Home |
Help |
Advanced search
2024-04-19 08:44:14, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001256549 7164 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens polycomb group ring finger 5 (PCGF5), transcript
variant 2, mRNA.
ACCESSION NM_001256549
VERSION NM_001256549.1 GI:375065845
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 7164)
AUTHORS Luo,T., Kuriakose,J.A., Zhu,B., Wakeel,A. and McBride,J.W.
TITLE Ehrlichia chaffeensis TRP120 interacts with a diverse array of
eukaryotic proteins involved in transcription, signaling, and
cytoskeleton organization
JOURNAL Infect. Immun. 79 (11), 4382-4391 (2011)
PUBMED 21859857
REFERENCE 2 (bases 1 to 7164)
AUTHORS Wakeel,A., Kuriakose,J.A. and McBride,J.W.
TITLE An Ehrlichia chaffeensis tandem repeat protein interacts with
multiple host targets involved in cell signaling, transcriptional
regulation, and vesicle trafficking
JOURNAL Infect. Immun. 77 (5), 1734-1745 (2009)
PUBMED 19273555
REFERENCE 3 (bases 1 to 7164)
AUTHORS Grupe,A., Li,Y., Rowland,C., Nowotny,P., Hinrichs,A.L., Smemo,S.,
Kauwe,J.S., Maxwell,T.J., Cherny,S., Doil,L., Tacey,K., van
Luchene,R., Myers,A., Wavrant-De Vrieze,F., Kaleem,M.,
Hollingworth,P., Jehu,L., Foy,C., Archer,N., Hamilton,G.,
Holmans,P., Morris,C.M., Catanese,J., Sninsky,J., White,T.J.,
Powell,J., Hardy,J., O'Donovan,M., Lovestone,S., Jones,L.,
Morris,J.C., Thal,L., Owen,M., Williams,J. and Goate,A.
TITLE A scan of chromosome 10 identifies a novel locus showing strong
association with late-onset Alzheimer disease
JOURNAL Am. J. Hum. Genet. 78 (1), 78-88 (2006)
PUBMED 16385451
REMARK GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
AK303014.1, AC026227.8 and BQ420347.1.
Transcript Variant: This variant (2) differs in the 5' UTR compared
to variant 1. Variants 1, 2 and 4 all encode the same protein.
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.
##Evidence-Data-START##
Transcript exon combination :: AK303014.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025084 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-1399 AK303014.1 2-1400
1400-7079 AC026227.8 100224-105903 c
7080-7164 BQ420347.1 307-391
FEATURES Location/Qualifiers
source 1..7164
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="10"
/map="10q23.32"
gene 1..7164
/gene="PCGF5"
/gene_synonym="RNF159"
/note="polycomb group ring finger 5"
/db_xref="GeneID:84333"
/db_xref="HGNC:28264"
exon 1..177
/gene="PCGF5"
/gene_synonym="RNF159"
/inference="alignment:Splign:1.39.8"
variation 78
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:141603371"
exon 178..472
/gene="PCGF5"
/gene_synonym="RNF159"
/inference="alignment:Splign:1.39.8"
variation 227
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:151125630"
variation 334
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:374274424"
variation 349
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:368638959"
misc_feature 352..354
/gene="PCGF5"
/gene_synonym="RNF159"
/note="upstream in-frame stop codon"
CDS 361..1131
/gene="PCGF5"
/gene_synonym="RNF159"
/note="ring finger protein (C3HC4 type) 159; RING finger
protein 159"
/codon_start=1
/product="polycomb group RING finger protein 5"
/protein_id="NP_001243478.1"
/db_xref="GI:375065846"
/db_xref="CCDS:CCDS7413.1"
/db_xref="GeneID:84333"
/db_xref="HGNC:28264"
/translation="
MATQRKHLVKDFNPYITCYICKGYLIKPTTVTECLHTFCKTCIVQHFEDSNDCPRCGNQVHETNPLEMLRLDNTLEEIIFKLVPGLREQELERESEFWKKNKPQENGQDDTSKADKPKVDEEGDENEDDKDYHRSDPQIAICLDCLRNNGQSGDNVVKGLMKKFIRCSTRVTVGTIKKFLSLKLKLPSSYELDVLCNGEIMGKDHTMEFIYMTRWRLRGENFRCLNCSASQVCSQDGPLYQSYPMVLQYRPRIDFG
"
misc_feature 409..528
/gene="PCGF5"
/gene_synonym="RNF159"
/note="RING-finger (Really Interesting New Gene) domain, a
specialized type of Zn-finger of 40 to 60 residues that
binds two atoms of zinc; defined by the 'cross-brace'
motif C-X2-C-X(9-39)-C-X(1-3)-
H-X(2-3)-(N/C/H)-X2-C-X(4-48)C-X2-C; probably involved
in...; Region: RING; cd00162"
/db_xref="CDD:29102"
misc_feature order(412..414,421..423,460..462,466..468,475..477,
484..486,517..519,526..528)
/gene="PCGF5"
/gene_synonym="RNF159"
/note="cross-brace motif; other site"
/db_xref="CDD:29102"
variation 416
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:372696858"
exon 473..569
/gene="PCGF5"
/gene_synonym="RNF159"
/inference="alignment:Splign:1.39.8"
variation 489
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:148710899"
variation 509
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:372569296"
variation 522
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="c"
/db_xref="dbSNP:142481328"
exon 570..625
/gene="PCGF5"
/gene_synonym="RNF159"
/inference="alignment:Splign:1.39.8"
variation 616
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:369012074"
variation 623
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:372777415"
exon 626..685
/gene="PCGF5"
/gene_synonym="RNF159"
/inference="alignment:Splign:1.39.8"
exon 686..834
/gene="PCGF5"
/gene_synonym="RNF159"
/inference="alignment:Splign:1.39.8"
variation 692
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:375287111"
variation 710
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:151323358"
variation 719
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:369899767"
variation 723
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:140669067"
variation 727
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="g"
/db_xref="dbSNP:373196380"
exon 835..933
/gene="PCGF5"
/gene_synonym="RNF159"
/inference="alignment:Splign:1.39.8"
variation 841
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:200475271"
variation 855
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:191760973"
exon 934..1023
/gene="PCGF5"
/gene_synonym="RNF159"
/inference="alignment:Splign:1.39.8"
exon 1024..1083
/gene="PCGF5"
/gene_synonym="RNF159"
/inference="alignment:Splign:1.39.8"
variation 1042
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:377561962"
variation 1050
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="g"
/replace="t"
/db_xref="dbSNP:144351361"
variation 1062
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:146460099"
exon 1084..7146
/gene="PCGF5"
/gene_synonym="RNF159"
/inference="alignment:Splign:1.39.8"
variation 1122
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:367608907"
variation 1125
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:191746944"
variation 1178
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:182483549"
variation 1182
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:186761917"
variation 1217
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="c"
/db_xref="dbSNP:113330131"
variation 1303
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="g"
/replace="t"
/db_xref="dbSNP:115710628"
variation 1326
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="t"
/db_xref="dbSNP:1061292"
variation 1512
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:192315041"
variation 1566
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="g"
/db_xref="dbSNP:369207455"
variation 1584
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:185855100"
variation 1588
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:2450445"
variation 1750
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:190416217"
variation 1795
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:142716800"
variation 1805
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:143433812"
variation 1892
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:193205144"
variation 2007..2008
/gene="PCGF5"
/gene_synonym="RNF159"
/replace=""
/replace="t"
/db_xref="dbSNP:369517487"
variation 2115
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:371532480"
variation 2134
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:374524017"
variation 2137
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:184608338"
variation 2184
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:41286928"
variation 2334
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:115091137"
variation 2338
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:147972947"
variation 2366
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:188924445"
variation 2436
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:11186527"
variation 2444
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:3758498"
variation 2553
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:181383797"
variation 2556
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:185615722"
variation 2575
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:117714148"
variation 2634
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:141793573"
variation 2671
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="g"
/replace="t"
/db_xref="dbSNP:150577718"
variation 2783
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:78753737"
variation 2814
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:138671662"
variation 2978
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:141746709"
variation 3265
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:150651081"
variation 3348
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:374075294"
variation 3406
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:371607692"
variation 3407
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:189639049"
variation 3409
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:375699378"
variation 3459
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:370238940"
variation 3506
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="g"
/db_xref="dbSNP:146104676"
variation 3559
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:73314513"
variation 3561
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:372967837"
variation 3562
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:180820131"
variation 3570
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:185903355"
variation 3630
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="g"
/db_xref="dbSNP:192037337"
variation 3697
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:181775076"
variation 3700
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:369073230"
variation 3775
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:374815810"
variation 3822
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:368134239"
variation 3828
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="g"
/db_xref="dbSNP:186011849"
variation 3834
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:190422800"
variation 3922
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:182708660"
variation 4131
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:77284033"
variation 4136
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:372684384"
variation 4147
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="g"
/db_xref="dbSNP:186979627"
variation 4150
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="g"
/db_xref="dbSNP:191257053"
variation 4152
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:75369883"
variation 4159
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="g"
/replace="t"
/db_xref="dbSNP:182578013"
variation 4175
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="t"
/db_xref="dbSNP:140071127"
variation 4202
/gene="PCGF5"
/gene_synonym="RNF159"
/replace=""
/replace="a"
/db_xref="dbSNP:376545723"
variation 4226
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:187750853"
variation 4371
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="g"
/replace="t"
/db_xref="dbSNP:193111647"
variation 4453
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:7902729"
variation 4454
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:184851487"
variation 4597
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="g"
/replace="t"
/db_xref="dbSNP:187609815"
variation 4611..4612
/gene="PCGF5"
/gene_synonym="RNF159"
/replace=""
/replace="t"
/db_xref="dbSNP:34602274"
variation 4698
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:192141310"
variation 4749
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="c"
/db_xref="dbSNP:117060235"
variation 4762
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="g"
/db_xref="dbSNP:184313387"
variation 4927
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:7074612"
variation 5009
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:189589853"
variation 5021
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="g"
/db_xref="dbSNP:181181369"
variation 5022
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:7091037"
variation 5027
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:61875626"
variation 5049..5050
/gene="PCGF5"
/gene_synonym="RNF159"
/replace=""
/replace="c"
/db_xref="dbSNP:34362692"
variation 5065
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:61875627"
variation 5071
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="t"
/db_xref="dbSNP:61875628"
variation 5170
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:375250914"
variation 5171
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:144690508"
variation 5285
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:148499126"
variation 5291
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="t"
/db_xref="dbSNP:142980825"
variation 5309
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="g"
/replace="t"
/db_xref="dbSNP:7075114"
variation 5366
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:147733453"
variation 5462
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:117231376"
variation 5493
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:115540244"
variation 5506
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:142578695"
variation 5715
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="g"
/replace="t"
/db_xref="dbSNP:375431648"
variation 5819
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="c"
/db_xref="dbSNP:184412430"
variation 5936
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="t"
/db_xref="dbSNP:11592412"
variation 6064
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:370759691"
variation 6080..6081
/gene="PCGF5"
/gene_synonym="RNF159"
/replace=""
/replace="aa"
/db_xref="dbSNP:370725076"
variation 6343
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:373030793"
variation 6506
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:144807100"
variation 6571
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="c"
/db_xref="dbSNP:189395525"
variation 6583
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:112689997"
variation 6819
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:147805190"
variation 6845
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:181980522"
STS 6861..7037
/gene="PCGF5"
/gene_synonym="RNF159"
/standard_name="RH80111"
/db_xref="UniSTS:92151"
variation 6909
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="t"
/db_xref="dbSNP:11541126"
variation 6916
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:13675"
variation 6952
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:2619614"
variation 6954
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:186252705"
variation 6987
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="t"
/db_xref="dbSNP:14611"
variation 7081
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:190667449"
ORIGIN
cacaacgttcccgtttgcttatagttgtcaacgaccatgatctctggacccacactacagtaacaagtttgtcagtcattttcagataaggtgcaaatcaagggatggctttgtccccacttcggcgcaggtgggacagacttggggaagacgcagctgaagagacaaattctcaggacatgggaaagcggaaccaccaaaaggagtgatgatcaacgatctcatgataaatctggatgctagttctcatgcctcaggacatcctactgggaacgacacaccagctcctgggatcagactttcatctacttaggacccctctttgcccagactactaaagccagtcttcactagccacgaatggctacccaaaggaaacacttggtgaaagattttaatccttacattacctgctatatctgtaaagggtatctgatcaagccaacaacagtgacggaatgcctccatacattctgtaagacttgtattgttcagcactttgaagatagcaatgattgcccaaggtgtggcaaccaagttcatgagacaaatccattagaaatgttgaggttggacaatacattagaggaaattatatttaagctggtccctggactacgagaacaagaacttgagcgtgaatctgaattttggaagaaaaataagcctcaagaaaatggacaagatgatacttcaaaagctgacaaaccgaaagtagatgaagaaggtgatgaaaatgaagatgataaagattatcacagaagtgacccacaaattgctatctgtctagattgtttacgaaataatgggcaatcaggggacaatgtagtaaagggtttaatgaagaaattcattcgatgttctacacgtgtaactgtgggaactattaaaaaatttctaagtttaaaactaaaacttccaagttcttatgagttggatgtgctgtgcaatggtgaaattatggggaaggatcatactatggaattcatctacatgacaagatggcgactaagaggcgaaaactttcggtgtctgaactgctcagcttcgcaagtctgctctcaggatggccctttgtatcagtcataccctatggtactgcagtatcgaccaagaattgatttcggttagaccaaggggcccagacctcactgagatgaatcctgcactatttgtttactcgtcaacagattgcacagttaacggtgtgtggactagaggaacacaaccagattttcagcatgcaaataaggccattgtctatctctaaattgtcagttgcattcatgttgtttctattaggagcaaaccaagtgccattctgctactgaaccatctgcataaggtatttgtgttgtctcaaagtgtgcaagtcatggtaaaaatcagttagctgtgccgccatgattcacccttctgaatattttgcttgcctgttccaagattgttctaatgtttaattacactagtaaaatggctcaatttttgtggtgttgcagttttcacatacttactcttttattcttgtttaaatagcgtactctacaagaaactaataattatatcttgaaattattttgtatggaagtatatttagaaaagtggtttttgagccactgtcttgttcttgataagctttttgtgtgaaaaaaagttcattcttgagtgtgcaagtccttttgccaagaattccaattattctgtaacattagagcacaatataattgtagacattctaagcatctgtccgtgtagtctaccaattgcacaaggaaggcatgttagccctccagattgaaaatgtatgtgacctcttgaactgaagttagattcccaaccattcaaaatgttggcagctgatcacatttacttctgataaaagtaatgtgtaagtaaggttaatcttctttcataatgccttatgacaagcaggtgctgcttcatgaaacgtcattgtatagcccatttcatgtatcattacattgttgctgttatttaatgagtgcattatttctctttttaagttggccttaggtatatgtcattgtggcatgcagagggttatgacgattttaaatattaggatttttagagcacataacattagctattttatggatttcaaaagtctcaaaacagttgtagattaaaactgttagttacctttcacatttccaaactatgtgcataaaatagaataaatgcagtatagaactatgctaaccaaaattaataggttaagggtattttattttaaatcctgtagtaattggggaaatgagaagattattattttatacatgagttcattaagatcagaaatacaaaatgtcctgtattttgcagttttgttaagtcttccattcgttttaggattagtctgcaagtcaaagaaagtcttgttaccttaaattatatgaaaactgtcattttaaatcttttaatatttacagttttcaaaaaccttacttggaaattgctttgaaacaaacaagctaacctttgaaacttaggaaaaaatcttgaaagttaggaaaaatatttgagaaatatgacgagcacaatctgtgtgttacacacatttagtttttatactgcatatgtggtaaatgtgtcacattttccagtaaaatgtatcagaaatcaatgccttctgaatttcaaaatgattcttagaaataagatattgtacaactctagcaaacatacaaagtacagctaaatcttaatatatttcactatgtaaaaggctgaaacttcataattatctgttccttctatctttttttgagtcaaaaagtctattaaatttttctgttgttgttccaactttggtgaaaaaggttatggcaatactttaactttgttttgttacattgtttttgttcttggaatggctcacaagcagaatttaaaaggcagattttcattaactataaatggctgaaaaaactgaatttactatctagctacagaaattatttttctatggtgtgaaactgttcccagacatccctaagaacttttacaaattattataaatttgtcacacctaggtcagcgattaaaatagtgttttgcaaatggaattttaattaactcaaaatgaattaagagtgcattttaaaaatcacaagtgagactttgatgttttggccccccagccaaaacttaatggtcataaatgaattttatctacaaaatctctttaaatttggctggttgccttgtcatatgtaatttcactattttccaaggaaatatataggaagcaattatgaaactgagaatagttttatatagaattcttttatttactgataatgcattaacatttttattgaaatgcaatggaatatgtgccaaaacacgtgaaaagcttacataaagaaaggcatcagttgtcgtttggagaaaggtacacatttttttgatggtcctaagtgatatggtattactactagaatcacagatttcttcaactgacttattttggtatattcaactacagctttctaaggataggactactttcatgtctagtaatacactgtattccccgttaattatcccttaagtcagattgtagaatttgcaagaaactaggtatagaaaaaatgtacaggcaacttttgtggttagctttataaatttagggtgcttataaaatgataaaatgaattctttaaataacctataggaatcatctgaatctgtaacatcagagactaaaactaaaagttttctttaatctgttgtttcttaagcaataaactgaaagacctttacttccataaaagattttgttatctcttttatctgccttagaaattataagtataaaagggtcaagggaacttagatataaagaatgactgtggtttataaacattactttaattgaagtaatcacatcagttaatagagaaatcaaaatatgtatggccttttctctagattagcaaaacagctttacaaagtatgaaaaaataaactaaaatgctcattgatgaggtaatactcagtctggagtacaggtaacttgggtaatgccttttaactactcttagaggagtatattatttctttatacattaaacatctatcccatagtaatgtgccacattttataaacgtaatgactttgctcaactacattacacactcaaatgtaatctaaatttaaactgattatttaaggaaaaaaagtgtgttatataatattgtgaactgtttagctttactgaaatatttaagagaaagtgcctcattactaaagtgcatttctgttttaaatttactgcataaagtttgagttatctgtacctgtctcttatgaatggtttcatatctaaataggctcttgtaagttaatttttttggaagattttcataagaatatagatatcaccaaagacattttacagtaaattaataaccatgttggagagacggttttaacagtttggaggttggaaatttttagattgcaatttaattttatatagttaggcaataaccttgattaattgctaaaatatcaccaaagaaaggctttaaactgaattttcttggtgagatcagtcaaatgcaggcttttcttgcaataatcagaacacacttcctttcaaatatgttcattgtttttcagcatcatctaacagatcttagtaaatctaaatcctcaaagatgagaaagaggtaaacacaacaaatagccttcctctgcatgaaaagtgagagaaatacatactttgaaaagaaagttcagatttttaatttgagagggtttttatttcatggaggcagtgttaactaaaattaagcttagatttagctcctgtattattcataatatgagaaattttattaaaggcagactttggtaaaagtgccaacacacttacttgtatagaaaagacttcattctatgggatttatataagtaagtgctttctctatattcaaaatatttcataaggacctgtggtttttttccccttaaaaagcaactctaggccgggcacagtggctcatgcctgtaatcccagcactttgggaggccaaggcaggtggatcacttgaggtcaggagttcgagaccagctggttaacatggtgaaaccccatctctactaaaaatacaaaaattagccaggtgtggtggcacgcgcctgtaatcccagctacatgggaggttgaggcaggagaatctcttgaacccaggaggtggaggttgcagtgagccgcaattacaccactgcactccagcctgggtgacacagcgagtctccatctccaaaaaaaattcaactcttggtcttgtttctcagcacttagtttattgttattagaatttagccatacagccaactttgacaaaatgggtcacagaacaagcatgtacatcaagaggaagttccatatcccccttgtaccatttctccttgggaactcatgctatgggctaccttaaaggtaaaactcatcttatggagtctttctgataggtcactaggtaaaactccttggatagggtgaaaatggatgcacactctattacatactctggtttatcataaggaattttccagaaagctaagctttatactaataagatattggttggtagtaggaacttcaaaaatgaatgagtttgccataactttaattttctggattagaaacacaaaacttgaaatgcaattatcaatattttgtaatatatattcctacagtttgggtagaaataaggaacatgtctgctagatctggtttatgaaaaagtgaaaaatattaaatacaccagagactcaaaccctttcaaggcacacaataactgttctggatttacctgacaaacctagttgagtagcattttgacagaaaatatcagactgaaagttcattcaaatgtacttaaatgtacaatacagtgttcaatagtttttattgcagtgatgtttttccaataatttaagtaattctcttcctagtataatacagttttcataaataatgtttacttgctttctttatattttcaaataaaattaaaatgctcgagcacttcctttcagaaagttataaaattaaaaataattattttaaatgctcattcaaatgtgtctgtatacttgctatgcccctttttctataattccaaactgagactgatttttcagagatttttaactttaataattttaaatctagaatcaagtgaaacagatatgttaaatactgagtctagttttcttccatcttatggagcttcatggaataagaaactaatctagtgcaaatgaagattaaatatttctgggtgatggagagatagtcaacaaatttatttatccatcctctgcacatcagtccactggagcaggagttctacacattaaaaatgtaatgggatcagcctagcattgtttggtgttcttttgttgtattttttagaatgggggtgggggcctaagtgtccttatgaagctgtggtccacgacaggagcttgttgggggagtaccagggttctgctgctttcctgcatctgagcaacacaacagagatcatcagttttaaatagagtagccctcacaatcaaaatatcatagaatatattgtaaagttatgttgctaattttcctttgaaatataaaatattttaagctttttgtcaaaagtggtaacatcttaatacaaataaaaacctttttgtggttgtaagatttagcttataaatcattcaaattgaagtgaaagaattaccaggtcattgttaatgacttagtctattaagaatatatgtatttttgtaaaggaaaagcacttgtagatatttaatcagtacaagatatgtcttttgcagaaataaaatgctgcttagagattctccttaaatattttttatttttgtgctcaaatgtattttctgttgatctatggaatgttctgtacaaagctgtataattgtactgttgggctagatactttttttttttaatctggacttagccaagtatatttcaccatgttaaaatacagtatctttgttattaaaaattaaattgcataatttattattgtttgtcatctttaatattagtcactgtagattgcagccttcattaaaaatatctcctttaaaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:84333 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
GeneID:84333 -> Molecular function: GO:0008270 [zinc ion binding] evidence: IEA
GeneID:84333 -> Biological process: GO:0006351 [transcription, DNA-dependent] evidence: IEA
GeneID:84333 -> Biological process: GO:0006355 [regulation of transcription, DNA-dependent] evidence: IEA
GeneID:84333 -> Cellular component: GO:0005634 [nucleus] evidence: IDA
GeneID:84333 -> Cellular component: GO:0005813 [centrosome] evidence: IDA
GeneID:84333 -> Cellular component: GO:0031519 [PcG protein complex] evidence: IDA
by
@meso_cacase at
DBCLS
This page is licensed under a Creative Commons Attribution 2.1 Japan License.