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2024-04-20 19:07:02, GGRNA : RefSeq release 60 (20130726)
LOCUS NR_073375 3522 bp RNA linear PRI 17-JUL-2013
DEFINITION Homo sapiens minichromosome maintenance complex component 2 (MCM2),
transcript variant 2, non-coding RNA.
ACCESSION NR_073375
VERSION NR_073375.1 GI:409971442
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 3522)
AUTHORS Toubaji,A., Sutcliffe,S., Chaux,A., Lecksell,K., Hicks,J., De
Marzo,A.M., Platz,E.A. and Netto,G.J.
TITLE Immunohistochemical expression of minichromosome maintenance
complex protein 2 predicts biochemical recurrence in prostate
cancer: a tissue microarray and digital imaging analysis-based
study of 428 cases
JOURNAL Hum. Pathol. 43 (11), 1852-1865 (2012)
PUBMED 22554381
REMARK GeneRIF: Immunohistochemical expression of minichromosome
maintenance complex protein 2 predicts biochemical recurrence in
prostate cancer.
REFERENCE 2 (bases 1 to 3522)
AUTHORS Kang,Y.H., Galal,W.C., Farina,A., Tappin,I. and Hurwitz,J.
TITLE Properties of the human Cdc45/Mcm2-7/GINS helicase complex and its
action with DNA polymerase epsilon in rolling circle DNA synthesis
JOURNAL Proc. Natl. Acad. Sci. U.S.A. 109 (16), 6042-6047 (2012)
PUBMED 22474384
REMARK GeneRIF: Data show that using a 200-nt primed circular DNA
substrate, the combined action of DNA polymerase epsilon and the
Cdc45/Mcm2-7/GINS (CMG complex) leads to the formation of products
>10 kb in length.
REFERENCE 3 (bases 1 to 3522)
AUTHORS Conesa-Zamora,P., Trujillo-Santos,J., Orantes-Casado,F.J.,
Ortiz-Reina,S., Torres-Moreno,D. and Perez-Guillermo,M.
TITLE Analysis of performance characteristics of five cell cycle-related
immunohistochemical markers and human papillomavirus genotyping in
the diagnosis of cervical squamous cell carcinoma precursor lesions
JOURNAL Anal. Quant. Cytol. Histol. 34 (1), 49-55 (2012)
PUBMED 22590819
REMARK GeneRIF: ProEx C showed the best specificity; p16 displayed the
highest sensitivity and area under receiver operating
characteristic curve for squamous intraepithelial lesions
diagnosis.
REFERENCE 4 (bases 1 to 3522)
AUTHORS Suzuki,S., Kurata,M., Abe,S., Miyazawa,R., Murayama,T., Hidaka,M.,
Yamamoto,K. and Kitagawa,M.
TITLE Overexpression of MCM2 in myelodysplastic syndromes: association
with bone marrow cell apoptosis and peripheral cytopenia
JOURNAL Exp. Mol. Pathol. 92 (1), 160-166 (2012)
PUBMED 22115939
REMARK GeneRIF: The up-regulated expression of MCM2 is associated with
frequent apoptosis in myelodysplastic syndromes (MDS) and may have
an important role in the pathogenesis of MDS.
REFERENCE 5 (bases 1 to 3522)
AUTHORS Guler,N., Comunoglu,N. and Cabbar,F.
TITLE Ki-67 and MCM-2 in dental follicle and odontogenic cysts: the
effects of inflammation on proliferative markers
JOURNAL ScientificWorldJournal 2012, 946060 (2012)
PUBMED 22778705
REMARK GeneRIF: The results of this study indicated that the higher MCM-2
expressions in RC than the KCOT might be related to the
inflammation and this protein might be more sensitive to
inflammation.
REFERENCE 6 (bases 1 to 3522)
AUTHORS Ishimi,Y., Ichinose,S., Omori,A., Sato,K. and Kimura,H.
TITLE Binding of human minichromosome maintenance proteins with histone
H3
JOURNAL J. Biol. Chem. 271 (39), 24115-24122 (1996)
PUBMED 8798650
REFERENCE 7 (bases 1 to 3522)
AUTHORS Nakatsuru,S., Sudo,K. and Nakamura,Y.
TITLE Isolation and mapping of a human gene (MCM2) encoding a product
homologous to yeast proteins involved in DNA replication
JOURNAL Cytogenet. Cell Genet. 68 (3-4), 226-230 (1995)
PUBMED 7842741
REFERENCE 8 (bases 1 to 3522)
AUTHORS Todorov,I.T., Pepperkok,R., Philipova,R.N., Kearsey,S.E.,
Ansorge,W. and Werner,D.
TITLE A human nuclear protein with sequence homology to a family of early
S phase proteins is required for entry into S phase and for cell
division
JOURNAL J. Cell. Sci. 107 (PT 1), 253-265 (1994)
PUBMED 8175912
REFERENCE 9 (bases 1 to 3522)
AUTHORS Mincheva,A., Todorov,I., Werner,D., Fink,T.M. and Lichter,P.
TITLE The human gene for nuclear protein BM28 (CDCL1), a new member of
the early S-phase family of proteins, maps to chromosome band 3q21
JOURNAL Cytogenet. Cell Genet. 65 (4), 276-277 (1994)
PUBMED 8258304
REFERENCE 10 (bases 1 to 3522)
AUTHORS Todorov,I.T., Lavigne,J., Sakr,F., Kaneva,R., Foisy,S. and
Bibor-Hardy,V.
TITLE Nuclear matrix protein mitotin messenger RNA is expressed at
constant levels during the cell cycle
JOURNAL Biochem. Biophys. Res. Commun. 177 (1), 395-400 (1991)
PUBMED 1710453
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from DB100427.1, AK299934.1 and
BC000300.2.
Summary: The protein encoded by this gene is one of the highly
conserved mini-chromosome maintenance proteins (MCM) that are
involved in the initiation of eukaryotic genome replication. The
hexameric protein complex formed by MCM proteins is a key component
of the pre-replication complex (pre_RC) and may be involved in the
formation of replication forks and in the recruitment of other DNA
replication related proteins. This protein forms a complex with
MCM4, 6, and 7, and has been shown to regulate the helicase
activity of the complex. This protein is phosphorylated, and thus
regulated by, protein kinases CDC2 and CDC7. Multiple alternatively
spliced transcript variants have been found, but the full-length
nature of some variants has not been defined. [provided by RefSeq,
Oct 2012].
Transcript Variant: This variant (2) has an additional segment in
the 5' region, compared to variant 1. This variant is represented
as non-coding because the use of the 5'-most expected translational
start codon, as used in variant 1, renders the transcript a
candidate for nonsense-mediated mRNA decay (NMD).
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 :: AK299934.1 [ECO:0000332]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-53 DB100427.1 1-53
54-1996 AK299934.1 1-1943
1997-3522 BC000300.2 242-1767
FEATURES Location/Qualifiers
source 1..3522
/organism="Homo sapiens"
/mol_type="transcribed RNA"
/db_xref="taxon:9606"
/chromosome="3"
/map="3q21"
gene 1..3522
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/note="minichromosome maintenance complex component 2"
/db_xref="GeneID:4171"
/db_xref="HGNC:6944"
/db_xref="MIM:116945"
misc_RNA 1..3522
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/product="minichromosome maintenance complex component 2,
transcript variant 2"
/db_xref="GeneID:4171"
/db_xref="HGNC:6944"
/db_xref="MIM:116945"
exon 1..116
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/inference="alignment:Splign:1.39.8"
variation 29..30
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace=""
/replace="c"
/db_xref="dbSNP:34940832"
variation 46
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:146365324"
variation 53
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:368605937"
variation 73
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:373148451"
variation 79
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="g"
/replace="t"
/db_xref="dbSNP:375179722"
variation 82
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="g"
/db_xref="dbSNP:369455363"
misc_feature 111..551
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/inference="COORDINATES:
alignment:Blast2seq::RefSeq|NM_004526.3"
/note="primary ORF has stop codon >50 nucleotides from the
terminal splice site; nonsense-mediated decay (NMD)
candidate"
exon 117..346
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/inference="alignment:Splign:1.39.8"
variation 125
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:148166817"
variation 152
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="g"
/db_xref="dbSNP:376102107"
variation 163
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="g"
/db_xref="dbSNP:185298481"
variation 207
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:144051770"
variation 208
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:142494006"
variation 236
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:140680894"
variation 240
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:375851208"
variation 310
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:201221422"
variation 314
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="g"
/replace="t"
/db_xref="dbSNP:3087452"
exon 347..522
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/inference="alignment:Splign:1.39.8"
variation 354
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:200588762"
variation 356
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:186022338"
variation 384
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="g"
/replace="t"
/db_xref="dbSNP:374471462"
variation 387
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:199660068"
variation 388
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="c"
/db_xref="dbSNP:150844852"
variation 453
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:201721106"
variation 463
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:139163788"
variation 464
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="g"
/replace="t"
/db_xref="dbSNP:373434842"
variation 487
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:149927939"
variation 488
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:2257836"
variation 505
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:201216288"
variation 508
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:34997321"
variation 513
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:2307314"
exon 523..802
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/inference="alignment:Splign:1.39.8"
variation 546
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:377197527"
variation 552
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="g"
/db_xref="dbSNP:145141037"
variation 559
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:139973267"
variation 565
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:200927653"
variation 566
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:190889381"
variation 575
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:35343063"
variation 584
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:200231306"
variation 587
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:368377044"
variation 603
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:369899498"
variation 609
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:2307312"
variation 612
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:372044409"
variation 625
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1048225"
variation 633
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:893293"
variation 642
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:62264117"
variation 703
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:199665704"
variation 705
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="g"
/db_xref="dbSNP:140577001"
variation 708
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:150457733"
variation 722
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:376214773"
variation 723
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:371840356"
variation 748
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:375722226"
variation 751
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:201424836"
variation 780
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:138251000"
variation 787
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:201262336"
exon 803..1022
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/inference="alignment:Splign:1.39.8"
variation 809
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:370122469"
variation 816
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:373076757"
variation 853
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:201515306"
variation 855
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:371226878"
variation 884
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:144115876"
variation 885
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:146895950"
variation 888
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:35749886"
variation 924
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:376345350"
variation 951
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:142980535"
variation 952
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:144753488"
variation 957
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:368230142"
variation 980
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:148533176"
variation 1016
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:199968234"
exon 1023..1230
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/inference="alignment:Splign:1.39.8"
variation 1063
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="g"
/db_xref="dbSNP:141867973"
variation 1080
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:150564590"
variation 1131
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:376347464"
variation 1154
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="c"
/db_xref="dbSNP:139899850"
variation 1203
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:143514266"
variation 1204
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:201802595"
variation 1221
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="g"
/db_xref="dbSNP:200752349"
exon 1231..1365
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/inference="alignment:Splign:1.39.8"
variation 1263
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:112997630"
variation 1277
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:146752036"
variation 1286
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:139136642"
variation 1287
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:149877642"
variation 1294
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:377581276"
variation 1296
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:369427101"
variation 1304
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:144869999"
variation 1315
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:3087450"
variation 1326
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:3087449"
variation 1327
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:371462307"
variation 1359
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:202032909"
variation 1360
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:373695678"
exon 1366..1557
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/inference="alignment:Splign:1.39.8"
variation 1368
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:187407254"
variation 1403
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="g"
/db_xref="dbSNP:371208727"
variation 1405
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="g"
/db_xref="dbSNP:369473650"
variation 1407
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:147725704"
variation 1411
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="c"
/db_xref="dbSNP:201123662"
variation 1418
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:372110727"
variation 1447
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="g"
/db_xref="dbSNP:372976124"
variation 1459
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:199539311"
variation 1500
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="g"
/db_xref="dbSNP:142512970"
variation 1501
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:376973485"
variation 1516
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="t"
/db_xref="dbSNP:190988564"
variation 1522
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:182603137"
variation 1533
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="g"
/db_xref="dbSNP:140620010"
exon 1558..1651
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/inference="alignment:Splign:1.39.8"
variation 1583
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:139336906"
variation 1614
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:375359892"
variation 1630
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:13087457"
variation 1639
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="c"
/db_xref="dbSNP:150403449"
exon 1652..1902
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/inference="alignment:Splign:1.39.8"
variation 1681
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:138119298"
variation 1682
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:149592386"
variation 1689
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:57045995"
variation 1719
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:377737717"
variation 1782
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:182677955"
variation 1785
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:138708920"
variation 1803
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:376837416"
variation 1814
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:199793381"
variation 1839
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="g"
/db_xref="dbSNP:373318008"
exon 1903..2029
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/inference="alignment:Splign:1.39.8"
variation 1996
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:372340490"
variation 2004
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:377688408"
variation 2016
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:141735401"
variation 2017
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:138684820"
exon 2030..2142
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/inference="alignment:Splign:1.39.8"
variation 2067
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:377306111"
variation 2074
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:377424967"
variation 2083
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:201684888"
variation 2115
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:138093592"
variation 2127
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:111530425"
variation 2128
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:2307311"
exon 2143..2394
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/inference="alignment:Splign:1.39.8"
variation 2150
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:142652347"
variation 2159
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:370006900"
variation 2179
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:201200738"
variation 2185
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:11541852"
variation 2200
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:150514271"
variation 2222
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:139449344"
variation 2231
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:149699620"
variation 2242
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:147793264"
variation 2256
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:199907942"
variation 2263
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:142890769"
variation 2270
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:201217644"
variation 2308
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:2307313"
variation 2327
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:374686602"
variation 2328
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:144817363"
variation 2363
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:376563084"
exon 2395..2577
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/inference="alignment:Splign:1.39.8"
variation 2396
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:147917433"
variation 2403
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:149009392"
variation 2429
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="g"
/replace="t"
/db_xref="dbSNP:12482"
variation 2444
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:372194428"
variation 2465
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:201828053"
variation 2493
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:376569612"
variation 2497
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:369079696"
variation 2499
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:143447982"
variation 2508
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:200244254"
variation 2510
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="g"
/db_xref="dbSNP:375684929"
variation 2518
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:376831247"
variation 2556
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:371014572"
variation 2557
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:140928153"
variation 2560
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:150230243"
variation 2564
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:185316647"
exon 2578..2733
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/inference="alignment:Splign:1.39.8"
variation 2587
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:138865006"
variation 2603
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:374590880"
variation 2606
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:201882833"
variation 2610
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="c"
/db_xref="dbSNP:368722217"
variation 2616
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:373238083"
variation 2655
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:141996483"
variation 2664
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:146246663"
variation 2672
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="g"
/replace="t"
/db_xref="dbSNP:137990158"
variation 2685
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:190121900"
variation 2699
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:140905579"
variation 2702
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:144122212"
variation 2709
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="g"
/db_xref="dbSNP:377692299"
variation 2715
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:201109342"
exon 2734..3507
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/inference="alignment:Splign:1.39.8"
variation 2807
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:368010365"
variation 2808
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:202207227"
variation 2811
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:6794323"
variation 2818
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="c"
/db_xref="dbSNP:142055220"
variation 2829
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:376562317"
variation 2845
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:368340805"
variation 2864
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="g"
/replace="t"
/db_xref="dbSNP:368920498"
variation 2989
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:201056689"
variation 2992
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="c"
/db_xref="dbSNP:116343860"
variation 3138
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:371969091"
variation 3160
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="g"
/replace="t"
/db_xref="dbSNP:138698648"
variation 3264
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="t"
/db_xref="dbSNP:141767294"
variation 3341
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:73861539"
variation 3357
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:188052534"
variation 3360
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:116989425"
variation 3365
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="a"
/replace="g"
/db_xref="dbSNP:12298"
variation 3381
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="g"
/replace="t"
/db_xref="dbSNP:189683455"
variation 3420
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:17538767"
variation 3475
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
/replace="c"
/replace="t"
/db_xref="dbSNP:182305027"
polyA_signal 3485..3490
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
polyA_site 3507
/gene="MCM2"
/gene_synonym="BM28; CCNL1; cdc19; CDCL1; D3S3194;
MITOTIN"
ORIGIN
atgacgtcgcgttccgtagggctcttcccgggctttggtgggtcacgtgaaccacttttcgcgcgaaacctggttgttgctgtagtggcggagaggatcgtggtactgctatggcggaatcatcggaatccttcaccatggcatccagcccggcccagcgtcggcgaggcaatgatcctctcacctccagccctggccgaagctcccggcgtactgatgccctcacctccagccctggccgtgaccttccaccatttgaggatgagtccgaggggctcctaggcacagaggggcccctggaggaagaagaggatggagaggagctcattggagatggcatggaaagggactaccgcgccatcccagagctggacgcctatgaggccgagggactggctctggatgatgaggacgtagaggagctgacggccagtcagagggaggcagcagagcgggccatgcggcagcgtgaccgggaggctggccggggcctgggccgcatgcgccgtgggctcctgtatggtgtctcttgcctccccagacagcgatgaggaggacgaggagcgccctgcccgcaagcgccgccaggtggagcgggccacggaggacggcgaggaggacgaggagatgatcgagagcatcgagaacctggaggatctcaaaggccactctgtgcgcgagtgggtgagcatggcgggcccccggctggagatccaccaccgcttcaagaacttcctgcgcactcacgtcgacagccacggccacaacgtcttcaaggagcgcatcagcgacatgtgcaaagagaaccgtgagagcctggtggtgaactatgaggacttggcagccagggagcacgtgctggcctacttcctgcctgaggcaccggcggagctgctgcagatctttgatgaggctgccctggaggtggtactggccatgtaccccaagtacgaccgcatcaccaaccacatccatgtccgcatctcccacctgcctctggtggaggagctgcgctcgctgaggcagctgcatctgaaccagctgatccgcaccagtggggtggtgaccagctgcactggcgtcctgccccagctcagcatggtcaagtacaactgcaacaagtgcaatttcgtcctgggtcctttctgccagtcccagaaccaggaggtgaaaccaggctcctgtcctgagtgccagtcggccggcccctttgaggtcaacatggaggagaccatctatcagaactaccagcgtatccgaatccaggagagtccaggcaaagtggcggctggccggctgccccgctccaaggacgccattctcctcgcagatctggtggacagctgcaagccaggagacgagatagagctgactggcatctatcacaacaactatgatggctccctcaacactgccaatggcttccctgtctttgccactgtcatcctagccaaccacgtggccaagaaggacaacaaggttgctgtaggggaactgaccgatgaagatgtgaagatgatcactagcctctccaaggatcagcagatcggagagaagatctttgccagcattgctccttccatctatggtcatgaagacatcaagagaggcctggctctggccctgttcggaggggagcccaaaaacccaggtggcaagcacaaggtacgtggtgatatcaacgtgctcttgtgcggagaccctggcacagcgaagtcgcagtttctcaagtatattgagaaagtgtccagccgagccatcttcaccactggccagggggcgtcggctgtgggcctcacggcgtatgtccagcggcaccctgtcagcagggagtggaccttggaggctggggccctggttctggctgaccgaggagtgtgtctcattgatgaatttgacaagatgaatgaccaggacagaaccagcatccatgaggccatggagcaacagagcatctccatctcgaaggctggcatcgtcacctccctgcaggctcgctgcacggtcattgctgccgccaaccccataggagggcgctacgacccctcgctgactttctctgagaacgtggacctcacagagcccatcatctcacgctttgacatcctgtgtgtggtgagggacaccgtggacccagtccaggacgagatgctggcccgcttcgtggtgggcagccacgtcagacaccaccccagcaacaaggaggaggaggggctggccaatggcagcgctgctgagcccgccatgcccaacacgtatggcgtggagcccctgccccaggaggtcctgaagaagtacatcatctacgccaaggagagggtccacccgaagctcaaccagatggaccaggacaaggtggccaagatgtacagtgacctgaggaaagaatctatggcgacaggcagcatccccattacggtgcggcacatcgagtccatgatccgcatggcggaggcccacgcgcgcatccatctgcgggactatgtgatcgaagacgacgtcaacatggccatccgcgtgatgctggagagcttcatagacacacagaagttcagcgtcatgcgcagcatgcgcaagacttttgcccgctacctttcattccggcgtgacaacaatgagctgttgctcttcatactgaagcagttagtggcagagcaggtgacatatcagcgcaaccgctttggggcccagcaggacactattgaggtccctgagaaggacttggtggataaggctcgtcagatcaacatccacaacctctctgcattttatgacagtgagctcttcaggatgaacaagttcagccacgacctgaaaaggaaaatgatcctgcagcagttctgaggccctatgccatccataaggattccttgggattctggtttggggtggtcagtgccctctgtgctttatggacacaaaaccagagcacttgatgaactcggggtactagggtcagggcttatagcaggatgtctggctgcacctggcatgactgtttgtttctccaagcctgctttgtgcttctcacctttgggtgggatgccttgccagtgtgtcttacttggttgctgaacatcttgccacctccgagtgctttgtctccactcagtaccttggatcagagctgctgagttcaggatgcctgcgtgtggtttaggtgttagccttcttacatggatgtcaggagagctgctgccctcttggcgtgagttgcgtattcaggctgcttttgctgcctttggccagagagctggttgaagatgtttgtaatcgttttcagtctcctgcaggtttctgtgcccctgtggtggaagagggcacgacagtgccagcgcagcgttctgggctcctcagtcgcaggggtgggatgtgagtcatgcggattatccactcgccacagttatcagctgccattgctccctgtctgtttccccactctcttatttgtgcattcggtttggtttctgtagttttaatttttaataaagttgaataaaatataaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:4171 -> Molecular function: GO:0003677 [DNA binding] evidence: TAS
GeneID:4171 -> Molecular function: GO:0003678 [DNA helicase activity] evidence: IEA
GeneID:4171 -> Molecular function: GO:0003688 [DNA replication origin binding] evidence: IEA
GeneID:4171 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
GeneID:4171 -> Molecular function: GO:0005524 [ATP binding] evidence: IEA
GeneID:4171 -> Molecular function: GO:0042393 [histone binding] evidence: IEA
GeneID:4171 -> Molecular function: GO:0046872 [metal ion binding] evidence: IEA
GeneID:4171 -> Biological process: GO:0000082 [G1/S transition of mitotic cell cycle] evidence: TAS
GeneID:4171 -> Biological process: GO:0000278 [mitotic cell cycle] evidence: TAS
GeneID:4171 -> Biological process: GO:0006260 [DNA replication] evidence: TAS
GeneID:4171 -> Biological process: GO:0006268 [DNA unwinding involved in DNA replication] evidence: IEA
GeneID:4171 -> Biological process: GO:0006270 [DNA replication initiation] evidence: IMP
GeneID:4171 -> Biological process: GO:0006271 [DNA strand elongation involved in DNA replication] evidence: TAS
GeneID:4171 -> Biological process: GO:0006334 [nucleosome assembly] evidence: IEA
GeneID:4171 -> Biological process: GO:0007049 [cell cycle] evidence: TAS
GeneID:4171 -> Biological process: GO:0071353 [cellular response to interleukin-4] evidence: IEA
GeneID:4171 -> Cellular component: GO:0000785 [chromatin] evidence: IDA
GeneID:4171 -> Cellular component: GO:0005634 [nucleus] evidence: IDA
GeneID:4171 -> Cellular component: GO:0005654 [nucleoplasm] evidence: TAS
GeneID:4171 -> Cellular component: GO:0005664 [nuclear origin of replication recognition complex] evidence: IEA
GeneID:4171 -> Cellular component: GO:0042555 [MCM complex] evidence: IDA
by
@meso_cacase at
DBCLS
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