2024-03-29 14:28:53, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001271043 5733 bp mRNA linear PRI 17-JUN-2013 DEFINITION Homo sapiens nuclear factor I/X (CCAAT-binding transcription factor) (NFIX), transcript variant 1, mRNA. ACCESSION NM_001271043 VERSION NM_001271043.1 GI:402534519 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 5733) AUTHORS Lee,H.J., Woo,H.G., Greenwood,T.A., Kripke,D.F. and Kelsoe,J.R. TITLE A genome-wide association study of seasonal pattern mania identifies NF1A as a possible susceptibility gene for bipolar disorder JOURNAL J Affect Disord 145 (2), 200-207 (2013) PUBMED 22925353 REFERENCE 2 (bases 1 to 5733) AUTHORS Yoneda,Y., Saitsu,H., Touyama,M., Makita,Y., Miyamoto,A., Hamada,K., Kurotaki,N., Tomita,H., Nishiyama,K., Tsurusaki,Y., Doi,H., Miyake,N., Ogata,K., Naritomi,K. and Matsumoto,N. TITLE Missense mutations in the DNA-binding/dimerization domain of NFIX cause Sotos-like features JOURNAL J. Hum. Genet. 57 (3), 207-211 (2012) PUBMED 22301465 REMARK GeneRIF: missense mutations in NFIX were able to cause Sotos-like features. REFERENCE 3 (bases 1 to 5733) AUTHORS Lee,H., Jaffe,A.E., Feinberg,J.I., Tryggvadottir,R., Brown,S., Montano,C., Aryee,M.J., Irizarry,R.A., Herbstman,J., Witter,F.R., Goldman,L.R., Feinberg,A.P. and Fallin,M.D. TITLE DNA methylation shows genome-wide association of NFIX, RAPGEF2 and MSRB3 with gestational age at birth JOURNAL Int J Epidemiol 41 (1), 188-199 (2012) PUBMED 22422452 REMARK GeneRIF: DNA methylation shows genome-wide association of NFIX, RAPGEF2 and MSRB3 with gestational age at birth. REFERENCE 4 (bases 1 to 5733) AUTHORS Singh,S.K., Bhardwaj,R., Wilczynska,K.M., Dumur,C.I. and Kordula,T. TITLE A complex of nuclear factor I-X3 and STAT3 regulates astrocyte and glioma migration through the secreted glycoprotein YKL-40 JOURNAL J. Biol. Chem. 286 (46), 39893-39903 (2011) PUBMED 21953450 REMARK GeneRIF: NFI-X3 and STAT3 control the migration of differentiating astrocytes as well as migration and invasion of glioma cells via regulating YKL-40 expression. REFERENCE 5 (bases 1 to 5733) AUTHORS Singh,S.K., Wilczynska,K.M., Grzybowski,A., Yester,J., Osrah,B., Bryan,L., Wright,S., Griswold-Prenner,I. and Kordula,T. TITLE The unique transcriptional activation domain of nuclear factor-I-X3 is critical to specifically induce marker gene expression in astrocytes JOURNAL J. Biol. Chem. 286 (9), 7315-7326 (2011) PUBMED 21189253 REMARK GeneRIF: NFI-X3 activates GFAP expression, in part, by inducing alterations in the nucleosome architecture that lead to the increased recruitment of RNA polymerase II REFERENCE 6 (bases 1 to 5733) AUTHORS Wendler,W.M., Kremmer,E., Forster,R. and Winnacker,E.L. TITLE Identification of pirin, a novel highly conserved nuclear protein JOURNAL J. Biol. Chem. 272 (13), 8482-8489 (1997) PUBMED 9079676 REFERENCE 7 (bases 1 to 5733) AUTHORS Sumner,C., Shinohara,T., Durham,L., Traub,R., Major,E.O. and Amemiya,K. TITLE Expression of multiple classes of the nuclear factor-1 family in the developing human brain: differential expression of two classes of NF-1 genes JOURNAL J. Neurovirol. 2 (2), 87-100 (1996) PUBMED 8799200 REFERENCE 8 (bases 1 to 5733) AUTHORS Qian,F., Kruse,U., Lichter,P. and Sippel,A.E. TITLE Chromosomal localization of the four genes (NFIA, B, C, and X) for the human transcription factor nuclear factor I by FISH JOURNAL Genomics 28 (1), 66-73 (1995) PUBMED 7590749 REFERENCE 9 (bases 1 to 5733) AUTHORS Apt,D., Liu,Y. and Bernard,H.U. TITLE Cloning and functional analysis of spliced isoforms of human nuclear factor I-X: interference with transcriptional activation by NFI/CTF in a cell-type specific manner JOURNAL Nucleic Acids Res. 22 (19), 3825-3833 (1994) PUBMED 7937100 REFERENCE 10 (bases 1 to 5733) AUTHORS Seisenberger,C., Winnacker,E.L. and Scherthan,H. TITLE Localisation of the human nuclear factor I/X (NFI/X) gene to chromosome 19p13 and detection of five other related loci at 1p21-22, 1q42-43, 5q15, 11p13 and 20q13 by FISH JOURNAL Hum. Genet. 91 (6), 535-537 (1993) PUBMED 8340106 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AK295290.1 and AC007787.1. Summary: The protein encoded by this gene is a transcription factor that binds the palindromic sequence 5'-TTGGCNNNNNGCCAA-3 in viral and cellular promoters. The encoded protein can also stimulate adenovirus replication in vitro. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2012]. Transcript Variant: This variant (1) represents the longest transcript and encodes the longest isoform (1). Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## Transcript exon combination :: AK295290.1 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025082, ERS025085 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-1692 AK295290.1 1-1692 1693-5733 AC007787.1 32352-36392 FEATURES Location/Qualifiers source 1..5733 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="19" /map="19p13.3" gene 1..5733 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /note="nuclear factor I/X (CCAAT-binding transcription factor)" /db_xref="GeneID:4784" /db_xref="HGNC:7788" /db_xref="MIM:164005" exon 1..104 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /inference="alignment:Splign:1.39.8" misc_feature 48..50 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /note="upstream in-frame stop codon" CDS 54..1586 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /note="isoform 1 is encoded by transcript variant 1; nuclear factor 1 X-type; CTF; NF1-X; NF-I/X; nuclear factor 1/X; TGGCA-binding protein; CCAAT-box-binding transcription factor" /codon_start=1 /product="nuclear factor 1 X-type isoform 1" /protein_id="NP_001257972.1" /db_xref="GI:402534520" /db_xref="GeneID:4784" /db_xref="HGNC:7788" /db_xref="MIM:164005" /translation="
MEMSWARQSLAGIPAACDEFHPFIEALLPHVRAFSYTWFNLQARKRKYFKKHEKRMSKDEERAVKDELLGEKPEIKQKWASRLLAKLRKDIRPEFREDFVLTITGKKPPCCVLSNPDQKGKIRRIDCLRQADKVWRLDLVMVILFKGIPLESTDGERLYKSPQCSNPGLCVQPHHIGVTIKELDLYLAYFVHTPESGQSDSSNQQGDADIKPLPNGHLSFQDCFVTSGVWNVTELVRVSQTPVATASGPNFSLADLESPSYYNINQVTLGRRSITSPPSTSTTKRPKSIDDSEMESPVDDVFYPGTGRSPAAGSSQSSGWPNDVDAGPASLKKSGKLDFCSALSSQGSSPRMAFTHHPLPVLAGVRPGSPRATASALHFPSTSIIQQSSPYFTHPTIRYHHHHGQDSLKEFVQFVCSDGSGQATGQPNGSGQGKVPGSFLLPPPPPVARPVPLPMPDSKSTSTAPDGAALTPPSPSFATTGASSANRFVSIGPRDGNFLNIPQQSQSWFL
" misc_feature 87..215 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /note="Nuclear factor I protein pre-N-terminus; Region: NfI_DNAbd_pre-N; pfam10524" /db_xref="CDD:151076" misc_feature 279..587 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /note="N-terminal Mad Homology 1 (MH1) domain; Region: MH1; cl00055" /db_xref="CDD:241576" misc_feature 714..1583 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /note="CTF/NF-I family transcription modulation region; Region: CTF_NFI; pfam00859" /db_xref="CDD:144451" exon 105..636 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /inference="alignment:Splign:1.39.8" variation 149 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="t" /db_xref="dbSNP:368774795" variation 194 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="a" /replace="g" /db_xref="dbSNP:148229471" variation 210 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="" /replace="g" /db_xref="dbSNP:5827175" variation 218 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="a" /replace="g" /db_xref="dbSNP:375719449" variation 230 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="g" /db_xref="dbSNP:150443437" variation 256 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="t" /db_xref="dbSNP:387907254" variation 260 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="a" /replace="g" /db_xref="dbSNP:369196245" STS 276..520 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /standard_name="NFIX" /db_xref="UniSTS:504112" variation 335 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="a" /replace="g" /db_xref="dbSNP:375310739" variation 341 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="t" /db_xref="dbSNP:373938156" variation 386 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="t" /db_xref="dbSNP:376885081" variation 387 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="g" /replace="t" /db_xref="dbSNP:370482598" variation 437 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="a" /replace="g" /db_xref="dbSNP:369056833" variation 439 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="g" /db_xref="dbSNP:387907255" variation 459..460 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="" /replace="gggggg" /db_xref="dbSNP:149894387" variation 466 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="t" /db_xref="dbSNP:200603126" variation 470 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="a" /replace="g" /db_xref="dbSNP:200313486" variation 545 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="t" /db_xref="dbSNP:199762875" STS 567..1564 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /standard_name="Nfix" /db_xref="UniSTS:507089" variation 633 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="a" /replace="c" /db_xref="dbSNP:372477615" exon 637..699 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /inference="alignment:Splign:1.39.8" variation 645 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="t" /db_xref="dbSNP:387907253" variation 677 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="a" /replace="g" /db_xref="dbSNP:367591626" exon 700..774 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /inference="alignment:Splign:1.39.8" exon 775..895 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /inference="alignment:Splign:1.39.8" variation 818 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="a" /replace="c" /db_xref="dbSNP:201664313" variation 863 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="a" /replace="g" /db_xref="dbSNP:199590032" variation 890 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="t" /db_xref="dbSNP:369151512" exon 896..1032 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /inference="alignment:Splign:1.39.8" variation 920 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="t" /db_xref="dbSNP:201741871" variation 928 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="a" /replace="g" /db_xref="dbSNP:113721268" variation 932 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="g" /replace="t" /db_xref="dbSNP:1047135" variation 976 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="a" /replace="g" /db_xref="dbSNP:374776005" variation 1010 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="a" /replace="g" /db_xref="dbSNP:199631786" variation 1019 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="t" /db_xref="dbSNP:372881529" exon 1033..1155 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /inference="alignment:Splign:1.39.8" variation 1100 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="t" /db_xref="dbSNP:373603800" variation 1101 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="t" /db_xref="dbSNP:61754992" exon 1156..1331 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /inference="alignment:Splign:1.39.8" variation 1217 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="a" /replace="g" /db_xref="dbSNP:201174259" variation 1304 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="a" /replace="g" /db_xref="dbSNP:374101865" variation 1313 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="a" /replace="g" /db_xref="dbSNP:367955217" variation 1325 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="g" /db_xref="dbSNP:372077833" exon 1332..1479 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /inference="alignment:Splign:1.39.8" exon 1480..1571 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /inference="alignment:Splign:1.39.8" variation 1485 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="a" /replace="g" /db_xref="dbSNP:372257657" variation 1526 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="t" /db_xref="dbSNP:200499751" variation 1539 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="a" /replace="g" /db_xref="dbSNP:375287066" exon 1572..5733 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /inference="alignment:Splign:1.39.8" variation 1659 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="t" /db_xref="dbSNP:1047144" variation 1744..1745 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="" /replace="g" /db_xref="dbSNP:34095276" STS 1777..1897 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /standard_name="RH91530" /db_xref="UniSTS:86722" variation 1825 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="g" /replace="t" /db_xref="dbSNP:375166012" variation 1843 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="t" /db_xref="dbSNP:144975330" variation 1864 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="t" /db_xref="dbSNP:183935392" STS 1871..2078 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /standard_name="RH18298" /db_xref="UniSTS:30706" variation 1918 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:112643821" variation 2145 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="t" /db_xref="dbSNP:10416646" variation 2235 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="a" /replace="g" /db_xref="dbSNP:57359947" variation 2306 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="t" /db_xref="dbSNP:375305695" variation 2338 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="t" /db_xref="dbSNP:80090842" variation 2438..2457 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="" /replace="gagggcctccttcctgccac" /db_xref="dbSNP:375140220" variation 2451 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="t" /db_xref="dbSNP:369047813" variation 2611 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="g" /db_xref="dbSNP:145814634" variation 2726..2727 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="" /replace="a" /db_xref="dbSNP:34337363" variation 2730..2731 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="" /replace="a" /db_xref="dbSNP:5827180" variation 2774 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:77607471" variation 2833 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:113027509" variation 2834 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="a" /replace="g" /db_xref="dbSNP:111560188" variation 2906 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="g" /db_xref="dbSNP:188413501" variation 2937 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="t" /db_xref="dbSNP:181608618" variation 2999 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="a" /replace="c" /db_xref="dbSNP:372616189" variation 3003..3004 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="" /replace="c" /db_xref="dbSNP:201158408" variation 3004 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="" /replace="c" /db_xref="dbSNP:35992708" variation 3148 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="t" /db_xref="dbSNP:148149655" variation 3149..3152 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="" /replace="tctc" /db_xref="dbSNP:199726177" variation 3150..3153 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="" /replace="ctct" /db_xref="dbSNP:377649271" variation 3269 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="g" /db_xref="dbSNP:11555273" variation 3295 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="a" /replace="g" /db_xref="dbSNP:367898239" variation 3305 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="a" /replace="g" /db_xref="dbSNP:113396930" variation 3316 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="t" /db_xref="dbSNP:184187752" variation 3354 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="g" /db_xref="dbSNP:61270571" variation 3404 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="t" /db_xref="dbSNP:369984914" variation 3407 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="g" /db_xref="dbSNP:11555274" variation 3520 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="g" /db_xref="dbSNP:376300898" variation 3829 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="" /replace="c" /db_xref="dbSNP:71798576" variation 3888 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="" /replace="a" /db_xref="dbSNP:112879585" variation 3893..3894 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="" /replace="a" /db_xref="dbSNP:71841362" variation 3996..3997 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="" /replace="a" /db_xref="dbSNP:142626844" variation 4105 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="t" /db_xref="dbSNP:190683071" variation 4125..4126 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="" /replace="t" /db_xref="dbSNP:71719751" variation 4125 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="" /replace="t" /db_xref="dbSNP:112478002" variation 4195 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="g" /replace="t" /db_xref="dbSNP:182072517" polyA_signal 4412..4417 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" polyA_site 4443 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" variation 4588 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="a" /replace="g" /db_xref="dbSNP:150757731" variation 4660 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="t" /db_xref="dbSNP:117198656" variation 4800 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="t" /db_xref="dbSNP:75550675" variation 4860 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="a" /replace="t" /db_xref="dbSNP:10419483" variation 4906 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="a" /replace="g" /db_xref="dbSNP:137978145" variation 5279 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="c" /replace="t" /db_xref="dbSNP:186285075" variation 5286..5287 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="" /replace="a" /db_xref="dbSNP:34291647" variation 5544 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" /replace="g" /replace="t" /db_xref="dbSNP:112707286" polyA_signal 5705..5710 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" polyA_signal 5713..5718 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" polyA_site 5733 /gene="NFIX" /gene_synonym="MRSHSS; NF1A; SOTOS2" ORIGIN
agacggacactgtgccggggcgagctgacaggagttcacggctgcgatagaacatggagatgtcatgggcgcgacagagcctggcggggataccagcagcgtgtgatgagttccacccgttcatcgaggcactgctgcctcacgtccgcgctttctcctacacctggttcaacctgcaggcgcggaagcgcaagtacttcaagaagcatgaaaagcggatgtcgaaggacgaggagcgggcggtgaaggacgagctgctgggcgagaagcccgagatcaagcagaagtgggcatcccggctgctggccaagctgcgcaaggacatccggcccgagttccgcgaggacttcgtgctgaccatcacgggcaagaagcccccctgctgcgtgctctccaaccccgaccagaagggcaagatccggcggattgactgcctgcgccaggctgacaaggtgtggcggctggacctggtcatggtgattttgtttaaggggatccccctggaaagtactgatggggagcggctctacaagtcgcctcagtgctcgaaccccggcctgtgcgtccagccacatcacattggagtcacaatcaaagaactggatctttatctggcttactttgtccacactccggaatccggacaatcagatagttcaaaccagcaaggagatgcggacatcaaaccactgcccaacgggcacttaagtttccaggactgttttgtgacttccggggtctggaatgtgacggagctggtgagagtatcacagactcctgttgcaacagcatcagggcccaacttctccctggcggacctggagagtcccagctactacaacatcaaccaggtgaccctggggcggcggtccatcacctcccctccttccaccagcaccaccaagcgccccaagtccatcgatgacagtgagatggagagccctgttgatgacgtgttctatcccgggacaggccgttccccagcagctggcagcagccagtccagcgggtggcccaacgatgtggatgcaggcccggcttctctaaagaagtcaggaaagctggacttctgcagtgccctctcctctcagggcagctccccgcgcatggctttcacccaccacccgctgcctgtgcttgctggagtcagaccagggagcccccgggccacagcatcagccctgcacttcccctccacgtccatcatccagcagtcgagcccgtatttcacgcacccgaccatccgctaccaccaccaccacgggcaggactcactgaaggagtttgtgcagtttgtgtgctcggatggctcgggccaggccaccggacagcccaacggtagcggccagggcaaagtcccggggtcatttttgctaccgccgccgcctccagtggccagacctgtgccccttcctatgcctgattccaaatccaccagcactgccccagacggcgccgccttgactcctccatcaccttcattcgcaacgacaggcgcctcctctgccaaccggtttgtcagcatcggaccccgggacggcaactttctgaacatcccacagcagtctcagtcctggttcctctgataagatcgacaaaagaaacaacaaaatgagaagaagaggttcctcgaaaggggggagaagaaattttgagaatggaaaaatcccccagcccagcccagccccaccgaaaagcaaaaattacacgtcgtcagccactcagcccttctctcctccagcccggggacccccgcgggccccagaagcagcccagttctcagagagcccttggaaggggtctcggtggagctgtgcaccagcagccaagcagaaagaaacacgcgacatggactctgtcaagtagaggacagaaagcaagaaaggatgcagaactgccttcctccccctgaccccgccccggccttctggggaaggaacaaagtccccaaacaaagcaaccagcacaattctgaaggggcctggcctccaccctcaccccttcctaggggaaccccaccctccacacagccggagctgccctagggagcctggagggccagcttgtaaagatgatggggtttagatccctcaggctctcccctccagactccgcccttccctccctccctccctccctccctctctgccaaggctccagcttcttcccccagctgctcccgaccaggagggggagagcagcctccacttaccccaccccacccttgggctaaaagcccccaggcgggcagggggtgacccctggagctagttgcgtgtcccagaatggagggtgttctgacaccccaccctgagccgcaagagcagtcctggggccctggacccctctgtacagtccgtaggaaaaagtcggaatgctctcgacggcctcgtcccagcctgggacaggccccctttcccctctctctgcaggccaggagggcctccttcctgccacgagggaggggagtcgggccccaggtcgcccccgcccccagccctgcatgcaggtgccctcgctccgccccatcagttcctgcccctgcccctcatgcagactgccctgctggggccgggccggagggtggagcagaaaggggaccccggagccgagcgaggaggaccaggcagccgccgctgccgcgctaagccaccacctgcgcttaggtaggcgtcctgctcgccgactttcagttccttgggagggtgttgggtgtcgtccttttcaaaagtgttttggagctttctgtgccccccgactttcccccgcctccccgccccccacgtggccacttttctctggattttagctgtaatgtctttactctttatttaggggtggggcattcattgtttgggtcttttgctgttggaatgggaactcctcctccatttgagcaacttgggaacaatttggtaacacaccacaggaagtagctctcccccccagccccctcctccctcaagggagggttggggggcctgtccagagggtcttcagaagcccccctgggagggaggggaggatgagcacgcccagctcccctccagggtgtgacttggcccctctggcttgtctttctgtgccttactcctcctcctgcgtctcccgttcctggccccttcttgagtccttgtgcctctctctttctctctctttcttaattgtatgaaaacacaaagcacaggtcaggatcctctgagagaaaatcaacattgcaccacgtaggggtgggctatgggctgtatttattgtgaatctagtttgtgaggctgtggccccgagctggcggagggagggaagaggagggagtgacgggaggggaggaggtcagcgacctggggccgtagcggcaggcgaacggtgcctgctacccagctggaagccacaaggtggctggctccaggggcggcttttgttggaagttgagtgaagccctccccctgtcctcagcgtgcagccctagaggaccccagggctgaggggcagtggatcctgcgggagtctcccggggcgtggggagtaaggccccgggggtggggggccgggtgggccgggcgtgacgcgcggtcaaagtgcaatgatttttcagttcggttggctaaacagggtcagagctgagagcgaagcagaaggggctccctgtccggcccacgtgccctttccctcgacgacagtcgagggctcgggctctgtgggactgtgggagctagggtctgcggggcgcctgcccgggcgaggtcggaagctgcaggccagctgggcccgggccggagcgtgcccggcggggctgcccgggcgggcagggggtgggggctgctcctttcccaagtggtgttgtgaggggcaatgagggcaacaggagatgtggggacgtgttaggagagaaaaaaaaaaaaacaaaaatatatatgggggaaattaacttttttttttcattgaaccaagtgcaatgcatcagagagttttcctatctttgtatgttaagagattaagaaaaaaaaattctatttttgttgtaatgtcctcgcggctctggggacgctaaaagaaccgggcctgccccgccctgcgcggggataacgaaagctgagtgtttttcccttttttttgttcgtttttagtttttttttttttaagtcgttttcctgcgttgacgaggatgatctggggtttttatttgtttcgtcgttcgttctgtttcggtgggagggctgaaggaaacgttcacattttagagtttaaaaaaaacacctcgacatttaaaaaatcaaccaacacaagatcaaaaaggaaaaggacgagagaaaaattatttttaagataattaaacataaaaccctggtgcttcttacattataaagtacgttttaaagaacccacaaactattatacataagtttatgaatcaattaaatatcctgcacttgttaggaatacgcatatcccttctttgttgagtttaacggaacgggacagcggcgtgcccccggcggctggactgctccggccgcgggtctccccgggcgcccctccctggggcccagcacccctcctcgccccatccccgtccgggtacgggggcgcggcaggggtccccggcccctcccccgcagaggtcaatgccaacgaacaaacgtcccctccctccctccctctccgccccgagcgcccttctttgagccagacgccaacttgaccctcaccagcattatcaggagcgcgctcagcaagttggtagtttcctcccccctttcccggcgcccctcccgcccccattcaacatctctcatcctatccccgaccccctccggggaacaccgggaaggctcgacgctccaggacaggaccagccacgcagacaggtcgatttgcccaggcccgcgcccgcacgcacgcacgcacacggccccgcacacagccccgccccaccccgcaaccagccctgtcgactgccttatacacccgcccccgcgctggccggccgacctagtgccttgttctcacccccgtgctggcggagcggacgccgcgctctgggtcccagaggggccgggtggctcagacgacccaccactcccccaccctgaccgtgctgaacagacccccccacacgagagaaaataaaggagcaataaagtcacgagaactttcgtcccccaatcgagagcccgaggggcaccccagccccgcctctgctcccccccaccccacccaccctcggggcgcccccctccccccgcaagccagcctgggccagccccgcttcggcccctcccgggagatccgtgcgcccgaccagcaccagcatcgcggaccgcaaaggccgcccgtcccgtcaaacaagtttcttcttaggctaagaaacgcagtatatacgagtatctctatatatagtactaatggatttggtgtgcttcccccttagcgtccccctccctctgctcctcctccttcagcctggtctccccctcttctctgccctccacccccgtctctgcactgagatacataagaaacaagggtagtttactgtctgttttgttttctgggttttcagtgtcctagcggaatgcaagtaggcagccagcccgtctgttccctctccgccccgccccgccccgcccccgtcactgcgcttctgttataccatctttgcctgactctctccggcttctccattgaatggctaatgtgtatgtgaaataaagaaataaagaaaaacaaacgcga
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:4784 -> Molecular function: GO:0003677 [DNA binding] evidence: IEA GeneID:4784 -> Molecular function: GO:0003700 [sequence-specific DNA binding transcription factor activity] evidence: TAS GeneID:4784 -> Molecular function: GO:0003705 [RNA polymerase II distal enhancer sequence-specific DNA binding transcription factor activity] evidence: TAS GeneID:4784 -> Biological process: GO:0000122 [negative regulation of transcription from RNA polymerase II promoter] evidence: IDA GeneID:4784 -> Biological process: GO:0006260 [DNA replication] evidence: IEA GeneID:4784 -> Biological process: GO:0006366 [transcription from RNA polymerase II promoter] evidence: TAS GeneID:4784 -> Biological process: GO:0021680 [cerebellar Purkinje cell layer development] evidence: IEA GeneID:4784 -> Biological process: GO:0021707 [cerebellar granule cell differentiation] evidence: IEA GeneID:4784 -> Biological process: GO:0045944 [positive regulation of transcription from RNA polymerase II promoter] evidence: IDA GeneID:4784 -> Biological process: GO:0048708 [astrocyte differentiation] evidence: IEA GeneID:4784 -> Cellular component: GO:0005634 [nucleus] evidence: IEA
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