Home |
Help |
Advanced search
2024-04-25 08:33:49, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_032373 7222 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens polycomb group ring finger 5 (PCGF5), transcript
variant 1, mRNA.
ACCESSION NM_032373
VERSION NM_032373.4 GI:375065847
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 7222)
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 7222)
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 7222)
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
BI464238.1, AL832496.1, AC026227.8 and BQ420347.1.
On Feb 9, 2012 this sequence version replaced gi:83816965.
Transcript Variant: This variant (1) represents the longest
transcript. 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 :: AL832496.1 [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
1-186 BI464238.1 5-190
187-1645 AL832496.1 3-1461
1646-7137 AC026227.8 100224-105715 c
7138-7222 BQ420347.1 307-391
FEATURES Location/Qualifiers
source 1..7222
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="10"
/map="10q23.32"
gene 1..7222
/gene="PCGF5"
/gene_synonym="RNF159"
/note="polycomb group ring finger 5"
/db_xref="GeneID:84333"
/db_xref="HGNC:28264"
/db_xref="HPRD:17825"
exon 1..235
/gene="PCGF5"
/gene_synonym="RNF159"
/inference="alignment:Splign:1.39.8"
variation 51..52
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="c"
/db_xref="dbSNP:11541127"
variation 68
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="c"
/db_xref="dbSNP:374098752"
variation 157
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="g"
/replace="t"
/db_xref="dbSNP:367724730"
variation 189
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:11186504"
exon 236..530
/gene="PCGF5"
/gene_synonym="RNF159"
/inference="alignment:Splign:1.39.8"
variation 285
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:151125630"
variation 392
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:374274424"
variation 407
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:368638959"
misc_feature 410..412
/gene="PCGF5"
/gene_synonym="RNF159"
/note="upstream in-frame stop codon"
CDS 419..1189
/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_115749.2"
/db_xref="GI:33300663"
/db_xref="CCDS:CCDS7413.1"
/db_xref="GeneID:84333"
/db_xref="HGNC:28264"
/db_xref="HPRD:17825"
/translation="
MATQRKHLVKDFNPYITCYICKGYLIKPTTVTECLHTFCKTCIVQHFEDSNDCPRCGNQVHETNPLEMLRLDNTLEEIIFKLVPGLREQELERESEFWKKNKPQENGQDDTSKADKPKVDEEGDENEDDKDYHRSDPQIAICLDCLRNNGQSGDNVVKGLMKKFIRCSTRVTVGTIKKFLSLKLKLPSSYELDVLCNGEIMGKDHTMEFIYMTRWRLRGENFRCLNCSASQVCSQDGPLYQSYPMVLQYRPRIDFG
"
misc_feature 467..586
/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(470..472,479..481,518..520,524..526,533..535,
542..544,575..577,584..586)
/gene="PCGF5"
/gene_synonym="RNF159"
/note="cross-brace motif; other site"
/db_xref="CDD:29102"
variation 474
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:372696858"
exon 531..627
/gene="PCGF5"
/gene_synonym="RNF159"
/inference="alignment:Splign:1.39.8"
variation 547
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:148710899"
variation 567
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:372569296"
variation 580
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="c"
/db_xref="dbSNP:142481328"
exon 628..683
/gene="PCGF5"
/gene_synonym="RNF159"
/inference="alignment:Splign:1.39.8"
variation 674
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:369012074"
variation 681
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:372777415"
exon 684..743
/gene="PCGF5"
/gene_synonym="RNF159"
/inference="alignment:Splign:1.39.8"
exon 744..892
/gene="PCGF5"
/gene_synonym="RNF159"
/inference="alignment:Splign:1.39.8"
variation 750
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:375287111"
variation 768
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:151323358"
variation 777
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:369899767"
variation 781
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:140669067"
variation 785
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="g"
/db_xref="dbSNP:373196380"
exon 893..991
/gene="PCGF5"
/gene_synonym="RNF159"
/inference="alignment:Splign:1.39.8"
variation 899
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:200475271"
variation 913
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:191760973"
exon 992..1081
/gene="PCGF5"
/gene_synonym="RNF159"
/inference="alignment:Splign:1.39.8"
exon 1082..1141
/gene="PCGF5"
/gene_synonym="RNF159"
/inference="alignment:Splign:1.39.8"
variation 1100
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:377561962"
variation 1108
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="g"
/replace="t"
/db_xref="dbSNP:144351361"
variation 1120
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:146460099"
exon 1142..7204
/gene="PCGF5"
/gene_synonym="RNF159"
/inference="alignment:Splign:1.39.8"
variation 1180
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:367608907"
variation 1183
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:191746944"
variation 1236
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:182483549"
variation 1240
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:186761917"
variation 1275
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="c"
/db_xref="dbSNP:113330131"
variation 1361
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="g"
/replace="t"
/db_xref="dbSNP:115710628"
variation 1384
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="t"
/db_xref="dbSNP:1061292"
variation 1570
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:192315041"
variation 1624
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="g"
/db_xref="dbSNP:369207455"
variation 1642
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:185855100"
variation 1646
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:2450445"
variation 1808
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:190416217"
variation 1853
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:142716800"
variation 1863
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:143433812"
variation 1950
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:193205144"
variation 2065..2066
/gene="PCGF5"
/gene_synonym="RNF159"
/replace=""
/replace="t"
/db_xref="dbSNP:369517487"
variation 2173
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:371532480"
variation 2192
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:374524017"
variation 2195
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:184608338"
variation 2242
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:41286928"
variation 2392
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:115091137"
variation 2396
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:147972947"
variation 2424
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:188924445"
variation 2494
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:11186527"
variation 2502
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:3758498"
variation 2611
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:181383797"
variation 2614
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:185615722"
variation 2633
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:117714148"
variation 2692
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:141793573"
variation 2729
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="g"
/replace="t"
/db_xref="dbSNP:150577718"
variation 2841
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:78753737"
variation 2872
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:138671662"
variation 3036
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:141746709"
variation 3323
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:150651081"
variation 3406
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:374075294"
variation 3464
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:371607692"
variation 3465
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:189639049"
variation 3467
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:375699378"
variation 3517
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:370238940"
variation 3564
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="g"
/db_xref="dbSNP:146104676"
variation 3617
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:73314513"
variation 3619
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:372967837"
variation 3620
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:180820131"
variation 3628
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:185903355"
variation 3688
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="g"
/db_xref="dbSNP:192037337"
variation 3755
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:181775076"
variation 3758
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:369073230"
variation 3833
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:374815810"
variation 3880
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:368134239"
variation 3886
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="g"
/db_xref="dbSNP:186011849"
variation 3892
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:190422800"
variation 3980
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:182708660"
variation 4189
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:77284033"
variation 4194
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:372684384"
variation 4205
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="g"
/db_xref="dbSNP:186979627"
variation 4208
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="g"
/db_xref="dbSNP:191257053"
variation 4210
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:75369883"
variation 4217
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="g"
/replace="t"
/db_xref="dbSNP:182578013"
variation 4233
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="t"
/db_xref="dbSNP:140071127"
variation 4260
/gene="PCGF5"
/gene_synonym="RNF159"
/replace=""
/replace="a"
/db_xref="dbSNP:376545723"
variation 4284
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:187750853"
variation 4429
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="g"
/replace="t"
/db_xref="dbSNP:193111647"
variation 4511
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:7902729"
variation 4512
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:184851487"
variation 4655
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="g"
/replace="t"
/db_xref="dbSNP:187609815"
variation 4669..4670
/gene="PCGF5"
/gene_synonym="RNF159"
/replace=""
/replace="t"
/db_xref="dbSNP:34602274"
variation 4756
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:192141310"
variation 4807
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="c"
/db_xref="dbSNP:117060235"
variation 4820
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="g"
/db_xref="dbSNP:184313387"
variation 4985
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:7074612"
variation 5067
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:189589853"
variation 5079
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="g"
/db_xref="dbSNP:181181369"
variation 5080
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:7091037"
variation 5085
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:61875626"
variation 5107..5108
/gene="PCGF5"
/gene_synonym="RNF159"
/replace=""
/replace="c"
/db_xref="dbSNP:34362692"
variation 5123
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:61875627"
variation 5129
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="t"
/db_xref="dbSNP:61875628"
variation 5228
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:375250914"
variation 5229
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:144690508"
variation 5343
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:148499126"
variation 5349
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="t"
/db_xref="dbSNP:142980825"
variation 5367
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="g"
/replace="t"
/db_xref="dbSNP:7075114"
variation 5424
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:147733453"
variation 5520
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:117231376"
variation 5551
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:115540244"
variation 5564
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:142578695"
variation 5773
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="g"
/replace="t"
/db_xref="dbSNP:375431648"
variation 5877
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="c"
/db_xref="dbSNP:184412430"
variation 5994
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="t"
/db_xref="dbSNP:11592412"
variation 6122
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:370759691"
variation 6138..6139
/gene="PCGF5"
/gene_synonym="RNF159"
/replace=""
/replace="aa"
/db_xref="dbSNP:370725076"
variation 6401
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:373030793"
variation 6564
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:144807100"
variation 6629
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="c"
/db_xref="dbSNP:189395525"
variation 6641
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:112689997"
variation 6877
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:147805190"
variation 6903
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:181980522"
STS 6919..7095
/gene="PCGF5"
/gene_synonym="RNF159"
/standard_name="RH80111"
/db_xref="UniSTS:92151"
variation 6967
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="t"
/db_xref="dbSNP:11541126"
variation 6974
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:13675"
variation 7010
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:2619614"
variation 7012
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:186252705"
variation 7045
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="t"
/db_xref="dbSNP:14611"
variation 7139
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:190667449"
ORIGIN
agtgggtggagttgcccttggaggcggcaccggacctgggccccgaggcccgccgcgccctgtcgggcctgagccgagtggccccacagagccggcgcgctcccgcctgcagggggagagcagacggggcgcggggaccggccaggccgcggcgggtgctgtttctgtttcactttccttcactctgaggccggcgcgctggcgggcgaggagcggcggcggtggcggccgctggacatgggaaagcggaaccaccaaaaggagtgatgatcaacgatctcatgataaatctggatgctagttctcatgcctcaggacatcctactgggaacgacacaccagctcctgggatcagactttcatctacttaggacccctctttgcccagactactaaagccagtcttcactagccacgaatggctacccaaaggaaacacttggtgaaagattttaatccttacattacctgctatatctgtaaagggtatctgatcaagccaacaacagtgacggaatgcctccatacattctgtaagacttgtattgttcagcactttgaagatagcaatgattgcccaaggtgtggcaaccaagttcatgagacaaatccattagaaatgttgaggttggacaatacattagaggaaattatatttaagctggtccctggactacgagaacaagaacttgagcgtgaatctgaattttggaagaaaaataagcctcaagaaaatggacaagatgatacttcaaaagctgacaaaccgaaagtagatgaagaaggtgatgaaaatgaagatgataaagattatcacagaagtgacccacaaattgctatctgtctagattgtttacgaaataatgggcaatcaggggacaatgtagtaaagggtttaatgaagaaattcattcgatgttctacacgtgtaactgtgggaactattaaaaaatttctaagtttaaaactaaaacttccaagttcttatgagttggatgtgctgtgcaatggtgaaattatggggaaggatcatactatggaattcatctacatgacaagatggcgactaagaggcgaaaactttcggtgtctgaactgctcagcttcgcaagtctgctctcaggatggccctttgtatcagtcataccctatggtactgcagtatcgaccaagaattgatttcggttagaccaaggggcccagacctcactgagatgaatcctgcactatttgtttactcgtcaacagattgcacagttaacggtgtgtggactagaggaacacaaccagattttcagcatgcaaataaggccattgtctatctctaaattgtcagttgcattcatgttgtttctattaggagcaaaccaagtgccattctgctactgaaccatctgcataaggtatttgtgttgtctcaaagtgtgcaagtcatggtaaaaatcagttagctgtgccgccatgattcacccttctgaatattttgcttgcctgttccaagattgttctaatgtttaattacactagtaaaatggctcaatttttgtggtgttgcagttttcacatacttactcttttattcttgtttaaatagcgtactctacaagaaactaataattatatcttgaaattattttgtatggaagtatatttagaaaagtggtttttgagccactgtcttgttcttgataagctttttgtgtgaaaaaaagttcattcttgagtgtgcaagtccttttgccaagaattccaattattctgtaacattagagcacaatataattgtagacattctaagcatctgtccgtgtagtctaccaattgcacaaggaaggcatgttagccctccagattgaaaatgtatgtgacctcttgaactgaagttagattcccaaccattcaaaatgttggcagctgatcacatttacttctgataaaagtaatgtgtaagtaaggttaatcttctttcataatgccttatgacaagcaggtgctgcttcatgaaacgtcattgtatagcccatttcatgtatcattacattgttgctgttatttaatgagtgcattatttctctttttaagttggccttaggtatatgtcattgtggcatgcagagggttatgacgattttaaatattaggatttttagagcacataacattagctattttatggatttcaaaagtctcaaaacagttgtagattaaaactgttagttacctttcacatttccaaactatgtgcataaaatagaataaatgcagtatagaactatgctaaccaaaattaataggttaagggtattttattttaaatcctgtagtaattggggaaatgagaagattattattttatacatgagttcattaagatcagaaatacaaaatgtcctgtattttgcagttttgttaagtcttccattcgttttaggattagtctgcaagtcaaagaaagtcttgttaccttaaattatatgaaaactgtcattttaaatcttttaatatttacagttttcaaaaaccttacttggaaattgctttgaaacaaacaagctaacctttgaaacttaggaaaaaatcttgaaagttaggaaaaatatttgagaaatatgacgagcacaatctgtgtgttacacacatttagtttttatactgcatatgtggtaaatgtgtcacattttccagtaaaatgtatcagaaatcaatgccttctgaatttcaaaatgattcttagaaataagatattgtacaactctagcaaacatacaaagtacagctaaatcttaatatatttcactatgtaaaaggctgaaacttcataattatctgttccttctatctttttttgagtcaaaaagtctattaaatttttctgttgttgttccaactttggtgaaaaaggttatggcaatactttaactttgttttgttacattgtttttgttcttggaatggctcacaagcagaatttaaaaggcagattttcattaactataaatggctgaaaaaactgaatttactatctagctacagaaattatttttctatggtgtgaaactgttcccagacatccctaagaacttttacaaattattataaatttgtcacacctaggtcagcgattaaaatagtgttttgcaaatggaattttaattaactcaaaatgaattaagagtgcattttaaaaatcacaagtgagactttgatgttttggccccccagccaaaacttaatggtcataaatgaattttatctacaaaatctctttaaatttggctggttgccttgtcatatgtaatttcactattttccaaggaaatatataggaagcaattatgaaactgagaatagttttatatagaattcttttatttactgataatgcattaacatttttattgaaatgcaatggaatatgtgccaaaacacgtgaaaagcttacataaagaaaggcatcagttgtcgtttggagaaaggtacacatttttttgatggtcctaagtgatatggtattactactagaatcacagatttcttcaactgacttattttggtatattcaactacagctttctaaggataggactactttcatgtctagtaatacactgtattccccgttaattatcccttaagtcagattgtagaatttgcaagaaactaggtatagaaaaaatgtacaggcaacttttgtggttagctttataaatttagggtgcttataaaatgataaaatgaattctttaaataacctataggaatcatctgaatctgtaacatcagagactaaaactaaaagttttctttaatctgttgtttcttaagcaataaactgaaagacctttacttccataaaagattttgttatctcttttatctgccttagaaattataagtataaaagggtcaagggaacttagatataaagaatgactgtggtttataaacattactttaattgaagtaatcacatcagttaatagagaaatcaaaatatgtatggccttttctctagattagcaaaacagctttacaaagtatgaaaaaataaactaaaatgctcattgatgaggtaatactcagtctggagtacaggtaacttgggtaatgccttttaactactcttagaggagtatattatttctttatacattaaacatctatcccatagtaatgtgccacattttataaacgtaatgactttgctcaactacattacacactcaaatgtaatctaaatttaaactgattatttaaggaaaaaaagtgtgttatataatattgtgaactgtttagctttactgaaatatttaagagaaagtgcctcattactaaagtgcatttctgttttaaatttactgcataaagtttgagttatctgtacctgtctcttatgaatggtttcatatctaaataggctcttgtaagttaatttttttggaagattttcataagaatatagatatcaccaaagacattttacagtaaattaataaccatgttggagagacggttttaacagtttggaggttggaaatttttagattgcaatttaattttatatagttaggcaataaccttgattaattgctaaaatatcaccaaagaaaggctttaaactgaattttcttggtgagatcagtcaaatgcaggcttttcttgcaataatcagaacacacttcctttcaaatatgttcattgtttttcagcatcatctaacagatcttagtaaatctaaatcctcaaagatgagaaagaggtaaacacaacaaatagccttcctctgcatgaaaagtgagagaaatacatactttgaaaagaaagttcagatttttaatttgagagggtttttatttcatggaggcagtgttaactaaaattaagcttagatttagctcctgtattattcataatatgagaaattttattaaaggcagactttggtaaaagtgccaacacacttacttgtatagaaaagacttcattctatgggatttatataagtaagtgctttctctatattcaaaatatttcataaggacctgtggtttttttccccttaaaaagcaactctaggccgggcacagtggctcatgcctgtaatcccagcactttgggaggccaaggcaggtggatcacttgaggtcaggagttcgagaccagctggttaacatggtgaaaccccatctctactaaaaatacaaaaattagccaggtgtggtggcacgcgcctgtaatcccagctacatgggaggttgaggcaggagaatctcttgaacccaggaggtggaggttgcagtgagccgcaattacaccactgcactccagcctgggtgacacagcgagtctccatctccaaaaaaaattcaactcttggtcttgtttctcagcacttagtttattgttattagaatttagccatacagccaactttgacaaaatgggtcacagaacaagcatgtacatcaagaggaagttccatatcccccttgtaccatttctccttgggaactcatgctatgggctaccttaaaggtaaaactcatcttatggagtctttctgataggtcactaggtaaaactccttggatagggtgaaaatggatgcacactctattacatactctggtttatcataaggaattttccagaaagctaagctttatactaataagatattggttggtagtaggaacttcaaaaatgaatgagtttgccataactttaattttctggattagaaacacaaaacttgaaatgcaattatcaatattttgtaatatatattcctacagtttgggtagaaataaggaacatgtctgctagatctggtttatgaaaaagtgaaaaatattaaatacaccagagactcaaaccctttcaaggcacacaataactgttctggatttacctgacaaacctagttgagtagcattttgacagaaaatatcagactgaaagttcattcaaatgtacttaaatgtacaatacagtgttcaatagtttttattgcagtgatgtttttccaataatttaagtaattctcttcctagtataatacagttttcataaataatgtttacttgctttctttatattttcaaataaaattaaaatgctcgagcacttcctttcagaaagttataaaattaaaaataattattttaaatgctcattcaaatgtgtctgtatacttgctatgcccctttttctataattccaaactgagactgatttttcagagatttttaactttaataattttaaatctagaatcaagtgaaacagatatgttaaatactgagtctagttttcttccatcttatggagcttcatggaataagaaactaatctagtgcaaatgaagattaaatatttctgggtgatggagagatagtcaacaaatttatttatccatcctctgcacatcagtccactggagcaggagttctacacattaaaaatgtaatgggatcagcctagcattgtttggtgttcttttgttgtattttttagaatgggggtgggggcctaagtgtccttatgaagctgtggtccacgacaggagcttgttgggggagtaccagggttctgctgctttcctgcatctgagcaacacaacagagatcatcagttttaaatagagtagccctcacaatcaaaatatcatagaatatattgtaaagttatgttgctaattttcctttgaaatataaaatattttaagctttttgtcaaaagtggtaacatcttaatacaaataaaaacctttttgtggttgtaagatttagcttataaatcattcaaattgaagtgaaagaattaccaggtcattgttaatgacttagtctattaagaatatatgtatttttgtaaaggaaaagcacttgtagatatttaatcagtacaagatatgtcttttgcagaaataaaatgctgcttagagattctccttaaatattttttatttttgtgctcaaatgtattttctgttgatctatggaatgttctgtacaaagctgtataattgtactgttgggctagatactttttttttttaatctggacttagccaagtatatttcaccatgttaaaatacagtatctttgttattaaaaattaaattgcataatttattattgtttgtcatctttaatattagtcactgtagattgcagccttcattaaaaatatctcctttaaaaaaaaaaaaaaaaaaaa
//
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.