2024-03-29 19:50:45, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_013260 2519 bp mRNA linear PRI 17-APR-2013 DEFINITION Homo sapiens SAP30 binding protein (SAP30BP), mRNA. ACCESSION NM_013260 VERSION NM_013260.6 GI:156071507 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 2519) AUTHORS Xu,B., Roos,J.L., Dexheimer,P., Boone,B., Plummer,B., Levy,S., Gogos,J.A. and Karayiorgou,M. TITLE Exome sequencing supports a de novo mutational paradigm for schizophrenia JOURNAL Nat. Genet. 43 (9), 864-868 (2011) PUBMED 21822266 REMARK Publication Status: Online-Only REFERENCE 2 (bases 1 to 2519) AUTHORS Chen,J., Li,Y.M., Li,J.F., Liu,L.D., Liao,Y., Na,R.X., Wang,J.J., Wang,L.C. and Li,Q.H. TITLE Transcriptional regulation by HSV-1 induced HTRP via acetylation system JOURNAL Virol Sin 25 (6), 417-424 (2010) PUBMED 21221920 REMARK GeneRIF: The results indicate that HTRP could inhibit the transcription of a viral promoter, whose interaction with SAP30 synergistically affects transcriptional inhibition of the herpes simplex virus type 1 genes, and is related to HDAC enzyme activity. REFERENCE 3 (bases 1 to 2519) AUTHORS Naukkarinen,J., Surakka,I., Pietilainen,K.H., Rissanen,A., Salomaa,V., Ripatti,S., Yki-Jarvinen,H., van Duijn,C.M., Wichmann,H.E., Kaprio,J., Taskinen,M.R. and Peltonen,L. CONSRTM ENGAGE Consortium TITLE Use of genome-wide expression data to mine the 'Gray Zone' of GWA studies leads to novel candidate obesity genes JOURNAL PLoS Genet. 6 (6), E1000976 (2010) PUBMED 20532202 REMARK GeneRIF: Observational study and genome-wide association study of gene-disease association. (HuGE Navigator) Publication Status: Online-Only REFERENCE 4 (bases 1 to 2519) AUTHORS Gao,J., Li,W.X., Feng,S.Q., Yuan,Y.S., Wan,D.F., Han,W. and Yu,Y. TITLE A protein-protein interaction network of transcription factors acting during liver cell proliferation JOURNAL Genomics 91 (4), 347-355 (2008) PUBMED 18255255 REFERENCE 5 (bases 1 to 2519) AUTHORS Li,J.F., Liu,L.D., Ma,S.H., Che,Y.C., Wang,L.C., Dong,C.H., Zhao,H.L., Liao,Y. and Li,Q.H. TITLE HTRP--an immediate-early gene product induced by HSV1 infection in human embryo fibroblasts, is involved in cellular co-repressors JOURNAL J. Biochem. 136 (2), 169-176 (2004) PUBMED 15496587 REMARK GeneRIF: HTRP is involved in cellular co-repressors REFERENCE 6 (bases 1 to 2519) AUTHORS Hu,R.M., Han,Z.G., Song,H.D., Peng,Y.D., Huang,Q.H., Ren,S.X., Gu,Y.J., Huang,C.H., Li,Y.B., Jiang,C.L., Fu,G., Zhang,Q.H., Gu,B.W., Dai,M., Mao,Y.F., Gao,G.F., Rong,R., Ye,M., Zhou,J., Xu,S.H., Gu,J., Shi,J.X., Jin,W.R., Zhang,C.K., Wu,T.M., Huang,G.Y., Chen,Z., Chen,M.D. and Chen,J.L. TITLE Gene expression profiling in the human hypothalamus-pituitary-adrenal axis and full-length cDNA cloning JOURNAL Proc. Natl. Acad. Sci. U.S.A. 97 (17), 9543-9548 (2000) PUBMED 10931946 REFERENCE 7 (bases 1 to 2519) AUTHORS Zhang,Y., Sun,Z.W., Iratni,R., Erdjument-Bromage,H., Tempst,P., Hampsey,M. and Reinberg,D. TITLE SAP30, a novel protein conserved between human and yeast, is a component of a histone deacetylase complex JOURNAL Mol. Cell 1 (7), 1021-1031 (1998) PUBMED 9651585 COMMENT VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from AC087749.12. On Aug 16, 2007 this sequence version replaced gi:47834346. Sequence Note: The RefSeq transcript and protein were derived from genomic sequence to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on alignments. ##Evidence-Data-START## Transcript exon combination :: BC030233.1, AY082382.1 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025081, ERS025082 [ECO:0000348] ##Evidence-Data-END## PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-160 AC087749.12 111805-111964 161-270 AC087749.12 113002-113111 271-318 AC087749.12 116302-116349 319-361 AC087749.12 137926-137968 362-450 AC087749.12 144269-144357 451-542 AC087749.12 146966-147057 543-603 AC087749.12 147797-147857 604-655 AC087749.12 148294-148345 656-714 AC087749.12 149242-149300 715-799 AC087749.12 150494-150578 800-2519 AC087749.12 150826-152545 FEATURES Location/Qualifiers source 1..2519 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="17" /map="17q25.1" gene 1..2519 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /note="SAP30 binding protein" /db_xref="GeneID:29115" /db_xref="HGNC:30785" /db_xref="HPRD:17094" /db_xref="MIM:610218" exon 1..160 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /inference="alignment:Splign:1.39.8" variation 20 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="a" /replace="g" /db_xref="dbSNP:370904087" variation 27 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="g" /replace="t" /db_xref="dbSNP:375315996" variation 50 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="a" /replace="g" /db_xref="dbSNP:368616539" CDS 55..981 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /note="HSV-1 binding; transcriptional regulator protein HCNGP" /codon_start=1 /product="SAP30-binding protein" /protein_id="NP_037392.1" /db_xref="GI:9994179" /db_xref="CCDS:CCDS11726.1" /db_xref="GeneID:29115" /db_xref="HGNC:30785" /db_xref="HPRD:17094" /db_xref="MIM:610218" /translation="
MAGKKNVLSSLAVYAEDSEPESDGEAGIEAVGSAAEEKGGLVSDAYGEDDFSRLGGDEDGYEEEEDENSRQSEDDDSETEKPEADDPKDNTEAEKRDPQELVASFSERVRNMSPDEIKIPPEPPGRCSNHLQDKIQKLYERKIKEGMDMNYIIQRKKEFRNPSIYEKLIQFCAIDELGTNYPKDMFDPHGWSEDSYYEALAKAQKIEMDKLEKAKKERTKIEFVTGTKKGTTTNATSTTTTTASTAVADAQKRKSKWDSAIPVTTIAQPTILTTTATLPAVVTVTTSASGSKTTVISAVGTIVKKAKQ
" misc_feature 106..108 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /experiment="experimental evidence, no additional details recorded" /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot (Q9UHR5.1); phosphorylation site" misc_feature 118..120 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /experiment="experimental evidence, no additional details recorded" /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot (Q9UHR5.1); phosphorylation site" misc_feature 181..183 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /experiment="experimental evidence, no additional details recorded" /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot (Q9UHR5.1); phosphorylation site" misc_feature 208..210 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /experiment="experimental evidence, no additional details recorded" /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot (Q9UHR5.1); phosphorylation site" misc_feature 391..393 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /experiment="experimental evidence, no additional details recorded" /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot (Q9UHR5.1); phosphorylation site" misc_feature 409..699 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /note="HCNGP-like protein; Region: HCNGP; pfam07818" /db_xref="CDD:191863" variation 80 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="t" /db_xref="dbSNP:201680665" variation 81 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="a" /replace="g" /db_xref="dbSNP:375395105" variation 99 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="g" /db_xref="dbSNP:372925697" variation 126 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="t" /db_xref="dbSNP:8071553" exon 161..270 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /inference="alignment:Splign:1.39.8" variation 161 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="a" /replace="g" /db_xref="dbSNP:111336734" variation 163 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="g" /db_xref="dbSNP:367727956" variation 167 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="a" /replace="g" /db_xref="dbSNP:199944352" variation 180 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="a" /replace="g" /db_xref="dbSNP:138151640" variation 269 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="t" /db_xref="dbSNP:200034773" exon 271..318 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /inference="alignment:Splign:1.39.8" variation 280 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="a" /replace="g" /db_xref="dbSNP:374805218" variation 293 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="a" /replace="c" /db_xref="dbSNP:141727230" exon 319..361 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /inference="alignment:Splign:1.39.8" variation 319 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="g" /db_xref="dbSNP:373126274" variation 341 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="a" /replace="g" /db_xref="dbSNP:150596591" variation 357 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="t" /db_xref="dbSNP:139608518" exon 362..450 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /inference="alignment:Splign:1.39.8" variation 392 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="t" /db_xref="dbSNP:370083040" variation 393 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="a" /replace="g" /db_xref="dbSNP:373834045" variation 403 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="a" /replace="g" /db_xref="dbSNP:368000997" variation 423 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="t" /db_xref="dbSNP:113668113" variation 439 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="a" /replace="c" /db_xref="dbSNP:11558668" exon 451..542 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /inference="alignment:Splign:1.39.8" variation 462 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="a" /replace="g" /db_xref="dbSNP:376697317" exon 543..603 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /inference="alignment:Splign:1.39.8" variation 572 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="g" /db_xref="dbSNP:146045832" exon 604..655 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /inference="alignment:Splign:1.39.8" variation 623 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="g" /replace="t" /db_xref="dbSNP:140022461" variation 629 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="t" /db_xref="dbSNP:184496853" exon 656..714 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /inference="alignment:Splign:1.39.8" variation 706 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="t" /db_xref="dbSNP:372381855" exon 715..799 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /inference="alignment:Splign:1.39.8" variation 735 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="t" /db_xref="dbSNP:187342769" variation 738 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="a" /replace="g" /db_xref="dbSNP:374730171" variation 753 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="t" /db_xref="dbSNP:376398113" variation 760 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="a" /replace="g" /db_xref="dbSNP:143739015" variation 762 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="a" /replace="g" /db_xref="dbSNP:56144802" variation 772..774 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="" /replace="act" /db_xref="dbSNP:372648052" exon 800..2519 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /inference="alignment:Splign:1.39.8" variation 831 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="a" /replace="g" /db_xref="dbSNP:148987774" variation 854 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="g" /db_xref="dbSNP:200708050" variation 872 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="t" /db_xref="dbSNP:373102942" variation 890 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="t" /db_xref="dbSNP:201392633" variation 936 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="t" /db_xref="dbSNP:140985854" variation 960 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="t" /db_xref="dbSNP:376325673" variation 982 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="t" /db_xref="dbSNP:377404831" variation 984 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="g" /replace="t" /db_xref="dbSNP:143414711" variation 985 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="a" /replace="g" /db_xref="dbSNP:200431565" variation 988 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="a" /replace="g" /db_xref="dbSNP:199634823" variation 990 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="a" /replace="g" /db_xref="dbSNP:146566382" STS 1055..1212 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /standard_name="RH18255" /db_xref="UniSTS:17514" variation 1077 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="a" /replace="g" /db_xref="dbSNP:369889672" variation 1192 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="t" /db_xref="dbSNP:182731847" variation 1359 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="t" /db_xref="dbSNP:16968216" STS 1388..1541 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /standard_name="RH17466" /db_xref="UniSTS:9256" variation 1446 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="a" /replace="g" /db_xref="dbSNP:377376763" variation 1560..1563 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="" /replace="cacc" /db_xref="dbSNP:376979689" variation 1576 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="a" /replace="t" /db_xref="dbSNP:28562909" variation 1687 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="t" /db_xref="dbSNP:370361692" variation 1696 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="g" /db_xref="dbSNP:149170453" variation 1726..1728 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="" /replace="cct" /db_xref="dbSNP:72233484" variation 1739 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="t" /db_xref="dbSNP:374711763" variation 1740 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="a" /replace="g" /db_xref="dbSNP:143212085" variation 1747 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="t" /db_xref="dbSNP:188077540" variation 1768 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="g" /db_xref="dbSNP:191551152" variation 1825 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="t" /db_xref="dbSNP:375147206" variation 1895 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="t" /db_xref="dbSNP:376525684" variation 2024 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="a" /replace="g" /db_xref="dbSNP:115467173" variation 2101 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="t" /db_xref="dbSNP:370978777" variation 2197 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="g" /db_xref="dbSNP:374244975" variation 2203 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="g" /replace="t" /db_xref="dbSNP:140465078" variation 2241 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="g" /db_xref="dbSNP:182922408" variation 2325 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="t" /db_xref="dbSNP:115541056" variation 2343 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="t" /db_xref="dbSNP:372366921" variation 2355 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="a" /replace="c" /db_xref="dbSNP:1063092" STS 2370..2470 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /standard_name="Cda12b04" /db_xref="UniSTS:68883" variation 2373 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="a" /replace="c" /db_xref="dbSNP:1063093" variation 2407 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="t" /db_xref="dbSNP:187220320" variation 2424 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="t" /db_xref="dbSNP:1063094" variation 2437 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="a" /replace="c" /db_xref="dbSNP:1063095" variation 2469 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="a" /replace="g" /db_xref="dbSNP:1063096" variation 2475 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="a" /replace="g" /db_xref="dbSNP:1046554" variation 2486 /gene="SAP30BP" /gene_synonym="HCNGP; HTRG; HTRP" /replace="c" /replace="t" /db_xref="dbSNP:192084264" ORIGIN
gaagtcggcgtcttgagtcataggagtgagccacgcccgggctgtgggaataagatggcggggaagaagaatgttctgtcgtctctcgcagtttacgcggaagattcagagcccgagtctgatggcgaggctggaatcgaggcggtgggcagcgcggctgaggagaaaggcggattggtatctgatgcctatggggaggatgacttttctcgtctagggggtgatgaagatggttatgaagaagaagaagatgagaacagtagacagtcggaagatgacgattcagagactgaaaaacctgaggctgatgacccaaaggataatacagaagcagaaaagcgagacccccaggaactcgtggcctccttttctgaaagagttcggaacatgtcgcctgatgaaatcaagatcccgccagaaccccctggcagatgttcaaatcacttgcaagacaagatccagaagctttatgaacgaaagataaaggagggaatggatatgaactacattatccaaaggaagaaagaatttcggaaccctagcatctacgagaagctgatccagttctgtgccattgacgagcttggcaccaactacccaaaggatatgtttgatccccatggctggtctgaggactcctactatgaggcattagccaaggcccagaaaattgagatggacaaattggaaaaggccaaaaaggagcgaacaaaaattgagtttgtgacgggcaccaaaaaaggcaccacgaccaacgccacgtccaccaccactaccactgccagcacagctgttgcagatgctcagaagagaaagagcaagtgggattcggctatcccagtgacaacgatagcccagcccaccatcctcaccaccacagccaccctgccagctgttgtcacggtcaccaccagcgccagcggctccaagaccaccgtcatctctgctgtgggcaccattgtgaagaaggccaagcagtgacctgaggggccaccctaggacttgaaaggaccgtgcagcccagtgaccactgcccagtgggaggcgccactttgtatatttcaggactgggacctactccccagatgccacctgagaggagcttctgtttggcattccagatggaaggacaggcagcacgggagccaggcgctgtggacagggtctgtccacgcaccacctggggtctgccgcctattaaaagtgccgtattcttacctcttggcatctcagatgcactggcctctcctgcattctgtttgcaggcaaatgcttcagctcacatgtcccccaagactcaatagtcttggttgggactattgcctcagggttgacaacagggtgatggaggcctgggacgctgttcagaggggtgacccaagaagtcaccgttgttatccgtgtatgcctctgggcatggacaggcgggagtccccgagccccacgtatgccccatctgccgccttgatcccaaaacccagccagttctcgggtgatggtggagctgtgctcccttgagtgcacttgagcactccccagaccagatcactttttggacacacccaggaaggcttttgaagtcaagccagtttccagaagggctggggtgagatcctgacctgtgcagagagtggggaggcgtcagcgcctggccagggctgccccagtcctttggtgcccggtgagcgcagccagcaggagctgagcagcgggggagatgaatcacctcctgccttggcgaggcggcagctcattgtttacaggcaagccctgctcctgggagggctcctgccaccccacccttcctctgtgtgttatctctgccccacagcagcccctgggcagcaccagtggccactgggctccccccggggttgaaacgggtttcccagaccaggggttcagaggagactatttacccttcatgatctttggcgattctccactggagcggaagggctgtgtgtcaaaagaaggaagccaggctgtgaagggccgtgttgctttcagtgggtgggcagaggtttagaaaggtggttctgaaatggcacctggtactcttgtgggacctggggaatataaggaactctgtgcatgaggtttcaaaaataaaaattgagtccactctccccgtacacacacactcgggcacttcaggaggtcagttctcaccccttcctcgatggggctttaaagctctggggagaagagctgctccccactcatgccccagagggactgtgaaaaggcttcctgtgacctccgatggcggcccctcattggccaagggcactgtggatgttttgtgggaggcagcatggcaccgtggaaagggcagtagacgtggagccggcacctctggtctggattccacttaaaaccagttgagtggtctcaagcccttaacctctgtaagcctgtttcttctctgaaatcacagtaataaagcgtcgtaagatggttgggaagaaccagaggtgacttatgcaaaagctttataaactgtaaagttcctgcca
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:29115 -> Molecular function: GO:0005515 [protein binding] evidence: IPI GeneID:29115 -> Biological process: GO:0006351 [transcription, DNA-dependent] evidence: IEA GeneID:29115 -> Biological process: GO:0006355 [regulation of transcription, DNA-dependent] evidence: IEA GeneID:29115 -> Biological process: GO:0006915 [apoptotic process] evidence: IEA GeneID:29115 -> Biological process: GO:0006917 [induction of apoptosis] evidence: IDA GeneID:29115 -> Cellular component: GO:0005634 [nucleus] evidence: IDA GeneID:29115 -> Cellular component: GO:0005730 [nucleolus] evidence: IDA GeneID:29115 -> Cellular component: GO:0045111 [intermediate filament cytoskeleton] evidence: IDA
by
@meso_cacase at
DBCLS
This page is licensed under a Creative Commons Attribution 2.1 Japan License.