2024-03-29 16:24:00, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001143852 3111 bp mRNA linear PRI 15-JUN-2013 DEFINITION Homo sapiens trichoplein, keratin filament binding (TCHP), transcript variant 2, mRNA. ACCESSION NM_001143852 VERSION NM_001143852.1 GI:219803768 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 3111) AUTHORS Luykx,J.J., Bakker,S.C., Lentjes,E., Neeleman,M., Strengman,E., Mentink,L., Deyoung,J., de Jong,S., Sul,J.H., Eskin,E., van Eijk,K., van Setten,J., Buizer-Voskamp,J.E., Cantor,R.M., Lu,A., van Amerongen,M., van Dongen,E.P., Keijzers,P., Kappen,T., Borgdorff,P., Bruins,P., Derks,E.M., Kahn,R.S. and Ophoff,R.A. TITLE Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid JOURNAL Mol. Psychiatry (2013) In press PUBMED 23319000 REMARK Publication Status: Available-Online prior to print REFERENCE 2 (bases 1 to 3111) AUTHORS Ibi,M., Zou,P., Inoko,A., Shiromizu,T., Matsuyama,M., Hayashi,Y., Enomoto,M., Mori,D., Hirotsune,S., Kiyono,T., Tsukita,S., Goto,H. and Inagaki,M. TITLE Trichoplein controls microtubule anchoring at the centrosome by binding to Odf2 and ninein JOURNAL J. Cell. Sci. 124 (PT 6), 857-864 (2011) PUBMED 21325031 REMARK GeneRIF: Trichoplein controls microtubule anchoring at the centrosome by binding to Odf2 and ninein. REFERENCE 3 (bases 1 to 3111) AUTHORS Cerqua,C., Anesti,V., Pyakurel,A., Liu,D., Naon,D., Wiche,G., Baffa,R., Dimmer,K.S. and Scorrano,L. TITLE Trichoplein/mitostatin regulates endoplasmic reticulum-mitochondria juxtaposition JOURNAL EMBO Rep. 11 (11), 854-860 (2010) PUBMED 20930847 REMARK GeneRIF: Trichoplein/mitostatin is a new regulator of mitochondria-endoplasmic reticulum juxtaposition. REFERENCE 4 (bases 1 to 3111) AUTHORS Vecchione,A., Fassan,M., Anesti,V., Morrione,A., Goldoni,S., Baldassarre,G., Byrne,D., D'Arca,D., Palazzo,J.P., Lloyd,J., Scorrano,L., Gomella,L.G., Iozzo,R.V. and Baffa,R. TITLE MITOSTATIN, a putative tumor suppressor on chromosome 12q24.1, is downregulated in human bladder and breast cancer JOURNAL Oncogene 28 (2), 257-269 (2009) PUBMED 18931701 REMARK GeneRIF: MITOSTATIN was found within a 3.2-kb transcript for an approximately 62 kDa mitochondrial protein with tumor suppressor activity. It inhibits cell growth, is proapoptotic and downregulates Hsp27. REFERENCE 5 (bases 1 to 3111) AUTHORS Tokumasu,F., Fairhurst,R.M., Ostera,G.R., Brittain,N.J., Hwang,J., Wellems,T.E. and Dvorak,J.A. TITLE Band 3 modifications in Plasmodium falciparum-infected AA and CC erythrocytes assayed by autocorrelation analysis using quantum dots JOURNAL J. Cell. Sci. 118 (PT 5), 1091-1098 (2005) PUBMED 15731014 REFERENCE 6 (bases 1 to 3111) AUTHORS Nishizawa,M., Izawa,I., Inoko,A., Hayashi,Y., Nagata,K., Yokoyama,T., Usukura,J. and Inagaki,M. TITLE Identification of trichoplein, a novel keratin filament-binding protein JOURNAL J. Cell. Sci. 118 (PT 5), 1081-1090 (2005) PUBMED 15731013 REMARK GeneRIF: trichoplein is a keratin 8/18-binding protein that may be involved in the organization of the apical network of keratin filaments and desmosomes in simple epithelial cells REFERENCE 7 (bases 1 to 3111) AUTHORS Yu,J.Q., Zhuang,H., Xiu,Y., El-Haddad,G., Kumar,R. and Alavi,A. TITLE Small urine leak after renal transplantation: detection by delayed 99mTc-DTPA renography--a case report JOURNAL J Nucl Med Technol 33 (1), 31-33 (2005) PUBMED 15731018 REFERENCE 8 (bases 1 to 3111) AUTHORS Panzegrau,B., Gordon,L. and Goudy,G.H. TITLE Outpatient therapeutic 131I for thyroid cancer JOURNAL J Nucl Med Technol 33 (1), 28-30 (2005) PUBMED 15731017 REFERENCE 9 (bases 1 to 3111) AUTHORS Katanick,S.L. CONSRTM Intersocietal Commission for the Accrediation of Nuclear Medicine Laboratories TITLE Fundamentals of ICANL accreditation JOURNAL J Nucl Med Technol 33 (1), 19-23 (2005) PUBMED 15731016 REFERENCE 10 (bases 1 to 3111) AUTHORS Seibert,J.A. and Boone,J.M. TITLE X-ray imaging physics for nuclear medicine technologists. Part 2: X-ray interactions and image formation JOURNAL J Nucl Med Technol 33 (1), 3-18 (2005) PUBMED 15731015 REMARK Review article COMMENT VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from AK092736.1, BC004285.1, AY007230.1 and AK000079.1. Transcript Variant: This variant (2) differs in the 5' UTR compared to variant 1. Variants 1 and 2 both encode the same protein. ##Evidence-Data-START## Transcript exon combination :: BC004285.1 [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 1-19 AK092736.1 1-19 20-2101 BC004285.1 1-2082 2102-3090 AY007230.1 2164-3152 3091-3111 AK000079.1 537-557 FEATURES Location/Qualifiers source 1..3111 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="12" /map="12q24.11" gene 1..3111 /gene="TCHP" /gene_synonym="TpMs" /note="trichoplein, keratin filament binding" /db_xref="GeneID:84260" /db_xref="HGNC:28135" /db_xref="MIM:612654" exon 1..153 /gene="TCHP" /gene_synonym="TpMs" /inference="alignment:Splign:1.39.8" variation 21 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:367828019" variation 55 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="g" /db_xref="dbSNP:71458311" variation 79 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="g" /db_xref="dbSNP:371282167" variation 108 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:113295369" CDS 154..1650 /gene="TCHP" /gene_synonym="TpMs" /note="mitostatin; tumor suppressor protein; mitochondrial protein with oncostatic activity" /codon_start=1 /product="trichoplein keratin filament-binding protein" /protein_id="NP_001137324.1" /db_xref="GI:219803769" /db_xref="CCDS:CCDS9137.1" /db_xref="GeneID:84260" /db_xref="HGNC:28135" /db_xref="MIM:612654" /translation="
MALPTLPSYWCSQQRLNQQLARQREQEARLRQQWEQNSRYFRMSDICSSKQAEWSSKTSYQRSMHAYQREKMKEEKRRSLEARREKLRQLMQEEQDLLARELEELRLSMNLQERRIREQHGKLKSAKEEQRKLIAEQLLYEHWKKNNPKLREMELDLHQKHVVNSWEMQKEEKKQQEATAEQENKRYENEYERARREALERMKAEEERRQLEDKLQAEALLQQMEELKLKEVEATKLKKEQENLLKQRWELERLEEERKQMEAFRQKAELGRFLRHQYNAQLSRRTQQIQEELEADRRILQALLEKEDESQRLHLARREQVMADVAWMKQAIEEQLQLERAREAELQMLLREEAKEMWEKREAEWARERSARDRLMSEVLTGRQQQIQEKIEQNRRAQEESLKHREQLIRNLEEVRELARREKEESEKLKSARKQELEAQVAERRLQAWEADQQEEEEEEEARRVEQLSDALLQQEAETMAEQGYRPKPYGHPKIAWN
" misc_feature 370..1647 /gene="TCHP" /gene_synonym="TpMs" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (Q9BT92.1); Region: Interaction with keratin proteins" misc_feature 928..1428 /gene="TCHP" /gene_synonym="TpMs" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (Q9BT92.1); Region: Trichohyalin/plectin homology domain" exon 154..341 /gene="TCHP" /gene_synonym="TpMs" /inference="alignment:Splign:1.39.8" variation 158 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:145451565" variation 167 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:148814070" variation 168 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:199913167" variation 173 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:200993715" variation 174 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:11539159" variation 186 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="g" /db_xref="dbSNP:184702109" variation 207 /gene="TCHP" /gene_synonym="TpMs" /replace="g" /replace="t" /db_xref="dbSNP:11615957" variation 214 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:375945839" variation 217 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:199775799" variation 224 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:373497072" variation 247 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:377471034" variation 263 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="c" /db_xref="dbSNP:200334528" variation 269 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:370844769" variation 283 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:202208566" variation 337 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:373557911" variation 338 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:375977597" exon 342..552 /gene="TCHP" /gene_synonym="TpMs" /inference="alignment:Splign:1.39.8" variation 381 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:202040061" variation 400 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:201548733" variation 425 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:144765573" variation 430 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:200027650" variation 471 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:138719299" variation 476 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:200713074" variation 513 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:140383594" variation 533 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:10774978" exon 553..609 /gene="TCHP" /gene_synonym="TpMs" /inference="alignment:Splign:1.39.8" variation 559 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:372219544" variation 572 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:149555348" variation 573 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:144237003" variation 584 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="t" /db_xref="dbSNP:199975433" variation 594 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="c" /db_xref="dbSNP:139102098" variation 597 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:139923209" variation 604 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:186211529" variation 605 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:199860940" variation 609 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:74416240" exon 610..678 /gene="TCHP" /gene_synonym="TpMs" /inference="alignment:Splign:1.39.8" variation 633 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="g" /db_xref="dbSNP:371039378" variation 640 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:147510018" exon 679..852 /gene="TCHP" /gene_synonym="TpMs" /inference="alignment:Splign:1.39.8" variation 691 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:373115835" variation 737 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:140118187" variation 747 /gene="TCHP" /gene_synonym="TpMs" /replace="g" /replace="t" /db_xref="dbSNP:142930724" variation 763 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="g" /db_xref="dbSNP:149507169" variation 774 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="g" /db_xref="dbSNP:192394776" variation 780 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:201972129" variation 804 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:150684855" variation 805 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:111431053" variation 808 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:377730872" variation 828 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:144756698" exon 853..965 /gene="TCHP" /gene_synonym="TpMs" /inference="alignment:Splign:1.39.8" variation 854 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:149867465" variation 860 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:141026601" variation 867 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="g" /db_xref="dbSNP:140898875" variation 896 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:143297503" variation 901 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="g" /db_xref="dbSNP:200322531" variation 902 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:74774614" variation 917 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:78378786" variation 920 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:76909214" variation 925 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:146721398" variation 934 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:142436521" variation 965 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:140322997" exon 966..1032 /gene="TCHP" /gene_synonym="TpMs" /inference="alignment:Splign:1.39.8" variation 977 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:143927087" variation 990 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:143562682" variation 995 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:201307226" variation 1007 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:367967992" variation 1016 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:150998390" variation 1017 /gene="TCHP" /gene_synonym="TpMs" /replace="g" /replace="t" /db_xref="dbSNP:202170610" exon 1033..1205 /gene="TCHP" /gene_synonym="TpMs" /inference="alignment:Splign:1.39.8" variation 1058 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:185515212" variation 1060 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="g" /db_xref="dbSNP:368484225" variation 1065 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:377341846" variation 1074 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:189930408" variation 1075 /gene="TCHP" /gene_synonym="TpMs" /replace="g" /replace="t" /db_xref="dbSNP:201132176" variation 1077 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:376133712" variation 1104 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:200187202" variation 1118 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:199750932" variation 1122 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:140889513" variation 1125 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:80217590" variation 1172 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:150191186" variation 1175 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:373850905" exon 1206..1287 /gene="TCHP" /gene_synonym="TpMs" /inference="alignment:Splign:1.39.8" variation 1226 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="g" /db_xref="dbSNP:139087904" variation 1258 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:143091693" variation 1264 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:147052884" variation 1267 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:200855746" variation 1268 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:368644707" variation 1269 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:138408335" variation 1284 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:148581914" exon 1288..1473 /gene="TCHP" /gene_synonym="TpMs" /inference="alignment:Splign:1.39.8" variation 1316 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:371270223" variation 1317 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="t" /db_xref="dbSNP:144342640" variation 1331 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:148794659" variation 1335 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="c" /db_xref="dbSNP:373009867" variation 1336 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:141600308" variation 1341 /gene="TCHP" /gene_synonym="TpMs" /replace="g" /replace="t" /db_xref="dbSNP:145932761" variation 1347 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:200720472" variation 1371 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:139831562" variation 1402 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:16940680" variation 1411 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:79799419" variation 1415 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:139095320" variation 1416 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:375988733" variation 1417 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:149921078" variation 1445 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:145032664" variation 1448 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:375710026" exon 1474..1617 /gene="TCHP" /gene_synonym="TpMs" /inference="alignment:Splign:1.39.8" variation 1484 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:149111537" variation 1500 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:143201598" variation 1540 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:372458088" variation 1541 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:147853930" variation 1543 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:201935991" variation 1548 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:375438947" variation 1584 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:368260508" variation 1609 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:141514320" variation 1610 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:376800013" variation 1617 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="g" /db_xref="dbSNP:147036260" exon 1618..3096 /gene="TCHP" /gene_synonym="TpMs" /inference="alignment:Splign:1.39.8" variation 1619 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:138352827" variation 1630 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:192103139" variation 1661 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:201796711" variation 1664 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:183112449" variation 1694 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:370977423" variation 1708 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:371507165" variation 1745 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="g" /db_xref="dbSNP:79886630" variation 1748 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:187402786" variation 1758 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:17680262" variation 1765 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:146125935" variation 1802 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:140150392" variation 1829 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:191871970" variation 1858 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="c" /db_xref="dbSNP:1045802" variation 1921 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:112152670" variation 1981 /gene="TCHP" /gene_synonym="TpMs" /replace="g" /replace="t" /db_xref="dbSNP:115197347" variation 2063 /gene="TCHP" /gene_synonym="TpMs" /replace="" /replace="a" /db_xref="dbSNP:56268430" variation 2136 /gene="TCHP" /gene_synonym="TpMs" /replace="g" /replace="t" /db_xref="dbSNP:371653953" variation 2204..2205 /gene="TCHP" /gene_synonym="TpMs" /replace="" /replace="g" /db_xref="dbSNP:35636733" variation 2223..2224 /gene="TCHP" /gene_synonym="TpMs" /replace="" /replace="g" /db_xref="dbSNP:34772666" variation 2397 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:182668261" variation 2407 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:143793004" variation 2408 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:146702695" variation 2653 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:117176903" variation 2701 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="t" /db_xref="dbSNP:186945991" variation 2787 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="t" /db_xref="dbSNP:56304404" variation 2914 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:192354734" variation 2919 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="t" /db_xref="dbSNP:184252549" variation 2926 /gene="TCHP" /gene_synonym="TpMs" /replace="g" /replace="t" /db_xref="dbSNP:76133847" STS 2940..3091 /gene="TCHP" /gene_synonym="TpMs" /standard_name="STS-R42792" /db_xref="UniSTS:67294" variation 2948 /gene="TCHP" /gene_synonym="TpMs" /replace="c" /replace="g" /db_xref="dbSNP:142517442" variation 2959 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="g" /db_xref="dbSNP:150919850" variation 2994 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="t" /db_xref="dbSNP:140889414" variation 3075 /gene="TCHP" /gene_synonym="TpMs" /replace="a" /replace="t" /db_xref="dbSNP:77606151" ORIGIN
gtcgtcgggctcgttgccggtgcaaacagggaggaaacagccggcgttgctgtagcgcgtctgggaattacaccgggggactggccggcccgcttcgtgcctgcgggaagtcgggccgggggactcttcggaaactccgagcctcagagaaatatggcgctcccgacgctgccgtcctactggtgcagccagcagcgcctgaatcagcagctagcacgacagcgagagcaggaggcccggcttcggcagcagtgggagcagaacagccgttacttcaggatgtctgacatctgcagctccaaacaggcagaatggagctctaaaacctcctaccagcggagcatgcatgcctatcagcgggagaagatgaaggaggagaagaggaggagtctggaggcccgacgggaaaagctcaggcagctcatgcaggaggagcaggacctgctggccagagaactggaggagctgaggctgagcatgaacttgcaggaaagaagaatccgggagcagcacgggaagctgaaatcagccaaagaagagcagaggaaactgattgctgaacaacttttgtacgaacactggaaaaagaacaacccgaaacttcgagagatggagctggaccttcaccagaagcatgtcgtaaactcttgggaaatgcagaaagaagaaaaaaaacagcaagaagccaccgcagagcaagagaacaaacggtatgaaaatgaatatgaaagggcccgaagggaggcgctagaaaggatgaaagctgaagaggagaggaggcagctggaggacaagctccaggccgaggcactgctgcaacagatggaggagctgaagctgaaggaggtggaggcgaccaaactaaagaaggagcaggagaatctgttgaagcagcggtgggagctagagaggctggaggaagagcgaaagcagatggaagccttccggcagaaggcagagctggggcgtttcttgagacatcagtataacgctcaactcagcagacgcacacagcagatccaagaggagctggaggcagacaggcggatcctgcaggccctcctcgagaaggaggacgagagccagcgcctccacctggccaggcgggagcaggtcatggccgatgtggcctggatgaagcaggccattgaggagcagctgcagctggagcgggcgcgggaggcagagctgcagatgctgctgagggaggaggccaaggagatgtgggaaaagagagaggcagagtgggcccgagagcgcagcgcacgggacagactgatgagcgaggttctgacagggagacaacagcaaatacaagagaagattgagcagaaccgacgggcacaagaggaatccctgaaacacagggagcaacttattcgaaatcttgaggaggtgagagagttggctcgtcgcgagaaagaggagagtgaaaagctgaaatcggccaggaagcaggagctggaagcccaggttgcagagcgccggctgcaggcatgggaagcagaccagcaggaggaggaggaagaggaggaggcccggcgggtcgagcagctctcagatgccctgctgcagcaggaggcggagactatggctgagcagggctaccggcctaagccttacggacatccaaaaattgcttggaactgacttcatgggtaccataagtacagagaacaagggatgctgaggcttctgatcccagccgccaggcagttttacagggctctgttaacagtaagtgcccggggcactgtcagatggctcagcagtgcctgctcaggttcatcattgaaacatcccagtgtttggccagacattaaggtgtcgtgagagtccctttcatgcctttcttacccaagcaagggtctttgatgggcacgtgtttacagcgctgctgcatagtcttgtaatatattaacagtcacatcaactgaaggtcaatactaagagccacaggttgtacctgtgatggggcgtgtggtttcctgttgtctcacctttaattgtcaacctccagtgttgactctagaaatatgaggaaagcttttcagtttttaaaattgccatttaaatttagtctattaaaaacaaacctagaggtcttggtgcagttgatttcagagtttattaatttagtggtcccaaaagtattacatcttttatattctggaagaaaagaactgtgaacaaattagaaccccggaacactctgacgtccatggacgcattccagaaaagtggcaagagatgagtctttcctcctccaggaagcattttggtagaatttccatagagcattgtctgtgagtgactgatcccaacatgtatgttactaagccccaaaacgaacttcaaactgggtgtggtggcacgtgcctttagtcccagctacccgggaggctgcggcaagaggattgcttgagcccaggagttcgagtccaacctgggcaaaagagtgagaccccatctctaaaaccaaaaaggtaccttagaaggtcacctggttggctaaccttttaaaggcaggggcgtgacacgtaggacacattgggaatgtcttggctactacatgtagccttctgggatatatgtgcccagagggagaagcactgagcctgaagaaactagatgagtctcagaaccacagaccggccagaaatctctcccaccattatatcagcgtgatacaggtctacattcatttctacaaacaggaacaagttccttgcagcaataatattattttatgacttgtatttttactatacccttcctctgaggtttagttttcatcacattatgttcaagattccatatctccgtaaattacagctaattacagggcattgttccatggttattaaaaatcagagtttattaaaaatcctgagtcttaagggctgtcttacctttcacttccactgtcctgtagaaacagatcaagctgcaaaccacgtccttcatctgttgttcattttcttgcaactctttgactctgatcccctgagcagcacgttcatcacgcatgctctctgttgcgttccccatttcagatgtccagtaatggtgaaataaaatcctgcttcgacagcaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:84260 -> Molecular function: GO:0005515 [protein binding] evidence: IPI GeneID:84260 -> Biological process: GO:0006915 [apoptotic process] evidence: IDA GeneID:84260 -> Biological process: GO:0030308 [negative regulation of cell growth] evidence: IDA GeneID:84260 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA GeneID:84260 -> Cellular component: GO:0005739 [mitochondrion] evidence: IDA GeneID:84260 -> Cellular component: GO:0005813 [centrosome] evidence: IDA GeneID:84260 -> Cellular component: GO:0005886 [plasma membrane] evidence: IDA GeneID:84260 -> Cellular component: GO:0045095 [keratin filament] evidence: IDA GeneID:84260 -> Cellular component: GO:0045179 [apical cortex] evidence: IDA
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