GGRNA Home | Help | Advanced search

2024-03-29 20:20:01, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_173546               1999 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens kelch domain containing 8B (KLHDC8B), mRNA.
ACCESSION   NM_173546
VERSION     NM_173546.2  GI:300863121
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 1999)
  AUTHORS   Krem,M.M., Luo,P., Ing,B.I. and Horwitz,M.S.
  TITLE     The kelch protein KLHDC8B guards against mitotic errors,
            centrosomal amplification, and chromosomal instability
  JOURNAL   J. Biol. Chem. 287 (46), 39083-39093 (2012)
   PUBMED   22988245
  REMARK    GeneRIF: kelch protein KLHDC8B guards against mitotic errors,
            centrosomal amplification, and chromosomal instability
REFERENCE   2  (bases 1 to 1999)
  AUTHORS   Elks,C.E., Perry,J.R., Sulem,P., Chasman,D.I., Franceschini,N.,
            He,C., Lunetta,K.L., Visser,J.A., Byrne,E.M., Cousminer,D.L.,
            Gudbjartsson,D.F., Esko,T., Feenstra,B., Hottenga,J.J.,
            Koller,D.L., Kutalik,Z., Lin,P., Mangino,M., Marongiu,M.,
            McArdle,P.F., Smith,A.V., Stolk,L., van Wingerden,S.H., Zhao,J.H.,
            Albrecht,E., Corre,T., Ingelsson,E., Hayward,C., Magnusson,P.K.,
            Smith,E.N., Ulivi,S., Warrington,N.M., Zgaga,L., Alavere,H.,
            Amin,N., Aspelund,T., Bandinelli,S., Barroso,I., Berenson,G.S.,
            Bergmann,S., Blackburn,H., Boerwinkle,E., Buring,J.E., Busonero,F.,
            Campbell,H., Chanock,S.J., Chen,W., Cornelis,M.C., Couper,D.,
            Coviello,A.D., d'Adamo,P., de Faire,U., de Geus,E.J., Deloukas,P.,
            Doring,A., Smith,G.D., Easton,D.F., Eiriksdottir,G., Emilsson,V.,
            Eriksson,J., Ferrucci,L., Folsom,A.R., Foroud,T., Garcia,M.,
            Gasparini,P., Geller,F., Gieger,C., Gudnason,V., Hall,P.,
            Hankinson,S.E., Ferreli,L., Heath,A.C., Hernandez,D.G., Hofman,A.,
            Hu,F.B., Illig,T., Jarvelin,M.R., Johnson,A.D., Karasik,D.,
            Khaw,K.T., Kiel,D.P., Kilpelainen,T.O., Kolcic,I., Kraft,P.,
            Launer,L.J., Laven,J.S., Li,S., Liu,J., Levy,D., Martin,N.G.,
            McArdle,W.L., Melbye,M., Mooser,V., Murray,J.C., Murray,S.S.,
            Nalls,M.A., Navarro,P., Nelis,M., Ness,A.R., Northstone,K.,
            Oostra,B.A., Peacock,M., Palmer,L.J., Palotie,A., Pare,G.,
            Parker,A.N., Pedersen,N.L., Peltonen,L., Pennell,C.E., Pharoah,P.,
            Polasek,O., Plump,A.S., Pouta,A., Porcu,E., Rafnar,T., Rice,J.P.,
            Ring,S.M., Rivadeneira,F., Rudan,I., Sala,C., Salomaa,V., Sanna,S.,
            Schlessinger,D., Schork,N.J., Scuteri,A., Segre,A.V.,
            Shuldiner,A.R., Soranzo,N., Sovio,U., Srinivasan,S.R.,
            Strachan,D.P., Tammesoo,M.L., Tikkanen,E., Toniolo,D., Tsui,K.,
            Tryggvadottir,L., Tyrer,J., Uda,M., van Dam,R.M., van Meurs,J.B.,
            Vollenweider,P., Waeber,G., Wareham,N.J., Waterworth,D.M.,
            Weedon,M.N., Wichmann,H.E., Willemsen,G., Wilson,J.F., Wright,A.F.,
            Young,L., Zhai,G., Zhuang,W.V., Bierut,L.J., Boomsma,D.I.,
            Boyd,H.A., Crisponi,L., Demerath,E.W., van Duijn,C.M., Econs,M.J.,
            Harris,T.B., Hunter,D.J., Loos,R.J., Metspalu,A., Montgomery,G.W.,
            Ridker,P.M., Spector,T.D., Streeten,E.A., Stefansson,K.,
            Thorsteinsdottir,U., Uitterlinden,A.G., Widen,E., Murabito,J.M.,
            Ong,K.K. and Murray,A.
  CONSRTM   GIANT Consortium
  TITLE     Thirty new loci for age at menarche identified by a meta-analysis
            of genome-wide association studies
  JOURNAL   Nat. Genet. 42 (12), 1077-1085 (2010)
   PUBMED   21102462
REFERENCE   3  (bases 1 to 1999)
  AUTHORS   Krem,M.M., Salipante,S.J. and Horwitz,M.S.
  TITLE     Mutations in a gene encoding a midbody protein in binucleated
            Reed-Sternberg cells of Hodgkin lymphoma
  JOURNAL   Cell Cycle 9 (4), 670-675 (2010)
   PUBMED   20107318
  REMARK    GeneRIF: Deficiency of KLHDC8B leads to binucleated cells,
            implicating its involvement in Reed-Sternberg cell formation
REFERENCE   4  (bases 1 to 1999)
  AUTHORS   Salipante,S.J., Mealiffe,M.E., Wechsler,J., Krem,M.M., Liu,Y.,
            Namkoong,S., Bhagat,G., Kirchhoff,T., Offit,K., Lynch,H.,
            Wiernik,P.H., Roshal,M., McMaster,M.L., Tucker,M., Fromm,J.R.,
            Goldin,L.R. and Horwitz,M.S.
  TITLE     Mutations in a gene encoding a midbody kelch protein in familial
            and sporadic classical Hodgkin lymphoma lead to binucleated cells
  JOURNAL   Proc. Natl. Acad. Sci. U.S.A. 106 (35), 14920-14925 (2009)
   PUBMED   19706467
  REMARK    GeneRIF: Depletion of KLHDC8B through RNA interference leads to an
            increase in binucleated cells, implicating its reduced expression
            in the formation of classical Hodgkin lymphoma's signature
            Reed-Sternberg cell.
REFERENCE   5  (bases 1 to 1999)
  AUTHORS   Wan,D., Gong,Y., Qin,W., Zhang,P., Li,J., Wei,L., Zhou,X., Li,H.,
            Qiu,X., Zhong,F., He,L., Yu,J., Yao,G., Jiang,H., Qian,L., Yu,Y.,
            Shu,H., Chen,X., Xu,H., Guo,M., Pan,Z., Chen,Y., Ge,C., Yang,S. and
            Gu,J.
  TITLE     Large-scale cDNA transfection screening for genes related to cancer
            development and progression
  JOURNAL   Proc. Natl. Acad. Sci. U.S.A. 101 (44), 15724-15729 (2004)
   PUBMED   15498874
  REMARK    Erratum:[Proc Natl Acad Sci U S A. 2004 Dec 14:101(50):17565]
REFERENCE   6  (bases 1 to 1999)
  AUTHORS   Adams,M.D., Soares,M.B., Kerlavage,A.R., Fields,C. and Venter,J.C.
  TITLE     Rapid cDNA sequencing (expressed sequence tags) from a
            directionally cloned human infant brain cDNA library
  JOURNAL   Nat. Genet. 4 (4), 373-380 (1993)
   PUBMED   8401585
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from T08504.1, BC039083.1 and
            BC013110.2.
            This sequence is a reference standard in the RefSeqGene project.
            On Jul 20, 2010 this sequence version replaced gi:27734908.
            
            Summary: This gene encodes a protein which forms a distinct
            beta-propeller protein structure of kelch domains allowing for
            protein-protein interactions. Mutations in this gene have been
            associated with Hodgkin lymphoma. [provided by RefSeq, Sep 2010].
            
            ##Evidence-Data-START##
            Transcript exon combination :: AY129011.1, BC039083.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025081, ERS025083 [ECO:0000348]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-50                T08504.1           1-50
            51-1702             BC039083.1         1-1652
            1703-1999           BC013110.2         696-992
FEATURES             Location/Qualifiers
     source          1..1999
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="3"
                     /map="3p21.31"
     gene            1..1999
                     /gene="KLHDC8B"
                     /note="kelch domain containing 8B"
                     /db_xref="GeneID:200942"
                     /db_xref="HGNC:28557"
                     /db_xref="HPRD:14598"
                     /db_xref="MIM:613169"
     exon            1..101
                     /gene="KLHDC8B"
                     /inference="alignment:Splign:1.39.8"
     variation       40
                     /gene="KLHDC8B"
                     /replace="aa"
                     /replace="tc"
                     /db_xref="dbSNP:71627370"
     variation       40
                     /gene="KLHDC8B"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:34571182"
     variation       41
                     /gene="KLHDC8B"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:13096406"
     variation       78
                     /gene="KLHDC8B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:387906223"
     variation       92
                     /gene="KLHDC8B"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:116279850"
     exon            102..611
                     /gene="KLHDC8B"
                     /inference="alignment:Splign:1.39.8"
     variation       222
                     /gene="KLHDC8B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375412310"
     variation       232
                     /gene="KLHDC8B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201421481"
     CDS             236..1300
                     /gene="KLHDC8B"
                     /codon_start=1
                     /product="kelch domain-containing protein 8B"
                     /protein_id="NP_775817.1"
                     /db_xref="GI:27734909"
                     /db_xref="CCDS:CCDS2791.1"
                     /db_xref="GeneID:200942"
                     /db_xref="HGNC:28557"
                     /db_xref="HPRD:14598"
                     /db_xref="MIM:613169"
                     /translation="
MSAGGGRAFAWQVFPPMPTCRVYGTVAHQDGHLLVLGGCGRAGLPLDTAETLDMASHTWLALAPLPTARAGAAAVVLGKQVLVVGGVDEVQSPVAAVEAFLMDEGRWERRATLPQAAMGVATVERDGMVYALGGMGPDTAPQAQVRVYEPRRDCWLSLPSMPTPCYGASTFLHGNKIYVLGGRQGKLPVTAFEAFDLEARTWTRHPSLPSRRAFAGCAMAEGSVFSLGGLQQPGPHNFYSRPHFVNTVEMFDLEHGSWTKLPRSLRMRDKRADFVVGSLGGHIVAIGGLGNQPCPLGSVESFSLARRRWEALPAMPTARCSCSSLQAGPRLFVIGGVAQGPSQAVEALCLRDGV
"
     misc_feature    236..328
                     /gene="KLHDC8B"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q8IXV7.1);
                     Region: Kelch 1"
     misc_feature    329..472
                     /gene="KLHDC8B"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q8IXV7.1);
                     Region: Kelch 2"
     misc_feature    476..616
                     /gene="KLHDC8B"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q8IXV7.1);
                     Region: Kelch 3"
     misc_feature    617..760
                     /gene="KLHDC8B"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q8IXV7.1);
                     Region: Kelch 4"
     misc_feature    620..757
                     /gene="KLHDC8B"
                     /note="Kelch domain; Region: Kelch; smart00612"
                     /db_xref="CDD:128874"
     misc_feature    725..862
                     /gene="KLHDC8B"
                     /note="Kelch motif; Region: Kelch_1; pfam01344"
                     /db_xref="CDD:201739"
     misc_feature    761..901
                     /gene="KLHDC8B"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q8IXV7.1);
                     Region: Kelch 5"
     misc_feature    866..1021
                     /gene="KLHDC8B"
                     /note="Galactose oxidase, central domain; Region: Kelch_3;
                     cl02701"
                     /db_xref="CDD:207702"
     misc_feature    905..1078
                     /gene="KLHDC8B"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q8IXV7.1);
                     Region: Kelch 6"
     misc_feature    1046..1192
                     /gene="KLHDC8B"
                     /note="Kelch motif; Region: Kelch_6; pfam13964"
                     /db_xref="CDD:206134"
     misc_feature    1079..1222
                     /gene="KLHDC8B"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q8IXV7.1);
                     Region: Kelch 7"
     misc_feature    1226..1297
                     /gene="KLHDC8B"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q8IXV7.1);
                     Region: Kelch 8"
     variation       236
                     /gene="KLHDC8B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:11558200"
     variation       242
                     /gene="KLHDC8B"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:371827527"
     variation       243
                     /gene="KLHDC8B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376554410"
     variation       272
                     /gene="KLHDC8B"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:199565210"
     variation       277
                     /gene="KLHDC8B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201475255"
     variation       299
                     /gene="KLHDC8B"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:374978976"
     variation       332
                     /gene="KLHDC8B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370010051"
     variation       357
                     /gene="KLHDC8B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373852462"
     variation       423
                     /gene="KLHDC8B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376897933"
     variation       426
                     /gene="KLHDC8B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149050663"
     variation       435
                     /gene="KLHDC8B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368617575"
     variation       440
                     /gene="KLHDC8B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369834697"
     variation       493
                     /gene="KLHDC8B"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:148228673"
     variation       552
                     /gene="KLHDC8B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139300054"
     exon            612..776
                     /gene="KLHDC8B"
                     /inference="alignment:Splign:1.39.8"
     variation       637
                     /gene="KLHDC8B"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:141927816"
     variation       651
                     /gene="KLHDC8B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376929323"
     variation       652
                     /gene="KLHDC8B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370116447"
     variation       705
                     /gene="KLHDC8B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149570292"
     variation       706
                     /gene="KLHDC8B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375567221"
     variation       721
                     /gene="KLHDC8B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199808095"
     variation       754
                     /gene="KLHDC8B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199949878"
     variation       755
                     /gene="KLHDC8B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200254776"
     variation       767
                     /gene="KLHDC8B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201859787"
     exon            777..1001
                     /gene="KLHDC8B"
                     /inference="alignment:Splign:1.39.8"
     variation       799
                     /gene="KLHDC8B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140099356"
     variation       800
                     /gene="KLHDC8B"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:146245053"
     variation       838
                     /gene="KLHDC8B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368130572"
     variation       846
                     /gene="KLHDC8B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139371579"
     variation       851
                     /gene="KLHDC8B"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:139453635"
     variation       854
                     /gene="KLHDC8B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147796338"
     variation       890
                     /gene="KLHDC8B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372010655"
     variation       924
                     /gene="KLHDC8B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369228701"
     variation       952
                     /gene="KLHDC8B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146679886"
     variation       957
                     /gene="KLHDC8B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201206162"
     variation       966
                     /gene="KLHDC8B"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:200076809"
     variation       967
                     /gene="KLHDC8B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201696469"
     exon            1002..1103
                     /gene="KLHDC8B"
                     /inference="alignment:Splign:1.39.8"
     variation       1023
                     /gene="KLHDC8B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148999552"
     variation       1068
                     /gene="KLHDC8B"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:373274746"
     variation       1091
                     /gene="KLHDC8B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376185018"
     exon            1104..1985
                     /gene="KLHDC8B"
                     /inference="alignment:Splign:1.39.8"
     variation       1119
                     /gene="KLHDC8B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375754493"
     variation       1137
                     /gene="KLHDC8B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148176543"
     variation       1141
                     /gene="KLHDC8B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368331749"
     variation       1152
                     /gene="KLHDC8B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375296215"
     variation       1154
                     /gene="KLHDC8B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150205472"
     variation       1157
                     /gene="KLHDC8B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367857888"
     variation       1219
                     /gene="KLHDC8B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371934873"
     variation       1234
                     /gene="KLHDC8B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138843346"
     variation       1293
                     /gene="KLHDC8B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374910661"
     variation       1300
                     /gene="KLHDC8B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:111352447"
     variation       1341
                     /gene="KLHDC8B"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:150542030"
     variation       1343
                     /gene="KLHDC8B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372241018"
     variation       1515
                     /gene="KLHDC8B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139491293"
     variation       1577
                     /gene="KLHDC8B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143176164"
     variation       1671
                     /gene="KLHDC8B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146662619"
     variation       1703
                     /gene="KLHDC8B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:9586"
     STS             1746..1970
                     /gene="KLHDC8B"
                     /standard_name="RH79955"
                     /db_xref="UniSTS:88153"
     variation       1862
                     /gene="KLHDC8B"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:11552"
     polyA_site      1985
                     /gene="KLHDC8B"
ORIGIN      
ccggagccccgccagagcccgacttcagccccagccagatcccgcgtcaacggaggcggaacggcggaccccgtaccctggcagcatcggagcaccggcgggtgaaggcaaggtccctggactggtcatatacctcttgtggccctggcagaatcaagatgaggccctgtcatgcctccccagtgaggcctacagtctgagcagacagcatggcctgccactggcagtgaacaccatgtctgcaggaggtggccgggcctttgcttggcaagtgttcccccccatgcccacttgccgggtctatggcacagtggcacaccaagatgggcacctgctggtgttggggggttgtggccgggctggactgcccctggacactgctgagacactggacatggcctcgcacacatggctggcactggcacccctgcccactgcccgggctggtgcagctgcggtagttctgggcaagcaggtgctagtggtgggtggtgtggatgaggtccagagcccggtagctgctgtagaggccttcctgatggatgagggccgctgggagcgtcgggccaccctccctcaagcagccatgggggttgcaactgtggagagagatggtatggtgtatgctctggggggaatgggccctgacacggccccccaggcccaggtacgtgtgtatgagccccgtcgggactgctggctttcgctaccctccatgcccacaccctgctatggggcctccaccttcctgcacgggaacaagatctatgtcctggggggccgccagggcaagctcccggtgactgcttttgaagcctttgatctggaggcccgtacatggacccggcatccaagcctacccagccgtcgggcctttgctggctgcgccatggctgaaggcagcgtctttagcctgggtggcctgcagcagcctgggccccacaacttctactctcgcccacactttgtcaacactgtggagatgtttgacctggagcatgggtcctggaccaaattgccccgcagcctgcgcatgagggataagagggcagactttgtggttgggtcccttgggggccacattgtggccattgggggccttggaaaccagccatgtcctttgggctctgtggagagctttagccttgcacggcggcgctgggaggcattgcctgccatgcccactgcccgctgctcctgctctagtctgcaggctgggccccggctgtttgttattgggggtgtggcccagggccccagtcaagccgtggaggcactgtgtctgcgtgatggggtctgaaggcttggtgggagctgtccactggagcagctcattgccagaggcagctatttctatggctccttttgctgctgaggacactcactgtggctctgtgggatgagagaggcatgggggtgagcacttgaaacactgccttggggccttgggttaggggagcctttgtctttagtgcaggacacacatatgcttacacctacctttatcaccattcgttcatgaatcatgcctagctccatccttgccctgggacctactaggccttccatccaactgggaaatggggagaagcaaagctggcctcatgctcttcagggtcagttcctatctggagttgaccaggcctaccccagttgccattcctgaaaaatctcagctgccaggctgcctttagggtccctgcagacccaggagagttgagagggtgggggacacagagagaatagagaggatgtgggaactgccagagggccggagcgcaggagttcaagtggaggaatgctggctttgagccctctacactgctggttgtatgaccttggacaagtcacttcacctctctgtgcctcagcatcctcatctataaatggggatctctgaaaccttcctaccctacctacctcacagggctgttgtgaggacccagggagtttggatgtggaagtaaaagtgctgctaaaacctaaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:200942 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA

by @meso_cacase at DBCLS
This page is licensed under a Creative Commons Attribution 2.1 Japan License.