Home |
Help |
Advanced search
2024-04-26 14:49:33, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_003276 3690 bp mRNA linear PRI 07-JUL-2013
DEFINITION Homo sapiens thymopoietin (TMPO), transcript variant 1, mRNA.
ACCESSION NM_003276
VERSION NM_003276.2 GI:296434313
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 3690)
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 3690)
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 3690)
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 3690)
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 3690)
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 3690)
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 3690)
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 3690)
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 3690)
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 3690)
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, U09086.1,
BP423544.1, BU932961.1 and BM991833.1.
This sequence is a reference standard in the RefSeqGene project.
On May 21, 2010 this sequence version replaced gi:4507554.
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 (1) encodes the longest 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 :: U09086.1, AK315221.1 [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
594-2581 U09086.1 503-2490
2582-2894 BP423544.1 229-541
2895-3185 BU932961.1 295-585
3186-3690 BM991833.1 1-505 c
FEATURES Location/Qualifiers
source 1..3690
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="12"
/map="12q22"
gene 1..3690
/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..2380
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/note="isoform alpha is encoded by transcript variant 1;
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 alpha"
/protein_id="NP_003267.1"
/db_xref="GI:4507555"
/db_xref="CCDS:CCDS9064.1"
/db_xref="GeneID:7112"
/db_xref="HGNC:11875"
/db_xref="HPRD:01777"
/db_xref="MIM:188380"
/translation="
MPEFLEDPSVLTKDKLKSELVANNVTLPAGEQRKDVYVQLYLQHLTARNRPPLPAGTNSKGPPDFSSDEEREPTPVLGSGAAAAGRSRAAVGRKATKKTDKPRQEDKDDLDVTELTNEDLLDQLVKYGVNPGPIVGTTRKLYEKKLLKLREQGTESRSSTPLPTISSSAENTRQNGSNDSDRYSDNEEGKKKEHKKVKSTRDIVPFSELGTTPSGGGFFQGISFPEISTRPPLGSTELQAAKKVHTSKGDLPREPLVATNLPGRGQLQKLASERNLFISCKSSHDRCLEKSSSSSSQPEHSAMLVSTAASPSLIKETTTGYYKDIVENICGREKSGIQPLCPERSHISDQSPLSSKRKALEESESSQLISPPLAQAIRDYVNSLLVQGGVGSLPGTSNSMPPLDVENIQKRIDQSKFQETEFLSPPRKVPRLSEKSVEERDSGSFVAFQNIPGSELMSSFAKTVVSHSLTTLGLEVAKQSQHDKIDASELSFPFHESILKVIEEEWQQVDRQLPSLACKYPVSSREATQILSVPKVDDEILGFISEATPLGGIQAASTESCNQQLDLALCRAYEAAASALQIATHTAFVAKAMQADISQAAQILSSDPSRTHQALGILSKTYDAASYICEAAFDEVKMAAHTMGNATVGRRYLWLKDCKINLASKNKLASTPFKGGTLFGGEVCKVIKKRGNKH
"
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 (P42166.2);
Region: Linker"
misc_feature 464..466
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphothreonine; propagated from
UniProtKB/Swiss-Prot (P42166.2); phosphorylation site"
misc_feature 470..472
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P42166.2); phosphorylation site"
misc_feature 491..493
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P42166.2); 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 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="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P42166.2); 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="Phosphothreonine; propagated from
UniProtKB/Swiss-Prot (P42166.2); 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="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P42166.2); 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; pfam03020"
/db_xref="CDD:145916"
misc_feature 755..757
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphothreonine; propagated from
UniProtKB/Swiss-Prot (P42166.2); phosphorylation site"
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="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P42166.2); 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="Phosphothreonine; propagated from
UniProtKB/Swiss-Prot (P42166.2); 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="Phosphothreonine; propagated from
UniProtKB/Swiss-Prot (P42166.2); 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 797..799
/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
(P42166.2); 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 863..883
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (P42166.2);
Region: Nuclear localization signal (Potential)"
misc_feature 1346..1348
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P42166.2); phosphorylation site"
misc_feature 1346..1348
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1355..1357
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P42166.2); phosphorylation site"
misc_feature 1403..1405
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P42166.2); phosphorylation site"
misc_feature 1565..1567
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P42166.2); phosphorylation site"
misc_feature 1676..2377
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/note="Lamina-associated polypeptide 2 alpha; Region:
LAP2alpha; pfam11560"
/db_xref="CDD:151996"
misc_feature 2261..2263
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/experiment="experimental evidence, no additional details
recorded"
/note="N6-acetyllysine; propagated from
UniProtKB/Swiss-Prot (P42166.2); acetylation site"
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..3672
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/inference="alignment:Splign:1.39.8"
variation 875
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:138259721"
variation 933
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:138938727"
variation 963
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:201119852"
variation 979
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:188308994"
variation 981
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:138790561"
variation 1008
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="g"
/replace="t"
/db_xref="dbSNP:35998138"
variation 1013
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:375903462"
variation 1041
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="g"
/db_xref="dbSNP:191275106"
variation 1044
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="t"
/db_xref="dbSNP:370585407"
variation 1062
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="t"
/db_xref="dbSNP:146364154"
variation 1089
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:368211058"
variation 1108
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:369897433"
variation 1116
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:139700737"
variation 1122
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:144465114"
variation 1149
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:146158243"
variation 1172
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="g"
/replace="t"
/db_xref="dbSNP:35645287"
variation 1174
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:370939324"
variation 1177
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:375249647"
variation 1180
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="t"
/db_xref="dbSNP:142500409"
variation 1181
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="g"
/replace="t"
/db_xref="dbSNP:201730568"
variation 1193
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:376074187"
variation 1204
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="g"
/replace="t"
/db_xref="dbSNP:369208265"
STS 1210..2199
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/standard_name="Tmpo"
/db_xref="UniSTS:507284"
variation 1220
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="g"
/db_xref="dbSNP:114939776"
variation 1232
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:139512723"
variation 1237
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:185083543"
variation 1245
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="g"
/db_xref="dbSNP:35969221"
variation 1259
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:377711296"
variation 1285
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:371441559"
variation 1289
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:57670957"
STS 1339..1478
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/standard_name="PMC310794P39"
/db_xref="UniSTS:272729"
variation 1343
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:200124801"
variation 1344
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:202106275"
variation 1345
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:147812883"
variation 1348
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:375628010"
variation 1369
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:141347778"
variation 1407
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:199943517"
variation 1443
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:202166461"
variation 1460
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="g"
/db_xref="dbSNP:147002330"
variation 1492
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:147635314"
variation 1509
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:149120802"
variation 1517
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:143232629"
variation 1538
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="g"
/replace="t"
/db_xref="dbSNP:200367787"
variation 1541
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:11838270"
variation 1551
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:370366685"
variation 1572
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:141443652"
variation 1576
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:377277295"
variation 1585
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:374855899"
variation 1600
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="g"
/db_xref="dbSNP:181830203"
variation 1604
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="g"
/db_xref="dbSNP:145703021"
variation 1624
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="t"
/db_xref="dbSNP:138388686"
variation 1626
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="g"
/db_xref="dbSNP:142981381"
variation 1653
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="g"
/db_xref="dbSNP:368161386"
variation 1657
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:371731646"
variation 1686
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:146132228"
variation 1693
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:143185150"
variation 1700
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="g"
/db_xref="dbSNP:373861992"
variation 1724
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:34301677"
variation 1729
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="g"
/db_xref="dbSNP:35761089"
variation 1766
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="g"
/replace="t"
/db_xref="dbSNP:80325832"
variation 1783
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:372248802"
variation 1834
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="g"
/replace="t"
/db_xref="dbSNP:143845319"
variation 1873
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:375056835"
variation 1886
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:199979773"
variation 1905
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:200717863"
variation 1927
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="t"
/db_xref="dbSNP:12316677"
variation 1955
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:144269053"
variation 1969
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:151318988"
variation 1986..1987
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace=""
/replace="c"
/db_xref="dbSNP:34406338"
variation 2004
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:147803339"
variation 2025
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:34150443"
variation 2026
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:200856956"
variation 2072
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:369840957"
variation 2090
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="g"
/db_xref="dbSNP:17459334"
variation 2097
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:376075320"
variation 2100
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:34983516"
STS 2103..2754
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/standard_name="TMPO_3873"
/db_xref="UniSTS:462590"
variation 2117
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="c"
/db_xref="dbSNP:140881399"
variation 2123
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:369379490"
variation 2124
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:150445385"
variation 2129
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:201929673"
variation 2136
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:367769644"
variation 2137
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:373227285"
variation 2173
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:377465206"
variation 2226
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:369785592"
variation 2244
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:138295270"
variation 2252
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:202035749"
variation 2263
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:201034441"
variation 2315
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:200419485"
variation 2363
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:17028450"
variation 2380
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:145677259"
variation 2406
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:371325939"
variation 2434
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="g"
/db_xref="dbSNP:372009555"
variation 2537
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="t"
/db_xref="dbSNP:113105753"
variation 2566
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:139018373"
variation 2620
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="g"
/db_xref="dbSNP:114931887"
variation 2634
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2043923"
variation 2661
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:189841238"
variation 2712
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:75569613"
variation 2717
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:79909726"
variation 2736
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:75460359"
variation 2750
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="t"
/db_xref="dbSNP:17028453"
variation 2789
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="t"
/db_xref="dbSNP:369534215"
variation 2826
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:181477122"
variation 2853
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:185280612"
variation 2865
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="t"
/db_xref="dbSNP:377237104"
variation 2904
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:79502085"
variation 2906
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:11109520"
variation 2928
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:373459649"
variation 3161
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="g"
/replace="t"
/db_xref="dbSNP:376889618"
variation 3355..3360
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace=""
/replace="ctgtat"
/db_xref="dbSNP:371536928"
variation 3365
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:141356917"
variation 3374
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:17028456"
STS 3462..3611
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/standard_name="STS-T25858"
/db_xref="UniSTS:194"
STS 3464..3657
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/standard_name="STS-T25858"
/db_xref="UniSTS:7104"
STS 3480..3649
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/standard_name="RH47529"
/db_xref="UniSTS:21038"
variation 3493
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="c"
/replace="t"
/db_xref="dbSNP:189746139"
variation 3552
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
/replace="a"
/replace="g"
/db_xref="dbSNP:150771350"
polyA_signal 3647..3652
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
polyA_site 3672
/gene="TMPO"
/gene_synonym="CMD1T; LAP2; LEMD4; PRO0868; TP"
ORIGIN
gttcttggggcgtgggcgaagcaggctgctcgcctcctgcctgtagtgtgtgggctggggttggtgcgagcttccagcttggccgcagttggttcgtagttcggctctggggtcttttgtgtccgggtctggcttggctttgtgtccgcgagtttttgttccgctccgcagcgctcttcccgggcaggagccgtgaggctcggaggcggcagcgcggtccccggccaggagcaagcgcgccggcgtgagcggcggcggcaaaggctgtggggagggggcttcgcagatccccgagatgccggagttcctggaagacccctcggtcctgacaaaagacaagttgaagagtgagttggtcgccaacaatgtgacgctgccggccggggagcagcgcaaagacgtgtacgtccagctctacctgcagcacctcacggctcgcaaccggccgccgctccccgccggcaccaacagcaaggggcccccggacttctccagtgacgaagagcgcgagcccaccccggtcctcggctctggggccgccgccgcgggccggagccgagcagccgtcggcaggaaagccacaaaaaaaactgataaacccagacaagaagataaagatgatctagatgtaacagagctcactaatgaagatcttttggatcagcttgtgaaatacggagtgaatcctggtcctattgtgggaacaaccaggaagctatatgagaaaaagcttttgaaactgagggaacaaggaacagaatcaagatcttctactcctctgccaacaatttcttcttcagcagaaaatacaaggcagaatggaagtaatgattctgacagatacagtgacaatgaagaaggaaagaagaaagaacacaagaaagtgaagtccactagggatattgttcctttttctgaacttggaactactccctctggtggtggattttttcagggtatttcttttcctgaaatctccacccgtcctcctttgggcagtaccgaactacaggcagctaagaaagtacatacttctaagggagacctacctagggagcctcttgttgccacaaacttgcctggcaggggacagttgcagaagttagcctctgaaaggaatttgtttatttcatgcaagtctagccatgataggtgtttagagaaaagttcttcgtcatcttctcagcctgaacacagtgccatgttggtctctactgcagcttctccttcactgattaaagaaaccaccactggttactataaagacatagtagaaaatatttgcggtagagagaaaagtggaattcaaccattatgtcctgagaggtcccatatttcagatcaatcgcctctctccagtaaaaggaaagcactagaagagtctgagagctcacaactaatttctccgccacttgcccaggcaatcagagattatgtcaattctctgttggtccagggtggggtaggtagtttgcctggaacttctaactctatgcccccactggatgtagaaaacatacagaagagaattgatcagtctaagtttcaagaaactgaattcctgtctcctccaagaaaagtccctagactgagtgagaagtcagtggaggaaagggattcaggttcctttgtggcatttcagaacatacctggatccgaactgatgtcttcttttgccaaaactgttgtctctcattcactcactaccttaggtctagaagtggctaagcaatcacagcatgataaaatagatgcctcagaactatcttttcccttccatgaatctattttaaaagtaattgaagaagaatggcagcaagttgacaggcagctgccttcactggcatgcaaatatccagtttcttccagggaggcaacacagatattatcagttccaaaagtagatgatgaaatcctagggtttatttctgaagccactccactaggaggtattcaagcagcctccactgagtcttgcaatcagcagttggacttagcactctgtagagcatatgaagctgcagcatcagcattgcagattgcaactcacactgcctttgtagctaaggctatgcaggcagacattagtcaagctgcacagattcttagctcagatcctagtcgtacccaccaagcgcttgggattctgagcaaaacatatgatgcagcctcatatatttgtgaagctgcatttgatgaagtgaagatggctgcccataccatgggaaatgccactgtaggtcgtcgatacctctggctgaaggattgcaaaattaatttagcttctaagaataagctggcttccactccctttaaaggtggaacattatttggaggagaagtatgcaaagtaattaaaaagcgtggaaataaacactagtaaaattaaggacaaaaagacatctatcttatctttcaggtactttatgccaacattttcttttctgttaaggttgttttagtttccagatagggctaattacaaaatgttaagcttctacccatcaaattacagtataaaagtaattgcctgtgtagaactacttgtcttttctaaagatttgcgtagataggaagcctggtacaaacaatttaacgctttctagatcacatattagtctctaagttgttttctgtttcctgctttacttatgtttttacaattctccaaaactaagaaaattctaattaggatataaggagtatttactgttcaatagaataatatgcatcctcctttatacctaggacagaattaaacatttgttacacattcagaacagtgatgttgttctttttgatacttttatctcagtatcttttcacgttccataacttgtccatatttttgctcatattttcttacttttctttgttatttattcatgtctgcaacatcaatcatagtagtctagatcaatgcaactcaaagcaccagtctacaaactgttacttatccacaggcaagataagcatgcacaagaatttaaatctagagatactttttaggtcaatgacaggatttgattttttagcaaaattttattaatagctaaagcaatgtattgatttacactctgatgcaagtaatttatctcttcattgactggtagcaaccaattcatggaccagtaccatggaccacactttgagaaacacttctttggataataatagatatcctgggatagtgcatgttcaccatctattttgtcagataatggggccttttaaaaaataatactttgctttcatgatatattgtattttgtggaaagttaagtttagcaatatagactctaaaagcaaattaaatttttttaagccataagaaattatactatatcccagtatctgtatgtctgtataaagcagtgtattatcatgttttcatttctgtgattgtaagttaagagtcttaactgcagaggtattgtggaaagtagtagccttaagcataataaaatatggtctcttgggtactccctctggccattaccacattcttagattatatgtgtccatctttgcagctttctgagagtaattttatttgttgtcttctgaaatgtacatgtatacatgtacctactgagtgctatgtgatttttaaaaatgtattactgtagaatgcttctgcaaattcaataaagttgttaaatttgaacagtgaaaaaaaaaaaaaaaaaa
//
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
by
@meso_cacase at
DBCLS
This page is licensed under a Creative Commons Attribution 2.1 Japan License.