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2024-04-20 20:31:01, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_178584               3187 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens septin 10 (SEPT10), transcript variant 2, mRNA.
ACCESSION   NM_178584
VERSION     NM_178584.2  GI:384871590
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 3187)
  AUTHORS   Xu,M., Takanashi,M., Oikawa,K., Nishi,H., Isaka,K., Yoshimoto,T.,
            Ohyashiki,J. and Kuroda,M.
  TITLE     Identification of a novel role of Septin 10 in
            paclitaxel-resistance in cancers through a functional genomics
            screen
  JOURNAL   Cancer Sci. 103 (4), 821-827 (2012)
   PUBMED   22320903
  REMARK    GeneRIF: we found that paclitaxel-resistant tumors had decreased
            expression of SEPT10.
REFERENCE   2  (bases 1 to 3187)
  AUTHORS   Benedetti,D., Bomben,R., Dal-Bo,M., Marconi,D., Zucchetto,A.,
            Degan,M., Forconi,F., Del-Poeta,G., Gaidano,G. and Gattei,V.
  TITLE     Are surrogates of IGHV gene mutational status useful in B-cell
            chronic lymphocytic leukemia? The example of Septin-10
  JOURNAL   Leukemia 22 (1), 224-226 (2008)
   PUBMED   17657217
  REMARK    GeneRIF: Lack of SEPT10 transcript is associated with B-cell
            chronic lymphocytic leukemia
REFERENCE   3  (bases 1 to 3187)
  AUTHORS   Lamesch,P., Li,N., Milstein,S., Fan,C., Hao,T., Szabo,G., Hu,Z.,
            Venkatesan,K., Bethel,G., Martin,P., Rogers,J., Lawlor,S.,
            McLaren,S., Dricot,A., Borick,H., Cusick,M.E., Vandenhaute,J.,
            Dunham,I., Hill,D.E. and Vidal,M.
  TITLE     hORFeome v3.1: a resource of human open reading frames representing
            over 10,000 human genes
  JOURNAL   Genomics 89 (3), 307-315 (2007)
   PUBMED   17207965
REFERENCE   4  (bases 1 to 3187)
  AUTHORS   Hillier,L.W., Graves,T.A., Fulton,R.S., Fulton,L.A., Pepin,K.H.,
            Minx,P., Wagner-McPherson,C., Layman,D., Wylie,K., Sekhon,M.,
            Becker,M.C., Fewell,G.A., Delehaunty,K.D., Miner,T.L., Nash,W.E.,
            Kremitzki,C., Oddy,L., Du,H., Sun,H., Bradshaw-Cordum,H., Ali,J.,
            Carter,J., Cordes,M., Harris,A., Isak,A., van Brunt,A., Nguyen,C.,
            Du,F., Courtney,L., Kalicki,J., Ozersky,P., Abbott,S.,
            Armstrong,J., Belter,E.A., Caruso,L., Cedroni,M., Cotton,M.,
            Davidson,T., Desai,A., Elliott,G., Erb,T., Fronick,C., Gaige,T.,
            Haakenson,W., Haglund,K., Holmes,A., Harkins,R., Kim,K.,
            Kruchowski,S.S., Strong,C.M., Grewal,N., Goyea,E., Hou,S., Levy,A.,
            Martinka,S., Mead,K., McLellan,M.D., Meyer,R., Randall-Maher,J.,
            Tomlinson,C., Dauphin-Kohlberg,S., Kozlowicz-Reilly,A., Shah,N.,
            Swearengen-Shahid,S., Snider,J., Strong,J.T., Thompson,J.,
            Yoakum,M., Leonard,S., Pearman,C., Trani,L., Radionenko,M.,
            Waligorski,J.E., Wang,C., Rock,S.M., Tin-Wollam,A.M., Maupin,R.,
            Latreille,P., Wendl,M.C., Yang,S.P., Pohl,C., Wallis,J.W.,
            Spieth,J., Bieri,T.A., Berkowicz,N., Nelson,J.O., Osborne,J.,
            Ding,L., Meyer,R., Sabo,A., Shotland,Y., Sinha,P., Wohldmann,P.E.,
            Cook,L.L., Hickenbotham,M.T., Eldred,J., Williams,D., Jones,T.A.,
            She,X., Ciccarelli,F.D., Izaurralde,E., Taylor,J., Schmutz,J.,
            Myers,R.M., Cox,D.R., Huang,X., McPherson,J.D., Mardis,E.R.,
            Clifton,S.W., Warren,W.C., Chinwalla,A.T., Eddy,S.R., Marra,M.A.,
            Ovcharenko,I., Furey,T.S., Miller,W., Eichler,E.E., Bork,P.,
            Suyama,M., Torrents,D., Waterston,R.H. and Wilson,R.K.
  TITLE     Generation and annotation of the DNA sequences of human chromosomes
            2 and 4
  JOURNAL   Nature 434 (7034), 724-731 (2005)
   PUBMED   15815621
REFERENCE   5  (bases 1 to 3187)
  AUTHORS   Sui,L., Zhang,W., Liu,Q., Chen,T., Li,N., Wan,T., Yu,M. and Cao,X.
  TITLE     Cloning and functional characterization of human septin 10, a novel
            member of septin family cloned from dendritic cells
  JOURNAL   Biochem. Biophys. Res. Commun. 304 (2), 393-398 (2003)
   PUBMED   12711328
  REMARK    GeneRIF: Cloning and functional characterization of septin 10.
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from AK021681.1, AC011753.6,
            BC020502.1, AF146760.1 and AC140485.3.
            On Apr 20, 2012 this sequence version replaced gi:30795192.
            
            Summary: This gene encodes a member of the septin family of
            cytoskeletal proteins with GTPase activity. This protein localizes
            to the cytoplasm and nucleus and displays GTP-binding and GTPase
            activity. A pseudogene for this gene is located on chromosome 8.
            Alternative splicing results in multiple transcript variants.
            [provided by RefSeq, Apr 2012].
            
            Transcript Variant: This variant (2) lacks an in-frame segment in
            the coding region, compared to variant 1. Isoform 2 is shorter than
            isoform 1.
            
            ##Evidence-Data-START##
            Transcript exon combination :: AK092033.1 [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
            1-161               AK021681.1         1-161
            162-162             AC011753.6         69138-69138         c
            163-409             AK021681.1         163-409
            410-3002            BC020502.1         173-2765
            3003-3185           AF146760.1         2821-3003
            3186-3187           AC140485.3         45359-45360         c
FEATURES             Location/Qualifiers
     source          1..3187
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="2"
                     /map="2q13"
     gene            1..3187
                     /gene="SEPT10"
                     /note="septin 10"
                     /db_xref="GeneID:151011"
                     /db_xref="HGNC:14349"
                     /db_xref="MIM:611737"
     exon            1..409
                     /gene="SEPT10"
                     /inference="alignment:Splign:1.39.8"
     variation       291
                     /gene="SEPT10"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:3829700"
     misc_feature    344..346
                     /gene="SEPT10"
                     /note="upstream in-frame stop codon"
     CDS             380..1675
                     /gene="SEPT10"
                     /note="isoform 2 is encoded by transcript variant 2;
                     septin-10"
                     /codon_start=1
                     /product="septin-10 isoform 2"
                     /protein_id="NP_848699.1"
                     /db_xref="GI:30795193"
                     /db_xref="CCDS:CCDS42726.1"
                     /db_xref="GeneID:151011"
                     /db_xref="HGNC:14349"
                     /db_xref="MIM:611737"
                     /translation="
MASSEVARHLKRENIRSLTMSGHVGFESLPDQLVNRSIQQGFCFNILCVGETGIGKSTLIDTLFNTNFEDYESSHFCPNVKLKAQTYELQESNVQLKLTIVNTVGFGDQINKEESYQPIVDYIDAQFEAYLQEELKIKRSLFTYHDSRIHVCLYFISPTGHSLKTLDLLTMKNLDSKVNIIPVIAKADTVSKTELQKFKIKLMSELVSNGVQIYQFPTDDDTIAKVNAAMNGQLPFAVVGSMDEVKVGNKMVKARQYPWGVVQVENENHCDFVKLREMLICTNMEDLREQTHTRHYELYRRCKLEEMGFTDVGPENKPVSVQETYEAKRHEFHGERQRKEEEMKQMFVQRVKEKEAILKEAERELQAKFEHLKRLHQEERMKLEEKRRLLEEEIIAFSKKKATSEIFHSQSFLATGSNLRKDKDRKNSNFL
"
     misc_feature    497..1303
                     /gene="SEPT10"
                     /note="CDC/Septin GTPase family; Region: CDC_Septin;
                     cd01850"
                     /db_xref="CDD:206649"
     misc_feature    500..1303
                     /gene="SEPT10"
                     /note="Septin; Region: Septin; pfam00735"
                     /db_xref="CDD:201420"
     misc_feature    527..550
                     /gene="SEPT10"
                     /note="G1 box; other site"
                     /db_xref="CDD:206649"
     misc_feature    order(533..553,683..685,692..694,932..937,941..943,
                     1097..1102)
                     /gene="SEPT10"
                     /note="GTP/Mg2+ binding site [chemical binding]; other
                     site"
                     /db_xref="CDD:206649"
     misc_feature    617..634
                     /gene="SEPT10"
                     /note="Switch I region; other site"
                     /db_xref="CDD:206649"
     misc_feature    683..694
                     /gene="SEPT10"
                     /note="G3 box; other site"
                     /db_xref="CDD:206649"
     misc_feature    order(689..805,809..832)
                     /gene="SEPT10"
                     /note="Switch II region; other site"
                     /db_xref="CDD:206649"
     misc_feature    932..943
                     /gene="SEPT10"
                     /note="G4 box; other site"
                     /db_xref="CDD:206649"
     misc_feature    1097..1105
                     /gene="SEPT10"
                     /note="G5 box; other site"
                     /db_xref="CDD:206649"
     exon            410..527
                     /gene="SEPT10"
                     /inference="alignment:Splign:1.39.8"
     exon            528..723
                     /gene="SEPT10"
                     /inference="alignment:Splign:1.39.8"
     exon            724..910
                     /gene="SEPT10"
                     /inference="alignment:Splign:1.39.8"
     variation       876
                     /gene="SEPT10"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:3829701"
     exon            911..1072
                     /gene="SEPT10"
                     /inference="alignment:Splign:1.39.8"
     exon            1073..1169
                     /gene="SEPT10"
                     /inference="alignment:Splign:1.39.8"
     exon            1170..1338
                     /gene="SEPT10"
                     /inference="alignment:Splign:1.39.8"
     exon            1339..1471
                     /gene="SEPT10"
                     /inference="alignment:Splign:1.39.8"
     exon            1472..1659
                     /gene="SEPT10"
                     /inference="alignment:Splign:1.39.8"
     exon            1660..3187
                     /gene="SEPT10"
                     /inference="alignment:Splign:1.39.8"
     variation       2154
                     /gene="SEPT10"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:3886070"
ORIGIN      
cacttccggcctcgcgagggccgcaatcactgctccgcagttcccgcctgcattcctcgcgccgtcttcctggagtcccagctctccttcagcccgccccaacgctgacgctcagtcctcaggcgtcgagggtagctcctgtgaggggctcgcttggcgcaggcaaaacgctcagcgcgcaccacagggcgtccgccccaaccccgcccccggaggcctccagctcggccccgcccctgtcccttccccgtcgcggaggcagcctagcctcgcgccccgcccgttgcttctgccctccggccttcccgccgccgtcgccgggaccagccgctcggggccgggctgatacagccgcttcaccgtgcccctgcccgcgaccatggcctcctccgaggtggcgcggcacctgaaaagagaaaacattcgttcgttgactatgtctggccatgttggttttgagagtttgcctgatcagctggtgaacagatccattcagcaaggtttctgctttaatattctctgtgtgggggaaactggaattggaaaatcaacactgattgacacattgtttaatactaattttgaagactatgaatcctcacatttttgcccaaatgttaaacttaaagctcagacatatgaactccaggaaagtaatgttcaattgaaattgaccattgtgaatacagtgggatttggtgaccaaataaataaagaagagagctaccaaccaatagttgactacatagatgctcagtttgaggcctatctccaagaagaactgaagattaagcgttctctctttacctaccatgattctcgcatccatgtgtgtctctacttcatttcaccgacaggccactctctgaagacacttgatctcttaaccatgaagaaccttgacagcaaggtaaacattataccagtgattgccaaagcagatacggtttctaaaactgaattacagaagtttaagatcaagctcatgagtgaattggtcagcaatggcgtccagatataccagttcccaacggatgatgacactattgctaaggtcaacgctgcaatgaatggacagttgccgtttgctgttgtgggaagtatggatgaggtaaaagtcggaaacaagatggtcaaagctcgccagtacccttggggtgttgtacaagtggaaaatgaaaaccactgtgactttgtaaagctgcgggaaatgctcatttgtacaaatatggaggacctgcgagagcagacccataccaggcactatgagctttacaggcgctgcaaactggaggaaatgggctttacagatgtgggcccagaaaacaagccagtcagtgttcaagagacctatgaagccaaaagacatgagttccatggtgaacgtcagaggaaggaagaagaaatgaaacagatgtttgtgcagcgagtaaaggagaaagaagccatattgaaagaagctgagagagagctacaggccaaatttgagcaccttaagagacttcaccaagaagagagaatgaagcttgaagaaaagagaagacttttggaagaagaaataattgctttctctaaaaagaaagctacctccgagatatttcacagccagtcctttctggcaacaggcagcaacctgaggaaggacaaggaccgtaagaactccaattttttgtaaaacagaagttccagagcacagaaggtcatcatcacaagcaaactttattaaaaaaaaactagaagtgtgctttgattttgctgttatttgttttatcacttctatatttggtgaacagccacagttactgatatttatggaaaagtactttcaagtacaaggtcaatacataagccagagtgaatgatactacaagttgagcatctctaattcaaaaatctgaaatccagaagcttcaaaatctgaatctttttgagcactgacttgaccccacaagtggaaaattccccacccgacacctttgctttctgatggttcagtttaaacagattttgtttcttgcacaaaatttttgtataaattactttcaggctatatgtataaggtggatgtgaaacatgaattatgtaattagagtcgggtcccgttgtgtatatgcagatattccaaacctgaaatccaaaacacttctggtccctagcattttggataagggatactcagcttgtacctatatattcatatatattcactgttgttagaaatgtttaagttgctgttctgtgatgaatctaaatcttttctcttgctaccaagctattgtcactgcagtgcattataccaaagagcgaagtcagtgccactgaaaatacagaacccattaatatcgtggctatctgattacatttatattccaagatgaaccttttttatatatgctaaaaattttggggaatatgttttgggatgtattatggagctaaaactctaacctcttaatagttttatagaacttaaaaattttttatacaattacccaattggtgatatgatcttaagcttttgtgtcagattatttaatatgatgacttcatgctttattatgccttattatggctgacgtattactgtggtgaaacaaaatatctttaaaagttaaaacatccagatatataagctattttttcctaaggataaagtacctttgagcatgagtgtatcacagctttcattaggaaaacttttcattacatacttgtttaaactctgtcttccagggtaaaaataataaggttgaatcattttattaaaaatactttttaagaaaataactatgaacatctgaatattaaagatataaaaatgcacataattcatatttcaggtggtatttgcattcagtgccttactggtattctcagaacattttaatgatttctaacatttcttaacagtcatagatatatacattttcattttttgtacttgaatattctaaataaaactgacatttactcttgacaaataaaacatatatttactaaaatgtgtttaattttcctttctgaaaactctcattttaaaaacgttcatttaattatgtatttgaattattttggagatgaggtattttatgagtattttcagacaatgaaacttattagtctgtgtcagattctgagcaatcatagagtcatctaagttgtaaataaaaccttgcatagcacaatt
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:151011 -> Molecular function: GO:0005525 [GTP binding] evidence: IEA
            GeneID:151011 -> Biological process: GO:0007049 [cell cycle] evidence: IEA
            GeneID:151011 -> Biological process: GO:0051301 [cell division] evidence: IEA
            GeneID:151011 -> Cellular component: GO:0031105 [septin complex] evidence: IEA

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