2024-04-23 21:47:39, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001011515 2031 bp mRNA linear PRI 07-JUL-2013 DEFINITION Homo sapiens PDZ and LIM domain 5 (PDLIM5), transcript variant 4, mRNA. ACCESSION NM_001011515 VERSION NM_001011515.2 GI:374093204 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 2031) AUTHORS Hui,J., Wang,J.Y., Shi,X.H., Zhang,Y.G., Liu,M., Wang,X., Wang,N.N., Chen,X., Liang,S.Y., Wei,D., Zhao,F., Zhang,Y.H. and Yang,Z. TITLE [Association of prostate cancer with PDLIM5, SLC22A3 and NKX3-1 in Chinese men] JOURNAL Zhonghua Nan Ke Xue 18 (5), 404-411 (2012) PUBMED 22741436 REMARK GeneRIF: PDLIM5 (rs17021918,T), SLC22A3 (rs9364554,C) and NKX3-1 (rs1512268,A) SNPs might not be associated with prostate cancer in Chinese men. REFERENCE 2 (bases 1 to 2031) AUTHORS Zain,M.A., Jahan,S.N., Reynolds,G.P., Zainal,N.Z., Kanagasundram,S. and Mohamed,Z. TITLE Peripheral PDLIM5 expression in bipolar disorder and the effect of olanzapine administration JOURNAL BMC Med. Genet. 13, 91 (2012) PUBMED 23031404 REMARK GeneRIF: The significant difference in expression of PDLIM5 mRNA in the peripheral blood leukocytes of treatment-naive bipolar (BPD) patients versus that of healthy control subjects suggests that it may be a good biological marker for BPD. Publication Status: Online-Only REFERENCE 3 (bases 1 to 2031) AUTHORS Fox CS, Liu Y, White CC, Feitosa M, Smith AV, Heard-Costa N, Lohman K, Johnson AD, Foster MC, Greenawalt DM, Griffin P, Ding J, Newman AB, Tylavsky F, Miljkovic I, Kritchevsky SB, Launer L, Garcia M, Eiriksdottir G, Carr JJ, Gudnason V, Harris TB, Cupples LA and Borecki IB. CONSRTM GIANT Consortium; MAGIC Consortium; GLGC Consortium TITLE Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women JOURNAL PLoS Genet. 8 (5), E1002695 (2012) PUBMED 22589738 REFERENCE 4 (bases 1 to 2031) AUTHORS Lasorella,A. and Iavarone,A. TITLE The protein ENH is a cytoplasmic sequestration factor for Id2 in normal and tumor cells from the nervous system JOURNAL Proc. Natl. Acad. Sci. U.S.A. 103 (13), 4976-4981 (2006) PUBMED 16549780 REMARK GeneRIF: ENH is a restraining factor of the oncogenic activity of inhibitor of DNA binding 2 proteins in neural tumors REFERENCE 5 (bases 1 to 2031) AUTHORS Niederlander,N., Fayein,N.A., Auffray,C. and Pomies,P. TITLE Characterization of a new human isoform of the enigma homolog family specifically expressed in skeletal muscle JOURNAL Biochem. Biophys. Res. Commun. 325 (4), 1304-1311 (2004) PUBMED 15555569 REMARK GeneRIF: Western blot studies of muscle tissues revealed that ENH4 is present only in skeletal muscle and there is a specific distribution of ENH members between skeletal and cardiac muscles, which is different in human and mouse. REFERENCE 6 (bases 1 to 2031) AUTHORS Wu,M., Li,Y., Ji,C., Xu,J., Zheng,H., Zou,X., Gu,S., Lou,Y., Xie,Y. and Mao,Y. TITLE Cloning and identification of a novel human gene PDLIM5, a homolog of AD-associated neuronal thread protein (AD7c-NTP) JOURNAL DNA Seq. 15 (2), 144-147 (2004) PUBMED 15346770 REFERENCE 7 (bases 1 to 2031) AUTHORS Maeno-Hikichi,Y., Chang,S., Matsumura,K., Lai,M., Lin,H., Nakagawa,N., Kuroda,S. and Zhang,J.F. TITLE A PKC epsilon-ENH-channel complex specifically modulates N-type Ca2+ channels JOURNAL Nat. Neurosci. 6 (5), 468-475 (2003) PUBMED 12665800 REFERENCE 8 (bases 1 to 2031) AUTHORS Nakagawa,N., Hoshijima,M., Oyasu,M., Saito,N., Tanizawa,K. and Kuroda,S. TITLE ENH, containing PDZ and LIM domains, heart/skeletal muscle-specific protein, associates with cytoskeletal proteins through the PDZ domain JOURNAL Biochem. Biophys. Res. Commun. 272 (2), 505-512 (2000) PUBMED 10833443 REFERENCE 9 (bases 1 to 2031) AUTHORS Ueki,N., Seki,N., Yano,K., Masuho,Y., Saito,T. and Muramatsu,M. TITLE Isolation, tissue expression, and chromosomal assignment of a human LIM protein gene, showing homology to rat enigma homologue (ENH) JOURNAL J. Hum. Genet. 44 (4), 256-260 (1999) PUBMED 10429367 REFERENCE 10 (bases 1 to 2031) AUTHORS Kuroda,S., Tokunaga,C., Kiyohara,Y., Higuchi,O., Konishi,H., Mizuno,K., Gill,G.N. and Kikkawa,U. TITLE Protein-protein interaction of zinc finger LIM domains with protein kinase C JOURNAL J. Biol. Chem. 271 (49), 31029-31032 (1996) PUBMED 8940095 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from DA895978.1, AL833151.1, AC093778.3 and AA253314.1. On Jan 27, 2012 this sequence version replaced gi:58533158. Summary: This gene encodes a member of a family of proteins that possess a 100-amino acid PDZ domain at the N terminus and one to three LIM domains at the C-terminus. This family member functions as a scaffold protein that tethers protein kinases to the Z-disk in striated muscles. It is thought to function in cardiomyocyte expansion and in restraining postsynaptic growth of excitatory synapses. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jan 2012]. Transcript Variant: This variant (4) has multiple differences in the coding region, lacks several 3' exons but contains an alternate 3' exon, and it thus has an alternate 3' coding region and 3' UTR, compared to isoform a. The encoded isoform (d) has a distinct C-terminus and is shorter than isoform a. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments. 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 :: AL833151.1, AL833438.1 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025083, ERS025084 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-103 DA895978.1 1-103 104-332 AL833151.1 2-230 333-333 AC093778.3 42560-42560 334-708 AL833151.1 232-606 709-709 AC093778.3 104472-104472 710-944 AL833151.1 608-842 945-1772 AC093778.3 105922-106749 1773-2031 AA253314.1 1-259 c FEATURES Location/Qualifiers source 1..2031 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="4" /map="4q22" gene 1..2031 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /note="PDZ and LIM domain 5" /db_xref="GeneID:10611" /db_xref="HGNC:17468" /db_xref="MIM:605904" exon 1..139 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /inference="alignment:Splign:1.39.8" variation 24 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="c" /replace="g" /db_xref="dbSNP:138430072" variation 49 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="c" /replace="t" /db_xref="dbSNP:192733830" variation 63 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="g" /db_xref="dbSNP:184767586" variation 70 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="c" /replace="g" /db_xref="dbSNP:143611898" variation 79 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="g" /db_xref="dbSNP:28736374" variation 81 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="c" /replace="g" /db_xref="dbSNP:147199893" variation 113 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="g" /db_xref="dbSNP:369769495" exon 140..277 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /inference="alignment:Splign:1.39.8" variation 165 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="c" /replace="t" /db_xref="dbSNP:200141226" misc_feature 167..169 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /note="upstream in-frame stop codon" CDS 182..886 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /note="isoform d is encoded by transcript variant 4; enigma homolog; PDZ and LIM domain protein 5; enigma-like LIM domain protein; enigma-like PDZ and LIM domains protein" /codon_start=1 /product="PDZ and LIM domain protein 5 isoform d" /protein_id="NP_001011515.1" /db_xref="GI:58533159" /db_xref="CCDS:CCDS47103.1" /db_xref="GeneID:10611" /db_xref="HGNC:17468" /db_xref="MIM:605904" /translation="
MSNYSVSLVGPAPWGFRLQGGKDFNMPLTISSLKDGGKAAQANVRIGDVVLSIDGINAQGMTHLEAQNKIKGCTGSLNMTLQRASAAPKPEPVPVQKPTVTSVCSETSQELAEGQRRGSQGDSKQQNGKIPPKRPPRKHIVERYTEFYHVPTHSDASKKRLIEDTEDWRPRTGTTQSRSFRILAQITGTEHLKESEADNTKKAKEKIPLHVFSPKYTKLRDWHHEVSARALNVQ
" misc_feature 185..187 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /experiment="experimental evidence, no additional details recorded" /note="N-acetylserine; propagated from UniProtKB/Swiss-Prot (Q96HC4.5); acetylation site" misc_feature 209..427 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /note="PDZ domain found in a variety of Eumetazoan signaling molecules, often in tandem arrangements. May be responsible for specific protein-protein interactions, as most PDZ domains bind C-terminal polypeptides, and binding to internal (non-C-terminal)...; Region: PDZ_signaling; cd00992" /db_xref="CDD:29049" misc_feature order(218..229,233..235,377..382,389..394) /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /note="protein binding site [polypeptide binding]; other site" /db_xref="CDD:29049" misc_feature 623..625 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /experiment="experimental evidence, no additional details recorded" /note="phosphorylation site" variation 217 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="c" /replace="t" /db_xref="dbSNP:373896689" variation 241 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="c" /replace="t" /db_xref="dbSNP:145981438" variation 246 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="g" /db_xref="dbSNP:75841704" exon 278..429 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /inference="alignment:Splign:1.39.8" variation 288 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="g" /replace="t" /db_xref="dbSNP:376270307" variation 328 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="g" /replace="t" /db_xref="dbSNP:114621202" variation 355 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="t" /db_xref="dbSNP:368230269" variation 359 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="g" /db_xref="dbSNP:146671681" variation 366 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="c" /db_xref="dbSNP:151288647" variation 426 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="g" /db_xref="dbSNP:372541276" exon 430..472 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /inference="alignment:Splign:1.39.8" variation 431 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="g" /db_xref="dbSNP:371717002" variation 455 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="c" /replace="t" /db_xref="dbSNP:375778697" variation 456 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="c" /replace="t" /db_xref="dbSNP:200495769" variation 457 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="g" /db_xref="dbSNP:145853286" exon 473..564 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /inference="alignment:Splign:1.39.8" variation 538 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="c" /db_xref="dbSNP:1056807" variation 541 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="g" /db_xref="dbSNP:1135006" variation 549 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="g" /db_xref="dbSNP:1135007" variation 564 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="g" /replace="t" /db_xref="dbSNP:1135008" exon 565..582 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /inference="alignment:Splign:1.39.8" variation 581 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="c" /replace="t" /db_xref="dbSNP:370669920" exon 583..755 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /inference="alignment:Splign:1.39.8" variation 588 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="c" /replace="t" /db_xref="dbSNP:375364739" variation 608 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="c" /replace="t" /db_xref="dbSNP:201891054" variation 609 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="g" /replace="t" /db_xref="dbSNP:141403934" variation 638 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="c" /replace="g" /db_xref="dbSNP:150388657" variation 671 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="g" /db_xref="dbSNP:202231060" variation 687 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="g" /db_xref="dbSNP:113605096" variation 691 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="g" /db_xref="dbSNP:115214197" variation 694 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="g" /db_xref="dbSNP:11722955" variation 709 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="g" /db_xref="dbSNP:11097431" variation 739 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="c" /replace="t" /db_xref="dbSNP:371463583" exon 756..792 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /inference="alignment:Splign:1.39.8" variation 772 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="c" /replace="t" /db_xref="dbSNP:202092014" variation 783 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="g" /db_xref="dbSNP:115781887" exon 793..2023 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /inference="alignment:Splign:1.39.8" variation 804 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="c" /db_xref="dbSNP:368434732" variation 811 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="c" /replace="t" /db_xref="dbSNP:372509415" variation 812 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="g" /db_xref="dbSNP:375154089" variation 832 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="g" /db_xref="dbSNP:199798888" variation 840 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="g" /db_xref="dbSNP:369465325" variation 857 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="g" /db_xref="dbSNP:79765561" variation 877 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="c" /replace="t" /db_xref="dbSNP:181685632" STS 881..1060 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /standard_name="RH91416" /db_xref="UniSTS:88822" variation 890 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="t" /db_xref="dbSNP:373227250" variation 933 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="t" /db_xref="dbSNP:199977664" variation 935 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="c" /replace="t" /db_xref="dbSNP:201186480" variation 935 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="" /replace="t" /db_xref="dbSNP:5860367" variation 968 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="c" /replace="t" /db_xref="dbSNP:184470510" variation 978 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="c" /db_xref="dbSNP:189671146" variation 990 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="c" /replace="t" /db_xref="dbSNP:181104813" variation 1086 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="c" /db_xref="dbSNP:62316474" variation 1087..1089 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="" /replace="a" /db_xref="dbSNP:5860368" variation 1087 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="c" /db_xref="dbSNP:202245025" variation 1088 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="" /replace="a" /db_xref="dbSNP:66505111" variation 1088 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="c" /db_xref="dbSNP:78280282" variation 1131 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="g" /replace="t" /db_xref="dbSNP:2131456" variation 1154 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="g" /replace="t" /db_xref="dbSNP:2131457" variation 1179 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="c" /replace="t" /db_xref="dbSNP:145963690" variation 1203 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="c" /replace="t" /db_xref="dbSNP:138571118" variation 1267..1270 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="" /replace="tact" /db_xref="dbSNP:145075802" variation 1268..1271 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="" /replace="actt" /db_xref="dbSNP:367682604" variation 1271 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="" /replace="actt" /db_xref="dbSNP:75036921" variation 1294 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="c" /replace="t" /db_xref="dbSNP:185996529" variation 1380 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="c" /replace="t" /db_xref="dbSNP:191195682" variation 1408 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="c" /replace="t" /db_xref="dbSNP:12642449" variation 1442 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="c" /replace="t" /db_xref="dbSNP:11551408" variation 1462 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="g" /db_xref="dbSNP:369119823" STS 1474..1568 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /standard_name="SHGC-63474" /db_xref="UniSTS:15587" variation 1518 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="c" /replace="g" /db_xref="dbSNP:79700101" variation 1639 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="g" /db_xref="dbSNP:2637973" variation 1651 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="c" /replace="t" /db_xref="dbSNP:141657395" STS 1777..1908 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /standard_name="SHGC-63475" /db_xref="UniSTS:5487" STS 1779..1904 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /standard_name="RH91857" /db_xref="UniSTS:88158" polyA_signal 1911..1916 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" polyA_site 1931 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" variation 1985 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="a" /replace="g" /db_xref="dbSNP:377202992" polyA_signal 2005..2010 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" variation 2018 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" /replace="c" /replace="g" /db_xref="dbSNP:144318128" polyA_site 2023 /gene="PDLIM5" /gene_synonym="ENH; ENH1; L9; LIM" ORIGIN
gtgtcctgggtcgggggtggggcgagggagagccaggaggcggaagttcccgcgggcggtggggacggcgccctcaccgcgagtcacttgtcagcccttgtctgaggcggaggcagccccgcgccgcgccggacccgagcatatttcattttctgtcattggactttgagccattagaaccatgagcaactacagtgtgtcactggttggcccagctccttggggtttccggctgcagggcggtaaggatttcaacatgcctctgacaatctctagtctaaaagatggcggcaaggcagcccaggcaaatgtaagaataggcgatgtggttctcagcattgatggaataaatgcacaaggaatgactcatcttgaagcccagaataagattaagggttgtacaggctctttgaatatgactctgcaaagagcatctgctgcacccaagcctgagccggttcctgttcaaaagcccacagtcaccagcgtgtgttccgagacttctcaggagctagcagagggacagagaagaggatcccagggtgacagtaaacagcaaaatgggaaaatcccacctaaacgcccaccaagaaaacacattgtggagcgctatacagagttttatcatgtacccactcacagtgatgccagcaagaagagactgattgaggatactgaagactggcgtccaaggactggaacaactcagtctcgctctttccgaatccttgcccagatcactgggactgaacatttgaaagaatctgaagccgataatacaaagaaggcaaaggaaaagataccccttcacgtctttagtcccaaatacacaaaattacgtgactggcaccatgaagtttcagcacgtgctcttaacgtacagtgatttatgagccttgccccccaagcagccagcacataccttttcatttactttttttttttcaacttcatagcaaaatctgtattaaatttgccttatgaaaaaatagaactttttctatacttttctaacaatttcctattgttgtgagaaaaggaagatgaacatgttttgtgctagttggtagctcacaaatgtaaaaccaaaaaaaaaaaaaaatagaaaattaagggactagatctatttgtggatttgtatctgtttttgttgtgattagggtagtaatcttggaaaacgaattattttcataagttgaatttggttagttggttggttgaagcagaggataatgagcaaataaagtccttgtctaatttggaaaatactttctttatattattaacatctcccaagattactttttaagttcattattatgttacattcaaagttgattgtaaattattctaaataagtaaatataaggaggcaagaataaacaaagactttattaaagaagagtgcgtgcattgtagatttaggtatcttttaaagtaggtactattcaggatggctctatgaagaggaggaggtccagatttggctcctgaaaaaggaaagaagagaattttacccctatttgcaatggagaaatacagtattctttggtttggttggatttgcaaatcctatttcctatcaaaggaaatatctctagtggatatttttagaatatagacaatttctaggtattaactaataagatatggaaaagatagctttgctttttttaatcagaagaacataaaataaattacaatatgaatgattgtgagacatcagagaaatattttacttagtgacgtaaactactgtgcactgctgctattcctaggaagctgtgttttgggcaatacatggaagctaaatatatgaccagaaatgctttctgccttgtaatatagtgtattatatattagagctaaatttagtaataaatgcattttgaagtttggaaaagtattgtaataaagttgcctttaacttagctttgtacttgttctgtttccttgaggctagacacagtgccatccaggacttattacagtataactgggtaaaataaacaattctctgacaaaaaaaaa
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ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:10611 -> Molecular function: GO:0003779 [actin binding] evidence: ISS GeneID:10611 -> Molecular function: GO:0005080 [protein kinase C binding] evidence: ISS GeneID:10611 -> Molecular function: GO:0008270 [zinc ion binding] evidence: IEA GeneID:10611 -> Molecular function: GO:0042805 [actinin binding] evidence: ISS GeneID:10611 -> Biological process: GO:0051963 [regulation of synapse assembly] evidence: ISS GeneID:10611 -> Biological process: GO:0061001 [regulation of dendritic spine morphogenesis] evidence: ISS GeneID:10611 -> Cellular component: GO:0005829 [cytosol] evidence: ISS GeneID:10611 -> Cellular component: GO:0005886 [plasma membrane] evidence: IEA GeneID:10611 -> Cellular component: GO:0014069 [postsynaptic density] evidence: ISS GeneID:10611 -> Cellular component: GO:0015629 [actin cytoskeleton] evidence: IDA GeneID:10611 -> Cellular component: GO:0016020 [membrane] evidence: ISS GeneID:10611 -> Cellular component: GO:0030054 [cell junction] evidence: IEA GeneID:10611 -> Cellular component: GO:0043005 [neuron projection] evidence: IEA GeneID:10611 -> Cellular component: GO:0045211 [postsynaptic membrane] evidence: IEA
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