttcctttagaagatggcagtgattataatattaatatgatttcatttgttccagtgtttagacatgaaatcatcttccttgtctcatgaaaacctaaatataaaaaaaaggaaaatactggagtttttatttctcttgtctttgttacatcctctgtttattataattttagcaccaacttcacacctagctaatttttttcatcataaagtggatgaaatgagcaagtacctaaaaattttatttcagataaaagtcaggagttactgctaaaaaacagacatgtaggagacattcaacaggagtatgaaatgagagttagaccatatgggctgacaacaccataaataacaagaaaagggagtgctgaaataggagagaacagagcaaatgttagctcaaagtatagacttagaaatatcaaagtaagagctatctggataaatatatagatattgagtgcttggaatcctagcctactatgtgaaaattaagtctaatgtcagaataacttacagaaaaatagaaaatgcacagctttaaaatgggcagagttaaaatctattcccagctttatcacttatttagccatgctagcctaggcctctatttccttgtctccaaaatgagaataataaaatttaggtcaggattactatataaactaagataatacagtgattctcaaagttgttcagactgtatagtaaggagaaagtctggttgcactttgaagagcttgaagatttgaaagattcccaaaaaagcattttaaagtttacatttaagggaccttggacctcaaccctctcaagtttacaagtctgaaactttagacatcaaaagtttgagcagtttttccaaggcaacattgatagttagattcagggccaggctgtaagtctagaatttagatatcctgatcccccagataccgctcttctggttatacacagaccagctataatttgctaaacataaaatattgcagtgtattagccggctgtggctccagagtctgtgccctttaccaccgtgcccaactgtttcacatgctgtgtttggtagtttttcctagtactctccttaataatggtggtgtttagcaaattgtattacataaataaatatttatttcatggattgagttatgttgcatattaaattactttccttcccattgtcaataatgacttctttatgtcttaggctgtattataaattcaaacacaggaatgttattcttgcctttttccatcagaattacctaaagttttattagactttccccctacttgcaaatctgcctggaggttctggtctttaggaagtagcacttagcaagttctggataagcactccagaatttgggatgagttatccttgttgtttgtccagctctatcttggaccccagtgctgctaattagattcatgccttgttctttagggcataagttcctctcttggctatttttcctagtatgctgagaactaggattccctttcagtgacagagtcctgccctggaaccccaatcaagagcctaaagtttaactactctctgagatattagcctgatgccagcagcctgcctggatctctaaatattacccattctgggagttgttagtggtctctgctttcctgcagtgtcactcctgcttcctcattgggcctgctagccacagctacttggatgtacccgaacctgttgccttgccctacctctgtgggctggttcagttctgcattcccattccagtgtccactgccttctcgctatccctcccatctgtgcgccaccaccagcttatccccagccctgctaacatgacaaactattgtgcatttgagtgcccactatacaatgtgtgaatataaccgtgcttttaagcattgactttaatgtctgggatgatccgtctagagtccatggaaccctcctgtgttttttcatccctttcttagtaatcttggaaatccacttatgaaattctttttctaacatttctttgctgaacggcatttttaaaattactttcacggtgtttctttccagtttgatctctacacaaacacaactttattacttgcaccagaaatgatttcaaacactttaggaactgtggtaggcttaattatgacttcccaaaagatatccctataccaatccctggaacctggaaatgttctcttctatagcaaaagatatgattaagttaaagtcttgagatggagagattattctgggtaatctgggagtgccctaaatgcagctacatctatgcttatatagaagcaaagggagatattaccacacagaagaggagaaagcacagtgaccacagaggcagagattggagtgatggagccgcagcaaaggaatgctgacagccaccagaagctggaggaggcaaagaacagattcttccccagagcctcttccagcaggagcatggccctacagataccgataaaactgatattggacttcctggcctccagaactatgggaataaatttattgtttcaagctatcaagtttgtgattatttgttactgctgccatagtaaattaatacaggagcatgcaggacagatctgtaatggcctgaactgaatttcaaggggtgtggaaaacagttactctttaacaccactccgtcttccccattagccatttggataagtcaaagatagccttagccatctcctatcttagttacttttctccttcaactgtattttgccattgtcgttgccattgcctctgcctaactgcaagccatcatcatctctcacatggactatgacgacctcctcatctccctgtatcttctctaatgcttctctcatatacatgctctcagcagccacctggtttaaaacaaaaacaaaaaaaacactaatcatgtcattccctgcttgtcttcccgttctttccaactgtcattccctgcttgtcttccaattctttccaactgcagttaagatcaaaccaccaagacctcaccaggctcccatctacttttcagcctcaactcagtccacctgctctgccaatcacacctgtttctttttgttgttctttccctaggatatagatcctggcatacctgcattctgattcttcttggaacaagccaaattctttcccctgtcagtacgtttgcatgtgtagtacatgttgcatcccaggcctgtctgccttcttaccctattttattttcatcatagcacttactaccatctgaaatgatctcatttatggtttgtctcctcagtgattaacacagttcctgcacacagtaaatcagtagttctcaacaggaagtgaagaggtcatcctgaggggaacatttagcaatacctagagacatttctggttgtcataaccaggggaatgctcctagtggatagaagtcagggaggctgttaaacccattccacaatgcacaggactggaacaaagaatgatctctcactcagaatgtcagtgttgccaaggtggagacatcctgcagtagatgcttgtggcagagggtactggttgtaccccagtatccattctttcattcacctgtgttaatacatgctccagttttgtatttttttttataaacagctgtcaagcataaagataacattttccatctccttgtatgtaagtggaaataggactgtcatgtggggccagtttcttttttttcttcctctgtcctgctgcttgaaacatatgctgctatcttagatcatgaggtcgaggccatgcaaagtggagcaacaaggagctgtgtccctgacgccataagcaccacacctgtcctgaattgctgtgaatgacaccagctaactacaatgcattgtctcaacatcctagacataataaaaagccataaatatgtttgtcctatgcagcacaaaacctttgtatctttgccttttatgttgggatcttaattaaaaattacatcctctactgtcaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:55973 -> Biological process: GO:0006886 [intracellular protein transport] evidence: IEA
GeneID:55973 -> Biological process: GO:0006915 [apoptotic process] evidence: IEA
GeneID:55973 -> Biological process: GO:0016192 [vesicle-mediated transport] evidence: IEA
GeneID:55973 -> Cellular component: GO:0005789 [endoplasmic reticulum membrane] evidence: IEA
GeneID:55973 -> Cellular component: GO:0016021 [integral to membrane] evidence: IEA
by
@meso_cacase at
DBCLS
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