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2024-04-25 12:48:25, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_018844 6034 bp mRNA linear PRI 07-JUL-2013
DEFINITION Homo sapiens B-cell receptor-associated protein 29 (BCAP29),
transcript variant 2, mRNA.
ACCESSION NM_018844
VERSION NM_018844.3 GI:240255593
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 6034)
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 6034)
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 6034)
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 6034)
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 6034)
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 6034)
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 6034)
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 6034)
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
BG776708.1, DA717500.1, AK289401.1, 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:56549090.
Transcript Variant: This variant (2) differs in the 5' UTR, and
lacks an alternate exon in the 3' coding region that causes a
frameshift, compared to variant 1. The resulting isoform (b) is
shorter and has a distinct C-terminus, compared to isoform a.
##Evidence-Data-START##
Transcript exon combination :: BX647653.1, BC008478.1 [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
1-19 BG776708.1 2-20
20-156 DA717500.1 16-152
157-243 BG776708.1 157-243
244-1244 AK289401.1 1-1001
1245-2319 BX647653.1 955-2029
2320-3034 AK000878.1 503-1217
3035-3180 BF434482.1 6-151 c
3181-3218 AK000878.1 1364-1401
3219-3924 DA569360.1 22-727
3925-4572 EB388415.1 42-689
4573-4673 BE006248.1 335-435 c
4674-5173 AW994087.1 58-557
5174-5232 H40966.1 167-225
5233-5589 BM931263.1 18-374
5590-6014 AI684765.1 3-427 c
6015-6034 BX101190.1 653-672
FEATURES Location/Qualifiers
source 1..6034
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="7"
/map="7q22.3"
gene 1..6034
/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..325
/gene="BCAP29"
/gene_synonym="BAP29"
/inference="alignment:Splign:1.39.8"
variation 69
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="g"
/db_xref="dbSNP:114205169"
variation 86
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:79044539"
variation 208
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="t"
/db_xref="dbSNP:147124369"
variation 216
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:192628453"
misc_feature 217..219
/gene="BCAP29"
/gene_synonym="BAP29"
/note="upstream in-frame stop codon"
exon 326..431
/gene="BCAP29"
/gene_synonym="BAP29"
/inference="alignment:Splign:1.39.8"
variation 326
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:199849251"
CDS 340..1065
/gene="BCAP29"
/gene_synonym="BAP29"
/note="isoform b is encoded by transcript variant 2;
BCR-associated protein 29"
/codon_start=1
/product="B-cell receptor-associated protein 29 isoform b"
/protein_id="NP_061332.2"
/db_xref="GI:56549091"
/db_xref="CCDS:CCDS34731.1"
/db_xref="GeneID:55973"
/db_xref="HGNC:24131"
/db_xref="HPRD:16541"
/translation="
MTLQWAAVATFLYAEIGLILIFCLPFIPPQRWQKIFSFNVWGKIATFWNKAFLTIIILLIVLFLDAVREVRKYSSVHTIEKSSTSRPDAYEHTQMKLFRSQRNLYISGFSLFFWLVLRRLVTLITQLAKELSNKGVLKTQAENTNKAAKKFMEENEKLKRILKSHGKDEECVLEAENKKLVEDQEKLKTELRKTSDALSKAQNDVMEMKMQSERLSKEYDQLLKEHSELQDRLERGNKKRL
"
misc_feature 340..999
/gene="BCAP29"
/gene_synonym="BAP29"
/note="B-cell receptor-associated protein 31-like; Region:
Bap31; pfam05529"
/db_xref="CDD:203268"
misc_feature 358..420
/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 469..531
/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 649..711
/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 1051..1062
/gene="BCAP29"
/gene_synonym="BAP29"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q9UHQ4.2);
Region: Di-lysine motif"
variation 345
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:147480624"
variation 351
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:79851050"
variation 356
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="g"
/db_xref="dbSNP:373953226"
variation 380
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:377691627"
variation 385
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:199610383"
variation 423
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:112014287"
variation 429
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:371256945"
exon 432..532
/gene="BCAP29"
/gene_synonym="BAP29"
/inference="alignment:Splign:1.39.8"
variation 435
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="g"
/db_xref="dbSNP:139985744"
variation 439
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:115265641"
variation 441
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:145323623"
variation 452
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="t"
/db_xref="dbSNP:377633207"
variation 508
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:11538934"
variation 519
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="g"
/replace="t"
/db_xref="dbSNP:147672425"
exon 533..683
/gene="BCAP29"
/gene_synonym="BAP29"
/inference="alignment:Splign:1.39.8"
variation 545
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="t"
/db_xref="dbSNP:201232183"
variation 625
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="t"
/db_xref="dbSNP:139180117"
variation 646
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="c"
/db_xref="dbSNP:371275655"
exon 684..819
/gene="BCAP29"
/gene_synonym="BAP29"
/inference="alignment:Splign:1.39.8"
variation 695
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:115169101"
variation 704
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:145143247"
variation 707
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:372162991"
variation 739
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:202114958"
variation 755
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="g"
/db_xref="dbSNP:201575711"
variation 799
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:149083912"
variation 805
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:200507390"
exon 820..928
/gene="BCAP29"
/gene_synonym="BAP29"
/inference="alignment:Splign:1.39.8"
variation 833
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:369170874"
variation 834
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:377378599"
variation 843
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:143137459"
variation 867
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="c"
/db_xref="dbSNP:370040223"
variation 876
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="c"
/db_xref="dbSNP:374387001"
variation 879
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:146681774"
variation 895
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:140300975"
exon 929..1029
/gene="BCAP29"
/gene_synonym="BAP29"
/inference="alignment:Splign:1.39.8"
variation 990
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:374377179"
variation 1015
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:377663210"
exon 1030..6019
/gene="BCAP29"
/gene_synonym="BAP29"
/inference="alignment:Splign:1.39.8"
variation 1085
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="g"
/db_xref="dbSNP:374467600"
variation 1086
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:202191845"
variation 1100
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:115835071"
variation 1105
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:141644610"
variation 1113
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:10262001"
variation 1153
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:138972250"
variation 1161
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:146893215"
variation 1164
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:6958094"
variation 1167
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:201233658"
variation 1188
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="t"
/db_xref="dbSNP:139945433"
variation 1190
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:371866792"
variation 1192
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="g"
/replace="t"
/db_xref="dbSNP:143920431"
variation 1208
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:375907489"
variation 1242
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:199509606"
variation 1440
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:115864140"
variation 1544
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:118011218"
STS 1601..1791
/gene="BCAP29"
/gene_synonym="BAP29"
/standard_name="GDB:1318014"
/db_xref="UniSTS:16776"
variation 1978
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:68170813"
variation 1988
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:147958146"
STS 2033..2127
/gene="BCAP29"
/gene_synonym="BAP29"
/standard_name="SHGC-56363"
/db_xref="UniSTS:55878"
variation 2151
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:191943063"
variation 2277
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:183323764"
variation 2334..2335
/gene="BCAP29"
/gene_synonym="BAP29"
/replace=""
/replace="g"
/db_xref="dbSNP:35850975"
variation 2435
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="c"
/db_xref="dbSNP:73189586"
variation 2483
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="g"
/replace="t"
/db_xref="dbSNP:188276191"
variation 2507
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:192562234"
variation 2541
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:370655627"
variation 2597
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:79352300"
variation 2617
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:371509524"
variation 2650
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="g"
/replace="t"
/db_xref="dbSNP:79568400"
variation 2762
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="g"
/db_xref="dbSNP:115358300"
variation 2871
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:182351772"
variation 2937
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="g"
/db_xref="dbSNP:148109169"
variation 2953
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="c"
/db_xref="dbSNP:186580286"
STS 2961..3141
/gene="BCAP29"
/gene_synonym="BAP29"
/standard_name="D7S2317"
/db_xref="UniSTS:72190"
STS 2970..3075
/gene="BCAP29"
/gene_synonym="BAP29"
/standard_name="D7S2087E"
/db_xref="UniSTS:73734"
variation 2997
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:368214337"
variation 3035
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:2807"
variation 3039
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:376330557"
variation 3113
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:2808"
variation 3203
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:141906379"
variation 3268
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:114911391"
variation 3570
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:192636539"
variation 3572
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="c"
/db_xref="dbSNP:184760147"
variation 3595
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:145449126"
variation 3631
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:190265502"
variation 3746
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="g"
/db_xref="dbSNP:138067581"
variation 3813
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:10274041"
variation 3833
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:114397560"
variation 3834
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:73421411"
variation 3955
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="g"
/db_xref="dbSNP:142568228"
variation 3957
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:116989627"
variation 3993
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="c"
/db_xref="dbSNP:374497980"
variation 4024
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:146015616"
variation 4299
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="g"
/replace="t"
/db_xref="dbSNP:369775506"
variation 4307
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:374055501"
variation 4317
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="g"
/replace="t"
/db_xref="dbSNP:375535508"
variation 4350
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="g"
/db_xref="dbSNP:147280763"
variation 4408
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:148717090"
STS 4431..4558
/gene="BCAP29"
/gene_synonym="BAP29"
/standard_name="SGC30522"
/db_xref="UniSTS:2297"
variation 4508
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:139636749"
variation 4509
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="t"
/db_xref="dbSNP:369614689"
variation 4532
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:2518"
variation 4540
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:376481325"
variation 4584
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:193156110"
variation 4628..4629
/gene="BCAP29"
/gene_synonym="BAP29"
/replace=""
/replace="g"
/db_xref="dbSNP:34205693"
variation 4649
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:142296035"
variation 4666
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="g"
/db_xref="dbSNP:149241331"
variation 4694
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:371995630"
variation 4699
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:200826621"
variation 4775
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:61743132"
variation 4804
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:377003341"
variation 4815
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="t"
/db_xref="dbSNP:2894475"
variation 4835..4836
/gene="BCAP29"
/gene_synonym="BAP29"
/replace=""
/replace="a"
/db_xref="dbSNP:376161660"
variation 4863
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="g"
/db_xref="dbSNP:144458228"
variation 4865
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="g"
/db_xref="dbSNP:111437695"
variation 4869
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:75316272"
variation 4883
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="g"
/replace="t"
/db_xref="dbSNP:375227036"
variation 4930..4931
/gene="BCAP29"
/gene_synonym="BAP29"
/replace=""
/replace="a"
/db_xref="dbSNP:199722961"
variation 4939
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="c"
/db_xref="dbSNP:74364257"
variation 4940
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:148429040"
variation 4971
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:115631817"
variation 4981
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:373068762"
variation 5027
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:17154251"
variation 5065
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:113098309"
variation 5135
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:145176882"
variation 5183
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:78581752"
variation 5394
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="t"
/db_xref="dbSNP:184999321"
variation 5418
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:189996300"
variation 5452
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:73724554"
variation 5514
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:140873571"
variation 5582
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="c"
/db_xref="dbSNP:181278738"
variation 5590
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="c"
/db_xref="dbSNP:9691194"
variation 5674
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:114064780"
variation 5703
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:185436022"
variation 5749
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:73724555"
variation 5759
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="c"
/db_xref="dbSNP:78850321"
variation 5839
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:188232319"
STS 5841..5990
/gene="BCAP29"
/gene_synonym="BAP29"
/standard_name="WI-15161"
/db_xref="UniSTS:18528"
variation 5866
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:115944436"
variation 5875
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:151316901"
variation 5881
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:140636962"
variation 5897
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="c"
/replace="t"
/db_xref="dbSNP:113818720"
variation 5923
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="c"
/db_xref="dbSNP:118044052"
variation 5960
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="g"
/db_xref="dbSNP:180746547"
variation 5975
/gene="BCAP29"
/gene_synonym="BAP29"
/replace="a"
/replace="c"
/db_xref="dbSNP:187568187"
ORIGIN
agacctggaccccggcaccctcccgccggggccgcacttagcagtggaaagtctgtcctcctgaagaagttgcgctccgacctccaagcatcaggtcaaaagtctaactcattctctgacctgccgccaattagaaaacaactgttgccaataaacgtggtcgcgccgcctgtgacctcagccgggacggacccgcgggcgggagcctgcggggcgtgaggcggggtggggccctggctcccctcccccgcccagccgcggcgtctgacgtcccgcgcgtcggcggccgcggagcagcgcagggagccaggcgggctgccggcgggtgtgaagaaaaaaatgacactccaatgggctgcagtggcaacctttctttatgccgaaataggactcattttaatcttctgcctaccttttattcctcctcagagatggcagaagattttttcatttaatgtctggggtaaaattgcaactttttggaacaaggctttccttaccattatcatcctattgattgttctatttctagatgctgtgagagaagtaaggaaatattcctcagttcataccattgagaagagctccaccagcagacctgatgcctatgaacacacacagatgaaactttttaggtctcaaagaaatctttacatttctggattttccctatttttttggctagttttgagacgtctggttacgcttattactcaactggcaaaagaactgtcaaacaaaggtgtacttaaaactcaagcagaaaatactaacaaggctgccaaaaaatttatggaagaaaacgaaaaactaaaaaggattttgaaaagccatggtaaagatgaagaatgtgttttggaagcagaaaataaaaaactagtagaagaccaggagaaactgaaaactgaattaaggaagacttcagatgccctttctaaggcacaaaatgatgtgatggaaatgaagatgcagtcagagagactttcgaaagaatatgatcaactcctgaaagaacactctgaacttcaggatcgtttagaaagaggcaacaagaaaagactgtgaactttataaaagacacttgcaatatactgtgtcaaaatgataattttgttatgttagcctctagaaaatttaagttcagaaaaatgcactatgaccggttcgtaatttttttaatgccacacataggttgtattgtaatggcattatcaaaatatttgatgatgtttcagatatattgcaaagtctgtattccagctcttaagaaaaatataagcatgttaaataccatatttacatattgataatgtcattggtatatggtggctgtttaccaataaaaggaaaaaattcattaaccggttgcttccaaaattagaagttttaagttgcatgaaaccattaatagccttgaaagctttgataagttttcagtaataataacctatttaatcagatgatgatgtgtttgaaaatagtgttcaatatcagcaaatttgtacacagggaatgtaaataaggataactgatcagagttatccactgtatttataaggaagagtcggaaaaaacaatgaccttagttttttttaagcctgatgatactatggtttactctaataagatagctatattgataattatatttttgttactgtgcccttgcacattttggtctttttgttaatatttttattaataacacataattagtaaccactctactgtttcaagttaatctagtaatagagcttacatatatttgtataactgctataccactgaactgaatttattttacaacagtgtagaattcttgaaaagttaacgtagaaaatatccaaaaagcagtatttctagaaagtgtccaaaaagcagtatttctttcccttggttgtgagagtaactaattatataaatattacctcaaaaatacatacactggtatcacacagtctttctacaatgtttctgtattctgaaagctaaatattaagtactatttttccattcaaatattcatttagaatttcctttagaagatggcagtgattataatattaatatgatttcatttgttccagtgtttagacatgaaatcatcttccttgtctcatgaaaacctaaatataaaaaaaaggaaaatactggagtttttatttctcttgtctttgttacatcctctgtttattataattttagcaccaacttcacacctagctaatttttttcatcataaagtggatgaaatgagcaagtacctaaaaattttatttcagataaaagtcaggagttactgctaaaaaacagacatgtaggagacattcaacaggagtatgaaatgagagttagaccatatgggctgacaacaccataaataacaagaaaagggagtgctgaaataggagagaacagagcaaatgttagctcaaagtatagacttagaaatatcaaagtaagagctatctggataaatatatagatattgagtgcttggaatcctagcctactatgtgaaaattaagtctaatgtcagaataacttacagaaaaatagaaaatgcacagctttaaaatgggcagagttaaaatctattcccagctttatcacttatttagccatgctagcctaggcctctatttccttgtctccaaaatgagaataataaaatttaggtcaggattactatataaactaagataatacagtgattctcaaagttgttcagactgtatagtaaggagaaagtctggttgcactttgaagagcttgaagatttgaaagattcccaaaaaagcattttaaagtttacatttaagggaccttggacctcaaccctctcaagtttacaagtctgaaactttagacatcaaaagtttgagcagtttttccaaggcaacattgatagttagattcagggccaggctgtaagtctagaatttagatatcctgatcccccagataccgctcttctggttatacacagaccagctataatttgctaaacataaaatattgcagtgtattagccggctgtggctccagagtctgtgccctttaccaccgtgcccaactgtttcacatgctgtgtttggtagtttttcctagtactctccttaataatggtggtgtttagcaaattgtattacataaataaatatttatttcatggattgagttatgttgcatattaaattactttccttcccattgtcaataatgacttctttatgtcttaggctgtattataaattcaaacacaggaatgttattcttgcctttttccatcagaattacctaaagttttattagactttccccctacttgcaaatctgcctggaggttctggtctttaggaagtagcacttagcaagttctggataagcactccagaatttgggatgagttatccttgttgtttgtccagctctatcttggaccccagtgctgctaattagattcatgccttgttctttagggcataagttcctctcttggctatttttcctagtatgctgagaactaggattccctttcagtgacagagtcctgccctggaaccccaatcaagagcctaaagtttaactactctctgagatattagcctgatgccagcagcctgcctggatctctaaatattacccattctgggagttgttagtggtctctgctttcctgcagtgtcactcctgcttcctcattgggcctgctagccacagctacttggatgtacccgaacctgttgccttgccctacctctgtgggctggttcagttctgcattcccattccagtgtccactgccttctcgctatccctcccatctgtgcgccaccaccagcttatccccagccctgctaacatgacaaactattgtgcatttgagtgcccactatacaatgtgtgaatataaccgtgcttttaagcattgactttaatgtctgggatgatccgtctagagtccatggaaccctcctgtgttttttcatccctttcttagtaatcttggaaatccacttatgaaattctttttctaacatttctttgctgaacggcatttttaaaattactttcacggtgtttctttccagtttgatctctacacaaacacaactttattacttgcaccagaaatgatttcaaacactttaggaactgtggtaggcttaattatgacttcccaaaagatatccctataccaatccctggaacctggaaatgttctcttctatagcaaaagatatgattaagttaaagtcttgagatggagagattattctgggtaatctgggagtgccctaaatgcagctacatctatgcttatatagaagcaaagggagatattaccacacagaagaggagaaagcacagtgaccacagaggcagagattggagtgatggagccgcagcaaaggaatgctgacagccaccagaagctggaggaggcaaagaacagattcttccccagagcctcttccagcaggagcatggccctacagataccgataaaactgatattggacttcctggcctccagaactatgggaataaatttattgtttcaagctatcaagtttgtgattatttgttactgctgccatagtaaattaatacaggagcatgcaggacagatctgtaatggcctgaactgaatttcaaggggtgtggaaaacagttactctttaacaccactccgtcttccccattagccatttggataagtcaaagatagccttagccatctcctatcttagttacttttctccttcaactgtattttgccattgtcgttgccattgcctctgcctaactgcaagccatcatcatctctcacatggactatgacgacctcctcatctccctgtatcttctctaatgcttctctcatatacatgctctcagcagccacctggtttaaaacaaaaacaaaaaaaacactaatcatgtcattccctgcttgtcttcccgttctttccaactgtcattccctgcttgtcttccaattctttccaactgcagttaagatcaaaccaccaagacctcaccaggctcccatctacttttcagcctcaactcagtccacctgctctgccaatcacacctgtttctttttgttgttctttccctaggatatagatcctggcatacctgcattctgattcttcttggaacaagccaaattctttcccctgtcagtacgtttgcatgtgtagtacatgttgcatcccaggcctgtctgccttcttaccctattttattttcatcatagcacttactaccatctgaaatgatctcatttatggtttgtctcctcagtgattaacacagttcctgcacacagtaaatcagtagttctcaacaggaagtgaagaggtcatcctgaggggaacatttagcaatacctagagacatttctggttgtcataaccaggggaatgctcctagtggatagaagtcagggaggctgttaaacccattccacaatgcacaggactggaacaaagaatgatctctcactcagaatgtcagtgttgccaaggtggagacatcctgcagtagatgcttgtggcagagggtactggttgtaccccagtatccattctttcattcacctgtgttaatacatgctccagttttgtatttttttttataaacagctgtcaagcataaagataacattttccatctccttgtatgtaagtggaaataggactgtcatgtggggccagtttcttttttttcttcctctgtcctgctgcttgaaacatatgctgctatcttagatcatgaggtcgaggccatgcaaagtggagcaacaaggagctgtgtccctgacgccataagcaccacacctgtcctgaattgctgtgaatgacaccagctaactacaatgcattgtctcaacatcctagacataataaaaagccataaatatgtttgtcctatgcagcacaaaacctttgtatctttgccttttatgttgggatcttaattaaaaattacatcctctactgtcaaaaaaaaaaaaaaa
//
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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