Home |
Help |
Advanced search
2025-05-09 20:34:15, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001258024 2607 bp mRNA linear PRI 18-APR-2013
DEFINITION Homo sapiens SKI family transcriptional corepressor 1 (SKOR1),
mRNA.
ACCESSION NM_001258024
VERSION NM_001258024.1 GI:384407368
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 2607)
AUTHORS Winkelmann,J., Czamara,D., Schormair,B., Knauf,F., Schulte,E.C.,
Trenkwalder,C., Dauvilliers,Y., Polo,O., Hogl,B., Berger,K.,
Fuhs,A., Gross,N., Stiasny-Kolster,K., Oertel,W., Bachmann,C.G.,
Paulus,W., Xiong,L., Montplaisir,J., Rouleau,G.A., Fietze,I.,
Vavrova,J., Kemlink,D., Sonka,K., Nevsimalova,S., Lin,S.C.,
Wszolek,Z., Vilarino-Guell,C., Farrer,M.J., Gschliesser,V.,
Frauscher,B., Falkenstetter,T., Poewe,W., Allen,R.P., Earley,C.J.,
Ondo,W.G., Le,W.D., Spieler,D., Kaffe,M., Zimprich,A., Kettunen,J.,
Perola,M., Silander,K., Cournu-Rebeix,I., Francavilla,M.,
Fontenille,C., Fontaine,B., Vodicka,P., Prokisch,H., Lichtner,P.,
Peppard,P., Faraco,J., Mignot,E., Gieger,C., Illig,T.,
Wichmann,H.E., Muller-Myhsok,B. and Meitinger,T.
TITLE Genome-wide association study identifies novel restless legs
syndrome susceptibility loci on 2p14 and 16q12.1
JOURNAL PLoS Genet. 7 (7), E1002171 (2011)
PUBMED 21779176
REMARK Erratum:[PLoS Genet. 2011 Aug;7(8). doi:
10.1371/annotation/393ad2d3-df4f-4770-87bc-00bfabf79362]
REFERENCE 2 (bases 1 to 2607)
AUTHORS Arndt,S., Schmidt,J., Wacker,E., Karrer,S. and Bosserhoff,A.K.
TITLE Fussel-15, a new player in wound healing, is deregulated in keloid
and localized scleroderma
JOURNAL Am. J. Pathol. 178 (6), 2622-2631 (2011)
PUBMED 21641385
REMARK GeneRIF: Permanent expression of Fussel-15 in keloid and skin
sclerosis fibroblasts could be involved in the pathogenesis of
these conditions.
REFERENCE 3 (bases 1 to 2607)
AUTHORS Riviere,J.B., Xiong,L., Levchenko,A., St-Onge,J., Gaspar,C.,
Dion,Y., Lesperance,P., Tellier,G., Richer,F., Chouinard,S. and
Rouleau,G.A.
CONSRTM Montreal Tourette Study Group
TITLE Association of intronic variants of the BTBD9 gene with Tourette
syndrome
JOURNAL Arch. Neurol. 66 (10), 1267-1272 (2009)
PUBMED 19822783
REMARK GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
REFERENCE 4 (bases 1 to 2607)
AUTHORS Kemlink,D., Polo,O., Frauscher,B., Gschliesser,V., Hogl,B.,
Poewe,W., Vodicka,P., Vavrova,J., Sonka,K., Nevsimalova,S.,
Schormair,B., Lichtner,P., Silander,K., Peltonen,L., Gieger,C.,
Wichmann,H.E., Zimprich,A., Roeske,D., Muller-Myhsok,B.,
Meitinger,T. and Winkelmann,J.
TITLE Replication of restless legs syndrome loci in three European
populations
JOURNAL J. Med. Genet. 46 (5), 315-318 (2009)
PUBMED 19279021
REMARK GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
REFERENCE 5 (bases 1 to 2607)
AUTHORS Winkelmann,J.
TITLE Genetics of restless legs syndrome
JOURNAL Curr Neurol Neurosci Rep 8 (3), 211-216 (2008)
PUBMED 18541116
REMARK GeneRIF: MEIS1 and LBXCOR1 are developmental factors and raise new
pathophysiologic questions for RLS.
Review article
REFERENCE 6 (bases 1 to 2607)
AUTHORS Winkelmann,J., Schormair,B., Lichtner,P., Ripke,S., Xiong,L.,
Jalilzadeh,S., Fulda,S., Putz,B., Eckstein,G., Hauk,S.,
Trenkwalder,C., Zimprich,A., Stiasny-Kolster,K., Oertel,W.,
Bachmann,C.G., Paulus,W., Peglau,I., Eisensehr,I., Montplaisir,J.,
Turecki,G., Rouleau,G., Gieger,C., Illig,T., Wichmann,H.E.,
Holsboer,F., Muller-Myhsok,B. and Meitinger,T.
TITLE Genome-wide association study of restless legs syndrome identifies
common variants in three genomic regions
JOURNAL Nat. Genet. 39 (8), 1000-1006 (2007)
PUBMED 17637780
REMARK GeneRIF: Observational study and genome-wide association study of
gene-disease association. (HuGE Navigator)
REFERENCE 7 (bases 1 to 2607)
AUTHORS Arndt,S., Poser,I., Moser,M. and Bosserhoff,A.K.
TITLE Fussel-15, a novel Ski/Sno homolog protein, antagonizes BMP
signaling
JOURNAL Mol. Cell. Neurosci. 34 (4), 603-611 (2007)
PUBMED 17292623
REMARK GeneRIF: a novel gene, fussel-15 (functional smad suppressing
element on chromosome 15) with high homology to the recently
discovered Fussel-18 protein.
REFERENCE 8 (bases 1 to 2607)
AUTHORS Mizuhara,E., Nakatani,T., Minaki,Y., Sakamoto,Y. and Ono,Y.
TITLE Corl1, a novel neuronal lineage-specific transcriptional
corepressor for the homeodomain transcription factor Lbx1
JOURNAL J. Biol. Chem. 280 (5), 3645-3655 (2005)
PUBMED 15528197
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
AY669507.1.
##Evidence-Data-START##
Transcript exon combination :: AY669507.1 [ECO:0000332]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-2607 AY669507.1 1-2607
FEATURES Location/Qualifiers
source 1..2607
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="15"
/map="15q23"
gene 1..2607
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/note="SKI family transcriptional corepressor 1"
/db_xref="GeneID:390598"
/db_xref="HGNC:21326"
/db_xref="MIM:611273"
CDS 1..2607
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/note="corepressor for LBX1; ladybird homeobox corepressor
1; transcriptional corepressor CORL1; functional smad
suppressing element 15; fussel-15; LBX1 corepressor 1;
functional Smad-suppressing element on chromosome 15;
Lbxcor1 homolog"
/codon_start=1
/product="SKI family transcriptional corepressor 1"
/protein_id="NP_001244953.1"
/db_xref="GI:384407369"
/db_xref="CCDS:CCDS58374.1"
/db_xref="GeneID:390598"
/db_xref="HGNC:21326"
/db_xref="MIM:611273"
/translation="
MIPKSLVQAAETQRGLCEPGGKGREGRSGGKGETRPRGVGTQEGKGTIPGSPREKRGERGEGDPALLPAEDLWRLPGSKDRLRSSLLPPPGPPSSDSGPGPPSSHSGKTAQGPRTLNWARKQSARTSSNLCAWSLAMATKMAEIPSSPYEPGQRGMKDTQRGDAPQRGSPEPRILQLARVGNVYLKEESSRSGRLEAKKWIPTKFLENLSVPHVDLGGNQLWSGGMEALTTQLGPGREGSSSPNSKQELQPYSGSSALKPNQVGETSLYGVPIVSLVIDGQERLCLAQISNTLLKNYSYNEIHNRRVALGITCVQCTPVQLEILRRAGAMPISSRRCGMITKREAERLCKSFLGEHKPPKLPENFAFDVVHECAWGSRGSFIPARYNSSRAKCIKCGYCSMYFSPNKFIFHSHRTPDAKYTQPDAANFNSWRRHLKLSDKSATDELSHAWEDRGLGLATGASGPAGPGGPGGGAGVRSYPVIPVPSKGFGLLQKLPPPLFPHPYGFPTAFGLCPKKDDPVLGAGEPKGGSYVSAFRPVVKDTESIAKLYGSAREAYGAGPARGPGPGAGSGGYVSPDFLSEGSSSYNSASPDVDTADEPEVDVESNRFPDDEDAQEETEPSAPSAGGGPDAGRPAFGDLAAEDLVRRPERSPPSGGGGYELREPCGPLGGPAPAKVFAPERDEHVKSAAVALGPAASYVCTPEAHEPDKEDNHSPADDLETRKSYPDQRSISQPSPANTDRGEDGLTLDVTGTHLVEKDIENLAREELQKLLLEQMELRKKLEREFQSLKDNFQDQMKRELAYREEMVQQLQIVRDTLCNELDQERKARYAIQQKLKEAHDALHHFSCKMLTPRHCTGNCSFKPPLLP
"
misc_feature 763..1065
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/note="SKI/SNO/DAC family; Region: Ski_Sno; pfam02437"
/db_xref="CDD:145533"
misc_feature 1096..1356
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/note="c-SKI Smad4 binding domain; Region:
c-SKI_SMAD_bind; cl07406"
/db_xref="CDD:198898"
exon 1..42
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/inference="alignment:Splign:1.39.8"
variation 36
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="a"
/replace="c"
/db_xref="dbSNP:376842060"
exon 43..270
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/inference="alignment:Splign:1.39.8"
variation 261
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:61734073"
variation 264..265
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace=""
/replace="ccccccccc"
/db_xref="dbSNP:139069155"
variation 270
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:369184389"
exon 271..355
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/inference="alignment:Splign:1.39.8"
exon 356..665
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/inference="alignment:Splign:1.39.8"
variation 399
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368253306"
variation 452
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200685698"
variation 454
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:146830880"
variation 516
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:199633420"
variation 523
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:115047604"
variation 582
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="a"
/replace="c"
/db_xref="dbSNP:200031104"
variation 598
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="a"
/replace="t"
/db_xref="dbSNP:7170185"
variation 605
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="c"
/replace="g"
/db_xref="dbSNP:148949019"
variation 607
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:76620287"
variation 635
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:376577033"
exon 666..1356
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/inference="alignment:Splign:1.39.8"
variation 681
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201958154"
variation 708
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:374164977"
variation 730
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:143149450"
variation 815
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="c"
/replace="g"
/db_xref="dbSNP:370905136"
variation 905
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:80315297"
variation 909
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373981657"
variation 913
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:368613673"
variation 960
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:375607879"
variation 1033
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="g"
/replace="t"
/db_xref="dbSNP:371883029"
variation 1198
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:112240620"
variation 1227
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:142994786"
exon 1357..1585
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/inference="alignment:Splign:1.39.8"
variation 1399
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="a"
/replace="c"
/db_xref="dbSNP:113458822"
variation 1400
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="c"
/replace="g"
/db_xref="dbSNP:202009740"
variation 1449
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370291556"
variation 1490
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:374997595"
variation 1514
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:151027563"
variation 1582
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="c"
/replace="g"
/db_xref="dbSNP:184007521"
exon 1586..1891
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/inference="alignment:Splign:1.39.8"
variation 1668
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:62015251"
variation 1776
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:368785544"
variation 1828
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371282973"
variation 1855
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="c"
/replace="g"
/db_xref="dbSNP:374790671"
variation 1857
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="c"
/replace="g"
/db_xref="dbSNP:369158955"
variation 1887
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="a"
/replace="t"
/db_xref="dbSNP:371609590"
exon 1892..2025
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/inference="alignment:Splign:1.39.8"
variation 1897
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200956599"
variation 1999
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace=""
/replace="c"
/db_xref="dbSNP:35101671"
variation 2015
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:377719980"
exon 2026..2116
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/inference="alignment:Splign:1.39.8"
exon 2117..2224
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/inference="alignment:Splign:1.39.8"
variation 2127
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="c"
/replace="g"
/db_xref="dbSNP:145030258"
variation 2129
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:375931873"
variation 2135
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138872533"
variation 2145
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="a"
/replace="c"
/db_xref="dbSNP:140632257"
variation 2163
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:150139245"
variation 2220
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:138605791"
exon 2225..2296
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/inference="alignment:Splign:1.39.8"
variation 2226
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:202165325"
variation 2263
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="g"
/replace="t"
/db_xref="dbSNP:184089221"
variation 2280
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="a"
/replace="c"
/db_xref="dbSNP:377094576"
variation 2294..2295
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace=""
/replace="a"
/db_xref="dbSNP:34118838"
exon 2297..2371
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/inference="alignment:Splign:1.39.8"
variation 2317
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="a"
/replace="c"
/db_xref="dbSNP:371135892"
variation 2350
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="a"
/replace="c"
/db_xref="dbSNP:72751453"
exon 2372..2446
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/inference="alignment:Splign:1.39.8"
variation 2376
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:143609706"
variation 2380
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="c"
/replace="g"
/db_xref="dbSNP:137873737"
exon 2447..2512
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/inference="alignment:Splign:1.39.8"
variation 2482
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="g"
/replace="t"
/db_xref="dbSNP:369578582"
variation 2494
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:143419968"
exon 2513..2607
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/inference="alignment:Splign:1.39.8"
variation 2533
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:370329539"
variation 2553
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:147155241"
variation 2559
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:140401745"
variation 2560
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="c"
/replace="g"
/db_xref="dbSNP:372809122"
variation 2604
/gene="SKOR1"
/gene_synonym="CORL1; FUSSEL15; LBXCOR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:141220171"
ORIGIN
atgatcccaaagagcctggtccaggcagcggaaacccagaggggtctctgcgagccaggagggaaaggaagagaggggagaagtggaggaaaaggggagacacgccccagaggagttggaacgcaggagggaaaggggaccatacccggtagcccgagggaaaaacgaggcgagaggggagaaggcgaccccgcgctgctacccgcggaagatttatggcgcctcccgggttccaaggacaggctgcgttcgtcgctgctgccaccgccgggacccccttcttctgactccgggcccggacccccctcctctcactcagggaaaaccgcgcagggacccaggaccctcaactgggccagaaagcaaagtgcaaggaccagcagcaacttgtgtgcctggagccttgcaatggctacgaagatggctgagattccttctagcccatatgagccgggacagcgaggcatgaaggatactcagagaggtgatgcccctcaaagaggaagcccagagccccgaatcctgcagttggcccgagtgggaaacgtatatctgaaggaggaaagctcaaggagtgggcgactggaagctaagaagtggatcccaacaaagttccttgagaacctctctgtcccacacgttgacctcggtggaaaccagctttggagcggcggcatggaggctctcaccactcagctggggccggggcgcgagggcagttcctcgcccaactccaagcaggagctgcagccgtactcgggctccagcgctctcaaacccaaccaggtgggcgagacgtcgctgtacggggtgcccattgtgtcgctggtcatcgacggccaggagcgcctatgcctggcgcagatctccaacaccctcctcaagaactacagctataatgagatccacaaccgccgcgtggccctgggcatcacgtgcgtgcagtgcacgccggtacagctggagattctgcgtcgggccggggccatgcccatctcgtcgcgccgctgcggcatgatcactaagcgagaggccgaacgcctgtgcaagtcgttcctgggcgagcacaaaccacccaagctgcccgagaacttcgccttcgatgtggtgcacgagtgcgcgtggggctcgcgtggtagcttcatccctgcgcgttacaacagctctcgtgccaagtgcatcaagtgcggctactgcagcatgtacttctcgcccaacaagttcatcttccactcgcaccgaacacccgacgccaagtacacgcagcccgatgccgccaacttcaactcctggcgtcgtcacctcaaactcagtgacaagtcggccacagacgaactgagccatgcttgggaggaccgcggacttggcctggcgactggagctagtggcccggcgggcccaggagggcccggtggcggcgccggcgtacgaagctacccggtgatcccggtgcccagcaaaggctttgggctcctgcaaaagctgcccccaccacttttcccccatccttacggcttccctacggccttcggcctatgccccaaaaaggacgacccggttttaggcgcgggcgagccaaagggcggctcctacgtgtcggccttccggccggtggtcaaggacaccgagagcatcgctaagctctacgggagcgcccgggaggcgtacggcgcggggcctgctcgggggccgggacccggcgctgggagcggcggctacgtgagcccggactttctgagcgagggcagctccagctacaattccgcctcgcccgacgtggacaccgcggacgagcccgaggtggacgtggaatccaaccgcttccccgacgacgaggacgcccaagaggagaccgagcccagcgcacccagcgcagggggcggcccagacgctggccggcccgcatttggggacttggcagccgaagacttggtgcggagacctgagaggagcccgccaagcggcggcggcggctacgagctgcgagagccttgcgggcccctaggaggccccgcgccggccaaggtgttcgcgcccgagagggatgagcacgtgaagagcgcggcggtggcgctggggcccgcggcctcctacgtctgcacccccgaggcccacgagccagataaggaagacaatcactcgcccgccgatgatttggaaacgaggaaatcctatccagaccaaaggagtatctcccagccaagtcctgcaaatacagacagaggcgaagatgggcttaccttggatgtcacaggaactcatttggtggagaaagatatcgagaacctggccagagaggaattgcaaaaactgctcctggaacaaatggagctccgcaagaagctggaacgggaatttcagagtctcaaagataattttcaggatcaaatgaagagggaattggcttatcgagaagaaatggtgcaacagctgcaaattgtcagagataccctgtgtaacgaactcgaccaggagcggaaggcgcgctatgccatccagcagaaattgaaagaagcccacgacgccctgcaccatttctcctgcaagatgctgacgccccgccactgcactggcaactgctccttcaagccaccgctgttgccctag
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:390598 -> Molecular function: GO:0000166 [nucleotide binding] evidence: IEA
GeneID:390598 -> Molecular function: GO:0003714 [transcription corepressor activity] evidence: IEA
GeneID:390598 -> Molecular function: GO:0046332 [SMAD binding] evidence: IPI
GeneID:390598 -> Biological process: GO:0000122 [negative regulation of transcription from RNA polymerase II promoter] evidence: IBA
GeneID:390598 -> Biological process: GO:0006351 [transcription, DNA-dependent] evidence: IEA
GeneID:390598 -> Biological process: GO:0006355 [regulation of transcription, DNA-dependent] evidence: NAS
GeneID:390598 -> Biological process: GO:0030512 [negative regulation of transforming growth factor beta receptor signaling pathway] evidence: IBA
GeneID:390598 -> Biological process: GO:0030514 [negative regulation of BMP signaling pathway] evidence: IDA
GeneID:390598 -> Cellular component: GO:0005634 [nucleus] evidence: IBA
GeneID:390598 -> Cellular component: GO:0005634 [nucleus] evidence: NAS
GeneID:390598 -> Cellular component: GO:0005667 [transcription factor complex] evidence: IEA
GeneID:390598 -> Cellular component: GO:0005737 [cytoplasm] evidence: IBA
GeneID:390598 -> Cellular component: GO:0030425 [dendrite] evidence: IDA
GeneID:390598 -> Cellular component: GO:0043025 [neuronal cell body] evidence: IDA
by
@meso_cacase at
DBCLS
This page is licensed under a Creative Commons Attribution 2.1 Japan License.