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Aliases for MCM2 Gene

Aliases for MCM2 Gene

  • Minichromosome Maintenance Complex Component 2 2 3 5
  • Minichromosome Maintenance Protein 2 Homolog 3 4
  • Nuclear Protein BM28 3 4
  • Mitotin 2 3
  • CCNL1 3 4
  • CDCL1 3 4
  • BM28 3 4
  • MCM2 Minichromosome Maintenance Deficient 2, Mitotin (S. Cerevisiae) 2
  • Minichromosome Maintenance Deficient (S. Cerevisiae) 2 (Mitotin) 2
  • Minichromosome Maintenance Deficient 2 (Mitotin) 3
  • DNA Replication Licensing Factor MCM2 3
  • Cell Devision Cycle-Like 1 3
  • Cyclin-Like 1 3
  • EC 3.6.4.12 4
  • KIAA0030 4
  • D3S3194 3
  • DFNA70 3
  • Cdc19 3

External Ids for MCM2 Gene

Previous HGNC Symbols for MCM2 Gene

  • CCNL1
  • CDCL1

Previous GeneCards Identifiers for MCM2 Gene

  • GC03P124148
  • GC03P127476
  • GC03P128598
  • GC03P128638
  • GC03P128799
  • GC03P127317
  • GC03P124697

Summaries for MCM2 Gene

Entrez Gene Summary for MCM2 Gene

  • 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]

GeneCards Summary for MCM2 Gene

MCM2 (Minichromosome Maintenance Complex Component 2) is a Protein Coding gene. Diseases associated with MCM2 include Autosomal Dominant Nonsyndromic Deafness 70 and Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna. Among its related pathways are Telomere C-strand (Lagging Strand) Synthesis and E2F mediated regulation of DNA replication. GO annotations related to this gene include ATPase activity and DNA helicase activity. An important paralog of this gene is MCM9.

UniProtKB/Swiss-Prot for MCM2 Gene

  • Acts as component of the MCM2-7 complex (MCM complex) which is the putative replicative helicase essential for once per cell cycle DNA replication initiation and elongation in eukaryotic cells. The active ATPase sites in the MCM2-7 ring are formed through the interaction surfaces of two neighboring subunits such that a critical structure of a conserved arginine finger motif is provided in trans relative to the ATP-binding site of the Walker A box of the adjacent subunit. The six ATPase active sites, however, are likely to contribute differentially to the complex helicase activity. Required for the entry in S phase and for cell division. Plays a role in terminally differentiated hair cells development of the cochlea and induces cells apoptosis.

Gene Wiki entry for MCM2 Gene

No data available for CIViC summary , Tocris Summary , PharmGKB "VIP" Summary , fRNAdb sequence ontologies and piRNA Summary for MCM2 Gene

Genomics for MCM2 Gene

Regulatory Elements for MCM2 Gene

Enhancers for MCM2 Gene
GeneHancer Identifier Enhancer Score Enhancer Sources Gene-Enhancer Score TSS distance (kb) Number of Genes Away Size (kb) Transcription Factor Binding Sites within enhancer Gene Targets for Enhancer
GH03G127766 1.8 FANTOM5 Ensembl ENCODE dbSUPER 15.2 +174.8 174822 12.1 TBP RAD21 YY1 GATA2 SCRT2 ZNF143 RCOR1 FOS RELB IKZF2 MCM2 TPRA1 MGLL ABTB1 PODXL2
GH03G127574 1.1 Ensembl ENCODE 12 -23.0 -23016 1.3 HDGF HDAC1 RB1 CREB3L1 ZSCAN4 SIN3A ZNF2 RAD21 ZNF143 ZNF207 TPRA1 MCM2 PODXL2 MIR6825 ENSG00000282860
GH03G127910 1.1 Ensembl ENCODE 10.2 +313.2 313192 1.4 ZSCAN4 SIN3A ZNF2 ZNF335 GLIS2 ELK1 EGR2 ZBTB11 REST TBX21 MCM2 TPRA1 KBTBD12 PODXL2 GC03P127895
GH03G127683 0.9 Ensembl dbSUPER 10.6 +85.5 85512 0.7 ZNF263 SCRT1 CTCF ETV1 RAD21 SCRT2 SMC3 FOXP2 PODXL2 MCM2 TPRA1 ABTB1 MGLL
GH03G127764 0.8 dbSUPER 10.3 +167.2 167232 1.0 PKNOX1 BACH1 BMI1 RELA ARID3A POLR2A EED FOS RELB CREM PODXL2 MCM2 TPRA1 MGLL ABTB1
- Elite enhancer and/or Elite enhancer-gene association Download GeneHancer data dump

Enhancers around MCM2 on UCSC Golden Path with GeneCards custom track

Promoters for MCM2 Gene
Ensembl Regulatory Elements (ENSRs) TSS Distance (bp) Size (bp) Binding Sites for Transcription Factors within promoters
ENSR00000157964 177 1201 HDGF MLX CREB3L1 ZFP64 ARID4B SIN3A DMAP1 ZNF2 ZBTB7B YY1

Genomic Location for MCM2 Gene

Chromosome:
3
Start:
127,598,223 bp from pter
End:
127,622,436 bp from pter
Size:
24,214 bases
Orientation:
Plus strand

Genomic View for MCM2 Gene

Genes around MCM2 on UCSC Golden Path with GeneCards custom track

Cytogenetic band:
MCM2 Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
Genomic Location for MCM2 Gene
GeneLoc Logo Genomic Neighborhood Exon StructureGene Density

RefSeq DNA sequence for MCM2 Gene

Proteins for MCM2 Gene

  • Protein details for MCM2 Gene (UniProtKB/Swiss-Prot)

    Protein Symbol:
    P49736-MCM2_HUMAN
    Recommended name:
    DNA replication licensing factor MCM2
    Protein Accession:
    P49736
    Secondary Accessions:
    • Q14577
    • Q15023
    • Q8N2V1
    • Q969W7
    • Q96AE1
    • Q9BRM7

    Protein attributes for MCM2 Gene

    Size:
    904 amino acids
    Molecular mass:
    101896 Da
    Quaternary structure:
    • Component of the MCM2-7 complex. The complex forms a toroidal hexameric ring with the proposed subunit order MCM2-MCM6-MCM4-MCM7-MCM3-MCM5 (Probable). Interacts with DBF4 (By similarity). Interacts with KAT7. May interact with MCM10.
    Miscellaneous:
    • Early fractionation of eukaryotic MCM proteins yielded a variety of dimeric, trimeric and tetrameric complexes with unclear biological significance. Specifically a MCM467 subcomplex is shown to have in vitro helicase activity which is inhibited by the MCM2 subunit. The MCM2-7 hexamer is the proposed physiological active complex.
    SequenceCaution:
    • Sequence=BAA04642.1; Type=Erroneous initiation; Note=Translation N-terminally shortened.; Evidence={ECO:0000305}; Sequence=BAA12177.1; Type=Erroneous initiation; Note=Translation N-terminally extended.; Evidence={ECO:0000305}; Sequence=CAA47749.1; Type=Erroneous initiation; Note=Translation N-terminally shortened.; Evidence={ECO:0000305}; Sequence=CAA47749.1; Type=Frameshift; Positions=115, 124, 127, 129, 154, 158, 773, 811; Evidence={ECO:0000305};

    Three dimensional structures from OCA and Proteopedia for MCM2 Gene

neXtProt entry for MCM2 Gene

Post-translational modifications for MCM2 Gene

  • Phosphorylated on Ser-108 by ATR in proliferating cells. Ser-108 proliferation is increased by genotoxic agents. Ser-40 is mediated by the CDC7-DBF4 and CDC7-DBF4B complexes, while Ser-53 phosphorylation is only mediated by the CDC7-DBF4 complex. Phosphorylation by the CDC7-DBF4 complex during G1/S phase is required for the initiation of DNA replication.
  • Ubiquitination at Lys178, Lys469, Lys476, Lys492, Lys613, and Lys722
  • Modification sites at PhosphoSitePlus

Other Protein References for MCM2 Gene

No data available for DME Specific Peptides for MCM2 Gene

Domains & Families for MCM2 Gene

Gene Families for MCM2 Gene

Suggested Antigen Peptide Sequences for MCM2 Gene

GenScript: Design optimal peptide antigens:

Graphical View of Domain Structure for InterPro Entry

P49736

UniProtKB/Swiss-Prot:

MCM2_HUMAN :
  • Belongs to the MCM family.
Family:
  • Belongs to the MCM family.
genes like me logo Genes that share domains with MCM2: view

Function for MCM2 Gene

Molecular function for MCM2 Gene

GENATLAS Biochemistry:
cell division cycle,early S-phase-like 1,involved in an early step of DNA replication,participating in the cell cycle control of genome duplication
UniProtKB/Swiss-Prot CatalyticActivity:
ATP + H(2)O = ADP + phosphate.
UniProtKB/Swiss-Prot Function:
Acts as component of the MCM2-7 complex (MCM complex) which is the putative replicative helicase essential for once per cell cycle DNA replication initiation and elongation in eukaryotic cells. The active ATPase sites in the MCM2-7 ring are formed through the interaction surfaces of two neighboring subunits such that a critical structure of a conserved arginine finger motif is provided in trans relative to the ATP-binding site of the Walker A box of the adjacent subunit. The six ATPase active sites, however, are likely to contribute differentially to the complex helicase activity. Required for the entry in S phase and for cell division. Plays a role in terminally differentiated hair cells development of the cochlea and induces cells apoptosis.

Enzyme Numbers (IUBMB) for MCM2 Gene

Gene Ontology (GO) - Molecular Function for MCM2 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0000166 nucleotide binding IEA --
GO:0003677 DNA binding IEA,TAS 8175912
GO:0003678 DNA helicase activity IEA --
GO:0003688 DNA replication origin binding IEA --
GO:0004386 helicase activity IEA --
genes like me logo Genes that share ontologies with MCM2: view
genes like me logo Genes that share phenotypes with MCM2: view

Animal Model Products

No data available for Human Phenotype Ontology , Animal Models , Transcription Factor Targets and HOMER Transcription for MCM2 Gene

Localization for MCM2 Gene

Subcellular locations from UniProtKB/Swiss-Prot for MCM2 Gene

Subcellular locations from

COMPARTMENTS
Extracellular space Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi Apparatus Nucleus Mitochondrion 0 1 2 3 4 5 Confidence
COMPARTMENTS Subcellular localization image for MCM2 gene
Compartment Confidence
cytoskeleton 5
nucleus 5
cytosol 5

Gene Ontology (GO) - Cellular Components for MCM2 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0000784 nuclear chromosome, telomeric region IDA 19135898
GO:0000785 chromatin TAS,IDA 16899510
GO:0005634 nucleus IDA,IEA 16899510
GO:0005654 nucleoplasm IDA,TAS --
GO:0005664 nuclear origin of replication recognition complex IEA --
genes like me logo Genes that share ontologies with MCM2: view

Pathways & Interactions for MCM2 Gene

genes like me logo Genes that share pathways with MCM2: view

Pathways by source for MCM2 Gene

SIGNOR curated interactions for MCM2 Gene

Activates:
Is activated by:
Other effect:

Gene Ontology (GO) - Biological Process for MCM2 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0000082 G1/S transition of mitotic cell cycle TAS --
GO:0006260 DNA replication TAS,IEA --
GO:0006268 DNA unwinding involved in DNA replication IEA --
GO:0006270 DNA replication initiation IMP,IEA 16899510
GO:0006334 nucleosome assembly IEA --
genes like me logo Genes that share ontologies with MCM2: view

Drugs & Compounds for MCM2 Gene

(7) Drugs for MCM2 Gene - From: HMDB and Novoseek

Name Status Disease Links Group Role Mechanism of Action Clinical Trials
Phosphoric acid Approved Pharma 0
Water Approved Pharma 0
Adenosine triphosphate Approved Nutra 0

(2) Additional Compounds for MCM2 Gene - From: Novoseek and HMDB

Name Synonyms Role CAS Number PubChem IDs PubMed IDs
ADP
  • Adenosindiphosphorsaeure
  • Adenosine 5'-pyrophosphate
  • Adenosine diphosphate
  • Adenosine pyrophosphate
  • Adenosine-5'-diphosphate
Full agonist, Agonist 58-64-0
genes like me logo Genes that share compounds with MCM2: view

Transcripts for MCM2 Gene

Unigene Clusters for MCM2 Gene

Minichromosome maintenance complex component 2:
Representative Sequences:

Alternative Splicing Database (ASD) splice patterns (SP) for MCM2 Gene

ExUns: 1a · 1b ^ 2a · 2b ^ 3a · 3b ^ 4a · 4b ^ 5 ^ 6 ^ 7 ^ 8 ^ 9 ^ 10 ^ 11 ^ 12 ^ 13 ^ 14a · 14b ^ 15 ^ 16 ^ 17 ^ 18a · 18b
SP1: - - -
SP2: - - - - - -
SP3:
SP4:
SP5:

Relevant External Links for MCM2 Gene

GeneLoc Exon Structure for
MCM2
ECgene alternative splicing isoforms for
MCM2

Expression for MCM2 Gene

mRNA expression in normal human tissues from GTEx, Illumina, BioGPS, and CGAP SAGE for MCM2 Gene

mRNA expression in embryonic tissues and stem cells from LifeMap Discovery

Protein differential expression in normal tissues from HIPED for MCM2 Gene

This gene is overexpressed in Liver (39.1), Lymph node (7.1), and Fetal ovary (6.4).

Integrated Proteomics: protein expression in normal tissues and cell lines from ProteomicsDB, PaxDb, MaxQB, and MOPED for MCM2 Gene



Protein tissue co-expression partners for MCM2 Gene

- Elite partner

NURSA nuclear receptor signaling pathways regulating expression of MCM2 Gene:

MCM2

SOURCE GeneReport for Unigene cluster for MCM2 Gene:

Hs.477481

Evidence on tissue expression from TISSUES for MCM2 Gene

  • Nervous system(4.9)
  • Lung(4.6)
  • Liver(4.5)
  • Blood(4.4)
  • Muscle(4.4)
  • Bone marrow(4.3)
  • Intestine(3)
  • Skin(3)
  • Lymph node(2.4)
  • Eye(2.2)
genes like me logo Genes that share expression patterns with MCM2: view

Primer Products

No data available for mRNA differential expression in normal tissues , mRNA Expression by UniProt/SwissProt and Phenotype-based relationships between genes and organs from Gene ORGANizer for MCM2 Gene

Orthologs for MCM2 Gene

This gene was present in the common ancestor of eukaryotes.

Orthologs for MCM2 Gene

Organism Taxonomy Gene Similarity Type Details
chimpanzee
(Pan troglodytes)
Mammalia MCM2 34 35
  • 99.56 (n)
oppossum
(Monodelphis domestica)
Mammalia MCM2 35
  • 94 (a)
OneToOne
platypus
(Ornithorhynchus anatinus)
Mammalia MCM2 35
  • 94 (a)
OneToOne
dog
(Canis familiaris)
Mammalia MCM2 34 35
  • 89.95 (n)
mouse
(Mus musculus)
Mammalia Mcm2 16 35 34
  • 87.32 (n)
rat
(Rattus norvegicus)
Mammalia Mcm2 34
  • 86.91 (n)
cow
(Bos Taurus)
Mammalia MCM2 34 35
  • 85.89 (n)
chicken
(Gallus gallus)
Aves MCM2 34 35
  • 81.11 (n)
lizard
(Anolis carolinensis)
Reptilia MCM2 35
  • 89 (a)
OneToOne
tropical clawed frog
(Silurana tropicalis)
Amphibia mcm2 34
  • 75.16 (n)
Str.1626 34
African clawed frog
(Xenopus laevis)
Amphibia mcm2-prov 34
zebrafish
(Danio rerio)
Actinopterygii mcm2 34 35
  • 74.81 (n)
rainbow trout
(Oncorhynchus mykiss)
Actinopterygii Omy.7968 34
African malaria mosquito
(Anopheles gambiae)
Insecta AgaP_AGAP004275 34
  • 63.58 (n)
fruit fly
(Drosophila melanogaster)
Insecta Mcm2 36 34 35
  • 62.91 (n)
worm
(Caenorhabditis elegans)
Secernentea mcm-2 36 34 35
  • 57.36 (n)
A. gosspyii yeast
(Ashbya gossypii)
Saccharomycetes AGOS_AFR178W 34
  • 55.48 (n)
K. lactis yeast
(Kluyveromyces lactis)
Saccharomycetes KLLA0F12584g 34
  • 52.48 (n)
baker's yeast
(Saccharomyces cerevisiae)
Saccharomycetes MCM2 34 35 37
  • 51.96 (n)
thale cress
(Arabidopsis thaliana)
eudicotyledons MCM2 34
  • 54.2 (n)
soybean
(Glycine max)
eudicotyledons Gma.2371 34
rice
(Oryza sativa)
Liliopsida Os11g0484300 34
  • 56.54 (n)
Os.12974 34
barley
(Hordeum vulgare)
Liliopsida Hv.3981 34
wheat
(Triticum aestivum)
Liliopsida Ta.2860 34
sea squirt
(Ciona savignyi)
Ascidiacea -- 35
  • 66 (a)
OneToOne
bread mold
(Neurospora crassa)
Ascomycetes NCU04327 34
  • 58.69 (n)
fission yeast
(Schizosaccharomyces pombe)
Schizosaccharomycetes mcm2 34
  • 53.37 (n)
sea squirt
(Ciona intestinalis)
Ascidiacea Cin.647 34
Species where no ortholog for MCM2 was found in the sources mined by GeneCards:
  • Actinobacteria (Mycobacterium tuberculosis)
  • Alicante grape (Vitis vinifera)
  • alpha proteobacteria (Wolbachia pipientis)
  • amoeba (Dictyostelium discoideum)
  • Archea (Pyrococcus horikoshii)
  • beta proteobacteria (Neisseria meningitidis)
  • Chromalveolata (Phytophthora infestans)
  • common water flea (Daphnia pulex)
  • corn (Zea mays)
  • E. coli (Escherichia coli)
  • filamentous fungi (Aspergillus nidulans)
  • Firmicute bacteria (Streptococcus pneumoniae)
  • green algae (Chlamydomonas reinhardtii)
  • honey bee (Apis mellifera)
  • loblloly pine (Pinus taeda)
  • malaria parasite (Plasmodium falciparum)
  • medicago trunc (Medicago Truncatula)
  • moss (Physcomitrella patens)
  • orangutan (Pongo pygmaeus)
  • pig (Sus scrofa)
  • rice blast fungus (Magnaporthe grisea)
  • schistosome parasite (Schistosoma mansoni)
  • sea anemone (Nematostella vectensis)
  • sea urchin (Strongylocentrotus purpuratus)
  • sorghum (Sorghum bicolor)
  • stem rust fungus (Puccinia graminis)
  • sugarcane (Saccharum officinarum)
  • tomato (Lycopersicon esculentum)
  • toxoplasmosis (Toxoplasma gondii)
  • Trichoplax (Trichoplax adhaerens)

Evolution for MCM2 Gene

ENSEMBL:
Gene Tree for MCM2 (if available)
TreeFam:
Gene Tree for MCM2 (if available)

Paralogs for MCM2 Gene

Paralogs for MCM2 Gene

(6) SIMAP similar genes for MCM2 Gene using alignment to 7 proteins:

genes like me logo Genes that share paralogs with MCM2: view

Variants for MCM2 Gene

Sequence variations from dbSNP and Humsavar for MCM2 Gene

SNP ID Clin Chr 03 pos Sequence Context AA Info Type
rs375851208 Pathogenic, Deafness, autosomal dominant, 70 (DFNA70) [MIM:616968] 127,599,441(+) CTGGC(C/T)GTGAC nc-transcript-variant, upstream-variant-2KB, reference, missense
rs1000044439 -- 127,614,995(+) GAGAC(A/G)CCTCT intron-variant
rs1000111676 -- 127,609,669(+) ATTTA(A/T)GTTGC intron-variant
rs1000143031 -- 127,609,318(+) TGCGA(C/T)GAGAA intron-variant
rs1000201515 -- 127,621,520(+) GAAGC(C/T)CCTTA intron-variant, nc-transcript-variant

Structural Variations from Database of Genomic Variants (DGV) for MCM2 Gene

Variant ID Type Subtype PubMed ID
dgv8563n54 CNV loss 21841781
esv2102273 CNV deletion 18987734
esv2555442 CNV deletion 19546169
esv2653998 CNV deletion 19546169

Variation tolerance for MCM2 Gene

Residual Variation Intolerance Score: 8.02% of all genes are more intolerant (likely to be disease-causing)
Gene Damage Index Score: 4.27; 62.62% of all genes are more intolerant (likely to be disease-causing)

Relevant External Links for MCM2 Gene

Human Gene Mutation Database (HGMD)
MCM2
SNPedia medical, phenotypic, and genealogical associations of SNPs for
MCM2

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot for MCM2 Gene

Disorders for MCM2 Gene

MalaCards: The human disease database

(14) MalaCards diseases for MCM2 Gene - From: ClinVar, Orphanet, Swiss-Prot, DISEASES, Novoseek, and GeneCards

Disorder Aliases PubMed IDs
autosomal dominant nonsyndromic deafness 70
  • autosomal dominant deafness 70
autosomal dominant non-syndromic sensorineural deafness type dfna
  • autosomal dominant isolated neurosensory deafness type dfna
cervix endometriosis
  • cervical endometriosis
autosomal dominant nonsyndromic deafness
  • autosomal dominant deafness
follicular adenoma
  • follicular adenoma of the thyroid gland
- elite association - COSMIC cancer census association via MalaCards
Search MCM2 in MalaCards View complete list of genes associated with diseases

UniProtKB/Swiss-Prot

MCM2_HUMAN
  • Deafness, autosomal dominant, 70 (DFNA70) [MIM:616968]: A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. DFNA70 is characterized by slowly progressive, postlingual hearing impairment. {ECO:0000269 PubMed:26196677}. Note=The disease is caused by mutations affecting the gene represented in this entry.

Relevant External Links for MCM2

Genetic Association Database (GAD)
MCM2
Human Genome Epidemiology (HuGE) Navigator
MCM2
Atlas of Genetics and Cytogenetics in Oncology and Haematology:
MCM2
genes like me logo Genes that share disorders with MCM2: view

No data available for Genatlas for MCM2 Gene

Publications for MCM2 Gene

  1. The human gene for nuclear protein BM28 (CDCL1), a new member of the early S-phase family of proteins, maps to chromosome band 3q21. (PMID: 8258304) Mincheva A. … Lichter P. (Cytogenet. Cell Genet. 1994) 2 3 4 22 64
  2. Essential role of phosphorylation of MCM2 by Cdc7/Dbf4 in the initiation of DNA replication in mammalian cells. (PMID: 16899510) Tsuji T. … Jiang W. (Mol. Biol. Cell 2006) 3 4 22 64
  3. The human homolog of Saccharomyces cerevisiae Mcm10 interacts with replication factors and dissociates from nuclease-resistant nuclear structures in G(2) phase. (PMID: 11095689) Izumi M. … Hanaoka F. (Nucleic Acids Res. 2000) 3 4 22 64
  4. Nuclear matrix protein mitotin messenger RNA is expressed at constant levels during the cell cycle. (PMID: 1710453) Todorov I.T. … Bibor-Hardy V. (Biochem. Biophys. Res. Commun. 1991) 2 3 22 64
  5. Whole Exome Sequencing Identified MCM2 as a Novel Causative Gene for Autosomal Dominant Nonsyndromic Deafness in a Chinese Family. (PMID: 26196677) Gao J. … Liu Y. (PLoS ONE 2015) 3 4 64

Products for MCM2 Gene

Sources for MCM2 Gene

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