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2025-05-09 17:29:45, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_173544 2523 bp mRNA linear PRI 18-APR-2013
DEFINITION Homo sapiens family with sequence similarity 129, member C
(FAM129C), transcript variant 1, mRNA.
ACCESSION NM_173544
VERSION NM_173544.4 GI:148664195
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 2523)
AUTHORS Boyd,R.S., Adam,P.J., Patel,S., Loader,J.A., Berry,J.,
Redpath,N.T., Poyser,H.R., Fletcher,G.C., Burgess,N.A.,
Stamps,A.C., Hudson,L., Smith,P., Griffiths,M., Willis,T.G.,
Karran,E.L., Oscier,D.G., Catovsky,D., Terrett,J.A. and Dyer,M.J.
TITLE Proteomic analysis of the cell-surface membrane in chronic
lymphocytic leukemia: identification of two novel proteins, BCNP1
and MIG2B
JOURNAL Leukemia 17 (8), 1605-1612 (2003)
PUBMED 12886250
REMARK GeneRIF: Isolation and sequencing. Prediction of transmembrane
domains, with three alternatively spliced final exons.
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
AY254199.1, AA649002.1 and AI688885.1.
On Jun 7, 2007 this sequence version replaced gi:141801207.
Transcript Variant: This variant (1) represents the longer
transcript and encodes the longer isoform (a).
##Evidence-Data-START##
Transcript exon combination :: AY254199.1 [ECO:0000332]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-2242 AY254199.1 1-2242
2243-2309 AA649002.1 21-87 c
2310-2523 AI688885.1 1-214 c
FEATURES Location/Qualifiers
source 1..2523
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="19"
/map="19p13.11"
gene 1..2523
/gene="FAM129C"
/gene_synonym="BCNP1"
/note="family with sequence similarity 129, member C"
/db_xref="GeneID:199786"
/db_xref="HGNC:24130"
/db_xref="HPRD:16546"
/db_xref="MIM:609967"
exon 1..159
/gene="FAM129C"
/gene_synonym="BCNP1"
/inference="alignment:Splign:1.39.8"
variation 30
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:150025276"
variation 38
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:186618148"
variation 86
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:372435389"
variation 94
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:111557825"
variation 103
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369556688"
variation 104
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:116630557"
variation 113
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="g"
/db_xref="dbSNP:374999039"
variation 117
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200819562"
variation 118
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368905077"
misc_feature 127..129
/gene="FAM129C"
/gene_synonym="BCNP1"
/note="upstream in-frame stop codon"
CDS 139..2232
/gene="FAM129C"
/gene_synonym="BCNP1"
/note="isoform a is encoded by transcript variant 1;
niban-like protein 2; B-cell novel protein 1"
/codon_start=1
/product="niban-like protein 2 isoform a"
/protein_id="NP_775815.2"
/db_xref="GI:31542207"
/db_xref="CCDS:CCDS12362.1"
/db_xref="GeneID:199786"
/db_xref="HGNC:24130"
/db_xref="HPRD:16546"
/db_xref="MIM:609967"
/translation="
MGPDRKEVPLSRGTQAVVVGKGRGAPGDDSSMGGRPSSPLDKQQRQHLRGQVDTLLRNFLPCYRGQLAASVLRQISRELGPQEPTGSQLLRSKKLPRVREHRGPLTQLRGHPPRWQPIFCVLRGDGRLEWFSHKEEYENGGHCLGSTALTGYTLLTSQREYLRLLDALCPESLGDHTQEEPDSLLEVPVSFPLFLQHPFRRHLCFSAATREAQHAWRLALQGGIRLQGTVLQRSQAPAARAFLDAVRLYRQHQGHFGDDDVTLGSDAEVLTAVLMREQLPALRAQTLPGLRGAGRARAWAWTELLDAVHAAVLAGASAGLCAFQPEKDELLASLEKTIRPDVDQLLRQRARVAGRLRTDIRGPLESCLRREVDPQLPRVVQTLLRTVEASLEAVRTLLAQGMDRLSHRLRQSPSGTRLRREVYSFGEMPWDLALMQTCYREAERSRGRLGQLAAPFGFLGMQSLVFGAQDLAQQLMADAVATFLQLADQCLTTALNCDQAAQRLERVRGRVLKKFKSDSGLAQRRFIRGWGLCIFLPFVLSQLEPGCKKELPEFEGDVLAVGSQALTTEGIYEDVIRGCLLQRIDQELKKTLGANDVSCTLDGCLEVPWEQEGAAPNLNLVSSFLAGRQAFTDFLCLPAKSSANWILAASLLSCSCFRSGFHRDSRVFLVQLAEGLSHSLETVSSHSVWSFRPTPRQ
"
exon 160..286
/gene="FAM129C"
/gene_synonym="BCNP1"
/inference="alignment:Splign:1.39.8"
variation 187
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="g"
/replace="t"
/db_xref="dbSNP:377615680"
variation 192
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:144347016"
variation 193
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201992026"
variation 203
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138735905"
variation 215
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:370987487"
variation 222
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200808762"
variation 223
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:73504235"
variation 226
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="c"
/db_xref="dbSNP:200304763"
variation 236
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:147810248"
variation 241
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:141221433"
variation 248
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:370585817"
variation 256
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201383126"
exon 287..417
/gene="FAM129C"
/gene_synonym="BCNP1"
/inference="alignment:Splign:1.39.8"
variation 289
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="c"
/db_xref="dbSNP:145037648"
variation 300
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="g"
/db_xref="dbSNP:199639094"
variation 328
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:375693198"
variation 345
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:369418945"
variation 356
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201415239"
variation 366
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="t"
/db_xref="dbSNP:150918693"
variation 368
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:140895055"
variation 390
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:74336438"
variation 393
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:185897431"
variation 394
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:375422466"
variation 409
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:138634803"
variation 416
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="t"
/db_xref="dbSNP:371886240"
exon 418..543
/gene="FAM129C"
/gene_synonym="BCNP1"
/inference="alignment:Splign:1.39.8"
variation 434
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:140354498"
variation 443
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:376837341"
variation 456
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="c"
/db_xref="dbSNP:371234153"
variation 464
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:76766278"
variation 471
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:73504248"
variation 489
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:141997373"
variation 492
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="g"
/db_xref="dbSNP:187591525"
variation 513
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:143668756"
variation 517
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:111971153"
variation 540
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:372956322"
exon 544..658
/gene="FAM129C"
/gene_synonym="BCNP1"
/inference="alignment:Splign:1.39.8"
variation 556
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:150700269"
variation 582
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:74387759"
variation 597
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:140293166"
variation 612
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:143255653"
variation 614
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="g"
/replace="t"
/db_xref="dbSNP:201345901"
variation 625
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:184472022"
variation 626
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370043401"
variation 635
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:147499098"
exon 659..826
/gene="FAM129C"
/gene_synonym="BCNP1"
/inference="alignment:Splign:1.39.8"
variation 664
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:139561286"
variation 670
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="g"
/db_xref="dbSNP:200829044"
variation 682
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="g"
/replace="t"
/db_xref="dbSNP:113569844"
variation 699
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:144900974"
variation 713
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373318613"
variation 717
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:62126825"
variation 735
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="c"
/db_xref="dbSNP:376855441"
variation 739
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:148620566"
variation 781
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:377505484"
variation 811
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:114859428"
variation 824
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:8107859"
exon 827..942
/gene="FAM129C"
/gene_synonym="BCNP1"
/inference="alignment:Splign:1.39.8"
variation 849
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="g"
/replace="t"
/db_xref="dbSNP:372319496"
variation 874
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:202226577"
variation 921
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:74546231"
exon 943..1047
/gene="FAM129C"
/gene_synonym="BCNP1"
/inference="alignment:Splign:1.39.8"
variation 952
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:202025122"
variation 964
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="c"
/db_xref="dbSNP:371969596"
variation 986
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201425039"
variation 1007
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:181869656"
variation 1012
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="g"
/db_xref="dbSNP:115590519"
variation 1016
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="c"
/db_xref="dbSNP:114207587"
exon 1048..1210
/gene="FAM129C"
/gene_synonym="BCNP1"
/inference="alignment:Splign:1.39.8"
variation 1059
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="g"
/db_xref="dbSNP:200159429"
variation 1186
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:78631497"
variation 1189
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="g"
/db_xref="dbSNP:371269275"
variation 1208
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:59757874"
exon 1211..1401
/gene="FAM129C"
/gene_synonym="BCNP1"
/inference="alignment:Splign:1.39.8"
variation 1211
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:140392723"
variation 1235
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:116690925"
variation 1276
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201443040"
variation 1286
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:113762390"
variation 1336
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369599576"
variation 1348
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="g"
/db_xref="dbSNP:146478867"
variation 1361
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="g"
/replace="t"
/db_xref="dbSNP:140620586"
variation 1367
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="g"
/replace="t"
/db_xref="dbSNP:150439084"
variation 1380
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:11878663"
variation 1387
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="c"
/db_xref="dbSNP:376551112"
exon 1402..1560
/gene="FAM129C"
/gene_synonym="BCNP1"
/inference="alignment:Splign:1.39.8"
variation 1402
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="g"
/db_xref="dbSNP:369452509"
variation 1425
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:114849169"
variation 1436
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:199734357"
variation 1457
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201431632"
variation 1465
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:374484972"
variation 1468
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:368873219"
variation 1469
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:149574830"
variation 1478
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="g"
/db_xref="dbSNP:142486184"
variation 1481
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:372327001"
variation 1503
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:375779762"
variation 1531
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:191462652"
variation 1540
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:143233543"
exon 1561..1677
/gene="FAM129C"
/gene_synonym="BCNP1"
/inference="alignment:Splign:1.39.8"
variation 1583
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:374603681"
variation 1613
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:139360897"
variation 1616
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:45532635"
variation 1617
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:76814516"
variation 1627
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:140048862"
variation 1655
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="g"
/db_xref="dbSNP:369494726"
variation 1666
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373733258"
variation 1668
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:138987050"
variation 1669
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200100942"
exon 1678..1785
/gene="FAM129C"
/gene_synonym="BCNP1"
/inference="alignment:Splign:1.39.8"
variation 1696
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:141937404"
variation 1720
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201247329"
variation 1723
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:150542864"
variation 1725
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="g"
/db_xref="dbSNP:139512738"
variation 1729
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="g"
/replace="t"
/db_xref="dbSNP:149676710"
variation 1732
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="g"
/db_xref="dbSNP:140658814"
variation 1741
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:144132615"
variation 1765
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:10401716"
exon 1786..1897
/gene="FAM129C"
/gene_synonym="BCNP1"
/inference="alignment:Splign:1.39.8"
variation 1788
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:141041739"
variation 1816
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="g"
/replace="t"
/db_xref="dbSNP:192212740"
variation 1824
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:143130213"
variation 1831
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="g"
/replace="t"
/db_xref="dbSNP:202088970"
variation 1861
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:374460967"
variation 1871
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="g"
/replace="t"
/db_xref="dbSNP:151074024"
variation 1878
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:140969272"
exon 1898..1981
/gene="FAM129C"
/gene_synonym="BCNP1"
/inference="alignment:Splign:1.39.8"
variation 1929
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:372827884"
variation 1931
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="c"
/db_xref="dbSNP:150586223"
variation 1945
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:11666267"
exon 1982..2508
/gene="FAM129C"
/gene_synonym="BCNP1"
/inference="alignment:Splign:1.39.8"
variation 2123
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371879832"
variation 2126
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:147123061"
variation 2135
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="g"
/db_xref="dbSNP:200699370"
variation 2157
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="c"
/db_xref="dbSNP:199532721"
STS 2160..2283
/gene="FAM129C"
/gene_synonym="BCNP1"
/standard_name="SHGC-58046"
/db_xref="UniSTS:63748"
variation 2184
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:138526761"
variation 2185
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200266618"
variation 2223
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373133380"
variation 2225
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:375255515"
variation 2239
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="g"
/db_xref="dbSNP:201757380"
variation 2244
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="g"
/db_xref="dbSNP:200935218"
variation 2278
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:34631213"
variation 2344
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="c"
/db_xref="dbSNP:151316029"
variation 2356
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="g"
/replace="t"
/db_xref="dbSNP:78256011"
variation 2358
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="g"
/replace="t"
/db_xref="dbSNP:140449099"
variation 2374
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:112216671"
variation 2402
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="c"
/replace="g"
/db_xref="dbSNP:372083536"
variation 2404
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="g"
/replace="t"
/db_xref="dbSNP:147029596"
variation 2451
/gene="FAM129C"
/gene_synonym="BCNP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:372956480"
ORIGIN
gctgagcaggagatgggaattgaaacctgcgcagaggcggctgtgcagggtgagagtggagccgaaaccacagaaagtgaagtttgcttcaacgtcttgtcccggcaggccactcagatgtgagagtgaggaagtgggatggggcctgaccggaaggaggtgcccctgagccgaggaacgcaggcggtggtcgtggggaagggaagaggagccccgggagacgacagcagcatgggtgggcggccttcgagccctctggacaagcagcagcggcagcacctaaggggtcaggtggacaccctgctgaggaacttcctgccttgctaccgtgggcagctggcagcgtctgtcctgcggcagatctctcgagagctgggccctcaggagccgaccggaagccagttgctacgcagcaaaaagctgccccgagtccgtgagcaccgaggacccctgacccagcttcggggccacccaccccggtggcagccgatcttctgtgttctgcgtggggacggccgcctagagtggttcagccacaaggaggaatatgaaaacgggggccactgccttggctcaacagccctgacaggatacacgctcctgacttcccagcgagaatatctccgccttttggatgctctctgccctgaatccttgggagaccatactcaggaagagcctgactccctcttggaagtgcctgtgagcttcccgctgttcctgcagcaccccttccgccggcacctctgcttctctgcagccaccagggaggcacagcatgcctggaggctggccctgcagggtggcatccggcttcagggcacagtcctgcagcgaagccaggcccctgctgcccgggccttcctggacgccgtccgactctaccggcagcaccaaggccactttggcgacgacgacgtgaccctaggctcagacgccgaggtgctgaccgcggtgctgatgcgggagcaacttcccgcgctgcgagcccagacccttcctggcctgcggggggcaggccgcgcccgcgcctgggcctggaccgagcttctagacgccgttcacgcagctgtcctggccggggcctccgccgggctctgcgccttccagcccgaaaaggacgagctgcttgcgtcgctggagaagacgatccgcccggacgtggaccagctgctgcggcagcgggcgcgtgtggcggggcggctgaggacggatatcaggggaccgctcgagtcgtgcctgcgccgggaggtggacccgcagctgccccgggtcgtgcagaccctgctgcgcaccgtggaagcctcgctcgaggcggtgcggaccctcctggctcaaggcatggaccgactgtcccaccgcctgcgccagagcccctcaggcacgcggctgcgcagggaggtttactcatttggggagatgccgtgggacttggcgctgatgcagacatgctaccgtgaggccgagcggagccgggggcgcttggggcagctggcagcaccgtttggctttctggggatgcagagcctcgtgtttggggcccaagatcttgcacagcagctcatggctgacgccgtggccaccttcctgcagctggctgaccagtgtctgacgacggccctcaactgtgaccaggctgcccagaggctggagagagtcagggggcgcgtgctgaagaaattcaaatcggacagcgggttggcgcagaggaggttcatccgaggctggggtctctgcatctttttaccttttgtgctgagccaactcgagccaggctgcaaaaaggagctgcctgagttcgagggggatgtccttgccgtgggcagccaggctctgaccactgagggcatctatgaggacgtcatccgggggtgcttgctgcagaggattgaccaagaattgaaaaagacccttggtgccaatgatgtatcctgcactctggacggctgcttggaggtcccatgggaacaggagggagcagctccaaatcttaacttggtgtcaagtttcctggctgggagacaagcttttaccgacttcctctgcttgccagcaaagtcatctgctaactggatattggcagcttctctgctgtcttgcagctgcttccggagtgggttccacagggattcccgtgtgttcttggttcagcttgcagagggactttcacactccctggagaccgtttcctcccattctgtctggagttttcggcctaccccaagacaatgagatattcctgacctttccacctatttccctccaaccccaccttccgaaatacatttgctcaatacatttgcacttcataggcttctttagctgtcttccttttaccccggacgggatgtagatgttaattctggaacaattgcagctacaagaatttgtcatcctgccccttttgagaaaaacattgtttgcccttgggtctaaatccttccagatgggatgggatgtatcttgtcacctcctttttcttacttaatatgaaaagacctttcctcaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:199786 -> Molecular function: GO:0005543 [phospholipid binding] evidence: IEA
by
@meso_cacase at
DBCLS
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