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2024-04-26 02:42:21, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001256426 6219 bp mRNA linear PRI 07-JUL-2013
DEFINITION Homo sapiens PDZ and LIM domain 5 (PDLIM5), transcript variant 6,
mRNA.
ACCESSION NM_001256426
VERSION NM_001256426.1 GI:374093207
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 6219)
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 6219)
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 6219)
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 6219)
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 6219)
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 6219)
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 6219)
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 6219)
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 6219)
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 6219)
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, AL832686.1,
AC093778.3, AC108067.3 and AA614664.1.
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 (6) uses an alternate in-frame
splice site in the 5' coding region, and contains four additional
in-frame exons in the central coding region, compared to variant 1,
resulting in an isoform (f) that is longer 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 :: AL832686.1 [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
1-99 DA895978.1 1-99
100-708 AL832686.1 4-612
709-709 AC093778.3 104472-104472
710-1017 AL832686.1 614-921
1018-1018 AC093778.3 129047-129047
1019-1742 AL832686.1 923-1646
1743-1743 AC108067.3 35692-35692
1744-2065 AL832686.1 1648-1969
2066-5770 AC108067.3 42329-46033
5771-6219 AA614664.1 3-451 c
FEATURES Location/Qualifiers
source 1..6219
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="4"
/map="4q22"
gene 1..6219
/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..2059
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/note="isoform f is encoded by transcript variant 6;
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 f"
/protein_id="NP_001243355.1"
/db_xref="GI:374093208"
/db_xref="CCDS:CCDS58916.1"
/db_xref="GeneID:10611"
/db_xref="HGNC:17468"
/db_xref="MIM:605904"
/translation="
MSNYSVSLVGPAPWGFRLQGGKDFNMPLTISSLKDGGKAAQANVRIGDVVLSIDGINAQGMTHLEAQNKIKGCTGSLNMTLQRASAAPKPEPVPVQKPTVTSVCSETSQELAEGQRRGSQGDSKQQNGKIPPKRPPRKHIVERYTEFYHVPTHSDASKKRLIEDTEDWRPRTGTTQSRSFRILAQITGTEHLKESEADNTKKAKFDSALEDLPKSGPHPPATPQVLTIGSQVATLSKVATTYSSLSSSTGNVEDSFEGFRNFSTFSSPARYSAAVLSSAAATVSAVIATKTRLYTPERYHSLLDALCISPVSKPLAFSYLQSSRKSTGSIHVKKTSNSQEPSPQLASSVASTRSMPESLDSPTSGRPGVTSLTTAAAFKPVGSTGVIKSPSWQRPNQGVPSTGRISNSATYSGSVAPANSALGQTQPSDQDTLVQRAEHIPAGKRTPMCAHCNQVIRGPFLVALGKSWHPEEFNCAHCKNTMAYIGFVEEKGALYCELCYEKFFAPECGRCQRKILGEVISALKQTWHVSCFVCVACGKPIRNNVFHLEDGEPYCETDYYALFGTICHGCEFPIEAGDMFLEALGYTWHDTCFVCSVCCESLEGQTFFSKKDKPLCKKHAHSVNF
"
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 1526..1681
/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(1526..1528,1535..1537,1586..1588,1595..1597,
1604..1606,1613..1615,1667..1669,1676..1678)
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/note="Zn binding site [ion binding]; other site"
/db_xref="CDD:188837"
misc_feature 1703..1858
/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(1703..1705,1712..1714,1763..1765,1772..1774,
1781..1783,1790..1792,1844..1846,1853..1855)
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/note="Zn binding site [ion binding]; other site"
/db_xref="CDD:188711"
misc_feature 1880..2044
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/note="The third LIM domain of the Enigma Homolog (ENH)
family; Region: LIM3_ENH; cd09459"
/db_xref="CDD:188843"
misc_feature order(1880..1882,1889..1891,1946..1948,1955..1957,
1964..1966,1973..1975,2027..2029,2036..2038)
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/note="Zn binding site [ion binding]; other site"
/db_xref="CDD:188843"
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..912
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 819
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:180835231"
exon 913..1056
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 927
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:192429921"
variation 941
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:182234347"
variation 983..985
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="cct"
/db_xref="dbSNP:376754580"
variation 1018
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:10017461"
exon 1057..1188
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 1160
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:144181232"
variation 1164
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:374239277"
exon 1189..1376
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 1209
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:146000883"
variation 1210
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:139902919"
variation 1224
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1064238"
variation 1228
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:377407022"
variation 1238
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:141653509"
variation 1239
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:115018620"
variation 1249
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:116241517"
variation 1272
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:371181316"
variation 1301
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:966845"
variation 1312
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:116830271"
variation 1322
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:368387152"
variation 1337
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:370892974"
variation 1361
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:374739373"
exon 1377..1551
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 1400
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:148409775"
variation 1406
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:372735372"
variation 1409
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:7690296"
variation 1420
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:375931613"
variation 1430
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:7690464"
variation 1437
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:115386065"
variation 1452
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:114201587"
variation 1496
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:369761799"
variation 1521
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:139413367"
variation 1522
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:373251894"
variation 1539
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:376503569"
exon 1552..1732
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 1589
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:201156978"
variation 1592
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:377346480"
variation 1602
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:145633341"
variation 1606
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:201013535"
variation 1607
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:200640873"
variation 1617
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:373850074"
variation 1633
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:147724105"
variation 1643
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:142522131"
exon 1733..1853
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 1739
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:144752025"
variation 1743
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:13107595"
variation 1805
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:148939806"
variation 1807
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:200822536"
exon 1854..1969
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 1865
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:114255444"
variation 1867
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:143660655"
variation 1876
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:148074454"
variation 1879
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:115802510"
variation 1890
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:374091168"
variation 1900
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:140894265"
variation 1911
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:367629922"
variation 1936
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:144847144"
variation 1938
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:114713699"
exon 1970..6219
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 1977
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:201782564"
variation 1986
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:377023412"
variation 1995
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:141719357"
variation 2031
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:201326456"
variation 2038
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:146226694"
variation 2043
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:76352571"
variation 2066
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1056772"
variation 2093
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:372012549"
variation 2241
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:114319350"
variation 2314
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:189650582"
variation 2484
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="a"
/db_xref="dbSNP:33961001"
variation 2582
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:56746297"
variation 2589
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1802345"
STS 2602..3395
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/standard_name="D10S2448"
/db_xref="UniSTS:474444"
STS 2734..2816
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/standard_name="L18426"
/db_xref="UniSTS:34648"
variation 2791
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1134967"
variation 2792
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:374940031"
variation 2798
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:180795923"
variation 2828
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:141426145"
STS 2829..3240
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/standard_name="L17705"
/db_xref="UniSTS:66091"
variation 2837
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:370215027"
variation 2856
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1056773"
STS 2889..3011
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/standard_name="SHGC-67609"
/db_xref="UniSTS:54969"
variation 2890
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:377344916"
variation 2914
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:187628494"
variation 2927
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:137892930"
variation 2982
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:62316494"
variation 3065
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:14082"
variation 3107
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="t"
/db_xref="dbSNP:11339365"
variation 3113
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:201037096"
variation 3120
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:10590"
variation 3156
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:74599592"
variation 3246
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1134984"
variation 3474
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="a"
/replace="aaaaaaaa"
/db_xref="dbSNP:10706955"
variation 3491..3498
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="aaaaaaa"
/db_xref="dbSNP:71581598"
variation 3498
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="a"
/replace="aaaaaaaa"
/db_xref="dbSNP:11365933"
variation 3499..3501
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="gag"
/db_xref="dbSNP:141722289"
variation 3499
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:55845770"
variation 3501
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:58524187"
variation 3516
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:28709926"
variation 3558
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="c"
/db_xref="dbSNP:201923550"
variation 3567
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="g"
/db_xref="dbSNP:78150373"
variation 3568
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="g"
/db_xref="dbSNP:10706956"
variation 3568
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:75694017"
variation 3694
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:368604816"
variation 3696
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:115970344"
variation 3909
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:141649481"
variation 4100
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:11550270"
variation 4181
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:146120619"
variation 4348
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:190760822"
variation 4415
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:140154582"
variation 4428
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1048627"
variation 4504
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:141563714"
variation 4516
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1043848"
variation 4567..4570
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="tttg"
/db_xref="dbSNP:148752622"
variation 4570..4573
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="gttt"
/db_xref="dbSNP:371401737"
variation 4570
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="tttg"
/db_xref="dbSNP:34068251"
variation 4620
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:182959183"
variation 4679
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:371509832"
STS 4771..4841
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/standard_name="D4S2569E"
/db_xref="UniSTS:19561"
STS 4779..4949
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/standard_name="SHGC-24108"
/db_xref="UniSTS:4790"
variation 4818
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:150914060"
variation 4841
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:376838121"
variation 4862
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:185688185"
variation 4916
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:3943"
variation 4999
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1509617"
variation 5072..5073
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="ag"
/db_xref="dbSNP:368119740"
variation 5115
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1043853"
variation 5177
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:75854018"
variation 5290
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:13141591"
variation 5310
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:371683638"
variation 5406
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1139697"
variation 5466
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:114932838"
variation 5515
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:12294"
variation 5658
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:12650486"
variation 5664
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1043862"
variation 5790
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:139417946"
variation 5849
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:149975822"
variation 5853
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:190144928"
variation 5866
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:369868118"
variation 5877
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:115398076"
STS 6019..6113
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/standard_name="D9S1746E"
/db_xref="UniSTS:153922"
STS 6052..6181
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/standard_name="SHGC-59267"
/db_xref="UniSTS:57977"
variation 6079
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:140772832"
variation 6178
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:7285"
polyA_signal 6188..6193
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
polyA_signal 6192..6197
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
variation 6196
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:183448943"
polyA_site 6215
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
polyA_site 6219
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
ORIGIN
gtgtcctgggtcgggggtggggcgagggagagccaggaggcggaagttcccgcgggcggtggggacggcgccctcaccgcgagtcacttgtcagcccttgtctgaggcggaggcagccccgcgccgcgccggacccgagcatatttcattttctgtcattggactttgagccattagaaccatgagcaactacagtgtgtcactggttggcccagctccttggggtttccggctgcagggcggtaaggatttcaacatgcctctgacaatctctagtctaaaagatggcggcaaggcagcccaggcaaatgtaagaataggcgatgtggttctcagcattgatggaataaatgcacaaggaatgactcatcttgaagcccagaataagattaagggttgtacaggctctttgaatatgactctgcaaagagcatctgctgcacccaagcctgagccggttcctgttcaaaagcccacagtcaccagcgtgtgttccgagacttctcaggagctagcagagggacagagaagaggatcccagggtgacagtaaacagcaaaatgggaaaatcccacctaaacgcccaccaagaaaacacattgtggagcgctatacagagttttatcatgtacccactcacagtgatgccagcaagaagagactgattgaggatactgaagactggcgtccaaggactggaacaactcagtctcgctctttccgaatccttgcccagatcactgggactgaacatttgaaagaatctgaagccgataatacaaagaaggcaaagtttgacagtgctctggaagacctacctaagagtggacctcaccctcctgcaactcctcaggtgttaactattggtagccaagtggccacactttctaaagtagcaactacttattctagtttaagcagctccacaggaaatgtggaagattctttcgaaggttttcgaaacttttctaccttctcttctcctgctagatatagtgctgcagttctgagcagcgcagctgctactgtgtctgctgttattgctacaaaaaccaggctctacactcctgaaagatatcactcactcctggatgcactttgcatcagccctgtctccaagcctttagctttttcctatctgcagtcctcaaggaaatcaactggctctatccatgttaagaaaacaagtaactctcaggagccttctccgcagttggcttcctcggtagcttccacacggagcatgcccgagagcctggacagcccaacctctggcagaccaggggttaccagcctcacaactgcagctgccttcaagcctgtaggatccactggcgtcatcaagtcaccaagctggcaacggccaaaccaaggagtaccttccactggaagaatctcaaacagcgctacttactcaggatcagtggcaccagccaactcagctttgggacaaacccagccaagtgaccaggacactttagtgcaaagagctgagcacattccagcagggaaacgaactccgatgtgcgcccattgtaaccaggtcatcagaggaccattcttagtggcactggggaaatcttggcacccagaagaattcaactgcgctcactgcaaaaatacaatggcctacattggatttgtagaggagaaaggagccctgtattgtgagctgtgctatgagaaattctttgcccctgaatgtggtcgatgccaaaggaagatccttggagaagtcatcagtgcgttgaaacaaacttggcatgtttcctgttttgtgtgtgtagcctgtggaaagcccattcggaacaatgtttttcacttggaggatggtgaaccctactgtgagactgattattatgccctctttggtactatatgccatggatgtgaatttcccatagaagctggtgacatgttcctggaagctctgggctacacctggcatgacacttgctttgtatgctcagtgtgttgtgaaagtttggaaggtcagacctttttctccaagaaggacaagcccctgtgtaagaaacatgctcattctgtgaatttttgaaagtcaacagttcaggagaagagaaggaatttgaagagaaaaaggaaaattaaaattactaattaatttttagattcaatatttatatggagttttgaaaaataatagtggccctgaaggaataaattccagctttaaaaaccaagtctgaggaaatatttggcttcataaagtaaagagacggtttggcatttattattactttttcctgtattttatgcccataaaataagctttataaaaaccaatttcctgatggactattaaattcatcttagaataaattagtgaagaatttaattttagaataaataatccaatctgaaataattataccttctttccttgttaggtagttatgagtaaatctgcaaaaggcaatgaaaatgccttaaattttatcaataacagaattattgtatttaaaaaaaaactaatacttatctttaaaatagtaaataggattttaaacagagaattttatcagtaataggtgtcagtttttaaaaaattgcttgtaggctgagcgcggtggctcacgcctgtaatcccagcactttgggaggccaaggtgggtggaccacatgaggtcaggagtttgagatcagcctggccaacatggtgaaaccccatctctactaaaaatacaaaaattagccggacgcagtggcacgcgcctgtaatcccagctactcaagaggctgaggcacgagaatcacttgaacccgggagggagaggttgcagtgagccaagatcgtaccactgcactccagcctgggtgacagagtgagactctgtctccaaaaaaaaactttgcttgtatattatttttgccttacagtggatcattctagtaggaaaggacaataagattttttatcaaaatgtgtcatgccagtaagagatgttatattcttttctcatttcttccccacccaaaaataagctaccatatagcttataagtctcaaatttttgccttttactaaaatgtgattgtttctattcattgtgtatgcttcatcacctatattaggcaaattccatttttttcccttgtgctaaggtaaagatttaattaaataattttggcctctcatagttttctctctctttaaagagaataaatagagggccaggtgtggtggctcacgcctgtgatcccagcactttgggaggccaagacgggcggatcatgaggtcaagagatcaagatcatcctggccaacatggtgaaaccctgtctctactaaaaatacaaaaatgagctgggcatggtggggcgtgcctgtagtcccatgtacttgggaggctgaggcaggaaaattcttgaacccaggagacggaagttgcagtgagctgagatcacaccactgcactccagcctggtgacagagcaagactccggctcttaaaaaaaaaaaaaaaaaaaaaaaaagagagagagagaataaatagaaaagaatgtggctgggaattgtgaatcagaagattataccccccaattgtttttcaatccccttttctcaaataataaattagttaaatcagtttctgagttatgccactggctgatgaagagttgagaggtctctttgcagaatgatctttttgtttcgttttgtttcttcttctgcatttaaaaattaaaagattggtttgaggatgtgatgaaattgagactttttgtggttttctctcaataataagtgaaccaatttcaaatgtgatcacaaagtttggaaagcttttattcacagaggttgggtagtgttgggaggggagtttaattactcagattggcctgttatttgatttcctcctttgggaaaagaattatgtagataccacatggagacagggaaacaattgtggtaaaactgtggatcctgttgctatttgcccagtgagaaaacagattctggtatttgatttggtttttctctttgtttccagaatggatgaaagtccatgaacctcctaagttataatttaaatttgtttggggcaaggtgattttatagtcgagacagagccctaggtccttcctgccccatcactcacttacgacatcacttccattgtgtgcatgtttgttatagaggaggttttaggctacaatatttgtttaacctccctaagaactttcaaggcatctgtcctgaaagctgttaatttatggtctagcagatttatattatatgcagataataattaactggggataaaagaatggcaaggggtgacacaaagtagcaaactgaatacttctccaatagcaaccccaagctacctcctcaccctgcatcttggagggaggcaggaaatttcttttgaaataaagtgctggagctgaattctgcattatttatcgttgctgctgaaaccacctataaaagacttgctggctaatgtgcattgtcatataatgtacactgtcacatctttacagtcttgtatgttatagaatacaaaataagttgatggttttgtttggtgtgagctttttgtttgtttgtttagttttgccttcataggttatatgccaagatagtatttgataagtcaatgacatttggatgttttcttcaaagaattttatttgacccagatttcttataaagttatcttacattaaggatgtcattttcatcagaccttctttctacatattattcatgaagcataatgttgcatttctccaaattttatgcctgaaagggtagtgttgcttcctaaggtatcatgttgtctttgtgctttgtccatctcttccgtggcgaagctttatatctgttcctaaaacagttaatcctgtgaaataaatattgaacataatccagaagaatctctctgtttcccttggggaatgccatatttaattcaccagcagtaatcctttaataactggcagagcactttattcttctggtgagctccctgaatatttatttttctgattataaattttctatattagtagcattttttaattattacttcttcactatagagcatttacttttagtctctagatgtatattttggaatgctgtacttggcataacatagattaaaatcataatgcatgactaaaaactccttggatttatttcccattttaaaatttttagcggtaagttcagatttataatctttctctagacttccatggtctgaatgttgcctgctgaagtagcaacctaaaaagtatcccctgcttatgcttgtccagttggccctccatgtccataggcttcgcatctgtgattcagcccactgtgggtcaaaaatatttggggaaaaaaatggatggttgcgcctttgctgaacatgtacaaacttttttttgtcattaaacaatatagtataacaactatttacaaagcatttacattgtattagctattataggtaatctagagatgatttaaagtgtatggtaggatgtgcataggttatatgcaaatactacaccattttctataagggacttgaacatcatggactttagtatcctagggggttcttggaacccatcacccataggggcaccataggacaactatagtaccgtgtttatttcctattaattcaggttccgtttagagtctaaaactaaaacctaatcatttagtcacagtgtaaaaacaaatggaaataacagctcaaatcttcaaaatattactatagcattatgtttaaaataatctacaacaaaaatgtaccattttcaagcagtactacattaggagcccttttatagaaaataatttcttctttacccccgttccagtgtgaatctagtattctgttaacatttgtgtggcatttggagtttgtcatccccattgaagggagagccttctcagacatgaagcaagggaaacatactgaatagttttacacaaatttgatctggcttccatttgtccccctcatttcccaaatgtttaaatgtattggatttggattctcaatgtataagttgccttatctgttaatgtctatcttctgtctctttaattttgtatatctgctgttttgcttttggatacattttctaattagaagtcacatgataaatataatcagtatagtaataataccataatgtgcacatactcaataaataaatgactgcattgttgtaaatgag
//
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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