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2024-04-25 07:57:06, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001011513 5805 bp mRNA linear PRI 07-JUL-2013
DEFINITION Homo sapiens PDZ and LIM domain 5 (PDLIM5), transcript variant 2,
mRNA.
ACCESSION NM_001011513
VERSION NM_001011513.3 GI:374093200
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 5805)
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 5805)
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 5805)
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 5805)
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 5805)
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 5805)
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 5805)
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 5805)
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 5805)
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 5805)
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, AL832157.1,
AC108067.3 and AA614664.1.
On Jan 27, 2012 this sequence version replaced gi:197383099.
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 (2) uses an alternate in-frame
splice site in the 5' coding region, compared to variant 1,
resulting in an isoform (b) that is shorter than isoform a.
Sequence Note: This RefSeq record was created from transcript and
genomic sequence data to make the sequence consistent with the
reference genome assembly. The genomic coordinates used for the
transcript record were based on transcript alignments.
Publication Note: This RefSeq record includes a subset of the
publications that are available for this gene. Please see the Gene
record to access additional publications.
##Evidence-Data-START##
Transcript exon combination :: AL832157.1 [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
1-99 DA895978.1 1-99
100-1034 AL832157.1 2-936
1035-1035 AC108067.3 18603-18603
1036-1328 AL832157.1 938-1230
1329-1329 AC108067.3 35692-35692
1330-1446 AL832157.1 1232-1348
1447-1447 AC108067.3 40684-40684
1448-1704 AL832157.1 1350-1606
1705-5356 AC108067.3 42382-46033
5357-5805 AA614664.1 3-451 c
FEATURES Location/Qualifiers
source 1..5805
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="4"
/map="4q22"
gene 1..5805
/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..1645
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/note="isoform b is encoded by transcript variant 2;
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 b"
/protein_id="NP_001011513.3"
/db_xref="GI:374093201"
/db_xref="CCDS:CCDS47102.1"
/db_xref="GeneID:10611"
/db_xref="HGNC:17468"
/db_xref="MIM:605904"
/translation="
MSNYSVSLVGPAPWGFRLQGGKDFNMPLTISSLKDGGKAAQANVRIGDVVLSIDGINAQGMTHLEAQNKIKGCTGSLNMTLQRASAAPKPEPVPVQKPTVTSVCSETSQELAEGQRRGSQGDSKQQNGPPRKHIVERYTEFYHVPTHSDASKKRLIEDTEDWRPRTGTTQSRSFRILAQITGTEHLKESEADNTKKANNSQEPSPQLASSVASTRSMPESLDSPTSGRPGVTSLTTAAAFKPVGSTGVIKSPSWQRPNQGVPSTGRISNSATYSGSVAPANSALGQTQPSDQDTLVQRAEHIPAGKRTPMCAHCNQVIRGPFLVALGKSWHPEEFNCAHCKNTMAYIGFVEEKGALYCELCYEKFFAPECGRCQRKILGEVISALKQTWHVSCFVCVACGKPIRNNVFHLEDGEPYCETDYYALFGTICHGCEFPIEAGDMFLEALGYTWHDTCFVCSVCCESLEGQTFFSKKDKPLCKKHAHSVNF
"
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 1112..1267
/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(1112..1114,1121..1123,1172..1174,1181..1183,
1190..1192,1199..1201,1253..1255,1262..1264)
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/note="Zn binding site [ion binding]; other site"
/db_xref="CDD:188837"
misc_feature 1289..1444
/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(1289..1291,1298..1300,1349..1351,1358..1360,
1367..1369,1376..1378,1430..1432,1439..1441)
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/note="Zn binding site [ion binding]; other site"
/db_xref="CDD:188711"
misc_feature 1466..1630
/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(1466..1468,1475..1477,1532..1534,1541..1543,
1550..1552,1559..1561,1613..1615,1622..1624)
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/note="Zn binding site [ion binding]; other site"
/db_xref="CDD:188843"
variation 217
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:373896689"
variation 241
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:145981438"
variation 246
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:75841704"
exon 278..429
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 288
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:376270307"
variation 328
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:114621202"
variation 355
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:368230269"
variation 359
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:146671681"
variation 366
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:151288647"
variation 426
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:372541276"
exon 430..472
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 431
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:371717002"
variation 455
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:375778697"
variation 456
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:200495769"
variation 457
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:145853286"
exon 473..564
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 538
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1056807"
variation 541
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1135006"
variation 549
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1135007"
variation 564
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1135008"
exon 565..737
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 570
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:375364739"
variation 590
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:201891054"
variation 591
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:141403934"
variation 620
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:150388657"
variation 653
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:202231060"
variation 669
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:113605096"
variation 673
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:115214197"
variation 676
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:11722955"
variation 691
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:11097431"
variation 721
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:371463583"
exon 738..774
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 754
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:202092014"
variation 765
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:115781887"
exon 775..962
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 795
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:146000883"
variation 796
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:139902919"
variation 810
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1064238"
variation 814
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:377407022"
variation 824
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:141653509"
variation 825
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:115018620"
variation 835
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:116241517"
variation 858
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:371181316"
variation 887
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:966845"
variation 898
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:116830271"
variation 908
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:368387152"
variation 923
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:370892974"
variation 947
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:374739373"
exon 963..1137
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 986
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:148409775"
variation 992
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:372735372"
variation 995
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:7690296"
variation 1006
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:375931613"
variation 1016
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:7690464"
variation 1023
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:115386065"
variation 1038
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:114201587"
variation 1082
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:369761799"
variation 1107
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:139413367"
variation 1108
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:373251894"
variation 1125
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:376503569"
exon 1138..1318
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 1175
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:201156978"
variation 1178
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:377346480"
variation 1188
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:145633341"
variation 1192
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:201013535"
variation 1193
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:200640873"
variation 1203
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:373850074"
variation 1219
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:147724105"
variation 1229
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:142522131"
exon 1319..1439
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 1325
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:144752025"
variation 1329
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:13107595"
variation 1391
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:148939806"
variation 1393
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:200822536"
exon 1440..1555
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 1451
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:114255444"
variation 1453
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:143660655"
variation 1462
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:148074454"
variation 1465
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:115802510"
variation 1476
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:374091168"
variation 1486
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:140894265"
variation 1497
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:367629922"
variation 1522
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:144847144"
variation 1524
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:114713699"
exon 1556..5805
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/inference="alignment:Splign:1.39.8"
variation 1563
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:201782564"
variation 1572
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:377023412"
variation 1581
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:141719357"
variation 1617
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:201326456"
variation 1624
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:146226694"
variation 1629
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:76352571"
variation 1652
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1056772"
variation 1679
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:372012549"
variation 1827
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:114319350"
variation 1900
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:189650582"
variation 2070
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="a"
/db_xref="dbSNP:33961001"
variation 2168
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:56746297"
variation 2175
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1802345"
STS 2188..2981
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/standard_name="D10S2448"
/db_xref="UniSTS:474444"
STS 2320..2402
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/standard_name="L18426"
/db_xref="UniSTS:34648"
variation 2377
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1134967"
variation 2378
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:374940031"
variation 2384
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:180795923"
variation 2414
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:141426145"
STS 2415..2826
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/standard_name="L17705"
/db_xref="UniSTS:66091"
variation 2423
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:370215027"
variation 2442
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1056773"
STS 2475..2597
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/standard_name="SHGC-67609"
/db_xref="UniSTS:54969"
variation 2476
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:377344916"
variation 2500
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:187628494"
variation 2513
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:137892930"
variation 2568
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:62316494"
variation 2651
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:14082"
variation 2693
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="t"
/db_xref="dbSNP:11339365"
variation 2699
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:201037096"
variation 2706
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:10590"
variation 2742
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:74599592"
variation 2832
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1134984"
variation 3060
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="a"
/replace="aaaaaaaa"
/db_xref="dbSNP:10706955"
variation 3077..3084
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="aaaaaaa"
/db_xref="dbSNP:71581598"
variation 3084
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="a"
/replace="aaaaaaaa"
/db_xref="dbSNP:11365933"
variation 3085..3087
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="gag"
/db_xref="dbSNP:141722289"
variation 3085
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:55845770"
variation 3087
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:58524187"
variation 3102
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:28709926"
variation 3144
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="c"
/db_xref="dbSNP:201923550"
variation 3153
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="g"
/db_xref="dbSNP:78150373"
variation 3154
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="g"
/db_xref="dbSNP:10706956"
variation 3154
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:75694017"
variation 3280
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:368604816"
variation 3282
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:115970344"
variation 3495
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:141649481"
variation 3686
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:11550270"
variation 3767
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:146120619"
variation 3934
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:190760822"
variation 4001
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:140154582"
variation 4014
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1048627"
variation 4090
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:141563714"
variation 4102
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1043848"
variation 4153..4156
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="tttg"
/db_xref="dbSNP:148752622"
variation 4156..4159
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="gttt"
/db_xref="dbSNP:371401737"
variation 4156
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="tttg"
/db_xref="dbSNP:34068251"
variation 4206
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:182959183"
variation 4265
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:371509832"
STS 4357..4427
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/standard_name="D4S2569E"
/db_xref="UniSTS:19561"
STS 4365..4535
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/standard_name="SHGC-24108"
/db_xref="UniSTS:4790"
variation 4404
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:150914060"
variation 4427
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:376838121"
variation 4448
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:185688185"
variation 4502
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:3943"
variation 4585
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1509617"
variation 4658..4659
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace=""
/replace="ag"
/db_xref="dbSNP:368119740"
variation 4701
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1043853"
variation 4763
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:75854018"
variation 4876
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:13141591"
variation 4896
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:371683638"
variation 4992
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1139697"
variation 5052
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:114932838"
variation 5101
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:12294"
variation 5244
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:12650486"
variation 5250
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1043862"
variation 5376
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:139417946"
variation 5435
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:149975822"
variation 5439
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:190144928"
variation 5452
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:369868118"
variation 5463
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:115398076"
STS 5605..5699
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/standard_name="D9S1746E"
/db_xref="UniSTS:153922"
STS 5638..5767
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/standard_name="SHGC-59267"
/db_xref="UniSTS:57977"
variation 5665
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:140772832"
variation 5764
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:7285"
polyA_signal 5774..5779
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
polyA_signal 5778..5783
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
variation 5782
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:183448943"
polyA_site 5801
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
polyA_site 5805
/gene="PDLIM5"
/gene_synonym="ENH; ENH1; L9; LIM"
ORIGIN
gtgtcctgggtcgggggtggggcgagggagagccaggaggcggaagttcccgcgggcggtggggacggcgccctcaccgcgagtcacttgtcagcccttgtctgaggcggaggcagccccgcgccgcgccggacccgagcatatttcattttctgtcattggactttgagccattagaaccatgagcaactacagtgtgtcactggttggcccagctccttggggtttccggctgcagggcggtaaggatttcaacatgcctctgacaatctctagtctaaaagatggcggcaaggcagcccaggcaaatgtaagaataggcgatgtggttctcagcattgatggaataaatgcacaaggaatgactcatcttgaagcccagaataagattaagggttgtacaggctctttgaatatgactctgcaaagagcatctgctgcacccaagcctgagccggttcctgttcaaaagcccacagtcaccagcgtgtgttccgagacttctcaggagctagcagagggacagagaagaggatcccagggtgacagtaaacagcaaaatggcccaccaagaaaacacattgtggagcgctatacagagttttatcatgtacccactcacagtgatgccagcaagaagagactgattgaggatactgaagactggcgtccaaggactggaacaactcagtctcgctctttccgaatccttgcccagatcactgggactgaacatttgaaagaatctgaagccgataatacaaagaaggcaaataactctcaggagccttctccgcagttggcttcctcggtagcttccacacggagcatgcccgagagcctggacagcccaacctctggcagaccaggggttaccagcctcacaactgcagctgccttcaagcctgtaggatccactggcgtcatcaagtcaccaagctggcaacggccaaaccaaggagtaccttccactggaagaatctcaaacagcgctacttactcaggatcagtggcaccagccaactcagctttgggacaaacccagccaagtgaccaggacactttagtgcaaagagctgagcacattccagcagggaaacgaactccgatgtgcgcccattgtaaccaggtcatcagaggaccattcttagtggcactggggaaatcttggcacccagaagaattcaactgcgctcactgcaaaaatacaatggcctacattggatttgtagaggagaaaggagccctgtattgtgagctgtgctatgagaaattctttgcccctgaatgtggtcgatgccaaaggaagatccttggagaagtcatcagtgcgttgaaacaaacttggcatgtttcctgttttgtgtgtgtagcctgtggaaagcccattcggaacaatgtttttcacttggaggatggtgaaccctactgtgagactgattattatgccctctttggtactatatgccatggatgtgaatttcccatagaagctggtgacatgttcctggaagctctgggctacacctggcatgacacttgctttgtatgctcagtgtgttgtgaaagtttggaaggtcagacctttttctccaagaaggacaagcccctgtgtaagaaacatgctcattctgtgaatttttgaaagtcaacagttcaggagaagagaaggaatttgaagagaaaaaggaaaattaaaattactaattaatttttagattcaatatttatatggagttttgaaaaataatagtggccctgaaggaataaattccagctttaaaaaccaagtctgaggaaatatttggcttcataaagtaaagagacggtttggcatttattattactttttcctgtattttatgcccataaaataagctttataaaaaccaatttcctgatggactattaaattcatcttagaataaattagtgaagaatttaattttagaataaataatccaatctgaaataattataccttctttccttgttaggtagttatgagtaaatctgcaaaaggcaatgaaaatgccttaaattttatcaataacagaattattgtatttaaaaaaaaactaatacttatctttaaaatagtaaataggattttaaacagagaattttatcagtaataggtgtcagtttttaaaaaattgcttgtaggctgagcgcggtggctcacgcctgtaatcccagcactttgggaggccaaggtgggtggaccacatgaggtcaggagtttgagatcagcctggccaacatggtgaaaccccatctctactaaaaatacaaaaattagccggacgcagtggcacgcgcctgtaatcccagctactcaagaggctgaggcacgagaatcacttgaacccgggagggagaggttgcagtgagccaagatcgtaccactgcactccagcctgggtgacagagtgagactctgtctccaaaaaaaaactttgcttgtatattatttttgccttacagtggatcattctagtaggaaaggacaataagattttttatcaaaatgtgtcatgccagtaagagatgttatattcttttctcatttcttccccacccaaaaataagctaccatatagcttataagtctcaaatttttgccttttactaaaatgtgattgtttctattcattgtgtatgcttcatcacctatattaggcaaattccatttttttcccttgtgctaaggtaaagatttaattaaataattttggcctctcatagttttctctctctttaaagagaataaatagagggccaggtgtggtggctcacgcctgtgatcccagcactttgggaggccaagacgggcggatcatgaggtcaagagatcaagatcatcctggccaacatggtgaaaccctgtctctactaaaaatacaaaaatgagctgggcatggtggggcgtgcctgtagtcccatgtacttgggaggctgaggcaggaaaattcttgaacccaggagacggaagttgcagtgagctgagatcacaccactgcactccagcctggtgacagagcaagactccggctcttaaaaaaaaaaaaaaaaaaaaaaaaagagagagagagaataaatagaaaagaatgtggctgggaattgtgaatcagaagattataccccccaattgtttttcaatccccttttctcaaataataaattagttaaatcagtttctgagttatgccactggctgatgaagagttgagaggtctctttgcagaatgatctttttgtttcgttttgtttcttcttctgcatttaaaaattaaaagattggtttgaggatgtgatgaaattgagactttttgtggttttctctcaataataagtgaaccaatttcaaatgtgatcacaaagtttggaaagcttttattcacagaggttgggtagtgttgggaggggagtttaattactcagattggcctgttatttgatttcctcctttgggaaaagaattatgtagataccacatggagacagggaaacaattgtggtaaaactgtggatcctgttgctatttgcccagtgagaaaacagattctggtatttgatttggtttttctctttgtttccagaatggatgaaagtccatgaacctcctaagttataatttaaatttgtttggggcaaggtgattttatagtcgagacagagccctaggtccttcctgccccatcactcacttacgacatcacttccattgtgtgcatgtttgttatagaggaggttttaggctacaatatttgtttaacctccctaagaactttcaaggcatctgtcctgaaagctgttaatttatggtctagcagatttatattatatgcagataataattaactggggataaaagaatggcaaggggtgacacaaagtagcaaactgaatacttctccaatagcaaccccaagctacctcctcaccctgcatcttggagggaggcaggaaatttcttttgaaataaagtgctggagctgaattctgcattatttatcgttgctgctgaaaccacctataaaagacttgctggctaatgtgcattgtcatataatgtacactgtcacatctttacagtcttgtatgttatagaatacaaaataagttgatggttttgtttggtgtgagctttttgtttgtttgtttagttttgccttcataggttatatgccaagatagtatttgataagtcaatgacatttggatgttttcttcaaagaattttatttgacccagatttcttataaagttatcttacattaaggatgtcattttcatcagaccttctttctacatattattcatgaagcataatgttgcatttctccaaattttatgcctgaaagggtagtgttgcttcctaaggtatcatgttgtctttgtgctttgtccatctcttccgtggcgaagctttatatctgttcctaaaacagttaatcctgtgaaataaatattgaacataatccagaagaatctctctgtttcccttggggaatgccatatttaattcaccagcagtaatcctttaataactggcagagcactttattcttctggtgagctccctgaatatttatttttctgattataaattttctatattagtagcattttttaattattacttcttcactatagagcatttacttttagtctctagatgtatattttggaatgctgtacttggcataacatagattaaaatcataatgcatgactaaaaactccttggatttatttcccattttaaaatttttagcggtaagttcagatttataatctttctctagacttccatggtctgaatgttgcctgctgaagtagcaacctaaaaagtatcccctgcttatgcttgtccagttggccctccatgtccataggcttcgcatctgtgattcagcccactgtgggtcaaaaatatttggggaaaaaaatggatggttgcgcctttgctgaacatgtacaaacttttttttgtcattaaacaatatagtataacaactatttacaaagcatttacattgtattagctattataggtaatctagagatgatttaaagtgtatggtaggatgtgcataggttatatgcaaatactacaccattttctataagggacttgaacatcatggactttagtatcctagggggttcttggaacccatcacccataggggcaccataggacaactatagtaccgtgtttatttcctattaattcaggttccgtttagagtctaaaactaaaacctaatcatttagtcacagtgtaaaaacaaatggaaataacagctcaaatcttcaaaatattactatagcattatgtttaaaataatctacaacaaaaatgtaccattttcaagcagtactacattaggagcccttttatagaaaataatttcttctttacccccgttccagtgtgaatctagtattctgttaacatttgtgtggcatttggagtttgtcatccccattgaagggagagccttctcagacatgaagcaagggaaacatactgaatagttttacacaaatttgatctggcttccatttgtccccctcatttcccaaatgtttaaatgtattggatttggattctcaatgtataagttgccttatctgttaatgtctatcttctgtctctttaattttgtatatctgctgttttgcttttggatacattttctaattagaagtcacatgataaatataatcagtatagtaataataccataatgtgcacatactcaataaataaatgactgcattgttgtaaatgag
//
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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