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2024-03-29 16:51:57, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_001256487           11256 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens golgin B1 (GOLGB1), transcript variant 3, mRNA.
ACCESSION   NM_001256487
VERSION     NM_001256487.1  GI:374532820
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 11256)
  AUTHORS   Rosing,M., Ossendorf,E., Rak,A. and Barnekow,A.
  TITLE     Giantin interacts with both the small GTPase Rab6 and Rab1
  JOURNAL   Exp. Cell Res. 313 (11), 2318-2325 (2007)
   PUBMED   17475246
  REMARK    GeneRIF: Giantin binds to Rab6A and Rab1 proteins.
REFERENCE   2  (bases 1 to 11256)
  AUTHORS   Breuza,L., Halbeisen,R., Jeno,P., Otte,S., Barlowe,C., Hong,W. and
            Hauri,H.P.
  TITLE     Proteomics of endoplasmic reticulum-Golgi intermediate compartment
            (ERGIC) membranes from brefeldin A-treated HepG2 cells identifies
            ERGIC-32, a new cycling protein that interacts with human Erv46
  JOURNAL   J. Biol. Chem. 279 (45), 47242-47253 (2004)
   PUBMED   15308636
REFERENCE   3  (bases 1 to 11256)
  AUTHORS   Oka,T., Ungar,D., Hughson,F.M. and Krieger,M.
  TITLE     The COG and COPI complexes interact to control the abundance of
            GEARs, a subset of Golgi integral membrane proteins
  JOURNAL   Mol. Biol. Cell 15 (5), 2423-2435 (2004)
   PUBMED   15004235
REFERENCE   4  (bases 1 to 11256)
  AUTHORS   Ruan,Q., Wang,Q., Xie,S., Fang,Y., Darzynkiewicz,Z., Guan,K.,
            Jhanwar-Uniyal,M. and Dai,W.
  TITLE     Polo-like kinase 3 is Golgi localized and involved in regulating
            Golgi fragmentation during the cell cycle
  JOURNAL   Exp. Cell Res. 294 (1), 51-59 (2004)
   PUBMED   14980500
REFERENCE   5  (bases 1 to 11256)
  AUTHORS   Gillingham,A.K., Pfeifer,A.C. and Munro,S.
  TITLE     CASP, the alternatively spliced product of the gene encoding the
            CCAAT-displacement protein transcription factor, is a Golgi
            membrane protein related to giantin
  JOURNAL   Mol. Biol. Cell 13 (11), 3761-3774 (2002)
   PUBMED   12429822
  REMARK    GeneRIF: Data report the characterization of a mammalian
            coiled-coil protein, CASP, a Golgi protein that shares with giantin
            a conserved histidine in its transmembrane domain.
REFERENCE   6  (bases 1 to 11256)
  AUTHORS   Linstedt,A.D., Jesch,S.A., Mehta,A., Lee,T.H., Garcia-Mata,R.,
            Nelson,D.S. and Sztul,E.
  TITLE     Binding relationships of membrane tethering components. The giantin
            N terminus and the GM130 N terminus compete for binding to the p115
            C terminus
  JOURNAL   J. Biol. Chem. 275 (14), 10196-10201 (2000)
   PUBMED   10744704
REFERENCE   7  (bases 1 to 11256)
  AUTHORS   Sonnichsen,B., Lowe,M., Levine,T., Jamsa,E., Dirac-Svejstrup,B. and
            Warren,G.
  TITLE     A role for giantin in docking COPI vesicles to Golgi membranes
  JOURNAL   J. Cell Biol. 140 (5), 1013-1021 (1998)
   PUBMED   9490716
REFERENCE   8  (bases 1 to 11256)
  AUTHORS   Sohda,M., Misumi,Y., Fujiwara,T., Nishioka,M. and Ikehara,Y.
  TITLE     Molecular cloning and sequence analysis of a human 372-kDA protein
            localized in the Golgi complex
  JOURNAL   Biochem. Biophys. Res. Commun. 205 (2), 1399-1408 (1994)
   PUBMED   7802676
REFERENCE   9  (bases 1 to 11256)
  AUTHORS   Seelig,H.P., Schranz,P., Schroter,H., Wiemann,C. and Renz,M.
  TITLE     Macrogolgin--a new 376 kD Golgi complex outer membrane protein as
            target of antibodies in patients with rheumatic diseases and HIV
            infections
  JOURNAL   J. Autoimmun. 7 (1), 67-91 (1994)
   PUBMED   8198703
REFERENCE   10 (bases 1 to 11256)
  AUTHORS   Linstedt,A.D. and Hauri,H.P.
  TITLE     Giantin, a novel conserved Golgi membrane protein containing a
            cytoplasmic domain of at least 350 kDa
  JOURNAL   Mol. Biol. Cell 4 (7), 679-693 (1993)
   PUBMED   7691276
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            BP320001.1, D25542.1, AB593126.1 and AA127633.1.
            
            Transcript Variant: This variant (3) uses an alternate splice site
            at its 5' end and initiates translation at a downstream start
            codon, compared to variant 1. It also uses an alternate in-frame
            splice site in the 3' coding region compared to variant 1. The
            encoded isoform (3) is shorter than isoform 1.
            
            Publication Note:  This RefSeq record includes a subset of the
            publications that are available for this gene. Please see the Gene
            record to access additional publications.
            
            ##Evidence-Data-START##
            Transcript exon combination :: D25542.1 [ECO:0000332]
            RNAseq introns              :: mixed/partial sample support
                                           ERS025081, ERS025082 [ECO:0000350]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-45                BP320001.1         1-45
            46-1413             D25542.1           1-1368
            1414-1417           AB593126.1         1265-1268
            1418-9027           D25542.1           1373-8982
            9028-9029           AB593126.1         8879-8880
            9030-9876           D25542.1           8985-9831
            9877-11238          AB593126.1         9728-11089
            11239-11256         AA127633.1         1-18                c
FEATURES             Location/Qualifiers
     source          1..11256
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="3"
                     /map="3q13"
     gene            1..11256
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /note="golgin B1"
                     /db_xref="GeneID:2804"
                     /db_xref="HGNC:4429"
                     /db_xref="MIM:602500"
     exon            1..136
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /inference="alignment:Splign:1.39.8"
     exon            137..262
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /inference="alignment:Splign:1.39.8"
     misc_feature    251..253
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /note="upstream in-frame stop codon"
     exon            263..415
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /inference="alignment:Splign:1.39.8"
     CDS             284..9961
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /note="isoform 3 is encoded by transcript variant 3;
                     golgin B1, golgi integral membrane protein; macrogolgin;
                     golgi integral membrane protein 1; golgi autoantigen,
                     golgin subfamily b, macrogolgin (with transmembrane
                     signal), 1; golgin subfamily B member 1; giantin; 372 kDa
                     Golgi complex-associated protein"
                     /codon_start=1
                     /product="Golgin subfamily B member 1 isoform 3"
                     /protein_id="NP_001243416.1"
                     /db_xref="GI:374532821"
                     /db_xref="GeneID:2804"
                     /db_xref="HGNC:4429"
                     /db_xref="MIM:602500"
                     /translation="
MEFNNTTQEDVQERLAYAEQLVVELKDIIRQKDVQLQQKDEALQEERKAADNKIKKLKLHAKAKLTSLNKYIEEMKAQGGTVLPTEPQSEEQLSKHDKSSTEEEMEIEKIKHKLQEKEELISTLQAQLTQAQAEQPAQSSTEMEEFVMMKQQLQEKEEFISTLQAQLSQTQAEQAAQLSSMQQVVREKDARFETQVRLHEDELLQLVTQADVETEMQQKLRVLQRKLEEHEESLVGRAQVVDLLQQELTAAEQRNQILSQQLQQMEAEHNTLRNTVETEREESKILLEKMELEVAERKLSFHNLQEEMHHLLEQFEQAGQAQAELESRYSALEQKHKAEMEEKTSHILSLQKTGQELQSACDALKDQNSKLLQDKNEQAVQSAQTIQQLEDQLQQKSKEISQFLNRLPLQQHETASQTSFPDVYNEGTQAVTEENIASLQKRVVELENEKGALLLSSIELEELKAENEKLSSQITLLEAQNRTGEADREVSEISIVDIANKRSSSAEESGQDVLENTFSQKHKELSVLLLEMKEAQEEIAFLKLQLQGKRAEEADHEVLDQKEMKQMEGEGIAPIKMKVFLEDTGQDFPLMPNEESSLPAVEKEQASTEHQSRTSEEISLNDAGVELKSTKQDGDKSLSAVPDIGQCHQDELERLKSQILELELNFHKAQEIYEKNLDEKAKEISNLNQLIEEFKKNADNNSSAFTALSEERDQLLSQVKELSMVTELRAQVKQLEMNLAEAERQRRLDYESQTAHDNLLTEQIHSLSIEAKSKDVKIEVLQNELDDVQLQFSEQSTLIRSLQSQLQNKESEVLEGAERVRHISSKVEELSQALSQKELEITKMDQLLLEKKRDVETLQQTIEEKDQQVTEISFSMTEKMVQLNEEKFSLGVEIKTLKEQLNLLSRAEEAKKEQVEEDNEVSSGLKQNYDEMSPAGQISKEELQHEFDLLKKENEQRKRKLQAALINRKELLQRVSRLEEELANLKDESKKEIPLSETERGEVEEDKENKEYSEKCVTSKCQEIEIYLKQTISEKEVELQHIRKDLEEKLAAEEQFQALVKQMNQTLQDKTNQIDLLQAEISENQAIIQKLITSNTDASDGDSVALVKETVVISPPCTGSSEHWKPELEEKILALEKEKEQLQKKLQEALTSRKAILKKAQEKERHLREELKQQKDDYNRLQEQFDEQSKENENIGDQLRQLQIQVRESIDGKLPSTDQQESCSSTPGLEEPLFKATEQHHTQPVLESNLCPDWPSHSEDASALQGGTSVAQIKAQLKEIEAEKVELELKVSSTTSELTKKSEEVFQLQEQINKQGLEIESLKTVSHEAEVHAESLQQKLESSQLQIAGLEHLRELQPKLDELQKLISKKEEDVSYLSGQLSEKEAALTKIQTEIIEQEDLIKALHTQLEMQAKEHDERIKQLQVELCEMKQKPEEIGEESRAKQQIQRKLQAALISRKEALKENKSLQEELSLARGTIERLTKSLADVESQVSAQNKEKDTVLGRLALLQEERDKLITEMDRSLLENQSLSSSCESLKLALEGLTEDKEKLVKEIESLKSSKIAESTEWQEKHKELQKEYEILLQSYENVSNEAERIQHVVEAVRQEKQELYGKLRSTEANKKETEKQLQEAEQEMEEMKEKMRKFAKSKQQKILELEEENDRLRAEVHPAGDTAKECMETLLSSNASMKEELERVKMEYETLSKKFQSLMSEKDSLSEEVQDLKHQIEGNVSKQANLEATEKHDNQTNVTEEGTQSIPGETEEQDSLSMSTRPTCSESVPSAKSANPAVSKDFSSHDEINNYLQQIDQLKERIAGLEEEKQKNKEFSQTLENEKNTLLSQISTKDGELKMLQEEVTKMNLLNQQIQEELSRVTKLKETAEEEKDDLEERLMNQLAELNGSIGNYCQDVTDAQIKNELLESEMKNLKKCVSELEEEKQQLVKEKTKVESEIRKEYLEKIQGAQKEPGNKSHAKELQELLKEKQQEVKQLQKDCIRYQEKISALERTVKALEFVQTESQKDLEITKENLAQAVEHRKKAQAELASFKVLLDDTQSEAARVLADNLKLKKELQSNKESVKSQMKQKDEDLERRLEQAEEKHLKEKKNMQEKLDALRREKVHLEETIGEIQVTLNKKDKEVQQLQENLDSTVTQLAAFTKSMSSLQDDRDRVIDEAKKWERKFSDAIQSKEEEIRLKEDNCSVLKDQLRQMSIHMEELKINISRLEHDKQIWESKAQTEVQLQQKVCDTLQGENKELLSQLEETRHLYHSSQNELAKLESELKSLKDQLTDLSNSLEKCKEQKGNLEGIIRQQEADIQNSKFSYEQLETDLQASRELTSRLHEEINMKEQKIISLLSGKEEAIQVAIAELRQQHDKEIKELENLLSQEEEENIVLEEENKKAVDKTNQLMETLKTIKKENIQQKAQLDSFVKSMSSLQNDRDRIVGDYQQLEERHLSIILEKDQLIQEAAAENNKLKEEIRGLRSHMDDLNSENAKLDAELIQYREDLNQVITIKDSQQKQLLEVQLQQNKELENKYAKLEEKLKESEEANEDLRRSFNALQEEKQDLSKEIESLKVSISQLTRQVTALQEEGTLGLYHAQLKVKEEEVHRLSALFSSSQKRIAELEEELVCVQKEAAKKVGEIEDKLKKELKHLHHDAGIMRNETETAEERVAELARDLVEMEQKLLMVTKENKGLTAQIQSFGRSMSSLQNSRDHANEELDELKRKYDASLKELAQLKEQGLLNRERDALLSETAFSMNSTEENSLSHLEKLNQQLLSKDEQLLHLSSQLEDSYNQVQSFSKAMASLQNERDHLWNELEKFRKSEEGKQRSAAQPSTSPAEVQSLKKAMSSLQNDRDRLLKELKNLQQQYLQINQEITELHPLKAQLQEYQDKTKAFQIMQEELRQENLSWQHELHQLRMEKSSWEIHERRMKEQYLMAISDKDQQLSHLQNLIRELRSSSSQTQPLKVQYQRQASPETSASPDGSQNLVYETELLRTQLNDSLKEIHQKELRIQQLNSNFSQLLEEKNTLSIQLCDTSQSLRENQQHYGDLLNHCAVLEKQVQELQAGPLNIDVAPGAPQEKNGVHRKSDPEELREPQQSFSEAQQQLCNTRQEVNELRKLLEEERDQRVAAENALSVAEEQIRRLEHSEWDSSRTPIIGSCGTQEQALLIDLTSNSCRRTRSGVGWKRVLRSLCHSRTRVPLLAAIYFLMIHVLLILCFTGHL
"
     misc_feature    1817..>2776
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /note="chromosome segregation protein SMC, common
                     bacterial type; Region: SMC_prok_B; TIGR02168"
                     /db_xref="CDD:162739"
     misc_feature    <2318..3280
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /note="chromosome segregation protein SMC, common
                     bacterial type; Region: SMC_prok_B; TIGR02168"
                     /db_xref="CDD:162739"
     misc_feature    <4337..5473
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /note="Chromosome segregation ATPases [Cell division and
                     chromosome partitioning]; Region: Smc; COG1196"
                     /db_xref="CDD:31389"
     misc_feature    <5231..5845
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /note="Transmembrane protein; Region: Macoilin; pfam09726"
                     /db_xref="CDD:204294"
     misc_feature    6266..>7201
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /note="chromosome segregation protein SMC, common
                     bacterial type; Region: SMC_prok_B; TIGR02168"
                     /db_xref="CDD:162739"
     misc_feature    <6782..>7639
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /note="chromosome segregation protein SMC, common
                     bacterial type; Region: SMC_prok_B; TIGR02168"
                     /db_xref="CDD:162739"
     misc_feature    8060..>9007
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /note="chromosome segregation protein SMC, common
                     bacterial type; Region: SMC_prok_B; TIGR02168"
                     /db_xref="CDD:162739"
     misc_feature    <8864..>9724
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /note="chromosome segregation protein SMC, common
                     bacterial type; Region: SMC_prok_B; TIGR02168"
                     /db_xref="CDD:162739"
     exon            416..568
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /inference="alignment:Splign:1.39.8"
     exon            569..697
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /inference="alignment:Splign:1.39.8"
     exon            698..814
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /inference="alignment:Splign:1.39.8"
     exon            815..937
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /inference="alignment:Splign:1.39.8"
     exon            938..1051
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /inference="alignment:Splign:1.39.8"
     exon            1052..1454
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /inference="alignment:Splign:1.39.8"
     exon            1455..1570
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /inference="alignment:Splign:1.39.8"
     exon            1571..1685
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /inference="alignment:Splign:1.39.8"
     exon            1686..1759
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /inference="alignment:Splign:1.39.8"
     exon            1760..6948
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /inference="alignment:Splign:1.39.8"
     variation       2377
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:35093512"
     variation       3238
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:34938201"
     variation       3816
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:3732410"
     STS             4188..4387
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /standard_name="EST13C8"
                     /db_xref="UniSTS:263095"
     STS             4502..4651
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /standard_name="SHGC-37473"
                     /db_xref="UniSTS:5384"
     STS             4749..4888
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /standard_name="RH91267"
                     /db_xref="UniSTS:91746"
     variation       5319
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:35674179"
     variation       5475
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1127412"
     variation       5899
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:34833153"
     exon            6949..8860
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /inference="alignment:Splign:1.39.8"
     variation       7684
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:1127415"
     exon            8861..9039
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /inference="alignment:Splign:1.39.8"
     exon            9040..9205
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /inference="alignment:Splign:1.39.8"
     exon            9206..9343
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /inference="alignment:Splign:1.39.8"
     exon            9344..9487
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /inference="alignment:Splign:1.39.8"
     exon            9488..9585
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /inference="alignment:Splign:1.39.8"
     exon            9586..9720
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /inference="alignment:Splign:1.39.8"
     variation       9606
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1803633"
     exon            9721..9826
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /inference="alignment:Splign:1.39.8"
     exon            9827..11242
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /inference="alignment:Splign:1.39.8"
     variation       9991
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:7153"
     STS             10035..10297
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /standard_name="WI-22003"
                     /db_xref="UniSTS:50828"
     STS             10042..10176
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /standard_name="STS-X75304"
                     /db_xref="UniSTS:41855"
     STS             10077..10177
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /standard_name="D3S3940"
                     /db_xref="UniSTS:68839"
     STS             10185..10269
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /standard_name="RH69909"
                     /db_xref="UniSTS:82747"
     variation       10497
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:1043827"
     STS             10899..11156
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /standard_name="IB1423"
                     /db_xref="UniSTS:46407"
     STS             10973..11170
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /standard_name="A001X20"
                     /db_xref="UniSTS:60929"
     STS             10973..11170
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /standard_name="G19747"
                     /db_xref="UniSTS:60928"
     STS             10984..11149
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /standard_name="WIAF-2081"
                     /db_xref="UniSTS:12953"
     STS             11009..11139
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /standard_name="G59904"
                     /db_xref="UniSTS:137186"
     STS             11047..11148
                     /gene="GOLGB1"
                     /gene_synonym="GCP; GCP372; GOLIM1"
                     /standard_name="PMC311069P7"
                     /db_xref="UniSTS:272888"
ORIGIN      
atcttccgtcccaactgctagtggctgagtccctggcggggcgcggcggtggaaggtgtcgcgtacgggcttcccgagctgacgtggcttgaattgggaggggggcagctggagcctcaggcggcagcgcttctagaaatgctgagccgattatcaggattagcaaatgttgttttgcatgaattatcaggagatgatgacactgatcagaatatgagggctcccctagaccctgtgagtagttctgttctgatttaaactggaattacaccaagaatctgacatggaatttaataatactacacaagaagatgttcaggagcgcctggcttatgcagagcaattggtggtggagctaaaagatattattagacagaaggatgttcaactgcagcagaaagatgaagctctacaggaagagagaaaagctgctgataacaaaattaaaaaactaaaacttcatgcgaaggccaaattaacttctttgaataaatacatagaagaaatgaaagcacaaggagggactgttctgcctacagaacctcagtcagaggagcaactttccaagcatgacaagagttctacagaggaagagatggaaatagaaaagataaaacataagctccaggagaaggaggaactaatcagcactttgcaagcccagcttactcaggcacaggcagaacaacctgcacagagttctacagagatggaagaatttgtaatgatgaagcaacagctccaggagaaggaagaattcattagcactttacaagcccagctcagccagacacaggcagagcaagctgcacagttgagttccatgcagcaggtggtccgagagaaagatgcccgctttgaaacacaagttcgtcttcatgaagatgagcttcttcagttagtaacccaggcagatgtggaaacagagatgcaacagaaattgagggtgctgcaaaggaagcttgaggaacacgaagaatccttggtgggccgtgctcaggtcgttgacttgctgcaacaggagctgactgctgctgagcagagaaaccagattctctctcagcagttacagcagatggaagctgagcataatactttgaggaacactgtggaaacagaaagagaggagtccaagattctactggaaaagatggaacttgaagtggcagagagaaaattatccttccataatctgcaggaagaaatgcatcatcttttagaacagtttgagcaagcaggccaagcccaggctgaactagagtctcggtatagtgctttggagcagaagcacaaagcagaaatggaagagaagacctctcatattttgagtcttcaaaagactggacaagagctgcagtctgcctgtgatgctctaaaggatcaaaattcaaagcttctccaagataagaatgagcaagcagttcagtcagcccagaccattcagcaactggaagatcagctccagcaaaaatccaaagaaattagccaatttctaaatagactgcccttgcaacaacatgaaacagcatctcagacttctttcccagatgtttataatgagggcacacaggcagtcactgaggagaatattgcttctttgcagaagagagtggtagaactagagaatgaaaagggagccttgctccttagttctatagagctggaggagctgaaagctgagaatgaaaaactgtcttctcagattactctcctagaggctcagaatagaactggggaggcagacagagaagtcagtgagatcagcattgttgatattgccaacaagaggagctcttctgctgaggaaagtggacaagatgttctagaaaacacattttctcagaaacataaagaattatcagttttattgttggaaatgaaagaagctcaagaggaaattgcatttcttaaattacagctccagggaaaaagggctgaggaagcagatcatgaggtccttgaccagaaagaaatgaaacagatggagggtgagggaatagctccaattaaaatgaaagtatttcttgaagatacagggcaagattttcccttaatgccaaatgaagagagcagtcttccagcagttgaaaaagaacaggcgagcactgaacatcaaagtagaacatctgaggaaatatctttaaatgatgctggagtagaattgaaatcaacaaagcaggatggtgataaatccctttctgctgtaccagatattggtcagtgtcatcaggatgagttggaaaggttaaaaagtcaaattttggagctcgagctaaactttcataaagcacaagaaatctatgagaaaaatttagatgagaaagctaaggaaattagcaacctaaaccagttgattgaggagtttaagaaaaatgctgacaacaacagcagtgcattcactgctttgtctgaagaaagagaccagcttctctctcaggtgaaggaacttagcatggtaacagaattgagggctcaggtaaagcaactggaaatgaaccttgcagaagcagaaaggcaaagaagacttgattatgaaagccaaactgcccatgacaacctgctcactgaacagatccatagtctcagcatagaagccaaatctaaagatgtgaaaattgaagttttacagaatgaactggatgatgtgcagcttcagttttctgagcagagtaccctgataagaagcctgcaaagccagctgcaaaataaggaaagtgaagtgcttgagggggcagaacgtgtaaggcatatctcaagtaaagtggaagaactgtcccaggctctttcacagaaggaacttgaaataacaaaaatggatcagctcttactagagaaaaagagagatgtggaaaccctccaacaaaccatcgaggagaaggatcaacaagtgacagaaatcagctttagtatgactgagaaaatggttcagcttaatgaagagaagttttctcttggggttgaaattaagactcttaaagaacagctaaatttattatccagagctgaggaagcaaaaaaagagcaggtggaagaagataatgaagtttcttctggccttaaacaaaattatgatgagatgagcccagcaggacaaataagtaaggaagaacttcagcatgaatttgaccttctgaagaaagaaaatgagcagagaaagagaaagctccaggcagctcttattaacagaaaggagcttctgcaaagagtcagtagattggaagaagaattagccaacttgaaagatgaatctaagaaagaaatcccactcagtgagactgagaggggagaagtggaagaagataaagaaaacaaagaatactcagaaaaatgtgtgacttctaagtgccaagaaatagaaatttatttaaaacagacaatatctgagaaagaagtggaactacagcatataaggaaggatttggaagaaaagctggcagctgaagagcaattccaggctctggtcaaacagatgaatcagaccttgcaagataaaacaaaccaaatagatttgctccaagcagaaatcagtgaaaaccaagcaattatccagaagttaatcacaagtaacacggatgcaagtgatggggactccgtagcacttgtaaaggaaacagtggtgataagtccaccttgtacaggtagtagtgaacactggaaaccagaactagaagaaaagatactggcccttgaaaaagaaaaggagcaacttcaaaagaagctacaggaagccttaacctcccgcaaggcaattcttaaaaaggcacaggagaaagaaagacatctcagggaggagctaaagcaacagaaagatgactataatcgcttgcaagaacagtttgatgagcaaagcaaggaaaatgagaatattggagaccagctaaggcaactccagattcaagtaagggaatccatagacggaaaactcccaagcacagaccagcaggaatcgtgttcttccactccaggtttagaagaacctttattcaaagccacagaacagcatcacactcaacctgttttagagtccaacttgtgcccagactggccttctcattctgaagatgcgagtgctctgcagggcggaacttctgttgcccagattaaggcccagctgaaggaaatagaggctgagaaagtagagttagaattgaaagttagttctacaacaagtgagcttactaaaaaatcagaagaggtatttcagttacaagagcagataaataaacagggtttagaaatcgagagtctaaagacagtatcccatgaagctgaagtccatgccgaaagcctgcagcagaaattggaaagcagccaactacaaattgctggcctagaacatctaagagaattgcaacctaaactggatgaactgcaaaaactcataagcaaaaaggaagaagacgttagctacctttctggacaacttagtgagaaagaagcagctctcactaaaatacagacagagataatagaacaagaagatttaattaaggctctgcatacacagctagaaatgcaagccaaagagcatgatgagaggataaagcagctacaggtggaactttgtgaaatgaagcaaaaaccagaagagattggagaagaaagtagagcaaagcaacaaatacaaaggaaactgcaagctgcccttatttcccgaaaagaagcactaaaagaaaacaaaagtctccaagaggaattgtctttggccagaggtaccattgaacgtctcaccaagtctctggcagatgtggaaagccaagtttctgctcaaaataaagaaaaagatacggtcttaggaaggttagctcttcttcaagaagaaagagacaaactcattacagaaatggacaggtctttattggaaaatcagagtctcagcagctcctgtgaaagtctaaaactagctctagagggtcttactgaagacaaggaaaagttagtgaaggaaattgaatctttgaaatcttctaagattgcagaaagtactgagtggcaagaga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//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:2804 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
            GeneID:2804 -> Biological process: GO:0007030 [Golgi organization] evidence: TAS
            GeneID:2804 -> Cellular component: GO:0000139 [Golgi membrane] evidence: IEA
            GeneID:2804 -> Cellular component: GO:0005793 [endoplasmic reticulum-Golgi intermediate compartment] evidence: IDA
            GeneID:2804 -> Cellular component: GO:0005794 [Golgi apparatus] evidence: IDA
            GeneID:2804 -> Cellular component: GO:0005795 [Golgi stack] evidence: TAS
            GeneID:2804 -> Cellular component: GO:0016021 [integral to membrane] evidence: IEA

by @meso_cacase at DBCLS
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