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2024-04-20 01:51:58, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001256428 5980 bp mRNA linear PRI 07-JUL-2013
DEFINITION Homo sapiens PDZ and LIM domain 5 (PDLIM5), transcript variant 8,
mRNA.
ACCESSION NM_001256428
VERSION NM_001256428.1 GI:374093211
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 5980)
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 5980)
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 5980)
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 5980)
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 5980)
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 5980)
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 5980)
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 5980)
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 5980)
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 5980)
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, AK296980.1,
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 (8) lacks an alternate exon in the
5' coding region and uses a downstream in-frame start codon,
compared to variant 1. The encoded isoform (h) is shorter at the
N-terminus, compared to isoform a.
Sequence Note: This RefSeq record was created from transcript and
genomic sequence data to make the sequence consistent with the
reference genome assembly. The genomic coordinates used for the
transcript record were based on transcript alignments.
Publication Note: This RefSeq record includes a subset of the
publications that are available for this gene. Please see the Gene
record to access additional publications.
##Evidence-Data-START##
Transcript exon combination :: AK296980.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025091 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-86 DA895978.1 1-86
87-1169 AK296980.1 1-1083
1170-1170 AC108067.3 18563-18563
1171-1503 AK296980.1 1085-1417
1504-1504 AC108067.3 35692-35692
1505-1939 AK296980.1 1419-1853
1940-5531 AC108067.3 42442-46033
5532-5980 AA614664.1 3-451 c
FEATURES Location/Qualifiers
source 1..5980
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="4"
/map="4q22"
gene 1..5980
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/note="PDZ and LIM domain 5"
/db_xref="GeneID:10611"
/db_xref="HGNC:17468"
/db_xref="MIM:605904"
exon 1..139
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 24
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:138430072"
variation 49
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:192733830"
variation 63
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:184767586"
variation 70
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:143611898"
variation 79
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:28736374"
variation 81
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:147199893"
variation 113
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:369769495"
exon 140..277
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 165
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:200141226"
variation 217
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:373896689"
variation 241
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:145981438"
variation 246
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:75841704"
misc_feature 264..266
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/note="upstream in-frame stop codon"
exon 278..320
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 279
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:371717002"
variation 303
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:375778697"
variation 304
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:200495769"
variation 305
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:145853286"
exon 321..739
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 328
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:369525076"
variation 385
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:116676966"
CDS 396..1820
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/note="isoform h is encoded by transcript variant 8;
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 h"
/protein_id="NP_001243357.1"
/db_xref="GI:374093212"
/db_xref="CCDS:CCDS58918.1"
/db_xref="GeneID:10611"
/db_xref="HGNC:17468"
/db_xref="MIM:605904"
/translation="
MAYNKAPRPFGSVSSPKVTSIPSPSSAFTPAHATTSSHASPSPVAAVTPPLFAASGLHANANLSADQSPSALSAGKTAVNVPRQPTVTSVCSETSQELAEGQRRGSQGDSKQQNGPPRKHIVERYTEFYHVPTHSDASKKRLIEDTEDWRPRTGTTQSRSFRILAQITGTEHLKESEADNTKKANNSQEPSPQLASSVASTRSMPESLDSPTSGRPGVTSLTTAAAFKPVGSTGVIKSPSWQRPNQGVPSTGRISNSATYSGSVAPANSALGQTQPSDQDTLVQRAEHIPAGKRTPMCAHCNQVIRGPFLVALGKSWHPEEFNCAHCKNTMAYIGFVEEKGALYCELCYEKFFAPECGRCQRKILGEVISALKQTWHVSCFVCVACGKPIRNNVFHLEDGEPYCETDYYALFGTICHGCEFPIEAGDMFLEALGYTWHDTCFVCSVCCESLEGQTFFSKKDKPLCKKHAHSVNF
"
misc_feature 1287..1442
/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(1287..1289,1296..1298,1347..1349,1356..1358,
1365..1367,1374..1376,1428..1430,1437..1439)
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/note="Zn binding site [ion binding]; other site"
/db_xref="CDD:188837"
misc_feature 1464..1619
/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(1464..1466,1473..1475,1524..1526,1533..1535,
1542..1544,1551..1553,1605..1607,1614..1616)
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/note="Zn binding site [ion binding]; other site"
/db_xref="CDD:188711"
misc_feature 1641..1805
/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(1641..1643,1650..1652,1707..1709,1716..1718,
1725..1727,1734..1736,1788..1790,1797..1799)
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/note="Zn binding site [ion binding]; other site"
/db_xref="CDD:188843"
variation 404
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:115650786"
variation 417
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:201130166"
variation 427
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:200298588"
variation 432
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:375640209"
variation 436
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:2452600"
variation 443
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:373008913"
variation 469
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:147707993"
variation 470
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:376748585"
variation 472
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:370647247"
variation 481
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:200734812"
variation 493
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:376940621"
variation 494
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:115743950"
variation 515
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:370388744"
variation 524
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:116148450"
variation 551
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:368630474"
variation 552
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:111766454"
variation 577
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:371298021"
variation 580
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:111914798"
variation 615
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:139073948"
variation 642
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:375019235"
variation 713
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1056807"
variation 716
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1135006"
variation 724
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1135007"
variation 739
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1135008"
exon 740..912
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 745
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:375364739"
variation 765
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:201891054"
variation 766
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:141403934"
variation 795
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:150388657"
variation 828
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:202231060"
variation 844
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:113605096"
variation 848
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:115214197"
variation 851
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:11722955"
variation 866
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:11097431"
variation 896
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:371463583"
exon 913..949
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 929
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:202092014"
variation 940
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:115781887"
exon 950..1137
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 970
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:146000883"
variation 971
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:139902919"
variation 985
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1064238"
variation 989
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:377407022"
variation 999
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:141653509"
variation 1000
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:115018620"
variation 1010
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:116241517"
variation 1033
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:371181316"
variation 1062
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:966845"
variation 1073
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:116830271"
variation 1083
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:368387152"
variation 1098
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:370892974"
variation 1122
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:374739373"
exon 1138..1312
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 1161
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:148409775"
variation 1167
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:372735372"
variation 1170
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:7690296"
variation 1181
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:375931613"
variation 1191
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:7690464"
variation 1198
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:115386065"
variation 1213
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:114201587"
variation 1257
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:369761799"
variation 1282
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:139413367"
variation 1283
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:373251894"
variation 1300
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:376503569"
exon 1313..1493
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 1350
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:201156978"
variation 1353
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:377346480"
variation 1363
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:145633341"
variation 1367
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:201013535"
variation 1368
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:200640873"
variation 1378
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:373850074"
variation 1394
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:147724105"
variation 1404
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:142522131"
exon 1494..1614
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 1500
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:144752025"
variation 1504
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:13107595"
variation 1566
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:148939806"
variation 1568
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:200822536"
exon 1615..1730
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 1626
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:114255444"
variation 1628
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:143660655"
variation 1637
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:148074454"
variation 1640
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:115802510"
variation 1651
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:374091168"
variation 1661
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:140894265"
variation 1672
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:367629922"
variation 1697
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:144847144"
variation 1699
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:114713699"
exon 1731..5980
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 1738
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:201782564"
variation 1747
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:377023412"
variation 1756
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:141719357"
variation 1792
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:201326456"
variation 1799
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:146226694"
variation 1804
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:76352571"
variation 1827
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1056772"
variation 1854
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:372012549"
variation 2002
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:114319350"
variation 2075
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:189650582"
variation 2245
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="a"
/db_xref="dbSNP:33961001"
variation 2343
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:56746297"
variation 2350
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1802345"
STS 2363..3156
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/standard_name="D10S2448"
/db_xref="UniSTS:474444"
STS 2495..2577
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/standard_name="L18426"
/db_xref="UniSTS:34648"
variation 2552
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1134967"
variation 2553
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:374940031"
variation 2559
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:180795923"
variation 2589
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:141426145"
STS 2590..3001
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/standard_name="L17705"
/db_xref="UniSTS:66091"
variation 2598
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:370215027"
variation 2617
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1056773"
STS 2650..2772
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/standard_name="SHGC-67609"
/db_xref="UniSTS:54969"
variation 2651
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:377344916"
variation 2675
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:187628494"
variation 2688
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:137892930"
variation 2743
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:62316494"
variation 2826
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:14082"
variation 2868
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="t"
/db_xref="dbSNP:11339365"
variation 2874
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:201037096"
variation 2881
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:10590"
variation 2917
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:74599592"
variation 3007
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1134984"
variation 3235
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="a"
/replace="aaaaaaaa"
/db_xref="dbSNP:10706955"
variation 3252..3259
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="aaaaaaa"
/db_xref="dbSNP:71581598"
variation 3259
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="a"
/replace="aaaaaaaa"
/db_xref="dbSNP:11365933"
variation 3260..3262
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="gag"
/db_xref="dbSNP:141722289"
variation 3260
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:55845770"
variation 3262
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:58524187"
variation 3277
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:28709926"
variation 3319
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="c"
/db_xref="dbSNP:201923550"
variation 3328
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="g"
/db_xref="dbSNP:78150373"
variation 3329
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="g"
/db_xref="dbSNP:10706956"
variation 3329
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:75694017"
variation 3455
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:368604816"
variation 3457
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:115970344"
variation 3670
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:141649481"
variation 3861
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:11550270"
variation 3942
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:146120619"
variation 4109
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:190760822"
variation 4176
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:140154582"
variation 4189
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1048627"
variation 4265
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:141563714"
variation 4277
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1043848"
variation 4328..4331
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="tttg"
/db_xref="dbSNP:148752622"
variation 4331..4334
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="gttt"
/db_xref="dbSNP:371401737"
variation 4331
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="tttg"
/db_xref="dbSNP:34068251"
variation 4381
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:182959183"
variation 4440
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:371509832"
STS 4532..4602
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/standard_name="D4S2569E"
/db_xref="UniSTS:19561"
STS 4540..4710
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/standard_name="SHGC-24108"
/db_xref="UniSTS:4790"
variation 4579
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:150914060"
variation 4602
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:376838121"
variation 4623
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:185688185"
variation 4677
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:3943"
variation 4760
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1509617"
variation 4833..4834
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="ag"
/db_xref="dbSNP:368119740"
variation 4876
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1043853"
variation 4938
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:75854018"
variation 5051
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:13141591"
variation 5071
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:371683638"
variation 5167
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1139697"
variation 5227
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:114932838"
variation 5276
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:12294"
variation 5419
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:12650486"
variation 5425
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1043862"
variation 5551
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:139417946"
variation 5610
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:149975822"
variation 5614
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:190144928"
variation 5627
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:369868118"
variation 5638
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:115398076"
STS 5780..5874
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/standard_name="D9S1746E"
/db_xref="UniSTS:153922"
STS 5813..5942
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/standard_name="SHGC-59267"
/db_xref="UniSTS:57977"
variation 5840
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:140772832"
variation 5939
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:7285"
polyA_signal 5949..5954
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
polyA_signal 5953..5958
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
variation 5957
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:183448943"
polyA_site 5976
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
polyA_site 5980
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
ORIGIN
gtgtcctgggtcgggggtggggcgagggagagccaggaggcggaagttcccgcgggcggtggggacggcgccctcaccgcgagtcacttgtcagcccttgtctgaggcggaggcagccccgcgccgcgccggacccgagcatatttcattttctgtcattggactttgagccattagaaccatgagcaactacagtgtgtcactggttggcccagctccttggggtttccggctgcagggcggtaaggatttcaacatgcctctgacaatctctagtagcatctgctgcacccaagcctgagccggttcctgttcaaaagggagaacctaaagaagtagttaaacctgtgcccattacatctcctgctgtgtccaaagtcacttccacaaacaacatggcctacaataaggcaccacggccttttggttctgtgtcttcaccaaaagtcacatccatcccatcaccatcgtctgccttcaccccagcccatgcgaccacctcatcacatgcttccccttcacccgtggctgccgtcactcctcccctgttcgctgcatctggactgcatgctaatgccaatcttagtgctgaccagtctccatctgcactgagcgctggtaaaactgcagttaatgtcccacggcagcccacagtcaccagcgtgtgttccgagacttctcaggagctagcagagggacagagaagaggatcccagggtgacagtaaacagcaaaatggcccaccaagaaaacacattgtggagcgctatacagagttttatcatgtacccactcacagtgatgccagcaagaagagactgattgaggatactgaagactggcgtccaaggactggaacaactcagtctcgctctttccgaatccttgcccagatcactgggactgaacatttgaaagaatctgaagccgataatacaaagaaggcaaataactctcaggagccttctccgcagttggcttcctcggtagcttccacacggagcatgcccgagagcctggacagcccaacctctggcagaccaggggttaccagcctcacaactgcagctgccttcaagcctgtaggatccactggcgtcatcaagtcaccaagctggcaacggccaaaccaaggagtaccttccactggaagaatctcaaacagcgctacttactcaggatcagtggcaccagccaactcagctttgggacaaacccagccaagtgaccaggacactttagtgcaaagagctgagcacattccagcagggaaacgaactccgatgtgcgcccattgtaaccaggtcatcagaggaccattcttagtggcactggggaaatcttggcacccagaagaattcaactgcgctcactgcaaaaatacaatggcctacattggatttgtagaggagaaaggagccctgtattgtgagctgtgctatgagaaattctttgcccctgaatgtggtcgatgccaaaggaagatccttggagaagtcatcagtgcgttgaaacaaacttggcatgtttcctgttttgtgtgtgtagcctgtggaaagcccattcggaacaatgtttttcacttggaggatggtgaaccctactgtgagactgattattatgccctctttggtactatatgccatggatgtgaatttcccatagaagctggtgacatgttcctggaagctctgggctacacctggcatgacacttgctttgtatgctcagtgtgttgtgaaagtttggaaggtcagacctttttctccaagaaggacaagcccctgtgtaagaaacatgctcattctgtgaatttttgaaagtcaacagttcaggagaagagaaggaatttgaagagaaaaaggaaaattaaaattactaattaatttttagattcaatatttatatggagttttgaaaaataatagtggccctgaaggaataaattccagctttaaaaaccaagtctgaggaaatatttggcttcataaagtaaagagacggtttggcatttattattactttttcctgtattttatgcccataaaataagctttataaaaaccaatttcctgatggactattaaattcatcttagaataaattagtgaagaatttaattttagaataaataatccaatctgaaataattataccttctttccttgttaggtagttatgagtaaatctgcaaaaggcaatgaaaatgccttaaattttatcaataacagaattattgtatttaaaaaaaaactaatacttatctttaaaatagtaaataggattttaaacagagaattttatcagtaataggtgtcagtttttaaaaaattgcttgtaggctgagcgcggtggctcacgcctgtaatcccagcactttgggaggccaaggtgggtggaccacatgaggtcaggagtttgagatcagcctggccaacatggtgaaaccccatctctactaaaaatacaaaaattagccggacgcagtggcacgcgcctgtaatcccagctactcaagaggctgaggcacgagaatcacttgaacccgggagggagaggttgcagtgagccaagatcgtaccactgcactccagcctgggtgacagagtgagactctgtctccaaaaaaaaactttgcttgtatattatttttgccttacagtggatcattctagtaggaaaggacaataagattttttatcaaaatgtgtcatgccagtaagagatgttatattcttttctcatttcttccccacccaaaaataagctaccatatagcttataagtctcaaatttttgccttttactaaaatgtgattgtttctattcattgtgtatgcttcatcacctatattaggcaaattccatttttttcccttgtgctaaggtaaagatttaattaaataattttggcctctcatagttttctctctctttaaagagaataaatagagggccaggtgtggtggctcacgcctgtgatcccagcactttgggaggccaagacgggcggatcatgaggtcaagagatcaagatcatcctggccaacatggtgaaaccctgtctctactaaaaatacaaaaatgagctgggcatggtggggcgtgcctgtagtcccatgtacttgggaggctgaggcaggaaaattcttgaacccaggagacggaagttgcagtgagctgagatcacaccactgcactccagcctggtgacagagcaagactccggctcttaaaaaaaaaaaaaaaaaaaaaaaaagagagagagagaataaatagaaaagaatgtggctgggaattgtgaatcagaagattataccccccaattgtttttcaatccccttttctcaaataataaattagttaaatcagtttctgagttatgccactggctgatgaagagttgagaggtctctttgcagaatgatctttttgtttcgttttgtttcttcttctgcatttaaaaattaaaagattggtttgaggatgtgatgaaattgagactttttgtggttttctctcaataataagtgaaccaatttcaaatgtgatcacaaagtttggaaagcttttattcacagaggttgggtagtgttgggaggggagtttaattactcagattggcctgttatttgatttcctcctttgggaaaagaattatgtagataccacatggagacagggaaacaattgtggtaaaactgtggatcctgttgctatttgcccagtgagaaaacagattctggtatttgatttggtttttctctttgtttccagaatggatgaaagtccatgaacctcctaagttataatttaaatttgtttggggcaaggtgattttatagtcgagacagagccctaggtccttcctgccccatcactcacttacgacatcacttccattgtgtgcatgtttgttatagaggaggttttaggctacaatatttgtttaacctccctaagaactttcaaggcatctgtcctgaaagctgttaatttatggtctagcagatttatattatatgcagataataattaactggggataaaagaatggcaaggggtgacacaaagtagcaaactgaatacttctccaatagcaaccccaagctacctcctcaccctgcatcttggagggaggcaggaaatttcttttgaaataaagtgctggagctgaattctgcattatttatcgttgctgctgaaaccacctataaaagacttgctggctaatgtgcattgtcatataatgtacactgtcacatctttacagtcttgtatgttatagaatacaaaataagttgatggttttgtttggtgtgagctttttgtttgtttgtttagttttgccttcataggttatatgccaagatagtatttgataagtcaatgacatttggatgttttcttcaaagaattttatttgacccagatttcttataaagttatcttacattaaggatgtcattttcatcagaccttctttctacatattattcatgaagcataatgttgcatttctccaaattttatgcctgaaagggtagtgttgcttcctaaggtatcatgttgtctttgtgctttgtccatctcttccgtggcgaagctttatatctgttcctaaaacagttaatcctgtgaaataaatattgaacataatccagaagaatctctctgtttcccttggggaatgccatatttaattcaccagcagtaatcctttaataactggcagagcactttattcttctggtgagctccctgaatatttatttttctgattataaattttctatattagtagcattttttaattattacttcttcactatagagcatttacttttagtctctagatgtatattttggaatgctgtacttggcataacatagattaaaatcataatgcatgactaaaaactccttggatttatttcccattttaaaatttttagcggtaagttcagatttataatctttctctagacttccatggtctgaatgttgcctgctgaagtagcaacctaaaaagtatcccctgcttatgcttgtccagttggccctccatgtccataggcttcgcatctgtgattcagcccactgtgggtcaaaaatatttggggaaaaaaatggatggttgcgcctttgctgaacatgtacaaacttttttttgtcattaaacaatatagtataacaactatttacaaagcatttacattgtattagctattataggtaatctagagatgatttaaagtgtatggtaggatgtgcataggttatatgcaaatactacaccattttctataagggacttgaacatcatggactttagtatcctagggggttcttggaacccatcacccataggggcaccataggacaactatagtaccgtgtttatttcctattaattcaggttccgtttagagtctaaaactaaaacctaatcatttagtcacagtgtaaaaacaaatggaaataacagctcaaatcttcaaaatattactatagcattatgtttaaaataatctacaacaaaaatgtaccattttcaagcagtactacattaggagcccttttatagaaaataatttcttctttacccccgttccagtgtgaatctagtattctgttaacatttgtgtggcatttggagtttgtcatccccattgaagggagagccttctcagacatgaagcaagggaaacatactgaatagttttacacaaatttgatctggcttccatttgtccccctcatttcccaaatgtttaaatgtattggatttggattctcaatgtataagttgccttatctgttaatgtctatcttctgtctctttaattttgtatatctgctgttttgcttttggatacattttctaattagaagtcacatgataaatataatcagtatagtaataataccataatgtgcacatactcaataaataaatgactgcattgttgtaaatgag
//
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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