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2024-04-20 11:24:55, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001256425 5713 bp mRNA linear PRI 07-JUL-2013
DEFINITION Homo sapiens PDZ and LIM domain 5 (PDLIM5), transcript variant 3,
mRNA.
ACCESSION NM_001256425 NM_001011514 NR_024179
VERSION NM_001256425.1 GI:374093202
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 5713)
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 5713)
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 5713)
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 5713)
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 5713)
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 5713)
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 5713)
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 5713)
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 5713)
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 5713)
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, BC026029.2,
AC108067.3 and AA614664.1.
On or before Jan 27, 2012 this sequence version replaced
gi:207440659, gi:58533156.
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 (3) lacks an alternate exon in the
5' coding region and uses a downstream in-frame start codon,
compared to variant 1. The encoded isoform (c) is shorter at the
N-terminus, compared to 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##
CDS exon combination :: BC026029.2, AL832157.1 [ECO:0000331]
RNAseq introns :: single sample supports all introns
ERS025084, ERS025085 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-139 DA895978.1 1-139
140-902 BC026029.2 2-764
903-903 AC108067.3 18563-18563
904-1236 BC026029.2 766-1098
1237-1237 AC108067.3 35692-35692
1238-2364 BC026029.2 1100-2226
2365-5264 AC108067.3 43134-46033
5265-5713 AA614664.1 3-451 c
FEATURES Location/Qualifiers
source 1..5713
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="4"
/map="4q22"
gene 1..5713
/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"
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"
misc_feature 417..419
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/note="upstream in-frame stop codon"
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..645
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 478
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:375364739"
variation 498
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:201891054"
variation 499
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:141403934"
variation 528
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:150388657"
variation 561
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:202231060"
variation 577
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:113605096"
variation 581
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:115214197"
variation 584
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:11722955"
variation 599
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:11097431"
variation 629
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:371463583"
exon 646..682
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 662
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:202092014"
variation 673
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:115781887"
exon 683..870
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 703
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:146000883"
variation 704
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:139902919"
variation 718
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1064238"
variation 722
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:377407022"
variation 732
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:141653509"
variation 733
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:115018620"
CDS 738..1553
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/note="isoform c is encoded by transcript variant 3;
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 c"
/protein_id="NP_001243354.1"
/db_xref="GI:374093203"
/db_xref="GeneID:10611"
/db_xref="HGNC:17468"
/db_xref="MIM:605904"
/translation="
MPESLDSPTSGRPGVTSLTTAAAFKPVGSTGVIKSPSWQRPNQGVPSTGRISNSATYSGSVAPANSALGQTQPSDQDTLVQRAEHIPAGKRTPMCAHCNQVIRGPFLVALGKSWHPEEFNCAHCKNTMAYIGFVEEKGALYCELCYEKFFAPECGRCQRKILGEVISALKQTWHVSCFVCVACGKPIRNNVFHLEDGEPYCETDYYALFGTICHGCEFPIEAGDMFLEALGYTWHDTCFVCSVCCESLEGQTFFSKKDKPLCKKHAHSVNF
"
misc_feature 1020..1175
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/note="The first LIM domain of the Enigma Homolog (ENH)
family; Region: LIM1_ENH; cd09453"
/db_xref="CDD:188837"
misc_feature order(1020..1022,1029..1031,1080..1082,1089..1091,
1098..1100,1107..1109,1161..1163,1170..1172)
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/note="Zn binding site [ion binding]; other site"
/db_xref="CDD:188837"
misc_feature 1197..1352
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/note="LIM is a small protein-protein interaction domain,
containing two zinc fingers; Region: LIM; cl02475"
/db_xref="CDD:198684"
misc_feature order(1197..1199,1206..1208,1257..1259,1266..1268,
1275..1277,1284..1286,1338..1340,1347..1349)
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/note="Zn binding site [ion binding]; other site"
/db_xref="CDD:188711"
misc_feature 1374..1538
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/note="LIM is a small protein-protein interaction domain,
containing two zinc fingers; Region: LIM; cl02475"
/db_xref="CDD:198684"
misc_feature order(1374..1376,1383..1385,1440..1442,1449..1451,
1458..1460,1467..1469,1521..1523,1530..1532)
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/note="Zn binding site [ion binding]; other site"
/db_xref="CDD:188711"
variation 743
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:116241517"
variation 766
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:371181316"
variation 795
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:966845"
variation 806
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:116830271"
variation 816
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:368387152"
variation 831
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:370892974"
variation 855
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:374739373"
exon 871..1045
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 894
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:148409775"
variation 900
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:372735372"
variation 903
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:7690296"
variation 914
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:375931613"
variation 924
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:7690464"
variation 931
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:115386065"
variation 946
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:114201587"
variation 990
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:369761799"
variation 1015
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:139413367"
variation 1016
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:373251894"
variation 1033
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:376503569"
exon 1046..1226
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 1083
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:201156978"
variation 1086
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:377346480"
variation 1096
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:145633341"
variation 1100
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:201013535"
variation 1101
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:200640873"
variation 1111
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:373850074"
variation 1127
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:147724105"
variation 1137
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:142522131"
exon 1227..1347
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 1233
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:144752025"
variation 1237
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:13107595"
variation 1299
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:148939806"
variation 1301
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:200822536"
exon 1348..1463
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 1359
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:114255444"
variation 1361
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:143660655"
variation 1370
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:148074454"
variation 1373
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:115802510"
variation 1384
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:374091168"
variation 1394
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:140894265"
variation 1405
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:367629922"
variation 1430
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:144847144"
variation 1432
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:114713699"
exon 1464..5713
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 1471
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:201782564"
variation 1480
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:377023412"
variation 1489
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:141719357"
variation 1525
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:201326456"
variation 1532
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:146226694"
variation 1537
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:76352571"
variation 1560
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1056772"
variation 1587
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:372012549"
variation 1735
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:114319350"
variation 1808
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:189650582"
variation 1978
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="a"
/db_xref="dbSNP:33961001"
variation 2076
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:56746297"
variation 2083
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1802345"
STS 2096..2889
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/standard_name="D10S2448"
/db_xref="UniSTS:474444"
STS 2228..2310
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/standard_name="L18426"
/db_xref="UniSTS:34648"
variation 2285
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1134967"
variation 2286
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:374940031"
variation 2292
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:180795923"
variation 2322
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:141426145"
STS 2323..2734
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/standard_name="L17705"
/db_xref="UniSTS:66091"
variation 2331
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:370215027"
variation 2350
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1056773"
STS 2383..2505
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/standard_name="SHGC-67609"
/db_xref="UniSTS:54969"
variation 2384
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:377344916"
variation 2408
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:187628494"
variation 2421
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:137892930"
variation 2476
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:62316494"
variation 2559
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:14082"
variation 2601
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="t"
/db_xref="dbSNP:11339365"
variation 2607
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:201037096"
variation 2614
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:10590"
variation 2650
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:74599592"
variation 2740
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1134984"
variation 2968
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="a"
/replace="aaaaaaaa"
/db_xref="dbSNP:10706955"
variation 2985..2992
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="aaaaaaa"
/db_xref="dbSNP:71581598"
variation 2992
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="a"
/replace="aaaaaaaa"
/db_xref="dbSNP:11365933"
variation 2993..2995
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="gag"
/db_xref="dbSNP:141722289"
variation 2993
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:55845770"
variation 2995
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:58524187"
variation 3010
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:28709926"
variation 3052
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="c"
/db_xref="dbSNP:201923550"
variation 3061
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="g"
/db_xref="dbSNP:78150373"
variation 3062
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="g"
/db_xref="dbSNP:10706956"
variation 3062
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:75694017"
variation 3188
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:368604816"
variation 3190
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:115970344"
variation 3403
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:141649481"
variation 3594
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:11550270"
variation 3675
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:146120619"
variation 3842
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:190760822"
variation 3909
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:140154582"
variation 3922
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1048627"
variation 3998
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:141563714"
variation 4010
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1043848"
variation 4061..4064
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="tttg"
/db_xref="dbSNP:148752622"
variation 4064..4067
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="gttt"
/db_xref="dbSNP:371401737"
variation 4064
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="tttg"
/db_xref="dbSNP:34068251"
variation 4114
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:182959183"
variation 4173
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:371509832"
STS 4265..4335
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/standard_name="D4S2569E"
/db_xref="UniSTS:19561"
STS 4273..4443
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/standard_name="SHGC-24108"
/db_xref="UniSTS:4790"
variation 4312
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:150914060"
variation 4335
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:376838121"
variation 4356
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:185688185"
variation 4410
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:3943"
variation 4493
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1509617"
variation 4566..4567
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="ag"
/db_xref="dbSNP:368119740"
variation 4609
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1043853"
variation 4671
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:75854018"
variation 4784
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:13141591"
variation 4804
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:371683638"
variation 4900
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1139697"
variation 4960
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:114932838"
variation 5009
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:12294"
variation 5152
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:12650486"
variation 5158
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1043862"
variation 5284
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:139417946"
variation 5343
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:149975822"
variation 5347
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:190144928"
variation 5360
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:369868118"
variation 5371
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:115398076"
STS 5513..5607
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/standard_name="D9S1746E"
/db_xref="UniSTS:153922"
STS 5546..5675
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/standard_name="SHGC-59267"
/db_xref="UniSTS:57977"
variation 5573
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:140772832"
variation 5672
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:7285"
polyA_signal 5682..5687
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
polyA_signal 5686..5691
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
variation 5690
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:183448943"
polyA_site 5709
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
polyA_site 5713
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
ORIGIN
gtgtcctgggtcgggggtggggcgagggagagccaggaggcggaagttcccgcgggcggtggggacggcgccctcaccgcgagtcacttgtcagcccttgtctgaggcggaggcagccccgcgccgcgccggacccgagcatatttcattttctgtcattggactttgagccattagaaccatgagcaactacagtgtgtcactggttggcccagctccttggggtttccggctgcagggcggtaaggatttcaacatgcctctgacaatctctagtctaaaagatggcggcaaggcagcccaggcaaatgtaagaataggcgatgtggttctcagcattgatggaataaatgcacaaggaatgactcatcttgaagcccagaataagattaagggttgtacaggctctttgaatatgactctgcaaagagcatctgctgcacccaagcctgagccggttcctgttcaaaagcccaccaagaaaacacattgtggagcgctatacagagttttatcatgtacccactcacagtgatgccagcaagaagagactgattgaggatactgaagactggcgtccaaggactggaacaactcagtctcgctctttccgaatccttgcccagatcactgggactgaacatttgaaagaatctgaagccgataatacaaagaaggcaaataactctcaggagccttctccgcagttggcttcctcggtagcttccacacggagcatgcccgagagcctggacagcccaacctctggcagaccaggggttaccagcctcacaactgcagctgccttcaagcctgtaggatccactggcgtcatcaagtcaccaagctggcaacggccaaaccaaggagtaccttccactggaagaatctcaaacagcgctacttactcaggatcagtggcaccagccaactcagctttgggacaaacccagccaagtgaccaggacactttagtgcaaagagctgagcacattccagcagggaaacgaactccgatgtgcgcccattgtaaccaggtcatcagaggaccattcttagtggcactggggaaatcttggcacccagaagaattcaactgcgctcactgcaaaaatacaatggcctacattggatttgtagaggagaaaggagccctgtattgtgagctgtgctatgagaaattctttgcccctgaatgtggtcgatgccaaaggaagatccttggagaagtcatcagtgcgttgaaacaaacttggcatgtttcctgttttgtgtgtgtagcctgtggaaagcccattcggaacaatgtttttcacttggaggatggtgaaccctactgtgagactgattattatgccctctttggtactatatgccatggatgtgaatttcccatagaagctggtgacatgttcctggaagctctgggctacacctggcatgacacttgctttgtatgctcagtgtgttgtgaaagtttggaaggtcagacctttttctccaagaaggacaagcccctgtgtaagaaacatgctcattctgtgaatttttgaaagtcaacagttcaggagaagagaaggaatttgaagagaaaaaggaaaattaaaattactaattaatttttagattcaatatttatatggagttttgaaaaataatagtggccctgaaggaataaattccagctttaaaaaccaagtctgaggaaatatttggcttcataaagtaaagagacggtttggcatttattattactttttcctgtattttatgcccataaaataagctttataaaaaccaatttcctgatggactattaaattcatcttagaataaattagtgaagaatttaattttagaataaataatccaatctgaaataattataccttctttccttgttaggtagttatgagtaaatctgcaaaaggcaatgaaaatgccttaaattttatcaataacagaattattgtatttaaaaaaaaactaatacttatctttaaaatagtaaataggattttaaacagagaattttatcagtaataggtgtcagtttttaaaaaattgcttgtaggctgagcgcggtggctcacgcctgtaatcccagcactttgggaggccaaggtgggtggaccacatgaggtcaggagtttgagatcagcctggccaacatggtgaaaccccatctctactaaaaatacaaaaattagccggacgcagtggcacgcgcctgtaatcccagctactcaagaggctgaggcacgagaatcacttgaacccgggagggagaggttgcagtgagccaagatcgtaccactgcactccagcctgggtgacagagtgagactctgtctccaaaaaaaaactttgcttgtatattatttttgccttacagtggatcattctagtaggaaaggacaataagattttttatcaaaatgtgtcatgccagtaagagatgttatattcttttctcatttcttccccacccaaaaataagctaccatatagcttataagtctcaaatttttgccttttactaaaatgtgattgtttctattcattgtgtatgcttcatcacctatattaggcaaattccatttttttcccttgtgctaaggtaaagatttaattaaataattttggcctctcatagttttctctctctttaaagagaataaatagagggccaggtgtggtggctcacgcctgtgatcccagcactttgggaggccaagacgggcggatcatgaggtcaagagatcaagatcatcctggccaacatggtgaaaccctgtctctactaaaaatacaaaaatgagctgggcatggtggggcgtgcctgtagtcccatgtacttgggaggctgaggcaggaaaattcttgaacccaggagacggaagttgcagtgagctgagatcacaccactgcactccagcctggtgacagagcaagactccggctcttaaaaaaaaaaaaaaaaaaaaaaaaagagagagagagaataaatagaaaagaatgtggctgggaattgtgaatcagaagattataccccccaattgtttttcaatccccttttctcaaataataaattagttaaatcagtttctgagttatgccactggctgatgaagagttgagaggtctctttgcagaatgatctttttgtttcgttttgtttcttcttctgcatttaaaaattaaaagattggtttgaggatgtgatgaaattgagactttttgtggttttctctcaataataagtgaaccaatttcaaatgtgatcacaaagtttggaaagcttttattcacagaggttgggtagtgttgggaggggagtttaattactcagattggcctgttatttgatttcctcctttgggaaaagaattatgtagataccacatggagacagggaaacaattgtggtaaaactgtggatcctgttgctatttgcccagtgagaaaacagattctggtatttgatttggtttttctctttgtttccagaatggatgaaagtccatgaacctcctaagttataatttaaatttgtttggggcaaggtgattttatagtcgagacagagccctaggtccttcctgccccatcactcacttacgacatcacttccattgtgtgcatgtttgttatagaggaggttttaggctacaatatttgtttaacctccctaagaactttcaaggcatctgtcctgaaagctgttaatttatggtctagcagatttatattatatgcagataataattaactggggataaaagaatggcaaggggtgacacaaagtagcaaactgaatacttctccaatagcaaccccaagctacctcctcaccctgcatcttggagggaggcaggaaatttcttttgaaataaagtgctggagctgaattctgcattatttatcgttgctgctgaaaccacctataaaagacttgctggctaatgtgcattgtcatataatgtacactgtcacatctttacagtcttgtatgttatagaatacaaaataagttgatggttttgtttggtgtgagctttttgtttgtttgtttagttttgccttcataggttatatgccaagatagtatttgataagtcaatgacatttggatgttttcttcaaagaattttatttgacccagatttcttataaagttatcttacattaaggatgtcattttcatcagaccttctttctacatattattcatgaagcataatgttgcatttctccaaattttatgcctgaaagggtagtgttgcttcctaaggtatcatgttgtctttgtgctttgtccatctcttccgtggcgaagctttatatctgttcctaaaacagttaatcctgtgaaataaatattgaacataatccagaagaatctctctgtttcccttggggaatgccatatttaattcaccagcagtaatcctttaataactggcagagcactttattcttctggtgagctccctgaatatttatttttctgattataaattttctatattagtagcattttttaattattacttcttcactatagagcatttacttttagtctctagatgtatattttggaatgctgtacttggcataacatagattaaaatcataatgcatgactaaaaactccttggatttatttcccattttaaaatttttagcggtaagttcagatttataatctttctctagacttccatggtctgaatgttgcctgctgaagtagcaacctaaaaagtatcccctgcttatgcttgtccagttggccctccatgtccataggcttcgcatctgtgattcagcccactgtgggtcaaaaatatttggggaaaaaaatggatggttgcgcctttgctgaacatgtacaaacttttttttgtcattaaacaatatagtataacaactatttacaaagcatttacattgtattagctattataggtaatctagagatgatttaaagtgtatggtaggatgtgcataggttatatgcaaatactacaccattttctataagggacttgaacatcatggactttagtatcctagggggttcttggaacccatcacccataggggcaccataggacaactatagtaccgtgtttatttcctattaattcaggttccgtttagagtctaaaactaaaacctaatcatttagtcacagtgtaaaaacaaatggaaataacagctcaaatcttcaaaatattactatagcattatgtttaaaataatctacaacaaaaatgtaccattttcaagcagtactacattaggagcccttttatagaaaataatttcttctttacccccgttccagtgtgaatctagtattctgttaacatttgtgtggcatttggagtttgtcatccccattgaagggagagccttctcagacatgaagcaagggaaacatactgaatagttttacacaaatttgatctggcttccatttgtccccctcatttcccaaatgtttaaatgtattggatttggattctcaatgtataagttgccttatctgttaatgtctatcttctgtctctttaattttgtatatctgctgttttgcttttggatacattttctaattagaagtcacatgataaatataatcagtatagtaataataccataatgtgcacatactcaataaataaatgactgcattgttgtaaatgag
//
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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