2024-04-25 04:13:56, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001130047 3914 bp mRNA linear PRI 17-APR-2013 DEFINITION Homo sapiens tubulin folding cofactor E-like (TBCEL), transcript variant 2, mRNA. ACCESSION NM_001130047 VERSION NM_001130047.1 GI:194239700 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 3914) AUTHORS Sellin,M.E., Holmfeldt,P., Stenmark,S. and Gullberg,M. TITLE Op18/Stathmin counteracts the activity of overexpressed tubulin-disrupting proteins in a human leukemia cell line JOURNAL Exp. Cell Res. 314 (6), 1367-1377 (2008) PUBMED 18262179 REMARK GeneRIF: Depletion of Op18 by means of RNA interference increased the susceptibility of tubulin to TBCE or E-like mediated disruption, while overexpressed Op18 exerted a tubulin-protective effect. REFERENCE 2 (bases 1 to 3914) AUTHORS Bartolini,F., Tian,G., Piehl,M., Cassimeris,L., Lewis,S.A. and Cowan,N.J. TITLE Identification of a novel tubulin-destabilizing protein related to the chaperone cofactor E JOURNAL J. Cell. Sci. 118 (PT 6), 1197-1207 (2005) PUBMED 15728251 REMARK GeneRIF: Leucine rich repeat containing 35 (E-like) is a novel regulator of tubulin stability with overexpression causing depolymerization of microtubules and suppression resulting in an increase in the number of stable microtubules. COMMENT VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from AK313324.1, BC020501.1, DN602255.1, AI128257.1 and BX091943.1. Transcript Variant: This variant (2) differs in the 5' UTR, compared to variant 1. Variants 1 and 2 encode the same protein. ##Evidence-Data-START## Transcript exon combination :: AK313324.1 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025098 [ECO:0000348] ##Evidence-Data-END## PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-569 AK313324.1 23-591 570-2772 BC020501.1 606-2808 2773-3228 DN602255.1 355-810 3229-3496 AI128257.1 40-307 c 3497-3914 BX091943.1 1-418 c FEATURES Location/Qualifiers source 1..3914 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="11" /map="11q23.3" gene 1..3914 /gene="TBCEL" /gene_synonym="El; LRRC35" /note="tubulin folding cofactor E-like" /db_xref="GeneID:219899" /db_xref="HGNC:28115" /db_xref="MIM:610451" exon 1..61 /gene="TBCEL" /gene_synonym="El; LRRC35" /inference="alignment:Splign:1.39.8" variation 28 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="t" /db_xref="dbSNP:370834296" exon 62..211 /gene="TBCEL" /gene_synonym="El; LRRC35" /inference="alignment:Splign:1.39.8" misc_feature 67..69 /gene="TBCEL" /gene_synonym="El; LRRC35" /note="upstream in-frame stop codon" CDS 79..1353 /gene="TBCEL" /gene_synonym="El; LRRC35" /note="catastrophin; leucine rich repeat containing 35; tubulin-specific chaperone e-like; E-like; leucine-rich repeat-containing protein 35" /codon_start=1 /product="tubulin-specific chaperone cofactor E-like protein" /protein_id="NP_001123519.1" /db_xref="GI:194239701" /db_xref="CCDS:CCDS31692.1" /db_xref="GeneID:219899" /db_xref="HGNC:28115" /db_xref="MIM:610451" /translation="
MDQPSGRSFMQVLCEKYSPENFPYRRGPGMGVHVPATPQGSPMKDRLNLPSVLVLNSCGITCAGDEKEIAAFCAHVSELDLSDNKLEDWHEVSKIVSNVPQLEFLNLSSNPLNLSVLERTCAGSFSGVRKLVLNNSKASWETVHMILQELPDLEELFLCLNDYETVSCPSICCHSLKLLHITDNNLQDWTEIRKLGVMFPSLDTLVLANNHLNAIEEPDDSLARLFPNLRSISLHKSGLQSWEDIDKLNSFPKLEEVRLLGIPLLQPYTTEERRKLVIARLPSVSKLNGSVVTDGEREDSERFFIRYYVDVPQEEVPFRYHELITKYGKLEPLAEVDLRPQSSAKVEVHFNDQVEEMSIRLDQTVAELKKQLKTLVQLPTSNMLLYYFDHEAPFGPEEMKYSSRALHSFGIRDGDKIYVESKTK
" misc_feature 295..372 /gene="TBCEL" /gene_synonym="El; LRRC35" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (Q5QJ74.2); Region: LRR 1" misc_feature 373..447 /gene="TBCEL" /gene_synonym="El; LRRC35" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (Q5QJ74.2); Region: LRR 2" misc_feature 448..519 /gene="TBCEL" /gene_synonym="El; LRRC35" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (Q5QJ74.2); Region: LRR 3" misc_feature 526..594 /gene="TBCEL" /gene_synonym="El; LRRC35" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (Q5QJ74.2); Region: LRR 4" misc_feature 595..669 /gene="TBCEL" /gene_synonym="El; LRRC35" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (Q5QJ74.2); Region: LRR 5" misc_feature 598..729 /gene="TBCEL" /gene_synonym="El; LRRC35" /note="Leucine Rich repeats (2 copies); Region: LRR_4; pfam12799" /db_xref="CDD:205079" misc_feature 673..750 /gene="TBCEL" /gene_synonym="El; LRRC35" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (Q5QJ74.2); Region: LRR 6" misc_feature 754..828 /gene="TBCEL" /gene_synonym="El; LRRC35" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (Q5QJ74.2); Region: LRR 7" misc_feature 1111..1335 /gene="TBCEL" /gene_synonym="El; LRRC35" /note="Ubiquitin-like proteins; Region: UBQ; cl00155" /db_xref="CDD:212176" misc_feature order(1183..1185,1228..1230) /gene="TBCEL" /gene_synonym="El; LRRC35" /note="charged pocket; other site" /db_xref="CDD:176352" misc_feature 1234..1245 /gene="TBCEL" /gene_synonym="El; LRRC35" /note="hydrophobic patch; other site" /db_xref="CDD:176352" variation 126 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="g" /db_xref="dbSNP:372493054" variation 152 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="c" /replace="g" /db_xref="dbSNP:138695287" variation 162 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="g" /db_xref="dbSNP:114354179" variation 166 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="g" /db_xref="dbSNP:376097465" variation 177 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="c" /replace="t" /db_xref="dbSNP:150702205" variation 185 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="c" /replace="t" /db_xref="dbSNP:185489274" exon 212..351 /gene="TBCEL" /gene_synonym="El; LRRC35" /inference="alignment:Splign:1.39.8" variation 229 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="g" /db_xref="dbSNP:144833842" variation 300 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="c" /replace="t" /db_xref="dbSNP:202229726" exon 352..533 /gene="TBCEL" /gene_synonym="El; LRRC35" /inference="alignment:Splign:1.39.8" variation 352 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="g" /db_xref="dbSNP:376267533" variation 479 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="g" /db_xref="dbSNP:377422079" variation 513 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="g" /replace="t" /db_xref="dbSNP:140003630" variation 514 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="t" /db_xref="dbSNP:78944388" variation 529 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="c" /replace="t" /db_xref="dbSNP:370948390" exon 534..790 /gene="TBCEL" /gene_synonym="El; LRRC35" /inference="alignment:Splign:1.39.8" variation 620 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="t" /db_xref="dbSNP:76061220" variation 621 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="g" /db_xref="dbSNP:374778286" variation 680 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="c" /replace="t" /db_xref="dbSNP:112262968" variation 694 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="g" /db_xref="dbSNP:368110919" variation 725 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="c" /db_xref="dbSNP:370713023" variation 748 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="g" /db_xref="dbSNP:373756527" variation 773 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="c" /replace="t" /db_xref="dbSNP:113070356" exon 791..917 /gene="TBCEL" /gene_synonym="El; LRRC35" /inference="alignment:Splign:1.39.8" variation 798 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="g" /db_xref="dbSNP:368859055" variation 810 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="c" /replace="t" /db_xref="dbSNP:368689002" variation 811 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="g" /db_xref="dbSNP:372851892" variation 888 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:35380371" variation 909 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="g" /db_xref="dbSNP:375999211" exon 918..1034 /gene="TBCEL" /gene_synonym="El; LRRC35" /inference="alignment:Splign:1.39.8" variation 967 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="c" /replace="t" /db_xref="dbSNP:377427847" variation 1018 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="g" /db_xref="dbSNP:146743853" exon 1035..3904 /gene="TBCEL" /gene_synonym="El; LRRC35" /inference="alignment:Splign:1.39.8" variation 1107 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="c" /replace="t" /db_xref="dbSNP:368786975" variation 1128 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="c" /replace="t" /db_xref="dbSNP:372272358" variation 1132 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="g" /db_xref="dbSNP:139578794" variation 1153 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="g" /db_xref="dbSNP:144345151" variation 1176 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="g" /db_xref="dbSNP:146540306" variation 1208 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="g" /db_xref="dbSNP:375282149" variation 1209 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="g" /db_xref="dbSNP:140041201" variation 1248 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="c" /replace="t" /db_xref="dbSNP:142279664" variation 1291 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="g" /db_xref="dbSNP:373338413" variation 1296 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="g" /db_xref="dbSNP:151214090" variation 1432 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="g" /db_xref="dbSNP:11602226" variation 1771 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="c" /db_xref="dbSNP:112522932" variation 1805 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="g" /db_xref="dbSNP:187013426" variation 1821 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="c" /replace="t" /db_xref="dbSNP:192223056" variation 1838..1839 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="" /replace="t" /db_xref="dbSNP:376175003" variation 1838 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="g" /db_xref="dbSNP:78898111" variation 1838 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="gt" /db_xref="dbSNP:374037889" variation 1893..1894 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="" /replace="a" /db_xref="dbSNP:35880364" variation 2056 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="" /replace="a" /db_xref="dbSNP:35274310" variation 2065 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="g" /db_xref="dbSNP:368819132" variation 2233 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="c" /replace="t" /db_xref="dbSNP:182842834" variation 2249 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="g" /replace="t" /db_xref="dbSNP:151150784" variation 2294 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="t" /db_xref="dbSNP:188225607" variation 2338 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="c" /replace="t" /db_xref="dbSNP:193272452" variation 2349 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="g" /db_xref="dbSNP:7109612" variation 2478 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="c" /replace="t" /db_xref="dbSNP:185388669" variation 2505 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="c" /replace="t" /db_xref="dbSNP:369691016" variation 2586 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="g" /db_xref="dbSNP:1063101" variation 2610 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="c" /replace="t" /db_xref="dbSNP:111981178" variation 2716 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="c" /db_xref="dbSNP:140115272" variation 2773 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="g" /db_xref="dbSNP:11218139" variation 2922 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="g" /replace="t" /db_xref="dbSNP:189501439" variation 3011 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="t" /db_xref="dbSNP:17124764" variation 3131 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="c" /replace="t" /db_xref="dbSNP:114126817" variation 3143 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="g" /db_xref="dbSNP:111781066" variation 3179 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="t" /db_xref="dbSNP:112596169" variation 3184 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="g" /db_xref="dbSNP:377402403" variation 3228 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="c" /replace="t" /db_xref="dbSNP:137987759" variation 3254 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="" /replace="t" /db_xref="dbSNP:147288817" variation 3268 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="" /replace="a" /db_xref="dbSNP:35834454" variation 3348 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="c" /replace="t" /db_xref="dbSNP:2298491" variation 3506 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="g" /db_xref="dbSNP:191396363" variation 3602 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="g" /db_xref="dbSNP:75050717" variation 3699..3701 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="" /replace="aat" /db_xref="dbSNP:370560199" variation 3707 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="c" /db_xref="dbSNP:184340231" variation 3735 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="a" /replace="g" /db_xref="dbSNP:111848290" variation 3805 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="c" /replace="t" /db_xref="dbSNP:188593117" variation 3852 /gene="TBCEL" /gene_synonym="El; LRRC35" /replace="c" /replace="t" /db_xref="dbSNP:367758300" ORIGIN
ggaaagctgcttccgggtcaatgcaggacactgggctccggcggccagagtgggggactagcattttaagaaagaaagatggatcaacctagtggaagaagtttcatgcaagtattatgtgaaaaatatagtcctgaaaattttccttatcgccgtggcccggggatgggagtccatgtcccagccacacctcagggctctcctatgaaagatcgcctcaacctcccaagtgtactagtgttgaacagctgtggaataacctgtgcaggagatgaaaaagaaattgctgctttctgcgctcatgtgtcggaactagatctttctgacaacaaactcgaagactggcatgaggtcagtaaaattgtgtcaaatgttcctcagttggagtttctaaacctgagttccaaccctctgaatttgtcggttttagaaagaacatgtgctgggtccttctctggggttcgcaaacttgtcctcaacaacagcaaagcttcttgggagacggtccacatgatactacaggagttaccagatttggaggagctcttcctgtgccttaatgactatgaaacagtgtcttgtccttctatttgctgtcattctcttaagctactacatataacagacaataacctccaagactggactgaaatacgaaagttaggagttatgtttccttcactggataccctcgtcctggccaacaatcatttgaatgctattgaggagcctgatgattcattggccaggttgtttcctaatcttcgatccatcagcctccacaagtcaggtttgcagtcctgggaagacattgataaactaaattcatttcccaaactggaagaagtgagattgttaggaattcctcttctgcagccatataccaccgaggagcgaaggaaattggtaatagccagattgccatcagtttccaaacttaatggcagcgttgttactgatggtgaacgagaagattctgagagattttttattcgttactatgtggatgttccacaggaagaagtgccattcaggtatcatgaactgatcactaaatatgggaagttggagcctttggcagaagtggacctaagaccccagagcagtgcaaaagtagaagtccactttaacgatcaggtggaagaaatgagcattcgtctggaccaaacagtggcagaactaaagaaacagttaaaaactctagtacaattacccacaagcaacatgcttctctactattttgaccatgaagcaccctttggcccagaggaaatgaagtacagctctcgggcattgcattcctttggcattagggatggagataaaatttacgtggaatccaaaacaaaataacctctaccagccttgtgaaaaacatacacataaggacttgttgcagggcatttgtttttaatgtggttttctttaggagggagaggttgtttttgttttgttttgttctgtttaggtttgggaaggattttgtatatttttccccctggagtgagtaggggccatttttgggtgttttctaccacagattgatttggctcagccagcggaattggccacatttccagtgtatgtgccctctctaaggaaagatgacaaagaaatcaccgacttcttactgtgttcactgggatttgcctgccacttggttatcattactgttgggtgaacctgtgaagataacatgaacactgtagccccttagaagggtctcatagagaatttaaacagggtgacaaggaatcttcacaggaagggccagaacttctctctcccagttcttccttccgctaccctccctccttggcttttttggttcagttccatttttttttcattttgacatgtggtttacctaatagttttgttctgttcataattcttatttctcaacctgggtgatttttttgttctcatttctcccttttgaaataattgaaagtgttttaagcatttttaacctgattctaatctcaggtacgcagtaagaagctataactctgttagaacctcgaagagtagatgtagaatgaaaactccaggaaaacttgcagttattctggaagcaccggcagaacagtctgatctctttgtatgttactaactcacttttaatgtccctgtacattatgtcagccattactttcataacatgaaatatgtcagattccagagttcttttatttttgcttattgaatgtatttcctcatatctttctttttcattactttaaactattgggaattgaggcctgacttcataaataattcaatagagtcctggatacgtgcaccaggagagttgagaattagctcataaactatctgtggtgtgtgtggggaatgaagttgggggatgtgggggaagagcttatgactttcccacctgtgtcatccattggaagcccttgctcttgcactttgcattaaaagtgggaaacattaatcaaagggagattttattcccaggttttccctgggactttgtgatatcataattgaacagttcttttgttttacatttcaatttagttgcctcatagaagtataactgcccaatctatgagtaaagtgtaagtgtcaaaactttacaattgcctccaagtcatattttttgcagaagcacatttaaagcacttttctgtaaaagctagttccttacctgcttggaaatctttttgtttgttcttctattcctttgttaatcagatgtaatccctttctttaatgtgtatttttcttggtccaccatgtttacagatgggagacttgagagatacttagcataactggggcagaaagtgtgtaagtgaagtatttttcaaagaatgcagttattatctgattgcatttgaccttttgacctttgttacataattctacccctcctacaaatttaatttttttatgaaatttttaggtgacttgtaaattcttcatgtatgaggagttgtgtttattaatgctactttttaaattttcctgtgccatgtggcagatgtttattctcttaatgcacttcaggtttgctatctgtaaagcctttgacccaggcctactgagtcaaatctacattcagtgtaacattaaaggtggaaaccaaagggtttgagaaagacgaataaggcctattctccttctgctgcagactttatctttcaaaatcataaaaatgagcaatggagatccaggctgggtatagacaagaataattattttgcaaacacattttcctgacagatttttggaagtaggaaaaaagtatggcaacagtgtcatgaagattgaaactgtaggtgctttgtgtatgtatgcatgagtgcagatgagtttgagagagaaaaagtgtaattgagccctttgcttttgtcagcctgggaaacagatgcgttcttattttttgaagttgtgtgaccctggactgtcccacagcagaaggcagaacaaacacttatgttatgctttaatcataagtggaatggtcacaattaataagatattttatatatggcaaagttttatgaaatgcttttttactattagagacctgtttcttctgttattacagaacacagtgtttatcaactgcggacataattcttttattatacagttgcatgtaaagggagcttctcatttaattcagcggatgtgggtatttttagggcattgtaattgatggttttaataattgctgaataatttttgattaagagaaaaatgtaatacaattactggtctgagttacagaacagaagttaatgaaaaaggctatttgagcatgtgtacttatagattcatttgggtggctgagaaaagatgctgcttttgaaataaaattggtgctgtgtagacacttgtaaccaaaattatttttataacagaactaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:219899 -> Cellular component: GO:0005737 [cytoplasm] evidence: IEA GeneID:219899 -> Cellular component: GO:0005856 [cytoskeleton] evidence: IEA
by
@meso_cacase at
DBCLS
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