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2020-10-24 07:00:02, 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:

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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