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2024-04-19 07:52:41, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001257101 7057 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens polycomb group ring finger 5 (PCGF5), transcript
variant 4, mRNA.
ACCESSION NM_001257101
VERSION NM_001257101.1 GI:380036032
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 7057)
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 7057)
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 7057)
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
AL731553.12, BC051845.1, AC026227.8 and BQ420347.1.
Transcript Variant: This variant (4) 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 :: BC051845.1 [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
1-70 AL731553.12 85048-85117
71-3687 BC051845.1 46-3662
3688-6682 AC026227.8 100514-103508 c
6683-7057 BQ420347.1 17-391
FEATURES Location/Qualifiers
source 1..7057
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="10"
/map="10q23.32"
gene 1..7057
/gene="PCGF5"
/gene_synonym="RNF159"
/note="polycomb group ring finger 5"
/db_xref="GeneID:84333"
/db_xref="HGNC:28264"
exon 1..70
/gene="PCGF5"
/gene_synonym="RNF159"
/inference="alignment:Splign:1.39.8"
variation 64
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="g"
/db_xref="dbSNP:12784538"
exon 71..365
/gene="PCGF5"
/gene_synonym="RNF159"
/inference="alignment:Splign:1.39.8"
variation 120
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:151125630"
variation 227
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:374274424"
variation 242
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:368638959"
misc_feature 245..247
/gene="PCGF5"
/gene_synonym="RNF159"
/note="upstream in-frame stop codon"
CDS 254..1024
/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_001244030.1"
/db_xref="GI:380036033"
/db_xref="CCDS:CCDS7413.1"
/db_xref="GeneID:84333"
/db_xref="HGNC:28264"
/translation="
MATQRKHLVKDFNPYITCYICKGYLIKPTTVTECLHTFCKTCIVQHFEDSNDCPRCGNQVHETNPLEMLRLDNTLEEIIFKLVPGLREQELERESEFWKKNKPQENGQDDTSKADKPKVDEEGDENEDDKDYHRSDPQIAICLDCLRNNGQSGDNVVKGLMKKFIRCSTRVTVGTIKKFLSLKLKLPSSYELDVLCNGEIMGKDHTMEFIYMTRWRLRGENFRCLNCSASQVCSQDGPLYQSYPMVLQYRPRIDFG
"
misc_feature 302..421
/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(305..307,314..316,353..355,359..361,368..370,
377..379,410..412,419..421)
/gene="PCGF5"
/gene_synonym="RNF159"
/note="cross-brace motif; other site"
/db_xref="CDD:29102"
variation 309
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:372696858"
exon 366..462
/gene="PCGF5"
/gene_synonym="RNF159"
/inference="alignment:Splign:1.39.8"
variation 382
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:148710899"
variation 402
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:372569296"
variation 415
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="c"
/db_xref="dbSNP:142481328"
exon 463..518
/gene="PCGF5"
/gene_synonym="RNF159"
/inference="alignment:Splign:1.39.8"
variation 509
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:369012074"
variation 516
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:372777415"
exon 519..578
/gene="PCGF5"
/gene_synonym="RNF159"
/inference="alignment:Splign:1.39.8"
exon 579..727
/gene="PCGF5"
/gene_synonym="RNF159"
/inference="alignment:Splign:1.39.8"
variation 585
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:375287111"
variation 603
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:151323358"
variation 612
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:369899767"
variation 616
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:140669067"
variation 620
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="g"
/db_xref="dbSNP:373196380"
exon 728..826
/gene="PCGF5"
/gene_synonym="RNF159"
/inference="alignment:Splign:1.39.8"
variation 734
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:200475271"
variation 748
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:191760973"
exon 827..916
/gene="PCGF5"
/gene_synonym="RNF159"
/inference="alignment:Splign:1.39.8"
exon 917..976
/gene="PCGF5"
/gene_synonym="RNF159"
/inference="alignment:Splign:1.39.8"
variation 935
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:377561962"
variation 943
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="g"
/replace="t"
/db_xref="dbSNP:144351361"
variation 955
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:146460099"
exon 977..7039
/gene="PCGF5"
/gene_synonym="RNF159"
/inference="alignment:Splign:1.39.8"
variation 1015
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:367608907"
variation 1018
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:191746944"
variation 1071
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:182483549"
variation 1075
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:186761917"
variation 1110
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="c"
/db_xref="dbSNP:113330131"
variation 1196
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="g"
/replace="t"
/db_xref="dbSNP:115710628"
variation 1219
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="t"
/db_xref="dbSNP:1061292"
variation 1405
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:192315041"
variation 1459
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="g"
/db_xref="dbSNP:369207455"
variation 1477
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:185855100"
variation 1481
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:2450445"
variation 1643
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:190416217"
variation 1688
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:142716800"
variation 1698
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:143433812"
variation 1785
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:193205144"
variation 1900..1901
/gene="PCGF5"
/gene_synonym="RNF159"
/replace=""
/replace="t"
/db_xref="dbSNP:369517487"
variation 2008
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:371532480"
variation 2027
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:374524017"
variation 2030
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:184608338"
variation 2077
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:41286928"
variation 2227
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:115091137"
variation 2231
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:147972947"
variation 2259
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:188924445"
variation 2329
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:11186527"
variation 2337
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:3758498"
variation 2446
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:181383797"
variation 2449
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:185615722"
variation 2468
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:117714148"
variation 2527
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:141793573"
variation 2564
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="g"
/replace="t"
/db_xref="dbSNP:150577718"
variation 2676
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:78753737"
variation 2707
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:138671662"
variation 2871
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:141746709"
variation 3158
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:150651081"
variation 3241
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:374075294"
variation 3299
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:371607692"
variation 3300
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:189639049"
variation 3302
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:375699378"
variation 3352
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:370238940"
variation 3399
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="g"
/db_xref="dbSNP:146104676"
variation 3452
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:73314513"
variation 3454
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:372967837"
variation 3455
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:180820131"
variation 3463
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:185903355"
variation 3523
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="g"
/db_xref="dbSNP:192037337"
variation 3590
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:181775076"
variation 3593
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:369073230"
variation 3668
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:374815810"
variation 3715
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:368134239"
variation 3721
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="g"
/db_xref="dbSNP:186011849"
variation 3727
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:190422800"
variation 3815
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:182708660"
variation 4024
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:77284033"
variation 4029
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:372684384"
variation 4040
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="g"
/db_xref="dbSNP:186979627"
variation 4043
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="g"
/db_xref="dbSNP:191257053"
variation 4045
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:75369883"
variation 4052
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="g"
/replace="t"
/db_xref="dbSNP:182578013"
variation 4068
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="t"
/db_xref="dbSNP:140071127"
variation 4095
/gene="PCGF5"
/gene_synonym="RNF159"
/replace=""
/replace="a"
/db_xref="dbSNP:376545723"
variation 4119
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:187750853"
variation 4264
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="g"
/replace="t"
/db_xref="dbSNP:193111647"
variation 4346
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:7902729"
variation 4347
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:184851487"
variation 4490
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="g"
/replace="t"
/db_xref="dbSNP:187609815"
variation 4504..4505
/gene="PCGF5"
/gene_synonym="RNF159"
/replace=""
/replace="t"
/db_xref="dbSNP:34602274"
variation 4591
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:192141310"
variation 4642
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="c"
/db_xref="dbSNP:117060235"
variation 4655
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="g"
/db_xref="dbSNP:184313387"
variation 4820
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:7074612"
variation 4902
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:189589853"
variation 4914
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="g"
/db_xref="dbSNP:181181369"
variation 4915
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:7091037"
variation 4920
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:61875626"
variation 4942..4943
/gene="PCGF5"
/gene_synonym="RNF159"
/replace=""
/replace="c"
/db_xref="dbSNP:34362692"
variation 4958
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:61875627"
variation 4964
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="t"
/db_xref="dbSNP:61875628"
variation 5063
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:375250914"
variation 5064
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:144690508"
variation 5178
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:148499126"
variation 5184
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="t"
/db_xref="dbSNP:142980825"
variation 5202
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="g"
/replace="t"
/db_xref="dbSNP:7075114"
variation 5259
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:147733453"
variation 5355
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:117231376"
variation 5386
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:115540244"
variation 5399
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:142578695"
variation 5608
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="g"
/replace="t"
/db_xref="dbSNP:375431648"
variation 5712
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="c"
/db_xref="dbSNP:184412430"
variation 5829
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="t"
/db_xref="dbSNP:11592412"
variation 5957
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:370759691"
variation 5973..5974
/gene="PCGF5"
/gene_synonym="RNF159"
/replace=""
/replace="aa"
/db_xref="dbSNP:370725076"
variation 6236
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:373030793"
variation 6399
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:144807100"
variation 6464
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="c"
/db_xref="dbSNP:189395525"
variation 6476
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:112689997"
variation 6712
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:147805190"
variation 6738
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:181980522"
STS 6754..6930
/gene="PCGF5"
/gene_synonym="RNF159"
/standard_name="RH80111"
/db_xref="UniSTS:92151"
variation 6802
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="t"
/db_xref="dbSNP:11541126"
variation 6809
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:13675"
variation 6845
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:2619614"
variation 6847
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="g"
/db_xref="dbSNP:186252705"
variation 6880
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="a"
/replace="t"
/db_xref="dbSNP:14611"
variation 6974
/gene="PCGF5"
/gene_synonym="RNF159"
/replace="c"
/replace="t"
/db_xref="dbSNP:190667449"
ORIGIN
cccacgcgcgcgcgctcgcgcaccacgcgccccgcgcggcccgcccggatcgtggcctctcgagagcaagacatgggaaagcggaaccaccaaaaggagtgatgatcaacgatctcatgataaatctggatgctagttctcatgcctcaggacatcctactgggaacgacacaccagctcctgggatcagactttcatctacttaggacccctctttgcccagactactaaagccagtcttcactagccacgaatggctacccaaaggaaacacttggtgaaagattttaatccttacattacctgctatatctgtaaagggtatctgatcaagccaacaacagtgacggaatgcctccatacattctgtaagacttgtattgttcagcactttgaagatagcaatgattgcccaaggtgtggcaaccaagttcatgagacaaatccattagaaatgttgaggttggacaatacattagaggaaattatatttaagctggtccctggactacgagaacaagaacttgagcgtgaatctgaattttggaagaaaaataagcctcaagaaaatggacaagatgatacttcaaaagctgacaaaccgaaagtagatgaagaaggtgatgaaaatgaagatgataaagattatcacagaagtgacccacaaattgctatctgtctagattgtttacgaaataatgggcaatcaggggacaatgtagtaaagggtttaatgaagaaattcattcgatgttctacacgtgtaactgtgggaactattaaaaaatttctaagtttaaaactaaaacttccaagttcttatgagttggatgtgctgtgcaatggtgaaattatggggaaggatcatactatggaattcatctacatgacaagatggcgactaagaggcgaaaactttcggtgtctgaactgctcagcttcgcaagtctgctctcaggatggccctttgtatcagtcataccctatggtactgcagtatcgaccaagaattgatttcggttagaccaaggggcccagacctcactgagatgaatcctgcactatttgtttactcgtcaacagattgcacagttaacggtgtgtggactagaggaacacaaccagattttcagcatgcaaataaggccattgtctatctctaaattgtcagttgcattcatgttgtttctattaggagcaaaccaagtgccattctgctactgaaccatctgcataaggtatttgtgttgtctcaaagtgtgcaagtcatggtaaaaatcagttagctgtgccgccatgattcacccttctgaatattttgcttgcctgttccaagattgttctaatgtttaattacactagtaaaatggctcaatttttgtggtgttgcagttttcacatacttactcttttattcttgtttaaatagcgtactctacaagaaactaataattatatcttgaaattattttgtatggaagtatatttagaaaagtggtttttgagccactgtcttgttcttgataagctttttgtgtgaaaaaaagttcattcttgagtgtgcaagtccttttgccaagaattccaattattctgtaacattagagcacaatataattgtagacattctaagcatctgtccgtgtagtctaccaattgcacaaggaaggcatgttagccctccagattgaaaatgtatgtgacctcttgaactgaagttagattcccaaccattcaaaatgttggcagctgatcacatttacttctgataaaagtaatgtgtaagtaaggttaatcttctttcataatgccttatgacaagcaggtgctgcttcatgaaacgtcattgtatagcccatttcatgtatcattacattgttgctgttatttaatgagtgcattatttctctttttaagttggccttaggtatatgtcattgtggcatgcagagggttatgacgattttaaatattaggatttttagagcacataacattagctattttatggatttcaaaagtctcaaaacagttgtagattaaaactgttagttacctttcacatttccaaactatgtgcataaaatagaataaatgcagtatagaactatgctaaccaaaattaataggttaagggtattttattttaaatcctgtagtaattggggaaatgagaagattattattttatacatgagttcattaagatcagaaatacaaaatgtcctgtattttgcagttttgttaagtcttccattcgttttaggattagtctgcaagtcaaagaaagtcttgttaccttaaattatatgaaaactgtcattttaaatcttttaatatttacagttttcaaaaaccttacttggaaattgctttgaaacaaacaagctaacctttgaaacttaggaaaaaatcttgaaagttaggaaaaatatttgagaaatatgacgagcacaatctgtgtgttacacacatttagtttttatactgcatatgtggtaaatgtgtcacattttccagtaaaatgtatcagaaatcaatgccttctgaatttcaaaatgattcttagaaataagatattgtacaactctagcaaacatacaaagtacagctaaatcttaatatatttcactatgtaaaaggctgaaacttcataattatctgttccttctatctttttttgagtcaaaaagtctattaaatttttctgttgttgttccaactttggtgaaaaaggttatggcaatactttaactttgttttgttacattgtttttgttcttggaatggctcacaagcagaatttaaaaggcagattttcattaactataaatggctgaaaaaactgaatttactatctagctacagaaattatttttctatggtgtgaaactgttcccagacatccctaagaacttttacaaattattataaatttgtcacacctaggtcagcgattaaaatagtgttttgcaaatggaattttaattaactcaaaatgaattaagagtgcattttaaaaatcacaagtgagactttgatgttttggccccccagccaaaacttaatggtcataaatgaattttatctacaaaatctctttaaatttggctggttgccttgtcatatgtaatttcactattttccaaggaaatatataggaagcaattatgaaactgagaatagttttatatagaattcttttatttactgataatgcattaacatttttattgaaatgcaatggaatatgtgccaaaacacgtgaaaagcttacataaagaaaggcatcagttgtcgtttggagaaaggtacacatttttttgatggtcctaagtgatatggtattactactagaatcacagatttcttcaactgacttattttggtatattcaactacagctttctaaggataggactactttcatgtctagtaatacactgtattccccgttaattatcccttaagtcagattgtagaatttgcaagaaactaggtatagaaaaaatgtacaggcaacttttgtggttagctttataaatttagggtgcttataaaatgataaaatgaattctttaaataacctataggaatcatctgaatctgtaacatcagagactaaaactaaaagttttctttaatctgttgtttcttaagcaataaactgaaagacctttacttccataaaagattttgttatctcttttatctgccttagaaattataagtataaaagggtcaagggaacttagatataaagaatgactgtggtttataaacattactttaattgaagtaatcacatcagttaatagagaaatcaaaatatgtatggccttttctctagattagcaaaacagctttacaaagtatgaaaaaataaactaaaatgctcattgatgaggtaatactcagtctggagtacaggtaacttgggtaatgccttttaactactcttagaggagtatattatttctttatacattaaacatctatcccatagtaatgtgccacattttataaacgtaatgactttgctcaactacattacacactcaaatgtaatctaaatttaaactgattatttaaggaaaaaaagtgtgttatataatattgtgaactgtttagctttactgaaatatttaagagaaagtgcctcattactaaagtgcatttctgttttaaatttactgcataaagtttgagttatctgtacctgtctcttatgaatggtttcatatctaaataggctcttgtaagttaatttttttggaagattttcataagaatatagatatcaccaaagacattttacagtaaattaataaccatgttggagagacggttttaacagtttggaggttggaaatttttagattgcaatttaattttatatagttaggcaataaccttgattaattgctaaaatatcaccaaagaaaggctttaaactgaattttcttggtgagatcagtcaaatgcaggcttttcttgcaataatcagaacacacttcctttcaaatatgttcattgtttttcagcatcatctaacagatcttagtaaatctaaatcctcaaagatgagaaagaggtaaacacaacaaatagccttcctctgcatgaaaagtgagagaaatacatactttgaaaagaaagttcagatttttaatttgagagggtttttatttcatggaggcagtgttaactaaaattaagcttagatttagctcctgtattattcataatatgagaaattttattaaaggcagactttggtaaaagtgccaacacacttacttgtatagaaaagacttcattctatgggatttatataagtaagtgctttctctatattcaaaatatttcataaggacctgtggtttttttccccttaaaaagcaactctaggccgggcacagtggctcatgcctgtaatcccagcactttgggaggccaaggcaggtggatcacttgaggtcaggagttcgagaccagctggttaacatggtgaaaccccatctctactaaaaatacaaaaattagccaggtgtggtggcacgcgcctgtaatcccagctacatgggaggttgaggcaggagaatctcttgaacccaggaggtggaggttgcagtgagccgcaattacaccactgcactccagcctgggtgacacagcgagtctccatctccaaaaaaaattcaactcttggtcttgtttctcagcacttagtttattgttattagaatttagccatacagccaactttgacaaaatgggtcacagaacaagcatgtacatcaagaggaagttccatatcccccttgtaccatttctccttgggaactcatgctatgggctaccttaaaggtaaaactcatcttatggagtctttctgataggtcactaggtaaaactccttggatagggtgaaaatggatgcacactctattacatactctggtttatcataaggaattttccagaaagctaagctttatactaataagatattggttggtagtaggaacttcaaaaatgaatgagtttgccataactttaattttctggattagaaacacaaaacttgaaatgcaattatcaatattttgtaatatatattcctacagtttgggtagaaataaggaacatgtctgctagatctggtttatgaaaaagtgaaaaatattaaatacaccagagactcaaaccctttcaaggcacacaataactgttctggatttacctgacaaacctagttgagtagcattttgacagaaaatatcagactgaaagttcattcaaatgtacttaaatgtacaatacagtgttcaatagtttttattgcagtgatgtttttccaataatttaagtaattctcttcctagtataatacagttttcataaataatgtttacttgctttctttatattttcaaataaaattaaaatgctcgagcacttcctttcagaaagttataaaattaaaaataattattttaaatgctcattcaaatgtgtctgtatacttgctatgcccctttttctataattccaaactgagactgatttttcagagatttttaactttaataattttaaatctagaatcaagtgaaacagatatgttaaatactgagtctagttttcttccatcttatggagcttcatggaataagaaactaatctagtgcaaatgaagattaaatatttctgggtgatggagagatagtcaacaaatttatttatccatcctctgcacatcagtccactggagcaggagttctacacattaaaaatgtaatgggatcagcctagcattgtttggtgttcttttgttgtattttttagaatgggggtgggggcctaagtgtccttatgaagctgtggtccacgacaggagcttgttgggggagtaccagggttctgctgctttcctgcatctgagcaacacaacagagatcatcagttttaaatagagtagccctcacaatcaaaatatcatagaatatattgtaaagttatgttgctaattttcctttgaaatataaaatattttaagctttttgtcaaaagtggtaacatcttaatacaaataaaaacctttttgtggttgtaagatttagcttataaatcattcaaattgaagtgaaagaattaccaggtcattgttaatgacttagtctattaagaatatatgtatttttgtaaaggaaaagcacttgtagatatttaatcagtacaagatatgtcttttgcagaaataaaatgctgcttagagattctccttaaatattttttatttttgtgctcaaatgtattttctgttgatctatggaatgttctgtacaaagctgtataattgtactgttgggctagatactttttttttttaatctggacttagccaagtatatttcaccatgttaaaatacagtatctttgttattaaaaattaaattgcataatttattattgtttgtcatctttaatattagtcactgtagattgcagccttcattaaaaatatctcctttaaaaaaaaaaaaaaaaaaaa
//
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
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