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2024-03-29 10:23:28, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_006457               6132 bp    mRNA    linear   PRI 07-JUL-2013
DEFINITION  Homo sapiens PDZ and LIM domain 5 (PDLIM5), transcript variant 1,
            mRNA.
ACCESSION   NM_006457
VERSION     NM_006457.4  GI:374092019
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 6132)
  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 6132)
  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 6132)
  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 6132)
  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 6132)
  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 6132)
  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 6132)
  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 6132)
  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 6132)
  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 6132)
  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, BC008741.2,
            AY598328.1, BF954250.1, AC108067.3 and AA614664.1.
            On Jan 26, 2012 this sequence version replaced gi:197383076.
            
            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 (1) encodes isoform a (also known
            as ENH1).
            
            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 :: AF061258.1, BC008741.2 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025081, ERS025082 [ECO:0000348]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-61                DA895978.1         1-61
            62-1321             BC008741.2         1-1260
            1322-1655           AY598328.1         1141-1474
            1656-1925           BF954250.1         27-296              c
            1926-5683           AC108067.3         42276-46033
            5684-6132           AA614664.1         3-451               c
FEATURES             Location/Qualifiers
     source          1..6132
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="4"
                     /map="4q22"
     gene            1..6132
                     /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..1972
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /note="isoform a is encoded by transcript variant 1;
                     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 a"
                     /protein_id="NP_006448.4"
                     /db_xref="GI:374092020"
                     /db_xref="CCDS:CCDS3641.1"
                     /db_xref="GeneID:10611"
                     /db_xref="HGNC:17468"
                     /db_xref="MIM:605904"
                     /translation="
MSNYSVSLVGPAPWGFRLQGGKDFNMPLTISSLKDGGKAAQANVRIGDVVLSIDGINAQGMTHLEAQNKIKGCTGSLNMTLQRASAAPKPEPVPVQKGEPKEVVKPVPITSPAVSKVTSTNNMAYNKAPRPFGSVSSPKVTSIPSPSSAFTPAHATTSSHASPSPVAAVTPPLFAASGLHANANLSADQSPSALSAGKTAVNVPRQPTVTSVCSETSQELAEGQRRGSQGDSKQQNGPPRKHIVERYTEFYHVPTHSDASKKRLIEDTEDWRPRTGTTQSRSFRILAQITGTEHLKESEADNTKKANNSQEPSPQLASSVASTRSMPESLDSPTSGRPGVTSLTTAAAFKPVGSTGVIKSPSWQRPNQGVPSTGRISNSATYSGSVAPANSALGQTQPSDQDTLVQRAEHIPAGKRTPMCAHCNQVIRGPFLVALGKSWHPEEFNCAHCKNTMAYIGFVEEKGALYCELCYEKFFAPECGRCQRKILGEVISALKQTWHVSCFVCVACGKPIRNNVFHLEDGEPYCETDYYALFGTICHGCEFPIEAGDMFLEALGYTWHDTCFVCSVCCESLEGQTFFSKKDKPLCKKHAHSVNF
"
     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    512..514
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (Q96HC4.5); phosphorylation site"
     misc_feature    590..592
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (Q96HC4.5); phosphorylation site"
     misc_feature    1106..1108
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (Q96HC4.5); phosphorylation site"
     misc_feature    1118..1120
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (Q96HC4.5); phosphorylation site"
     misc_feature    1439..1594
                     /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(1439..1441,1448..1450,1499..1501,1508..1510,
                     1517..1519,1526..1528,1580..1582,1589..1591)
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /note="Zn binding site [ion binding]; other site"
                     /db_xref="CDD:188837"
     misc_feature    1616..1771
                     /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(1616..1618,1625..1627,1676..1678,1685..1687,
                     1694..1696,1703..1705,1757..1759,1766..1768)
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /note="Zn binding site [ion binding]; other site"
                     /db_xref="CDD:188711"
     misc_feature    1793..1957
                     /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(1793..1795,1802..1804,1859..1861,1868..1870,
                     1877..1879,1886..1888,1940..1942,1949..1951)
                     /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..891
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /inference="alignment:Splign:1.39.8"
     variation       480
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:369525076"
     variation       537
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:116676966"
     variation       556
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:115650786"
     variation       569
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201130166"
     variation       579
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200298588"
     variation       584
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:375640209"
     variation       588
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:2452600"
     variation       595
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373008913"
     variation       621
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147707993"
     variation       622
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376748585"
     variation       624
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:370647247"
     variation       633
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200734812"
     variation       645
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376940621"
     variation       646
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:115743950"
     variation       667
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370388744"
     variation       676
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:116148450"
     variation       703
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368630474"
     variation       704
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:111766454"
     variation       729
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371298021"
     variation       732
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:111914798"
     variation       767
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139073948"
     variation       794
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375019235"
     variation       865
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:1056807"
     variation       868
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1135006"
     variation       876
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1135007"
     variation       891
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:1135008"
     exon            892..1064
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /inference="alignment:Splign:1.39.8"
     variation       897
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375364739"
     variation       917
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201891054"
     variation       918
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:141403934"
     variation       947
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:150388657"
     variation       980
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:202231060"
     variation       996
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:113605096"
     variation       1000
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:115214197"
     variation       1003
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:11722955"
     variation       1018
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:11097431"
     variation       1048
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371463583"
     exon            1065..1101
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /inference="alignment:Splign:1.39.8"
     variation       1081
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202092014"
     variation       1092
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:115781887"
     exon            1102..1289
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /inference="alignment:Splign:1.39.8"
     variation       1122
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146000883"
     variation       1123
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:139902919"
     variation       1137
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1064238"
     variation       1141
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377407022"
     variation       1151
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141653509"
     variation       1152
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:115018620"
     variation       1162
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:116241517"
     variation       1185
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371181316"
     variation       1214
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:966845"
     variation       1225
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:116830271"
     variation       1235
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368387152"
     variation       1250
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370892974"
     variation       1274
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374739373"
     exon            1290..1464
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /inference="alignment:Splign:1.39.8"
     variation       1313
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:148409775"
     variation       1319
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:372735372"
     variation       1322
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:7690296"
     variation       1333
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:375931613"
     variation       1343
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:7690464"
     variation       1350
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:115386065"
     variation       1365
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:114201587"
     variation       1409
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369761799"
     variation       1434
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139413367"
     variation       1435
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:373251894"
     variation       1452
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376503569"
     exon            1465..1645
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /inference="alignment:Splign:1.39.8"
     variation       1502
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201156978"
     variation       1505
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:377346480"
     variation       1515
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145633341"
     variation       1519
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201013535"
     variation       1520
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200640873"
     variation       1530
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373850074"
     variation       1546
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147724105"
     variation       1556
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142522131"
     exon            1646..1766
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /inference="alignment:Splign:1.39.8"
     variation       1652
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144752025"
     variation       1656
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:13107595"
     variation       1718
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148939806"
     variation       1720
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200822536"
     exon            1767..1882
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /inference="alignment:Splign:1.39.8"
     variation       1778
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:114255444"
     variation       1780
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143660655"
     variation       1789
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148074454"
     variation       1792
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:115802510"
     variation       1803
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374091168"
     variation       1813
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140894265"
     variation       1824
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:367629922"
     variation       1849
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:144847144"
     variation       1851
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:114713699"
     exon            1883..6132
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /inference="alignment:Splign:1.39.8"
     variation       1890
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201782564"
     variation       1899
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377023412"
     variation       1908
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:141719357"
     variation       1944
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:201326456"
     variation       1951
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146226694"
     variation       1956
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:76352571"
     variation       1979
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1056772"
     variation       2006
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372012549"
     variation       2154
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:114319350"
     variation       2227
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:189650582"
     variation       2397
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:33961001"
     variation       2495
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:56746297"
     variation       2502
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1802345"
     STS             2515..3308
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /standard_name="D10S2448"
                     /db_xref="UniSTS:474444"
     STS             2647..2729
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /standard_name="L18426"
                     /db_xref="UniSTS:34648"
     variation       2704
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:1134967"
     variation       2705
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374940031"
     variation       2711
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:180795923"
     variation       2741
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141426145"
     STS             2742..3153
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /standard_name="L17705"
                     /db_xref="UniSTS:66091"
     variation       2750
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370215027"
     variation       2769
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1056773"
     STS             2802..2924
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /standard_name="SHGC-67609"
                     /db_xref="UniSTS:54969"
     variation       2803
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377344916"
     variation       2827
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:187628494"
     variation       2840
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:137892930"
     variation       2895
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:62316494"
     variation       2978
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:14082"
     variation       3020
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:11339365"
     variation       3026
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201037096"
     variation       3033
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:10590"
     variation       3069
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:74599592"
     variation       3159
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:1134984"
     variation       3387
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace=""
                     /replace="a"
                     /replace="aaaaaaaa"
                     /db_xref="dbSNP:10706955"
     variation       3404..3411
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace=""
                     /replace="aaaaaaa"
                     /db_xref="dbSNP:71581598"
     variation       3411
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace=""
                     /replace="a"
                     /replace="aaaaaaaa"
                     /db_xref="dbSNP:11365933"
     variation       3412..3414
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace=""
                     /replace="gag"
                     /db_xref="dbSNP:141722289"
     variation       3412
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:55845770"
     variation       3414
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:58524187"
     variation       3429
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="c"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:28709926"
     variation       3471
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:201923550"
     variation       3480
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:78150373"
     variation       3481
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:10706956"
     variation       3481
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:75694017"
     variation       3607
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368604816"
     variation       3609
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:115970344"
     variation       3822
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141649481"
     variation       4013
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:11550270"
     variation       4094
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146120619"
     variation       4261
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:190760822"
     variation       4328
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140154582"
     variation       4341
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1048627"
     variation       4417
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:141563714"
     variation       4429
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1043848"
     variation       4480..4483
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace=""
                     /replace="tttg"
                     /db_xref="dbSNP:148752622"
     variation       4483..4486
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace=""
                     /replace="gttt"
                     /db_xref="dbSNP:371401737"
     variation       4483
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace=""
                     /replace="tttg"
                     /db_xref="dbSNP:34068251"
     variation       4533
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:182959183"
     variation       4592
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:371509832"
     STS             4684..4754
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /standard_name="D4S2569E"
                     /db_xref="UniSTS:19561"
     STS             4692..4862
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /standard_name="SHGC-24108"
                     /db_xref="UniSTS:4790"
     variation       4731
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:150914060"
     variation       4754
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:376838121"
     variation       4775
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:185688185"
     variation       4829
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:3943"
     variation       4912
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:1509617"
     variation       4985..4986
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace=""
                     /replace="ag"
                     /db_xref="dbSNP:368119740"
     variation       5028
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1043853"
     variation       5090
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:75854018"
     variation       5203
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:13141591"
     variation       5223
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:371683638"
     variation       5319
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:1139697"
     variation       5379
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:114932838"
     variation       5428
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:12294"
     variation       5571
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:12650486"
     variation       5577
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1043862"
     variation       5703
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139417946"
     variation       5762
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149975822"
     variation       5766
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:190144928"
     variation       5779
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369868118"
     variation       5790
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:115398076"
     STS             5932..6026
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /standard_name="D9S1746E"
                     /db_xref="UniSTS:153922"
     STS             5965..6094
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /standard_name="SHGC-59267"
                     /db_xref="UniSTS:57977"
     variation       5992
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:140772832"
     variation       6091
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:7285"
     polyA_signal    6101..6106
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
     polyA_signal    6105..6110
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
     variation       6109
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:183448943"
     polyA_site      6128
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
     polyA_site      6132
                     /gene="PDLIM5"
                     /gene_synonym="ENH; ENH1; L9; LIM"
ORIGIN      
gtgtcctgggtcgggggtggggcgagggagagccaggaggcggaagttcccgcgggcggtggggacggcgccctcaccgcgagtcacttgtcagcccttgtctgaggcggaggcagccccgcgccgcgccggacccgagcatatttcattttctgtcattggactttgagccattagaaccatgagcaactacagtgtgtcactggttggcccagctccttggggtttccggctgcagggcggtaaggatttcaacatgcctctgacaatctctagtctaaaagatggcggcaaggcagcccaggcaaatgtaagaataggcgatgtggttctcagcattgatggaataaatgcacaaggaatgactcatcttgaagcccagaataagattaagggttgtacaggctctttgaatatgactctgcaaagagcatctgctgcacccaagcctgagccggttcctgttcaaaagggagaacctaaagaagtagttaaacctgtgcccattacatctcctgctgtgtccaaagtcacttccacaaacaacatggcctacaataaggcaccacggccttttggttctgtgtcttcaccaaaagtcacatccatcccatcaccatcgtctgccttcaccccagcccatgcgaccacctcatcacatgcttccccttcacccgtggctgccgtcactcctcccctgttcgctgcatctggactgcatgctaatgccaatcttagtgctgaccagtctccatctgcactgagcgctggtaaaactgcagttaatgtcccacggcagcccacagtcaccagcgtgtgttccgagacttctcaggagctagcagagggacagagaagaggatcccagggtgacagtaaacagcaaaatggcccaccaagaaaacacattgtggagcgctatacagagttttatcatgtacccactcacagtgatgccagcaagaagagactgattgaggatactgaagactggcgtccaaggactggaacaactcagtctcgctctttccgaatccttgcccagatcactgggactgaacatttgaaagaatctgaagccgataatacaaagaaggcaaataactctcaggagccttctccgcagttggcttcctcggtagcttccacacggagcatgcccgagagcctggacagcccaacctctggcagaccaggggttaccagcctcacaactgcagctgccttcaagcctgtaggatccactggcgtcatcaagtcaccaagctggcaacggccaaaccaaggagtaccttccactggaagaatctcaaacagcgctacttactcaggatcagtggcaccagccaactcagctttgggacaaacccagccaagtgaccaggacactttagtgcaaagagctgagcacattccagcagggaaacgaactccgatgtgcgcccattgtaaccaggtcatcagaggaccattcttagtggcactggggaaatcttggcacccagaagaattcaactgcgctcactgcaaaaatacaatggcctacattggatttgtagaggagaaaggagccctgtattgtgagctgtgctatgagaaattctttgcccctgaatgtggtcgatgccaaaggaagatccttggagaagtcatcagtgcgttgaaacaaacttggcatgtttcctgttttgtgtgtgtagcctgtggaaagcccattcggaacaatgtttttcacttggaggatggtgaaccctactgtgagactgattattatgccctctttggtactatatgccatggatgtgaatttcccatagaagctggtgacatgttcctggaagctctgggctacacctggcatgacacttgctttgtatgctcagtgtgttgtgaaagtttggaaggtcagacctttttctccaagaaggacaagcccctgtgtaagaaacatgctcattctgtgaatttttgaaagtcaacagttcaggagaagagaaggaatttgaagagaaaaaggaaaattaaaattactaattaatttttagattcaatatttatatggagttttgaaaaataatagtggccctgaaggaataaattccagctttaaaaaccaagtctgaggaaatatttggcttcataaagtaaagagacggtttggcatttattattactttttcctgtattttatgcccataaaataagctttataaaaaccaatttcctgatggactattaaattcatcttagaataaattagtgaagaatttaattttagaataaataatccaatctgaaataattataccttctttccttgttaggtagttatgagtaaatctgcaaaaggcaatgaaaatgccttaaattttatcaataacagaattattgtatttaaaaaaaaactaatacttatctttaaaatagtaaataggattttaaacagagaattttatcagtaataggtgtcagtttttaaaaaattgcttgtaggctgagcgcggtggctcacgcctgtaatcccagcactttgggaggccaaggtgggtggaccacatgaggtcaggagtttgagatcagcctggccaacatggtgaaaccccatctctactaaaaatacaaaaattagccggacgcagtggcacgcgcctgtaatcccagctactcaagaggctgaggcacgagaatcacttgaacccgggagggagaggttgcagtgagccaagatcgtaccactgcactccagcctgggtgacagagtgagactctgtctccaaaaaaaaactttgcttgtatattatttttgccttacagtggatcattctagtaggaaaggacaataagattttttatcaaaatgtgtcatgccagtaagagatgttatattcttttctcatttcttccccacccaaaaataagctaccatatagcttataagtctcaaatttttgccttttactaaaatgtgattgtttctattcattgtgtatgcttcatcacctatattaggcaaattccatttttttcccttgtgctaaggtaaagatttaattaaataattttggcctctcatagttttctctctctttaaagagaataaatagagggccaggtgtggtggctcacgcctgtgatcccagcactttgggaggccaagacgggcggatcatgaggtcaagagatcaagatcatcctggccaacatggtgaaaccctgtctctactaaaaatacaaaaatgagctgggcatggtggggcgtgcctgtagtcccatgtacttgggaggctgaggcaggaaaattcttgaacccaggagacggaagttgcagtgagctgagatcacaccactgcactccagcctggtgacagagcaagactccggctcttaaaaaaaaaaaaaaaaaaaaaaaaagagagagagagaataaatagaaaagaatgtggctgggaattgtgaatcagaagattataccccccaattgtttttcaatccccttttctcaaataataaattagttaaatcagtttctgagttatgccactggctgatgaagagttgagaggtctctttgcagaatgatctttttgtttcgttttgtttcttcttctgcatttaaaaattaaaagattggtttgaggatgtgatgaaattgagactttttgtggttttctctcaataataagtgaaccaatttcaaatgtgatcacaaagtttggaaagcttttattcacagaggttgggtagtgttgggaggggagtttaattactcagattggcctgttatttgatttcctcctttgggaaaagaattatgtagataccacatggagacagggaaacaattgtggtaaaactgtggatcctgttgctatttgcccagtgagaaaacagattctggtatttgatttggtttttctctttgtttccagaatggatgaaagtccatgaacctcctaagttataatttaaatttgtttggggcaaggtgattttatagtcgagacagagccctaggtccttcctgccccatcactcacttacgacatcacttccattgtgtgcatgtttgttatagaggaggttttaggctacaatatttgtttaacctccctaagaactttcaaggcatctgtcctgaaagctgttaatttatggtctagcagatttatattatatgcagataataattaactggggataaaagaatggcaaggggtgacacaaagtagcaaactgaatacttctccaatagcaaccccaagctacctcctcaccctgcatcttggagggaggcaggaaatttcttttgaaataaagtgctggagctgaattctgcattatttatcgttgctgctgaaaccacctataaaagacttgctggctaatgtgcattgtcatataatgtacactgtcacatctttacagtcttgtatgttatagaatacaaaataagttgatggttttgtttggtgtgagctttttgtttgtttgtttagttttgccttcataggttatatgccaagatagtatttgataagtcaatgacatttggatgttttcttcaaagaattttatttgacccagatttcttataaagttatcttacattaaggatgtcattttcatcagaccttctttctacatattattcatgaagcataatgttgcatttctccaaattttatgcctgaaagggtagtgttgcttcctaaggtatcatgttgtctttgtgctttgtccatctcttccgtggcgaagctttatatctgttcctaaaacagttaatcctgtgaaataaatattgaacataatccagaagaatctctctgtttcccttggggaatgccatatttaattcaccagcagtaatcctttaataactggcagagcactttattcttctggtgagctccctgaatatttatttttctgattataaattttctatattagtagcattttttaattattacttcttcactatagagcatttacttttagtctctagatgtatattttggaatgctgtacttggcataacatagattaaaatcataatgcatgactaaaaactccttggatttatttcccattttaaaatttttagcggtaagttcagatttataatctttctctagacttccatggtctgaatgttgcctgctgaagtagcaacctaaaaagtatcccctgcttatgcttgtccagttggccctccatgtccataggcttcgcatctgtgattcagcccactgtgggtcaaaaatatttggggaaaaaaatggatggttgcgcctttgctgaacatgtacaaacttttttttgtcattaaacaatatagtataacaactatttacaaagcatttacattgtattagctattataggtaatctagagatgatttaaagtgtatggtaggatgtgcataggttatatgcaaatactacaccattttctataagggacttgaacatcatggactttagtatcctagggggttcttggaacccatcacccataggggcaccataggacaactatagtaccgtgtttatttcctattaattcaggttccgtttagagtctaaaactaaaacctaatcatttagtcacagtgtaaaaacaaatggaaataacagctcaaatcttcaaaatattactatagcattatgtttaaaataatctacaacaaaaatgtaccattttcaagcagtactacattaggagcccttttatagaaaataatttcttctttacccccgttccagtgtgaatctagtattctgttaacatttgtgtggcatttggagtttgtcatccccattgaagggagagccttctcagacatgaagcaagggaaacatactgaatagttttacacaaatttgatctggcttccatttgtccccctcatttcccaaatgtttaaatgtattggatttggattctcaatgtataagttgccttatctgttaatgtctatcttctgtctctttaattttgtatatctgctgttttgcttttggatacattttctaattagaagtcacatgataaatataatcagtatagtaataataccataatgtgcacatactcaataaataaatgactgcattgttgtaaatgag
//

Annotations:

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

by @meso_cacase at DBCLS
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