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2024-04-20 17:36:17, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001032283 4186 bp mRNA linear PRI 07-JUL-2013
DEFINITION Homo sapiens thymopoietin (TMPO), transcript variant 2, mRNA.
ACCESSION NM_001032283
VERSION NM_001032283.2 GI:296434314
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 4186)
AUTHORS Ward,M.C., van der Watt,P.J., Tzoneva,G. and Leaner,V.D.
TITLE Deregulated LAP2alpha expression in cervical cancer associates with
aberrant E2F and p53 activities
JOURNAL IUBMB Life 63 (11), 1018-1026 (2011)
PUBMED 21990273
REMARK GeneRIF: this study provides evidence for elevated LAP2alpha
expression in cervical cancer and suggests that E2F and p53
activities associate with the positive and negative regulation of
LAP2alpha expression, respectively
REFERENCE 2 (bases 1 to 4186)
AUTHORS Bailey SD, Xie C, Do R, Montpetit A, Diaz R, Mohan V, Keavney B,
Yusuf S, Gerstein HC, Engert JC and Anand S.
CONSRTM DREAM investigators
TITLE Variation at the NFATC2 locus increases the risk of
thiazolidinedione-induced edema in the Diabetes REduction
Assessment with ramipril and rosiglitazone Medication (DREAM) study
JOURNAL Diabetes Care 33 (10), 2250-2253 (2010)
PUBMED 20628086
REMARK GeneRIF: Observational study of gene-disease association,
gene-environment interaction, and pharmacogenomic / toxicogenomic.
(HuGE Navigator)
REFERENCE 3 (bases 1 to 4186)
AUTHORS Davila,S., Froeling,F.E., Tan,A., Bonnard,C., Boland,G.J.,
Snippe,H., Hibberd,M.L. and Seielstad,M.
TITLE New genetic associations detected in a host response study to
hepatitis B vaccine
JOURNAL Genes Immun. 11 (3), 232-238 (2010)
PUBMED 20237496
REMARK GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
REFERENCE 4 (bases 1 to 4186)
AUTHORS Craig,D.W., Millis,M.P. and DiStefano,J.K.
TITLE Genome-wide SNP genotyping study using pooled DNA to identify
candidate markers mediating susceptibility to end-stage renal
disease attributed to Type 1 diabetes
JOURNAL Diabet. Med. 26 (11), 1090-1098 (2009)
PUBMED 19929986
REMARK GeneRIF: Observational study and genome-wide association study of
gene-disease association. (HuGE Navigator)
REFERENCE 5 (bases 1 to 4186)
AUTHORS Talmud PJ, Drenos F, Shah S, Shah T, Palmen J, Verzilli C, Gaunt
TR, Pallas J, Lovering R, Li K, Casas JP, Sofat R, Kumari M,
Rodriguez S, Johnson T, Newhouse SJ, Dominiczak A, Samani NJ,
Caulfield M, Sever P, Stanton A, Shields DC, Padmanabhan S,
Melander O, Hastie C, Delles C, Ebrahim S, Marmot MG, Smith GD,
Lawlor DA, Munroe PB, Day IN, Kivimaki M, Whittaker J, Humphries SE
and Hingorani AD.
CONSRTM ASCOT investigators; NORDIL investigators; BRIGHT Consortium
TITLE Gene-centric association signals for lipids and apolipoproteins
identified via the HumanCVD BeadChip
JOURNAL Am. J. Hum. Genet. 85 (5), 628-642 (2009)
PUBMED 19913121
REMARK GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
REFERENCE 6 (bases 1 to 4186)
AUTHORS Hara,H., Hayashi,K., Ohta,K., Itoh,N. and Ohta,M.
TITLE A new thymopoietin precursor gene from human thymus
JOURNAL Biochem. Mol. Biol. Int. 34 (5), 927-933 (1994)
PUBMED 7703909
REFERENCE 7 (bases 1 to 4186)
AUTHORS Harris,C.A., Andryuk,P.J., Cline,S., Chan,H.K., Natarajan,A.,
Siekierka,J.J. and Goldstein,G.
TITLE Three distinct human thymopoietins are derived from alternatively
spliced mRNAs
JOURNAL Proc. Natl. Acad. Sci. U.S.A. 91 (14), 6283-6287 (1994)
PUBMED 7517549
REFERENCE 8 (bases 1 to 4186)
AUTHORS Heavner,G.A., Audhya,T. and Goldstein,G.
TITLE Peptide analogs of thymopentin distinguish distinct thymopoietin
receptor specificities on two human T cell lines
JOURNAL Regul. Pept. 27 (2), 257-262 (1990)
PUBMED 2158125
REFERENCE 9 (bases 1 to 4186)
AUTHORS Fuccello,A., Audhya,T., Talle,M.A. and Goldstein,G.
TITLE Immunoassay for bovine serum thymopoietin: discrimination from
splenin by monoclonal antibodies
JOURNAL Arch. Biochem. Biophys. 228 (1), 292-298 (1984)
PUBMED 6364989
REFERENCE 10 (bases 1 to 4186)
AUTHORS Twomey,J.J., Goldstein,G., Lewis,V.M., Bealmear,P.M. and Good,R.A.
TITLE Bioassay determinations of thymopoietin and thymic hormone levels
in human plasma
JOURNAL Proc. Natl. Acad. Sci. U.S.A. 74 (6), 2541-2545 (1977)
PUBMED 302007
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from DB239672.1, BC053675.1,
AB209297.1, BQ232508.1, BG676381.1, BM802949.1, AI055921.1 and
AA992204.1.
This sequence is a reference standard in the RefSeqGene project.
On May 21, 2010 this sequence version replaced gi:73760404.
Summary: The protein encoded by this gene resides in the nucleus
and may play a role in the assembly of the nuclear lamina, and thus
help maintain the structural organization of the nuclear envelope.
It may function as a receptor for the attachment of lamin filaments
to the inner nuclear membrane. Mutations in this gene are
associated with dilated cardiomyopathy. Alternatively spliced
transcript variants encoding different isoforms have been noted for
this gene. [provided by RefSeq, May 2010].
Transcript Variant: This variant (2) differs at the 3' end compared
to variant 1, resulting in a shorter isoform (beta) with a distinct
C-terminus compared to isoform alpha.
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 :: BC053675.1, U09087.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025081, ERS025083 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-593 DB239672.1 1-593
594-2596 BC053675.1 540-2542
2597-2829 AB209297.1 2206-2438
2830-3101 BQ232508.1 73-344
3102-3126 AB209297.1 2492-2516
3127-3549 BG676381.1 204-626
3550-3941 BM802949.1 384-775
3942-4114 AI055921.1 4-176 c
4115-4186 AA992204.1 1-72 c
FEATURES Location/Qualifiers
source 1..4186
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="12"
/map="12q22"
gene 1..4186
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/note="thymopoietin"
/db_xref="GeneID:7112"
/db_xref="HGNC:11875"
/db_xref="HPRD:01777"
/db_xref="MIM:188380"
exon 1..574
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/inference="alignment:Splign:1.39.8"
variation 125
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="g"
/db_xref="dbSNP:186697764"
misc_feature 194..196
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/note="upstream in-frame stop codon"
variation 244
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:370309699"
variation 283
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:374345638"
variation 285
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="c"
/db_xref="dbSNP:377404642"
variation 294
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="t"
/db_xref="dbSNP:144959639"
CDS 296..1660
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/note="isoform beta is encoded by transcript variant 2;
LEM domain containing 4; lamina-associated polypeptide 2;
TP beta/gamma; TP alpha; thymopoietin-related peptide
isoform alpha; thymopoietin-related peptide isoforms
beta/gamma"
/codon_start=1
/product="thymopoietin isoform beta"
/protein_id="NP_001027454.1"
/db_xref="GI:73760405"
/db_xref="CCDS:CCDS31879.1"
/db_xref="GeneID:7112"
/db_xref="HGNC:11875"
/db_xref="HPRD:01777"
/db_xref="MIM:188380"
/translation="
MPEFLEDPSVLTKDKLKSELVANNVTLPAGEQRKDVYVQLYLQHLTARNRPPLPAGTNSKGPPDFSSDEEREPTPVLGSGAAAAGRSRAAVGRKATKKTDKPRQEDKDDLDVTELTNEDLLDQLVKYGVNPGPIVGTTRKLYEKKLLKLREQGTESRSSTPLPTISSSAENTRQNGSNDSDRYSDNEEDSKIELKLEKREPLKGRAKTPVTLKQRRVEHNQSYSQAGITETEWTSGSSKGGPLQALTRESTRGSRRTPRKRVETSEHFRIDGPVISESTPIAETIMASSNESLVVNRVTGNFKHASPILPITEFSDIPRRAPKKPLTRAEVGEKTEERRVERDILKEMFPYEASTPTGISASCRRPIKGAAGRPLELSDFRMEESFSSKYVPKYVPLADVKSEKTKKGRSIPVWIKILLFVVVAVFLFLVYQAMETNQVNPFSNFLHVDPRKSN
"
misc_feature 296..1525
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (P42167.2);
Region: Nucleoplasmic (Potential)"
misc_feature 299..445
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/note="Thymopoietin protein; Region: Thymopoietin;
pfam08198"
/db_xref="CDD:149323"
misc_feature 440..619
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (P42167.2);
Region: Linker"
misc_feature 491..493
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 491..493
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 494..496
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 515..517
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 530..532
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 623..>709
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/note="LEM domain; Region: LEM; cl02649"
/db_xref="CDD:155036"
misc_feature 707..1024
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (P42167.2);
Region: NAKAP95-binding N"
misc_feature 755..757
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 761..763
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 767..769
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 770..772
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 773..775
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 785..787
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 824..826
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P42167.2); phosphorylation site"
misc_feature 833..835
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P42167.2); phosphorylation site"
misc_feature 833..835
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 842..844
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 845..847
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P42167.2); phosphorylation site"
misc_feature 845..847
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 917..919
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphothreonine; propagated from
UniProtKB/Swiss-Prot (P42167.2); phosphorylation site"
misc_feature 926..928
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphothreonine; propagated from
UniProtKB/Swiss-Prot (P42167.2); phosphorylation site"
misc_feature 1088..1090
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P42167.2); phosphorylation site"
misc_feature 1169..1171
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P42167.2); phosphorylation site"
misc_feature 1190..1408
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (P42167.2);
Region: Binds lamins B"
misc_feature 1193..1417
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (P42167.2);
Region: NAKAP95-binding C"
misc_feature 1211..1213
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P42167.2); phosphorylation site"
misc_feature 1211..1213
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1229..1231
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphothreonine; propagated from
UniProtKB/Swiss-Prot (P42167.2); phosphorylation site"
misc_feature 1238..1240
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P42167.2); phosphorylation site"
misc_feature 1379..1381
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P42167.2); phosphorylation site"
misc_feature 1427..1429
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1448..1450
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P42167.2); phosphorylation site"
misc_feature 1526..1597
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (P42167.2);
transmembrane region"
variation 308
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:149067616"
variation 322
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="g"
/replace="t"
/db_xref="dbSNP:190115355"
variation 367
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="g"
/replace="t"
/db_xref="dbSNP:201960762"
variation 379
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:199549942"
variation 382
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:114074541"
variation 409
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="c"
/db_xref="dbSNP:200619128"
variation 411
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:374578351"
variation 421
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:372903897"
variation 423
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:371427406"
variation 455
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:376363219"
variation 456..457
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="cc"
/replace="g"
/db_xref="dbSNP:368465288"
variation 520
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:59027673"
variation 526
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:139576816"
variation 560
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="g"
/db_xref="dbSNP:200177466"
exon 575..701
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/inference="alignment:Splign:1.39.8"
variation 626
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:201838047"
variation 645
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:141387097"
variation 650
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="g"
/replace="t"
/db_xref="dbSNP:113967157"
variation 653
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="c"
/db_xref="dbSNP:200420073"
variation 665
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:375619307"
variation 676
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:370093524"
variation 677
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:200943582"
exon 702..860
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/inference="alignment:Splign:1.39.8"
variation 771
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:183244086"
variation 792
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="c"
/db_xref="dbSNP:147012167"
variation 829
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:200016687"
variation 852
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:200923649"
exon 861..958
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/inference="alignment:Splign:1.39.8"
STS 903..1024
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/standard_name="SHGC-58801"
/db_xref="UniSTS:94447"
variation 907
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="c"
/db_xref="dbSNP:377624930"
variation 931
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="g"
/db_xref="dbSNP:371253652"
variation 949
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:138298699"
exon 959..1078
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/inference="alignment:Splign:1.39.8"
variation 1072
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:200238614"
exon 1079..1174
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/inference="alignment:Splign:1.39.8"
variation 1101
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:142891873"
variation 1107
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="c"
/db_xref="dbSNP:190515788"
variation 1151
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:199594991"
STS 1152..1301
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/standard_name="RH48814"
/db_xref="UniSTS:39587"
variation 1154
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="g"
/db_xref="dbSNP:7133258"
exon 1175..1285
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/inference="alignment:Splign:1.39.8"
variation 1222
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="g"
/replace="t"
/db_xref="dbSNP:374561277"
variation 1244
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="t"
/db_xref="dbSNP:368800243"
variation 1275
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="g"
/db_xref="dbSNP:372379540"
exon 1286..1374
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/inference="alignment:Splign:1.39.8"
variation 1303
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace=""
/replace="g"
/db_xref="dbSNP:34204719"
variation 1319
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="t"
/db_xref="dbSNP:147928797"
variation 1339
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="g"
/db_xref="dbSNP:141552430"
exon 1375..4181
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/inference="alignment:Splign:1.39.8"
variation 1414
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:144913822"
variation 1438
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="g"
/replace="t"
/db_xref="dbSNP:373609093"
variation 1456
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:370301550"
variation 1472
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:199545670"
variation 1523..1524
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace=""
/replace="c"
/db_xref="dbSNP:34001294"
variation 1532
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:115843977"
variation 1562
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="g"
/replace="t"
/db_xref="dbSNP:368180278"
variation 1568..1569
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace=""
/replace="gtttttttt"
/db_xref="dbSNP:144209787"
variation 1576
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="g"
/replace="t"
/db_xref="dbSNP:1058288"
variation 1582
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="c"
/db_xref="dbSNP:200202696"
STS 1589..1780
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/standard_name="RH11218"
/db_xref="UniSTS:90434"
variation 1591
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:61744201"
variation 1592
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:368843309"
variation 1644
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="g"
/db_xref="dbSNP:200273530"
variation 1661
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:1058300"
variation 1665
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:140261783"
variation 1678
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:371223654"
variation 1765
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:7966614"
polyA_signal 1771..1776
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
variation 1775
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="c"
/db_xref="dbSNP:1802615"
polyA_site 1805
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
variation 1871
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:192775311"
variation 1947..1948
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace=""
/replace="a"
/db_xref="dbSNP:372357069"
variation 1948
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace=""
/replace="a"
/db_xref="dbSNP:35567478"
variation 2092
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="g"
/replace="t"
/db_xref="dbSNP:184293463"
variation 2113
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:188145139"
variation 2143
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:181982566"
variation 2213
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="t"
/db_xref="dbSNP:1058309"
variation 2221..2223
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace=""
/replace="tgt"
/db_xref="dbSNP:375546327"
variation 2231
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:11109526"
variation 2271
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:137958470"
variation 2285
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:371174437"
variation 2395
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:374141361"
STS 2447..2587
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/standard_name="WI-18798"
/db_xref="UniSTS:26994"
variation 2572
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:75544449"
STS 2662..3242
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/standard_name="GDB:631802"
/db_xref="UniSTS:158429"
STS 2663..2765
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/standard_name="D11S3114"
/db_xref="UniSTS:152207"
STS 2734..2873
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/standard_name="D16S325"
/db_xref="UniSTS:147089"
variation 2741
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="g"
/replace="t"
/db_xref="dbSNP:12816564"
STS 2747..2837
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/standard_name="D8S2279"
/db_xref="UniSTS:473907"
variation 2864
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="c"
/db_xref="dbSNP:186285844"
variation 2921..2922
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace=""
/replace="a"
/db_xref="dbSNP:200555771"
variation 2931
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="t"
/db_xref="dbSNP:189099847"
variation 2978
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="g"
/replace="t"
/db_xref="dbSNP:181561458"
variation 3009
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:149485655"
variation 3099
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:186744278"
variation 3100
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:191087791"
variation 3102
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:28535939"
variation 3115
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:183137615"
STS 3123..3241
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/standard_name="D10S2448"
/db_xref="UniSTS:474444"
variation 3175
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:186047886"
variation 3176
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="c"
/db_xref="dbSNP:7973946"
variation 3183
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:147137090"
variation 3211
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:3177178"
variation 3216
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="t"
/db_xref="dbSNP:138693048"
variation 3225
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:3177180"
variation 3244
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:143292209"
variation 3248
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="g"
/replace="t"
/db_xref="dbSNP:112838469"
variation 3259
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:189533759"
variation 3304..3307
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace=""
/replace="tgga"
/db_xref="dbSNP:374509575"
variation 3432
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="c"
/db_xref="dbSNP:373125491"
variation 3525
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:370919987"
variation 3536
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="g"
/replace="t"
/db_xref="dbSNP:371728742"
variation 3576
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:148592104"
variation 3608
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:142900397"
variation 3609
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:73140468"
variation 3646..3647
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace=""
/replace="aa"
/db_xref="dbSNP:57778879"
variation 3647..3648
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace=""
/replace="aa"
/db_xref="dbSNP:67347959"
variation 3701
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace=""
/replace="g"
/db_xref="dbSNP:71704696"
variation 3718
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="g"
/db_xref="dbSNP:1044435"
variation 3736
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="c"
/db_xref="dbSNP:183276162"
variation 3771..3774
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace=""
/replace="tttc"
/db_xref="dbSNP:368618126"
STS 3868..4073
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/standard_name="RH44347"
/db_xref="UniSTS:67628"
variation 3964..3966
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace=""
/replace="tta"
/db_xref="dbSNP:57900732"
STS 3966..4066
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/standard_name="WI-11271"
/db_xref="UniSTS:35646"
variation 3998
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:371446465"
variation 4006
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:369299135"
polyA_signal 4013..4018
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
variation 4030
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:1044514"
polyA_site 4041
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
variation 4071
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:200354667"
variation 4081
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="t"
/db_xref="dbSNP:150669486"
polyA_signal 4093..4098
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
polyA_site 4114
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
polyA_signal 4128..4133
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
variation 4128
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:34963912"
polyA_site 4181
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
ORIGIN
gttcttggggcgtgggcgaagcaggctgctcgcctcctgcctgtagtgtgtgggctggggttggtgcgagcttccagcttggccgcagttggttcgtagttcggctctggggtcttttgtgtccgggtctggcttggctttgtgtccgcgagtttttgttccgctccgcagcgctcttcccgggcaggagccgtgaggctcggaggcggcagcgcggtccccggccaggagcaagcgcgccggcgtgagcggcggcggcaaaggctgtggggagggggcttcgcagatccccgagatgccggagttcctggaagacccctcggtcctgacaaaagacaagttgaagagtgagttggtcgccaacaatgtgacgctgccggccggggagcagcgcaaagacgtgtacgtccagctctacctgcagcacctcacggctcgcaaccggccgccgctccccgccggcaccaacagcaaggggcccccggacttctccagtgacgaagagcgcgagcccaccccggtcctcggctctggggccgccgccgcgggccggagccgagcagccgtcggcaggaaagccacaaaaaaaactgataaacccagacaagaagataaagatgatctagatgtaacagagctcactaatgaagatcttttggatcagcttgtgaaatacggagtgaatcctggtcctattgtgggaacaaccaggaagctatatgagaaaaagcttttgaaactgagggaacaaggaacagaatcaagatcttctactcctctgccaacaatttcttcttcagcagaaaatacaaggcagaatggaagtaatgattctgacagatacagtgacaatgaagaagactctaaaatagagctcaagcttgagaagagagaaccactaaagggcagagcaaagactccagtaacactcaagcaaagaagagttgagcacaatcagagctattctcaagctggaataactgagactgaatggacaagtggatcttcaaaaggcggacctctgcaggcattaactagggaatctacaagagggtcaagaagaactccaaggaaaagggtggaaacttcagaacattttcgtatagatggtccagtaatttcagagagtactcccatagctgaaactataatggcttcaagcaacgaatccttagttgtcaatagggtgactggaaatttcaagcatgcatctcctattctgccaatcactgaattctcagacatacccagaagagcaccaaagaaaccattgacaagagctgaagtgggagaaaaaacagaggaaagaagagtagaaagggatattcttaaggaaatgttcccctatgaagcatctacaccaacaggaattagtgctagttgccgcagaccaatcaaaggggctgcaggccggccattagaactcagtgatttcaggatggaggagtctttttcatctaaatatgttcctaagtatgttcccttggcagatgtcaagtcagaaaagacaaaaaagggacgctccattcccgtatggataaaaattttgctgtttgttgttgtggcagtttttttgtttttggtctatcaagctatggaaaccaaccaagtaaatcccttctctaattttcttcatgttgaccctagaaaatccaactgaatggtatctctttggcacgttcaacttggtctcctattttcaataactgttgaaaaacatttgtgtacacttgttgactccaagaactaaaaataatgtgatttcgcctcaataaatgtagtatttcattgaaaagcaaacaaaatatatataaatggacttcattaaaatgtttttgaactttggactagtaggagatcactttgtgccatatgaataatcttttttagctctggaactttttgtaggctttatttttttaatgtgggcatcttatttcatttttgaaaaaatgtatatgttttttgtgtatttgggaaacgaagggtgaaacatggtagtataatgtgaagctacacatttaaatacttagaattcttacagaaaagattttaagaattattctctgctgaataaaaactgcaaatatgtgaaacataatgaaattcagtaagaggaaaagtaacttggttgtactttttgtaactgcaacaaagtttgatggtgtttatgaggaaaagtacagcaataatctcttctgtaacctttattaatagtaatgttgttgtagccctatcatactcactttttaagacacagtatcatgaaagtcctatttcagtaagacccatttacatacagtagatttttagcagagatcttttagtgtaacatacatattttagagaattgttggctagctgtacatgttttgaaaagctgtttagctagctataaggctataattggaaatttgtattttttatttacagcaaaacatttattcagtcatccagtttgctaccaaaatatgttttagataagtgtgtgtatgtttgtttagaagttagaaattgtaaacactggtcttatgtttcatttggattcattattgcattgtcttgttaccagaaacaaattttgccgagctttttttgccctatatttcccagcataatttgattagaaagtacaaaaagggccaggcgcggtggcttacgcctgtaatcccagcactttgggaggccagggcgggtggatcacgaggtcaagagatcaagaccatcctggccaacatggtgaaaccccgtctctactaaaaatacaaaaaaattagctgggcgtgatgatgtgcgcctgtagtcctgtctactagggagactgaggcaggagaatcgtttgaacccaggaggcagaggttgcagtgagcagagattacgtcactgcactgtagcctggcgacagagcaagactccatctcaaaaaaaataaaaaagtacaaaaagtacttgcttttatattacatcataagcagtagttaataaagttgtatactcttaagaggtgggcattatgattattttttatttttttattttttatgagatggagtctcactcttgtcacccagactgtagtgcagtggcacgatctgggctcgatgcaacctctgcctcccaggttcaagcaattttcctgcctcggcagagacggggtttcaccatgttggccaggctggtctcgaacccctgacctcaagtgatcagcccacctcagcttcccaaagtgctgggattacaggtgtgatccactgcacccggccggcattatgattttgtgtactcttgaaatggttatctttgtggatgatttttttttttaagctgaaacttacctcatgaataacttgattaaagtagtaggtgattaaaatttcaatagaatcaaatgagacaaaaattttaaactgactcatttgagtttcaactttacagtcattgaccataaagcacactaaaaatgtaagttatttttaaatacatctgaaataaaaatacttactaaaaaggaagaagccgaagatgtatatttagaccagcacacaattttgatttcaattagccttattctaatatttagcttttagatctttcatacacattttcacgtactttgcaattgagaccagaaagacttgtaggtctttctgcagaatgagtgggtccttgcaaagtgagtgggaaacttactcctagatcagaaatgtttgcctctctgagtaaaatgtttctttcagatgagccatagagggggcaccttttactcaacttttctttgttttgaaactttgtttcccatactgttttcagccttttgtttataattagaaattgtgagaagcttcatttagtgtttaaaaatgtggggagataaatcagacttaacatgtatgtaagatcaattcacttaaaagtatggtccaaatagcaaaaataggaccaggtgaaacatgtagtcattttttaaaaacatgtacttggtcttttgtgtgtgtctgttttattccattagaataaatgtgtccttgatgtaaatgcaaagcatttcttcctgattaaattgtagatgtagactttacaatataattcaataataaaaagtaattaacctctagttttgtcgttgcaataaatggttttcagatagcacaaactgtgatttctggataacatttcttatgaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:7112 -> Molecular function: GO:0003677 [DNA binding] evidence: IEA
GeneID:7112 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
GeneID:7112 -> Molecular function: GO:0005521 [lamin binding] evidence: TAS
GeneID:7112 -> Biological process: GO:0006355 [regulation of transcription, DNA-dependent] evidence: IEA
GeneID:7112 -> Cellular component: GO:0000785 [chromatin] evidence: IDA
GeneID:7112 -> Cellular component: GO:0005634 [nucleus] evidence: IDA
GeneID:7112 -> Cellular component: GO:0005634 [nucleus] evidence: TAS
GeneID:7112 -> Cellular component: GO:0005635 [nuclear envelope] evidence: TAS
GeneID:7112 -> Cellular component: GO:0005637 [nuclear inner membrane] evidence: IEA
GeneID:7112 -> Cellular component: GO:0016021 [integral to membrane] evidence: IEA
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