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2024-04-27 04:33:27, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_005318 2336 bp mRNA linear PRI 05-MAY-2013
DEFINITION Homo sapiens H1 histone family, member 0 (H1F0), mRNA.
ACCESSION NM_005318
VERSION NM_005318.3 GI:85838503
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 2336)
AUTHORS Vyas,P. and Brown,D.T.
TITLE N- and C-terminal domains determine differential nucleosomal
binding geometry and affinity of linker histone isotypes H1(0) and
H1c
JOURNAL J. Biol. Chem. 287 (15), 11778-11787 (2012)
PUBMED 22334665
REMARK GeneRIF: The N-terminal domain contributes toward the differential
chromatin binding affinity, whereas the C-terminal domain
contributes toward distinct nucleosomal interface of isotypes H10
and H1c.
REFERENCE 2 (bases 1 to 2336)
AUTHORS Johnatty,S.E., Beesley,J., Chen,X., Macgregor,S., Duffy,D.L.,
Spurdle,A.B., deFazio,A., Gava,N., Webb,P.M., Rossing,M.A.,
Doherty,J.A., Goodman,M.T., Lurie,G., Thompson,P.J., Wilkens,L.R.,
Ness,R.B., Moysich,K.B., Chang-Claude,J., Wang-Gohrke,S.,
Cramer,D.W., Terry,K.L., Hankinson,S.E., Tworoger,S.S.,
Garcia-Closas,M., Yang,H., Lissowska,J., Chanock,S.J.,
Pharoah,P.D., Song,H., Whitemore,A.S., Pearce,C.L., Stram,D.O.,
Wu,A.H., Pike,M.C., Gayther,S.A., Ramus,S.J., Menon,U.,
Gentry-Maharaj,A., Anton-Culver,H., Ziogas,A., Hogdall,E.,
Kjaer,S.K., Hogdall,C., Berchuck,A., Schildkraut,J.M.,
Iversen,E.S., Moorman,P.G., Phelan,C.M., Sellers,T.A.,
Cunningham,J.M., Vierkant,R.A., Rider,D.N., Goode,E.L., Haviv,I.
and Chenevix-Trench,G.
CONSRTM Ovarian Cancer Association Consortium; Australian Ovarian Cancer
Study Group; Australian Cancer Study (Ovarian Cancer)
TITLE Evaluation of candidate stromal epithelial cross-talk genes
identifies association between risk of serous ovarian cancer and
TERT, a cancer susceptibility 'hot-spot'
JOURNAL PLoS Genet. 6 (7), E1001016 (2010)
PUBMED 20628624
REMARK GeneRIF: Meta-analysis of gene-disease association. (HuGE
Navigator)
Publication Status: Online-Only
REFERENCE 3 (bases 1 to 2336)
AUTHORS Ninios,Y.P., Sekeri-Pataryas,K.E. and Sourlingas,T.G.
TITLE Histone H1 subtype preferences of DFF40 and possible nuclear
localization of DFF40/45 in normal and trichostatin A-treated NB4
leukemic cells
JOURNAL Apoptosis 15 (2), 128-138 (2010)
PUBMED 19882353
REFERENCE 4 (bases 1 to 2336)
AUTHORS Collins,J.E., Wright,C.L., Edwards,C.A., Davis,M.P., Grinham,J.A.,
Cole,C.G., Goward,M.E., Aguado,B., Mallya,M., Mokrab,Y.,
Huckle,E.J., Beare,D.M. and Dunham,I.
TITLE A genome annotation-driven approach to cloning the human ORFeome
JOURNAL Genome Biol. 5 (10), R84 (2004)
PUBMED 15461802
REFERENCE 5 (bases 1 to 2336)
AUTHORS Dame,C., Sola,M.C., Fandrey,J., Rimsza,L.M., Freitag,P.,
Knopfle,G., Christensen,R.D. and Bungert,J.
TITLE Developmental changes in the expression of transcription factors
GATA-1, -2 and -3 during the onset of human medullary
haematopoiesis
JOURNAL Br. J. Haematol. 119 (2), 510-515 (2002)
PUBMED 12406094
REFERENCE 6 (bases 1 to 2336)
AUTHORS Lindner,H., Sarg,B., Hoertnagl,B. and Helliger,W.
TITLE The microheterogeneity of the mammalian H1(0) histone. Evidence for
an age-dependent deamidation
JOURNAL J. Biol. Chem. 273 (21), 13324-13330 (1998)
PUBMED 9582379
REFERENCE 7 (bases 1 to 2336)
AUTHORS Parseghian,M.H., Clark,R.F., Hauser,L.J., Dvorkin,N., Harris,D.A.
and Hamkalo,B.A.
TITLE Fractionation of human H1 subtypes and characterization of a
subtype-specific antibody exhibiting non-uniform nuclear staining
JOURNAL Chromosome Res. 1 (2), 127-139 (1993)
PUBMED 7511470
REFERENCE 8 (bases 1 to 2336)
AUTHORS Albig,W., Drabent,B., Kunz,J., Kalff-Suske,M., Grzeschik,K.H. and
Doenecke,D.
TITLE All known human H1 histone genes except the H1(0) gene are
clustered on chromosome 6
JOURNAL Genomics 16 (3), 649-654 (1993)
PUBMED 8325638
REFERENCE 9 (bases 1 to 2336)
AUTHORS Doenecke,D. and Tonjes,R.
TITLE Differential distribution of lysine and arginine residues in the
closely related histones H1 and H5. Analysis of a human H1 gene
JOURNAL J. Mol. Biol. 187 (3), 461-464 (1986)
PUBMED 3084796
REFERENCE 10 (bases 1 to 2336)
AUTHORS Dreikorn,K. and Rohl,L.
TITLE Preservation and transplantation of human cadaver kidneys.
Experiences with the Gamgro perfusion unit
JOURNAL Scand. J. Urol. Nephrol. 8 (1), 19-26 (1974)
PUBMED 4595808
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from BI462123.1, BX490432.1,
BC000145.1, Z97630.11, BC029046.1 and AA206831.1.
On Jan 27, 2006 this sequence version replaced gi:20336758.
Summary: Histones are basic nuclear proteins that are responsible
for the nucleosome structure of the chromosomal fiber in
eukaryotes. Nucleosomes consist of approximately 146 bp of DNA
wrapped around a histone octamer composed of pairs of each of the
four core histones (H2A, H2B, H3, and H4). The chromatin fiber is
further compacted through the interaction of a linker histone, H1,
with the DNA between the nucleosomes to form higher order chromatin
structures. This gene is intronless and encodes a member of the
histone H1 family. [provided by RefSeq, Jul 2008].
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.
COMPLETENESS: full length.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-179 BI462123.1 17-195
180-307 BX490432.1 58-185
308-1297 BC000145.1 155-1144
1298-1621 Z97630.11 14273-14596
1622-2191 BC000145.1 1468-2037
2192-2326 BC029046.1 2037-2171
2327-2336 AA206831.1 1-10 c
FEATURES Location/Qualifiers
source 1..2336
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="22"
/map="22q13.1"
gene 1..2336
/gene="H1F0"
/gene_synonym="H10; H1FV"
/note="H1 histone family, member 0"
/db_xref="GeneID:3005"
/db_xref="HGNC:4714"
/db_xref="HPRD:00819"
/db_xref="MIM:142708"
exon 1..2330
/gene="H1F0"
/gene_synonym="H10; H1FV"
/inference="alignment:Splign:1.39.8"
misc_feature 94..96
/gene="H1F0"
/gene_synonym="H10; H1FV"
/note="upstream in-frame stop codon"
variation 136
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="a"
/replace="g"
/db_xref="dbSNP:181731528"
variation 142
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="a"
/replace="g"
/db_xref="dbSNP:186080346"
variation 143
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="a"
/replace="g"
/db_xref="dbSNP:192306490"
variation 159..164
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace=""
/replace="gaggca"
/db_xref="dbSNP:202179193"
variation 163
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="c"
/replace="t"
/db_xref="dbSNP:183668620"
variation 164
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="a"
/replace="g"
/db_xref="dbSNP:186786865"
variation 177..188
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace=""
/replace="gaggcagagccc"
/db_xref="dbSNP:112389913"
variation 180..191
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace=""
/replace="gcagagcccgag"
/db_xref="dbSNP:371238242"
variation 180
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace=""
/replace="gcagagcccgag"
/db_xref="dbSNP:56234808"
variation 186
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="c"
/replace="g"
/db_xref="dbSNP:369141990"
variation 188
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="a"
/replace="c"
/db_xref="dbSNP:9607493"
variation 234
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="c"
/replace="t"
/db_xref="dbSNP:12165311"
variation 383
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="c"
/replace="t"
/db_xref="dbSNP:186139362"
STS 405..1059
/gene="H1F0"
/gene_synonym="H10; H1FV"
/standard_name="RH27824"
/db_xref="UniSTS:85317"
variation 408
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="c"
/replace="t"
/db_xref="dbSNP:374607983"
variation 416..417
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace=""
/replace="c"
/db_xref="dbSNP:140532092"
variation 423
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="a"
/replace="g"
/db_xref="dbSNP:368431497"
variation 425
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="c"
/replace="t"
/db_xref="dbSNP:371303008"
variation 427
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="a"
/replace="c"
/db_xref="dbSNP:374249786"
variation 429
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="a"
/replace="g"
/db_xref="dbSNP:190663843"
variation 430
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="c"
/replace="t"
/db_xref="dbSNP:372077183"
variation 432
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="a"
/replace="g"
/db_xref="dbSNP:373751761"
variation 433
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="a"
/replace="g"
/db_xref="dbSNP:182117701"
CDS 439..1023
/gene="H1F0"
/gene_synonym="H10; H1FV"
/note="H1.0, H1(0), H1-0; histone H1'; histone H1(0)"
/codon_start=1
/product="histone H1.0"
/protein_id="NP_005309.1"
/db_xref="GI:4885371"
/db_xref="CCDS:CCDS13956.1"
/db_xref="GeneID:3005"
/db_xref="HGNC:4714"
/db_xref="HPRD:00819"
/db_xref="MIM:142708"
/translation="
MTENSTSAPAAKPKRAKASKKSTDHPKYSDMIVAAIQAEKNRAGSSRQSIQKYIKSHYKVGENADSQIKLSIKRLVTTGVLKQTKGVGASGSFRLAKSDEPKKSVAFKKTKKEIKKVATPKKASKPKKAASKAPTKKPKATPVKKAKKKLAATPKKAKKPKTVKAKPVKASKPKKAKPVKPKAKSSAKRAGKKK
"
misc_feature 442..444
/gene="H1F0"
/gene_synonym="H10; H1FV"
/experiment="experimental evidence, no additional details
recorded"
/note="N-acetylthreonine; propagated from
UniProtKB/Swiss-Prot (P07305.3); acetylation site"
misc_feature 448..450
/gene="H1F0"
/gene_synonym="H10; H1FV"
/experiment="experimental evidence, no additional details
recorded"
/note="Deamidated asparagine, partial; propagated from
UniProtKB/Swiss-Prot (P07305.3); amidation site"
misc_feature 451..453
/gene="H1F0"
/gene_synonym="H10; H1FV"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 472..474
/gene="H1F0"
/gene_synonym="H10; H1FV"
/experiment="experimental evidence, no additional details
recorded"
/note="acetylation site"
misc_feature 511..756
/gene="H1F0"
/gene_synonym="H10; H1FV"
/note="linker histone 1 and histone 5 domains; the basic
subunit of chromatin is the nucleosome, consisting of an
octamer of core histones, two full turns of DNA, a linker
histone (H1 or H5) and a variable length of linker DNA;
H1/H5 are chromatin-associated...; Region: H15; cd00073"
/db_xref="CDD:28954"
misc_feature order(523..525,559..561,649..651,691..693)
/gene="H1F0"
/gene_synonym="H10; H1FV"
/note="DNA-binding site [nucleotide binding]; DNA binding
site"
/db_xref="CDD:28954"
misc_feature 634..669
/gene="H1F0"
/gene_synonym="H10; H1FV"
/note="DNA-binding site [nucleotide binding]; DNA binding
site"
/db_xref="CDD:28954"
misc_feature 634..636
/gene="H1F0"
/gene_synonym="H10; H1FV"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 727..756
/gene="H1F0"
/gene_synonym="H10; H1FV"
/note="AKP helix motif (fragment); other site"
/db_xref="CDD:28954"
misc_feature 808..810
/gene="H1F0"
/gene_synonym="H10; H1FV"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P07305.3); phosphorylation site"
misc_feature 808..810
/gene="H1F0"
/gene_synonym="H10; H1FV"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 949..951
/gene="H1F0"
/gene_synonym="H10; H1FV"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P07305.3); phosphorylation site"
variation 456
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="a"
/replace="g"
/db_xref="dbSNP:142834608"
variation 462
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="c"
/replace="t"
/db_xref="dbSNP:377253437"
variation 492
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="c"
/replace="t"
/db_xref="dbSNP:201578247"
variation 534
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="c"
/replace="t"
/db_xref="dbSNP:151035348"
variation 547
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="c"
/replace="t"
/db_xref="dbSNP:375796831"
variation 627
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="c"
/replace="t"
/db_xref="dbSNP:140898014"
variation 631
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="c"
/replace="g"
/db_xref="dbSNP:17855539"
variation 648
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="a"
/replace="g"
/db_xref="dbSNP:150162329"
variation 747
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="a"
/replace="g"
/db_xref="dbSNP:200068985"
variation 817
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="a"
/replace="g"
/db_xref="dbSNP:138891617"
variation 835
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="a"
/replace="g"
/db_xref="dbSNP:377660306"
variation 861
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="c"
/replace="t"
/db_xref="dbSNP:370894514"
variation 865
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="a"
/replace="g"
/db_xref="dbSNP:368543378"
variation 881
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="a"
/replace="g"
/db_xref="dbSNP:371918453"
variation 897
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="g"
/replace="t"
/db_xref="dbSNP:201818456"
variation 902
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="a"
/replace="g"
/db_xref="dbSNP:191676435"
variation 927
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="c"
/replace="g"
/db_xref="dbSNP:141353887"
variation 931
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="a"
/replace="g"
/db_xref="dbSNP:200902795"
STS 939..1166
/gene="H1F0"
/gene_synonym="H10; H1FV"
/standard_name="RH17516"
/db_xref="UniSTS:69594"
variation 1008
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="c"
/replace="t"
/db_xref="dbSNP:182905061"
variation 1043
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="a"
/replace="g"
/db_xref="dbSNP:369827028"
variation 1064
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="a"
/replace="g"
/db_xref="dbSNP:374321557"
STS 1092..1216
/gene="H1F0"
/gene_synonym="H10; H1FV"
/standard_name="G29683"
/db_xref="UniSTS:72511"
variation 1188
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="a"
/replace="t"
/db_xref="dbSNP:145575097"
variation 1213
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="a"
/replace="g"
/db_xref="dbSNP:188218991"
variation 1286..1291
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="cttgcg"
/replace="tttgc"
/db_xref="dbSNP:71322691"
variation 1286
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="c"
/replace="t"
/db_xref="dbSNP:6000898"
variation 1291
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace=""
/replace="g"
/db_xref="dbSNP:5845353"
variation 1298
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="c"
/replace="g"
/db_xref="dbSNP:199983827"
variation 1313..1314
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace=""
/replace="g"
/db_xref="dbSNP:34537258"
variation 1327
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="g"
/replace="t"
/db_xref="dbSNP:138070396"
variation 1439
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="c"
/replace="t"
/db_xref="dbSNP:1894644"
variation 1483
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="a"
/replace="g"
/db_xref="dbSNP:149530054"
variation 1529
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1894645"
variation 1621
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="c"
/replace="g"
/db_xref="dbSNP:1894646"
variation 1640
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="c"
/replace="t"
/db_xref="dbSNP:143155064"
variation 1652
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="a"
/replace="g"
/db_xref="dbSNP:148246524"
variation 1720
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="a"
/replace="t"
/db_xref="dbSNP:185448090"
variation 1779
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="a"
/replace="g"
/db_xref="dbSNP:143916364"
variation 1806
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="c"
/replace="t"
/db_xref="dbSNP:147261789"
variation 1814
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="a"
/replace="g"
/db_xref="dbSNP:80219930"
variation 1826
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="c"
/replace="t"
/db_xref="dbSNP:73411582"
variation 1916
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="g"
/replace="t"
/db_xref="dbSNP:142971115"
STS 1935..2062
/gene="H1F0"
/gene_synonym="H10; H1FV"
/standard_name="STS-W90034"
/db_xref="UniSTS:46658"
variation 2036
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="a"
/replace="g"
/db_xref="dbSNP:190553770"
STS 2041..2268
/gene="H1F0"
/gene_synonym="H10; H1FV"
/standard_name="G31469"
/db_xref="UniSTS:32448"
variation 2051
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="c"
/replace="t"
/db_xref="dbSNP:192459911"
variation 2104
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="g"
/replace="t"
/db_xref="dbSNP:191509238"
variation 2212
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="g"
/replace="t"
/db_xref="dbSNP:15973"
variation 2225..2226
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace=""
/replace="c"
/replace="cc"
/db_xref="dbSNP:71324880"
variation 2234..2235
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace=""
/replace="cc"
/replace="ccc"
/replace="ccca"
/db_xref="dbSNP:56665907"
variation 2235..2236
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace=""
/replace="cc"
/replace="ccc"
/replace="ccca"
/db_xref="dbSNP:67411801"
variation 2235
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="a"
/replace="c"
/db_xref="dbSNP:1050466"
variation 2262
/gene="H1F0"
/gene_synonym="H10; H1FV"
/replace="a"
/replace="g"
/db_xref="dbSNP:183751019"
polyA_signal 2305..2310
/gene="H1F0"
/gene_synonym="H10; H1FV"
polyA_site 2332
/gene="H1F0"
/gene_synonym="H10; H1FV"
ORIGIN
ggaagaaacacagatggcggcggcgcagcgccattccgggccgggagcaggcagccagcagccctgtcctcaccgcggtccgcccgccgccgctaaatacccggatgcgccgcccaagcgccagacgcggagctgggaaaagggaggcagaggaggcggaggcagaggcagaggcagaggcagagcccgagcccggtgccgagaccaagcgacagaccggcggggctgggcctcgcaaagccggctcggcgagctctcccgacacccgagccggggaggaaaagcagcgactcctcgctcgcatccccgggagccgcactccagactggcccggtagtcaggggctcaggagcagatcccgaggcaggctttgctcagcctccgacgagggctggccctttggaaggcgccttcaacagccggaccagacaggccaccatgaccgagaattccacgtccgcccctgcggccaagcccaagcgggccaaggcctccaagaagtccacagaccaccccaagtattcagacatgatcgtggctgccatccaggccgagaagaaccgcgctggctcctcgcgccagtccattcagaagtatatcaagagccactacaaggtgggtgagaacgctgactcgcagatcaagttgtccatcaagcgcctggtcaccaccggtgtcctcaagcagaccaaaggggtgggggcctcggggtccttccggctagccaagagcgacgaacccaagaagtcagtggccttcaagaagaccaagaaggaaatcaagaaggtagccacgccaaagaaggcatccaagcccaagaaggctgcctccaaagccccaaccaagaaacccaaagccaccccggtcaagaaggccaagaagaagctggctgccacgcccaagaaagccaaaaaacccaagactgtcaaagccaagccggtcaaggcatccaagcccaaaaaggccaaaccagtgaaacccaaagcaaagtccagtgccaagagggccggcaagaagaagtgacaatgaagtcttttcttgcggacactccctcctgtctcctattttctgtaaataattttctccttttttctctcttgatgctcaccaccaccttttgcccccttctgttctgactttataagagacaggatttggattcttcagaaattacagaataattcatttttccttaaccagttgtgcaaggacagcaacaaccaatctaatgatgagaatgtacttatattttgttttgctattaacctacttacggggttagggatttgcggggggggcttgtgtgttttgttggcttgtttgccatgaaggtagatgtgggtggggagaagacacaaggcagtttgttctggctagatgagagggaacccaggaattgtgaggttagcaggaatatctttagggtgagtgagttttctttgagttgggcacccgttgtgagagtttcagaacctttggccagcaggagagaggtggtagggagcagccagccggcaaaggaaggagggggaaaaaaaccgccaccgggctgacttccacctcccagtggtgagcagtgggggcccaaacccagtttccttctcatttttgttagtttgcgctttcggcctccctattttcttagggaaggggagtggggtccaagtgacagctggatgggagaagccatagtttctcccagtcagctaggatgtagccattgggggatctttgtggcttcagcaaattctcttgttaaaccggagtgaaaacttcaggggaagggtggggagtcagccaagtgcctcagtgtgccctgttgaaacttaggtttttccacgcaatcgatggattgtgtcctaggaagacttttcttttcctctggatttttgttcctcctgtacaagaggtgtctttgcttggtttggtggggctgcggccacttaaaacctcccgatctctttttgagtcctttattataagtagttgtagctgcgggagggggagggggagtgggcgggcagtggatagtaagacttactgcagtcgatttgggatttgctaagtagttttacagagctagatctgtgtgcatgtgtgtgtttgtgtatatatacatatctagggctagtacttagtttcacacccgggagctgggagaaaaaacctgtacagttgtctttctcttatttttaataaaatagaaaaatcgcgcacttgcgcgtcccccccccacccccttttttaaacaagtgttacttgtgccgggaaaattttgctgtctttgtaattttaaaactttaaaataaattggaaaagggagaaactgaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:3005 -> Molecular function: GO:0003677 [DNA binding] evidence: IEA
GeneID:3005 -> Biological process: GO:0006309 [apoptotic DNA fragmentation] evidence: TAS
GeneID:3005 -> Biological process: GO:0006334 [nucleosome assembly] evidence: IEA
GeneID:3005 -> Biological process: GO:0006915 [apoptotic process] evidence: TAS
GeneID:3005 -> Biological process: GO:0006921 [cellular component disassembly involved in execution phase of apoptosis] evidence: TAS
GeneID:3005 -> Cellular component: GO:0000786 [nucleosome] evidence: IEA
GeneID:3005 -> Cellular component: GO:0000790 [nuclear chromatin] evidence: IDA
GeneID:3005 -> Cellular component: GO:0005634 [nucleus] evidence: IDA
GeneID:3005 -> Cellular component: GO:0005654 [nucleoplasm] evidence: TAS
GeneID:3005 -> Cellular component: GO:0005794 [Golgi apparatus] evidence: IDA
by
@meso_cacase at
DBCLS
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