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2025-05-09 16:28:04, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_014865 4806 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens non-SMC condensin I complex, subunit D2 (NCAPD2),
mRNA.
ACCESSION NM_014865
VERSION NM_014865.3 GI:178056551
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 4806)
AUTHORS Olson,J.E., Wang,X., Pankratz,V.S., Fredericksen,Z.S., Vachon,C.M.,
Vierkant,R.A., Cerhan,J.R. and Couch,F.J.
TITLE Centrosome-related genes, genetic variation, and risk of breast
cancer
JOURNAL Breast Cancer Res. Treat. 125 (1), 221-228 (2011)
PUBMED 20508983
REMARK GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
REFERENCE 2 (bases 1 to 4806)
AUTHORS Kong,X., Stephens,J., Ball,A.R. Jr., Heale,J.T., Newkirk,D.A.,
Berns,M.W. and Yokomori,K.
TITLE Condensin I recruitment to base damage-enriched DNA lesions is
modulated by PARP1
JOURNAL PLoS ONE 6 (8), E23548 (2011)
PUBMED 21858164
REMARK GeneRIF: Data show that that DNA repear process is dictated by
PARP1 through its interaction with the chromosome-targeting domain
of the hCAP-D2 subunit of condensin I.
REFERENCE 3 (bases 1 to 4806)
AUTHORS Flachsbart,F., Franke,A., Kleindorp,R., Caliebe,A., Blanche,H.,
Schreiber,S. and Nebel,A.
TITLE Investigation of genetic susceptibility factors for human longevity
- a targeted nonsynonymous SNP study
JOURNAL Mutat. Res. 694 (1-2), 13-19 (2010)
PUBMED 20800603
REMARK GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
REFERENCE 4 (bases 1 to 4806)
AUTHORS Lee,J.H., Cheng,R., Rogaeva,E., Meng,Y., Stern,Y., Santana,V.,
Lantigua,R., Medrano,M., Jimenez-Velazquez,I.Z., Farrer,L.A., St
George-Hyslop,P. and Mayeux,R.
TITLE Further examination of the candidate genes in chromosome 12p13
locus for late-onset Alzheimer disease
JOURNAL Neurogenetics 9 (2), 127-138 (2008)
PUBMED 18340469
REMARK GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
REFERENCE 5 (bases 1 to 4806)
AUTHORS Beausoleil,S.A., Villen,J., Gerber,S.A., Rush,J. and Gygi,S.P.
TITLE A probability-based approach for high-throughput protein
phosphorylation analysis and site localization
JOURNAL Nat. Biotechnol. 24 (10), 1285-1292 (2006)
PUBMED 16964243
REFERENCE 6 (bases 1 to 4806)
AUTHORS Ball,A.R. Jr., Schmiesing,J.A., Zhou,C., Gregson,H.C., Okada,Y.,
Doi,T. and Yokomori,K.
TITLE Identification of a chromosome-targeting domain in the human
condensin subunit CNAP1/hCAP-D2/Eg7
JOURNAL Mol. Cell. Biol. 22 (16), 5769-5781 (2002)
PUBMED 12138188
REMARK GeneRIF: Data show the CNAP1 C-terminal region defines a novel
histone-binding domain that is responsible for targeting CNAP1, and
possibly condensin, to mitotic chromosomes.
REFERENCE 7 (bases 1 to 4806)
AUTHORS Kimura,K., Cuvier,O. and Hirano,T.
TITLE Chromosome condensation by a human condensin complex in Xenopus egg
extracts
JOURNAL J. Biol. Chem. 276 (8), 5417-5420 (2001)
PUBMED 11136719
REFERENCE 8 (bases 1 to 4806)
AUTHORS Schmiesing,J.A., Gregson,H.C., Zhou,S. and Yokomori,K.
TITLE A human condensin complex containing hCAP-C-hCAP-E and CNAP1, a
homolog of Xenopus XCAP-D2, colocalizes with phosphorylated histone
H3 during the early stage of mitotic chromosome condensation
JOURNAL Mol. Cell. Biol. 20 (18), 6996-7006 (2000)
PUBMED 10958694
REFERENCE 9 (bases 1 to 4806)
AUTHORS Collas,P., Le Guellec,K. and Tasken,K.
TITLE The A-kinase-anchoring protein AKAP95 is a multivalent protein with
a key role in chromatin condensation at mitosis
JOURNAL J. Cell Biol. 147 (6), 1167-1180 (1999)
PUBMED 10601332
REFERENCE 10 (bases 1 to 4806)
AUTHORS Simon,M.A.
TITLE Racial, ethnic, and gender diversity and the resident operative
experience. How can the Academic Orthopaedic Society shape the
future of orthopaedic surgery?
JOURNAL Clin. Orthop. Relat. Res. 360, 253-259 (1999)
PUBMED 10101332
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
AK022511.1, CN307514.1, BC028182.1, D63880.1, AK128354.1 and
AL548223.3.
On Apr 8, 2008 this sequence version replaced gi:41281520.
Publication Note: This RefSeq record includes a subset of the
publications that are available for this gene. Please see the Gene
record to access additional publications.
##Evidence-Data-START##
Transcript exon combination :: AK022511.1, D63880.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025081, ERS025083 [ECO:0000348]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-292 AK022511.1 1-292
293-725 CN307514.1 271-703
726-1965 BC028182.1 738-1977
1966-3231 D63880.1 2719-3984
3232-4006 AK128354.1 3144-3918
4007-4794 D63880.1 4760-5547
4795-4806 AL548223.3 761-772
FEATURES Location/Qualifiers
source 1..4806
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="12"
/map="12p13.3"
gene 1..4806
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/note="non-SMC condensin I complex, subunit D2"
/db_xref="GeneID:9918"
/db_xref="HGNC:24305"
exon 1..23
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/inference="alignment:Splign:1.39.8"
exon 24..173
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/inference="alignment:Splign:1.39.8"
misc_feature 29..31
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/note="upstream in-frame stop codon"
variation 38
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:375473393"
variation 43
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:112394925"
CDS 47..4252
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/note="chromosome condensation related SMC associated
protein 1; chromosome condensation-related SMC-associated
protein 1; XCAP-D2 homolog; chromosome-associated protein
D2"
/codon_start=1
/product="condensin complex subunit 1"
/protein_id="NP_055680.3"
/db_xref="GI:178056552"
/db_xref="CCDS:CCDS8548.1"
/db_xref="GeneID:9918"
/db_xref="HGNC:24305"
/translation="
MAPQMYEFHLPLSPEELLKSGGVNQYVVQEVLSIKHLPPQLRAFQAAFRAQGPLAMLQHFDTIYSILHHFRSIDPGLKEDTLQFLIKVVSRHSQELPAILDDTTLSGSDRNAHLNALKMNCYALIRLLESFETMASQTNLVDLDLGGKGKKARTKAAHGFDWEEERQPILQLLTQLLQLDIRHLWNHSIIEEEFVSLVTGCCYRLLENPTINHQKNRPTREAITHLLGVALTRYNHMLSATVKIIQMLQHFEHLAPVLVAAVSLWATDYGMKSIVGEIVREIGQKCPQELSRDPSGTKGFAAFLTELAERVPAILMSSMCILLDHLDGENYMMRNAVLAAMAEMVLQVLSGDQLEAAARDTRDQFLDTLQAHGHDVNSFVRSRVLQLFTRIVQQKALPLTRFQAVVALAVGRLADKSVLVCKNAIQLLASFLANNPFSCKLSDADLAGPLQKETQKLQEMRAQRRTAAASAVLDPEEEWEAMLPELKSTLQQLLQLPQGEEEIPEQIANTETTEDVKGRIYQLLAKASYKKAIILTREATGHFQESEPFSHIDPEESEETRLLNILGLIFKGPAASTQEKNPRESTGNMVTGQTVCKNKPNMSDPEESRGNDELVKQEMLVQYLQDAYSFSRKITEAIGIISKMMYENTTTVVQEVIEFFVMVFQFGVPQALFGVRRMLPLIWSKEPGVREAVLNAYRQLYLNPKGDSARAKAQALIQNLSLLLVDASVGTIQCLEEILCEFVQKDELKPAVTQLLWERATEKVACCPLERCSSVMLLGMMARGKPEIVGSNLDTLVSIGLDEKFPQDYRLAQQVCHAIANISDRRKPSLGKRHPPFRLPQEHRLFERLRETVTKGFVHPDPLWIPFKEVAVTLIYQLAEGPEVICAQILQGCAKQALEKLEEKRTSQEDPKESPAMLPTFLLMNLLSLAGDVALQQLVHLEQAVSGELCRRRVLREEQEHKTKDPKEKNTSSETTMEEELGLVGATADDTEAELIRGICEMELLDGKQTLAAFVPLLLKVCNNPGLYSNPDLSAAASLALGKFCMISATFCDSQLRLLFTMLEKSPLPIVRSNLMVATGDLAIRFPNLVDPWTPHLYARLRDPAQQVRKTAGLVMTHLILKDMVKVKGQVSEMAVLLIDPEPQIAALAKNFFNELSHKGNAIYNLLPDIISRLSDPELGVEEEPFHTIMKQLLSYITKDKQTESLVEKLCQRFRTSRTERQQRDLAYCVSQLPLTERGLRKMLDNFDCFGDKLSDESIFSAFLSVVGKLRRGAKPEGKAIIDEFEQKLRACHTRGLDGIKELEIGQAGSQRAPSAKKPSTGSRYQPLASTASDNDFVTPEPRRTTRRHPNTQQRASKKKPKVVFSSDESSEEDLSAEMTEDETPKKTTPILRASARRHRS
"
misc_feature 47..1855
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q15021.3);
Region: Interactions with SMC2 and SMC4"
misc_feature 104..106
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(Q15021.3); phosphorylation site"
misc_feature 266..769
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/note="non-SMC mitotic condensation complex subunit 1,
N-term; Region: Cnd1_N; pfam12922"
/db_xref="CDD:205148"
misc_feature 1799..1801
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(Q15021.3); phosphorylation site"
misc_feature 3251..3748
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/note="non-SMC mitotic condensation complex subunit 1;
Region: Cnd1; pfam12717"
/db_xref="CDD:205038"
misc_feature 3974..3976
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(Q15021.3); phosphorylation site"
misc_feature 4034..4036
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(Q15021.3); phosphorylation site"
misc_feature 4037..4039
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphothreonine; propagated from
UniProtKB/Swiss-Prot (Q15021.3); phosphorylation site"
misc_feature 4043..4045
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(Q15021.3); phosphorylation site"
misc_feature 4061..4063
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphothreonine; propagated from
UniProtKB/Swiss-Prot (Q15021.3); phosphorylation site"
misc_feature 4070..4132
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q15021.3);
Region: Bipartite nuclear localization signal"
misc_feature 4142..4144
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(Q15021.3); phosphorylation site"
misc_feature 4145..4147
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(Q15021.3); phosphorylation site"
misc_feature 4154..4156
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(Q15021.3); phosphorylation site"
misc_feature 4157..4159
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(Q15021.3); phosphorylation site"
misc_feature 4172..4174
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(Q15021.3); phosphorylation site"
variation 51
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="g"
/db_xref="dbSNP:149571298"
variation 54
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="c"
/db_xref="dbSNP:144221350"
variation 60
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:368305298"
variation 89
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:148279081"
variation 97
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:141314520"
variation 111
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="g"
/replace="t"
/db_xref="dbSNP:371605695"
variation 113
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="g"
/replace="t"
/db_xref="dbSNP:61753197"
variation 153
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:368159489"
exon 174..249
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/inference="alignment:Splign:1.39.8"
variation 174
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="g"
/db_xref="dbSNP:139616215"
variation 175
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="t"
/db_xref="dbSNP:145235239"
variation 235
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="g"
/db_xref="dbSNP:147643090"
exon 250..308
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/inference="alignment:Splign:1.39.8"
variation 258
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200920120"
variation 265
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:370628893"
variation 289
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:192059221"
variation 293
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="g"
/db_xref="dbSNP:714774"
variation 298
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:368645708"
exon 309..490
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/inference="alignment:Splign:1.39.8"
variation 314
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:79122711"
variation 318
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:12424437"
variation 325
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="g"
/db_xref="dbSNP:367995556"
variation 351
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="c"
/db_xref="dbSNP:149674449"
variation 412
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:12302888"
variation 445
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:371710232"
variation 446
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:372285001"
variation 490
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="g"
/db_xref="dbSNP:374658418"
exon 491..633
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/inference="alignment:Splign:1.39.8"
variation 511
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="g"
/db_xref="dbSNP:149220411"
variation 575
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:373617147"
variation 581
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:201452228"
variation 610
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="c"
/db_xref="dbSNP:61753198"
variation 622
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="c"
/db_xref="dbSNP:200260523"
variation 623
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:146876646"
variation 630
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:201246236"
exon 634..761
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/inference="alignment:Splign:1.39.8"
variation 647..648
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace=""
/replace="gggg"
/db_xref="dbSNP:144398305"
variation 649
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="g"
/replace="t"
/db_xref="dbSNP:200251936"
variation 656
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:201733141"
variation 657
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:374598691"
variation 683
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:372201069"
variation 693..694
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace=""
/replace="ac"
/db_xref="dbSNP:150849948"
variation 695
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:202035339"
variation 698
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="g"
/db_xref="dbSNP:201537317"
variation 701
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:192594761"
variation 703
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:200439617"
variation 705
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:201003099"
variation 728
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="g"
/db_xref="dbSNP:140685494"
variation 733
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="c"
/db_xref="dbSNP:199503063"
variation 755
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="c"
/db_xref="dbSNP:201164765"
exon 762..885
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/inference="alignment:Splign:1.39.8"
variation 805
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:200487561"
variation 829
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:145778768"
variation 830
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200088499"
variation 838
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:151070251"
variation 859
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:201656263"
exon 886..1033
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/inference="alignment:Splign:1.39.8"
variation 901
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="g"
/replace="t"
/db_xref="dbSNP:140976120"
variation 921
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:150197479"
variation 922
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:372316708"
variation 988
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="c"
/db_xref="dbSNP:138681507"
exon 1034..1231
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/inference="alignment:Splign:1.39.8"
variation 1055
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:143795587"
variation 1078
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:147023142"
variation 1101
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:370387241"
variation 1105
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:201334852"
variation 1119
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="g"
/db_xref="dbSNP:138198563"
variation 1186
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:202243696"
variation 1215
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:369341180"
exon 1232..1366
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/inference="alignment:Splign:1.39.8"
variation 1241
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:143666333"
variation 1270
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="t"
/db_xref="dbSNP:77013243"
variation 1280
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:201272617"
variation 1285
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:147187486"
variation 1292
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="t"
/db_xref="dbSNP:375941071"
variation 1324
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:71584848"
variation 1349
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200578810"
exon 1367..1454
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/inference="alignment:Splign:1.39.8"
variation 1370
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:373603488"
variation 1371
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="g"
/db_xref="dbSNP:35272924"
variation 1387
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:187474387"
variation 1392
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:141181063"
variation 1405
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200847598"
variation 1429
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:372666085"
variation 1452
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:374668663"
exon 1455..1635
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/inference="alignment:Splign:1.39.8"
variation 1518
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:199590135"
variation 1536
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="g"
/db_xref="dbSNP:150719071"
variation 1572
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:145893978"
variation 1592
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:375796466"
exon 1636..1760
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/inference="alignment:Splign:1.39.8"
variation 1643
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:368311206"
variation 1658
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="g"
/db_xref="dbSNP:139063293"
variation 1673
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="g"
/replace="t"
/db_xref="dbSNP:143983696"
variation 1675
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="c"
/db_xref="dbSNP:146888515"
variation 1684
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:201345518"
variation 1685
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200077145"
variation 1699
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:139746094"
variation 1709
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:201687848"
variation 1741
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="c"
/db_xref="dbSNP:116663267"
STS 1752..1878
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/standard_name="RH48486"
/db_xref="UniSTS:68822"
exon 1761..2000
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/inference="alignment:Splign:1.39.8"
variation 1766
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:115935399"
variation 1778
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:3180469"
variation 1785
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:17725914"
variation 1794
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:145828257"
variation 1812
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:151273606"
variation 1815
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="g"
/replace="t"
/db_xref="dbSNP:141590433"
variation 1839
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="t"
/db_xref="dbSNP:200329416"
variation 1842
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:147032879"
variation 1855
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:138222487"
variation 1872
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="g"
/db_xref="dbSNP:148221378"
variation 1888
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="t"
/db_xref="dbSNP:200533741"
variation 1929
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:369699402"
variation 1947
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:140245065"
variation 1949
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="c"
/db_xref="dbSNP:61751201"
variation 1966
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="c"
/db_xref="dbSNP:917634"
variation 1971
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:369598953"
exon 2001..2175
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/inference="alignment:Splign:1.39.8"
variation 2054
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:200624813"
variation 2066
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="g"
/replace="t"
/db_xref="dbSNP:376195353"
variation 2076
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:148424921"
variation 2084
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:142380498"
variation 2092
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:368606681"
variation 2104
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:370930042"
variation 2139
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:145931156"
exon 2176..2260
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/inference="alignment:Splign:1.39.8"
variation 2213
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:368048876"
variation 2230
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:372120618"
exon 2261..2394
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/inference="alignment:Splign:1.39.8"
variation 2269
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:375366285"
variation 2329
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:71579347"
variation 2330
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="g"
/db_xref="dbSNP:61763002"
exon 2395..2527
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/inference="alignment:Splign:1.39.8"
variation 2435
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:10849482"
variation 2446
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:115791107"
variation 2481
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:76687187"
variation 2514
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:369160973"
variation 2515
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:373388978"
exon 2528..2612
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/inference="alignment:Splign:1.39.8"
variation 2552
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:201468201"
variation 2553
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:73259178"
variation 2554
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="g"
/db_xref="dbSNP:200431803"
variation 2572
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="t"
/db_xref="dbSNP:375096381"
variation 2588
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:139932236"
variation 2594
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:200921592"
exon 2613..2780
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/inference="alignment:Splign:1.39.8"
variation 2622
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:113663520"
variation 2691
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:373969636"
variation 2692
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:370991665"
variation 2695
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:61751202"
variation 2702
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="g"
/replace="t"
/db_xref="dbSNP:376684532"
variation 2724
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="g"
/db_xref="dbSNP:149823221"
variation 2728
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:373683787"
variation 2778
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:145781104"
variation 2779
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:371088171"
exon 2781..2953
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/inference="alignment:Splign:1.39.8"
variation 2787
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:141629311"
variation 2803
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:11545056"
variation 2810
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="c"
/db_xref="dbSNP:375952478"
variation 2830
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="g"
/db_xref="dbSNP:201122686"
variation 2872
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:143514213"
variation 2897
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:145370494"
variation 2899
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:370594671"
variation 2901
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:373602126"
variation 2912
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:147656435"
variation 2945
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="c"
/db_xref="dbSNP:368743000"
exon 2954..3065
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/inference="alignment:Splign:1.39.8"
variation 2964
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:141891272"
variation 3046
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:142275546"
exon 3066..3189
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/inference="alignment:Splign:1.39.8"
variation 3109
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="g"
/db_xref="dbSNP:143208779"
variation 3137
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:148269816"
variation 3170
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:112784312"
exon 3190..3345
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/inference="alignment:Splign:1.39.8"
variation 3202
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:376232892"
variation 3233
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="g"
/db_xref="dbSNP:140333484"
variation 3239
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:376901782"
variation 3241
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:150344215"
variation 3288
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="t"
/db_xref="dbSNP:137946874"
variation 3299
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:199911941"
variation 3331
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="g"
/replace="t"
/db_xref="dbSNP:376577408"
variation 3337
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="g"
/db_xref="dbSNP:142419496"
variation 3345
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:145942484"
exon 3346..3523
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/inference="alignment:Splign:1.39.8"
variation 3346
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2072374"
variation 3351
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:201735986"
variation 3372
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:377720436"
variation 3382
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:149244253"
variation 3393
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:144412706"
variation 3421
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:76605012"
variation 3427
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="g"
/db_xref="dbSNP:148793704"
variation 3442
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:10849484"
variation 3463
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:371444456"
variation 3487
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:375019569"
variation 3507
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:199672478"
exon 3524..3618
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/inference="alignment:Splign:1.39.8"
variation 3529
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:740850"
variation 3534
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:376852566"
variation 3539
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:35819349"
variation 3546
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="t"
/db_xref="dbSNP:139998720"
variation 3553
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:373905082"
variation 3554
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="t"
/db_xref="dbSNP:145398040"
variation 3555
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:71579325"
variation 3556
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="c"
/db_xref="dbSNP:142367483"
variation 3564
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:183788505"
variation 3577
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:371282922"
variation 3605
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="g"
/db_xref="dbSNP:149767105"
exon 3619..3699
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/inference="alignment:Splign:1.39.8"
variation 3644
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:367671840"
variation 3645
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200410385"
variation 3681
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="c"
/db_xref="dbSNP:373223388"
variation 3699
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="g"
/replace="t"
/db_xref="dbSNP:61731148"
exon 3700..3883
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/inference="alignment:Splign:1.39.8"
variation 3707
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="g"
/db_xref="dbSNP:370458466"
variation 3708
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:199575493"
variation 3768
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:145700246"
variation 3784
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:148895571"
variation 3819
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="c"
/db_xref="dbSNP:143558583"
variation 3821
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:367748817"
variation 3845
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="g"
/db_xref="dbSNP:117693002"
variation 3846
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="g"
/replace="t"
/db_xref="dbSNP:137981914"
variation 3847
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1043262"
variation 3856
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="g"
/db_xref="dbSNP:368935958"
variation 3873
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace=""
/replace="c"
/db_xref="dbSNP:35079205"
variation 3874
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="g"
/replace="t"
/db_xref="dbSNP:61731147"
exon 3884..4010
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/inference="alignment:Splign:1.39.8"
variation 3915
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:368324917"
variation 3923
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:201167890"
variation 3963
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="g"
/db_xref="dbSNP:185696673"
variation 3988
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:144598859"
variation 4008
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2240871"
variation 4010
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200487459"
exon 4011..4166
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/inference="alignment:Splign:1.39.8"
variation 4021
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="g"
/db_xref="dbSNP:375102795"
variation 4050
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:150713925"
variation 4064
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:369464603"
variation 4067
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="g"
/db_xref="dbSNP:202123025"
variation 4084
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="c"
/db_xref="dbSNP:149422163"
variation 4085
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:373233854"
variation 4086
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:140382418"
variation 4093
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="t"
/db_xref="dbSNP:200908224"
variation 4110
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:370927177"
exon 4167..4806
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/inference="alignment:Splign:1.39.8"
variation 4193
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:61752289"
variation 4215
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:140130874"
variation 4239
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="g"
/replace="t"
/db_xref="dbSNP:202191153"
variation 4256
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="g"
/db_xref="dbSNP:371000555"
variation 4270
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="t"
/db_xref="dbSNP:201272523"
variation 4289
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:376231754"
variation 4336
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="g"
/replace="t"
/db_xref="dbSNP:190729237"
variation 4350..4351
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace=""
/replace="a"
/replace="t"
/db_xref="dbSNP:200984606"
variation 4350
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1043271"
variation 4351
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1127198"
variation 4368
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:148024858"
variation 4425
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="c"
/db_xref="dbSNP:141740035"
STS 4439..4565
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/standard_name="D15S1477"
/db_xref="UniSTS:474482"
STS 4453..4570
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/standard_name="D11S2560"
/db_xref="UniSTS:37928"
variation 4506
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:150206978"
variation 4517
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:71579331"
variation 4518
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:66671045"
variation 4584
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:112826761"
variation 4650
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1043282"
STS 4668..4767
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/standard_name="WI-21900"
/db_xref="UniSTS:11077"
variation 4753
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="a"
/replace="g"
/db_xref="dbSNP:186346773"
variation 4757
/gene="NCAPD2"
/gene_synonym="CAP-D2; CNAP1; hCAP-D2"
/replace="c"
/replace="t"
/db_xref="dbSNP:192059963"
ORIGIN
agagccgcgggtgagatccccagccctgtgagcctgtaggagtagaatggctccccaaatgtatgagttccatctgccattatccccagaggagttgttgaaaagtggaggggtgaatcagtatgttgtgcaagaggtactgtccatcaaacatcttccaccacagcttagagcttttcaggctgcctttcgagctcaggggcccctggctatgctgcagcactttgatactatctacagcattttgcatcactttcgaagtatagatcctggcctcaaagaagatactctgcaattcctgataaaagtggtatcccgccactcccaggagcttccagctatcctggatgatacaactttgagtggatcagatagaaacgcccatctaaatgccctcaaaatgaactgttatgctctgatacgtctcctggaatcctttgagaccatggccagccagacaaaccttgtggacctggaccttggtgggaagggtaagaaagctcggaccaaggcagcccatggctttgactgggaagaagagaggcaaccaattcttcagcttttaacacagctacttcagttggacatccgtcacctgtggaaccactcaataattgaagaagaatttgtcagtttggttactggctgttgctaccgccttctggagaatcccaccattaatcaccagaagaaccgccccactcgggaagccataacacacctgcttggtgtagccttgacccgttataaccatatgctcagtgctacagtgaagatcatccagatgctgcagcactttgaacacctggcacctgtactggttgcagccgtgagtctatgggcaactgactatggaatgaagagcatagtgggagagattgtaagagagattggacaaaagtgtccccaagagctgagtcgagacccttcagggacaaagggctttgcagcattcctgacagaactagcagaacgtgtcccagctatcctgatgtccagcatgtgcattttgctagatcacctggatggagaaaattacatgatgcgtaatgctgtgctggcagccatggcggagatggtgctgcaggttctcagtggcgatcaactggaagcagcagcccgagacaccagagaccagttcttggatactttacaagcccatggccatgatgtcaactcctttgtgcggagccgtgttttgcagctcttcacccgaattgtccagcagaaggctctccccctgacacgtttccaggcagtggtggctttagctgtgggacgtctggcagacaagtcagtgctagtatgtaaaaatgccatccagctgctggccagttttctagccaataatcctttctcctgcaagcttagtgatgctgaccttgccggaccactgcagaaggagacccagaaattacaagagatgagggcccagaggcgaactgcagcagcttctgcagtgctggacccagaggaggagtgggaagccatgctgccagagttgaagtctaccctgcagcagcttctacagcttccccagggagaggaggagattcctgagcaaattgccaatacagagacaactgaagatgtgaaaggacgcatctatcaactgcttgccaaagctagttacaaaaaggccatcattctcactcgagaagccacaggccacttccaggagtccgaacccttcagtcatatagacccagaggagtcagaggagaccaggctcttgaatatcttaggacttatcttcaaaggcccagcagcttccacacaagaaaagaatccccgggagtctacaggaaacatggtcacaggacagactgtctgtaaaaataaacccaatatgtcggatcctgaggaatccaggggaaatgatgaactagtgaagcaggagatgctggtacagtatctgcaggatgcctacagcttctcccggaagattacagaggccattggcatcatcagcaagatgatgtatgaaaacacaactacagtggtgcaggaggtgattgaattctttgtgatggtcttccaatttggggtaccccaggccctgtttggggtgcgccgtatgctgcctctcatctggtctaaggagcctggtgtccgggaagccgtgcttaatgcctaccgccaactctacctcaaccccaaaggggactctgccagagccaaggcccaggctttgattcagaatctctctctgctgctagtggatgcctcggttgggaccattcagtgtcttgaggaaattctctgtgagtttgtgcagaaggatgagttgaaaccagcagtgacccagctgctgtgggagcgggccaccgagaaggtcgcctgctgtcctctggagcgctgttcctctgtcatgcttcttggcatgatggcacgaggaaagccagaaattgtgggaagcaatttagacacactggtgagcatagggctggatgagaagtttccacaggactacaggctggcccagcaggtgtgccatgccattgccaacatctcggacaggagaaagccttctctgggcaaacgtcacccccccttccggctgcctcaggaacacaggttgtttgagcgactgcgggagacagtcacaaaaggctttgtccacccagacccactctggatcccattcaaagaggtggcagtgaccctcatttaccaactggcagagggccccgaagtgatctgtgcccagatattgcagggctgtgcaaaacaggccctggagaagctagaagagaagagaaccagtcaggaggacccgaaggagtcccccgcaatgctccccactttcctgttgatgaacctgctgtccctggctggggatgtggctctgcagcagctggtccacttggagcaggcagtgagtggagagctctgccggcgccgagttctccgggaagaacaggagcacaagaccaaagatcccaaggagaagaatacgagctctgagaccaccatggaggaggagctggggctggttggggcaacagcagatgacacagaggcagaactaatccgtggcatctgcgagatggaactgttggatggcaaacagacactggctgcctttgttccactcttgcttaaagtctgtaacaacccaggcctctatagcaacccagacctctctgcagctgcttcacttgcccttggcaagttctgcatgatcagtgccactttctgcgactcccagcttcgtcttctgttcaccatgctggaaaagtctccacttcccattgtccggtctaacctcatggttgccactggggatctggccatccgctttcccaatctggtggacccctggactcctcatctgtatgctcgtctccgggaccctgctcagcaagtgcggaaaacagcggggctggtgatgacccacctgatcctcaaggacatggtgaaggtgaaggggcaggtcagcgagatggcggtgctgctcatcgaccccgagcctcagattgctgccctggccaagaacttcttcaatgagctctcccacaagggcaacgcaatctataatctccttccagatatcatcagccgcctgtcagaccccgagctgggggtggaggaagagcctttccacaccatcatgaaacagctcctctcctacatcaccaaggacaagcagacagagagcctggtggaaaagctgtgtcagcggttccgcacatcccgaactgagcggcagcagcgagacctggcctactgtgtgtcacagctgcccctcacagagcgaggcctccgtaagatgcttgacaattttgactgttttggagacaaactgtcagatgagtccatcttcagtgcttttttgtcagttgtaggcaagctgcgacgtggggccaagcctgagggcaaggctataatagatgaatttgagcagaagcttcgggcctgtcataccagaggtttggatggaatcaaggagcttgagattggccaagcaggtagccagagagcgccatcagccaagaaaccatccactggttctaggtaccagcctctggcttctacagcctcagacaatgactttgtcacaccagagccccgccgtactacccgtcggcatccaaacacccagcagcgagcttccaaaaagaaacccaaagttgtcttctcaagtgatgagtccagtgaggaagatctttcagcagagatgacagaagacgagacacccaagaaaacaactcccattctcagagcatcggctcgcaggcacagatcctaggaagtctgttcctgtcctccctgtgcagggtatcctgtagggtgacctggaattcgaattctgtttcccttgtaaaatatttgtctgtctcttttttttaaaaaaaaaaaaggccgggcactgtggctcacgcctgtaatcccagcactttgcgataccaaggcgggtggataacctgaggtagggagttcgagaccagcctgaccaacatggagaaaccccatctctactaaaaataaaaaattagccgggcgtattggcgtgcgcctgtaatcccagctactcaagaggctgaggcaggagaatcgcctgaacccagaggcggaggttgtagtgagccgaaatcacaccattgcactccagcttgggcaacaatagcgaacctccatctcaaattaaaaaaaaaatgcctacacgctctttaaaatgcaaggctttctcttaaattagcctaactgaactgcgttgagctgcttcaactttggaatatatgtttgccaatctccttgttttctaatgaataaatgtttttatatacttttagacattttttc
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:9918 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
GeneID:9918 -> Molecular function: GO:0042393 [histone binding] evidence: IDA
GeneID:9918 -> Molecular function: GO:0042393 [histone binding] evidence: NAS
GeneID:9918 -> Biological process: GO:0000278 [mitotic cell cycle] evidence: TAS
GeneID:9918 -> Biological process: GO:0007076 [mitotic chromosome condensation] evidence: IDA
GeneID:9918 -> Biological process: GO:0007076 [mitotic chromosome condensation] evidence: NAS
GeneID:9918 -> Biological process: GO:0051301 [cell division] evidence: IEA
GeneID:9918 -> Cellular component: GO:0000228 [nuclear chromosome] evidence: IDA
GeneID:9918 -> Cellular component: GO:0000793 [condensed chromosome] evidence: IDA
GeneID:9918 -> Cellular component: GO:0000796 [condensin complex] evidence: IDA
GeneID:9918 -> Cellular component: GO:0000797 [condensin core heterodimer] evidence: NAS
GeneID:9918 -> Cellular component: GO:0005634 [nucleus] evidence: IDA
GeneID:9918 -> Cellular component: GO:0005634 [nucleus] evidence: NAS
GeneID:9918 -> Cellular component: GO:0005730 [nucleolus] evidence: IDA
GeneID:9918 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA
GeneID:9918 -> Cellular component: GO:0005737 [cytoplasm] evidence: NAS
GeneID:9918 -> Cellular component: GO:0005829 [cytosol] evidence: TAS
GeneID:9918 -> Cellular component: GO:0045120 [pronucleus] evidence: IEA
by
@meso_cacase at
DBCLS
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