MCM2 - minichromosome maintenance complex component 2 Gene

Also Known as BM28; CCNL1; CDCL1; cdc19; DFNA70; D3S3194; MITOTIN

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 4171

About MCM2

Cytogenetic location: 3q21.3 Genomic coordinates (GRCh38): 3:127,598,411-127,622,436 (from NCBI)

This gene has 9 transcripts (splice variants), 206 orthologues, 8 paralogues and is associated with 2 phenotypes. Broad expression in bone marrow (RPKM 27.3), lymph node (RPKM 14.9) and 23 other tissues.

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]

MCM2 Products (1)

mRNA Protein Name
NM_004526.4 NP_004517.2 DNA replication licensing factor MCM2
Molecular Function GO Annotation Evidence References Source
enables histone binding EXP
EXP: Inferred from Experiment
25618846 GOA
enables histone binding IPI
IPI: Inferred from physical interaction
25618846 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
11095689 GOA
Biological Process GO Annotation Evidence References Source
involved in DNA replication initiation IMP
IMP: Inferred from mutant phenotype
16899510 GOA
involved in DNA unwinding involved in DNA replication IDA
IDA: Inferred from direct assay
22474384 GOA
involved in apoptotic process IMP
IMP: Inferred from mutant phenotype
26196677 GOA
involved in cochlea development IMP
IMP: Inferred from mutant phenotype
26196677 GOA
Cellular Component GO Annotation Evidence References Source
part of CMG complex IPI
IPI: Inferred from physical interaction
22474384 GOA
part of MCM complex IDA
IDA: Inferred from direct assay
17296731 GOA
part of MCM complex IPI
IPI: Inferred from physical interaction
22540012 GOA
located in chromatin IDA
IDA: Inferred from direct assay
16899510 GOA
located in cytoplasm IDA
IDA: Inferred from direct assay
26196677 GOA
NOT located in nucleolus IDA
IDA: Inferred from direct assay
21383955 GOA
located in nucleus IDA
IDA: Inferred from direct assay
16899510 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

DNA replication licensing factor MCM2

  • cell devision cycle-like 1

MCM2 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
MCM2 P49736 AKAP8 Homo sapiens O43823 12740381
Intra
MCM2 P49736 CENPA Homo sapiens P49450 26167883
Intra
MCM2 P49736 CENPA Homo sapiens P49450 26167883
Intra
MCM2 P49736 GINS3 Homo sapiens Q9BRX5 19805216
Intra
MCM2 P49736 GINS3 Homo sapiens Q9BRX5 33961781
Intra
MCM2 P49736 H4C16 Homo sapiens P62805 26167883
Intra
MCM2 P49736 H4C16 Homo sapiens P62805 26167883
Intra
MCM2 P49736 H4C16 Homo sapiens P62805 19862764
Intra
MCM2 P49736 DONSON Homo sapiens Q9NYP3 32769987
Intra
MCM2 P49736 DONSON Homo sapiens Q9NYP3
PLA
32769987
Intra
MCM2 P49736 SSRP1 Homo sapiens Q08945 33961781
Intra
MCM2 P49736 MCM3 Homo sapiens P25205 17296731
Intra
MCM2 P49736 MCM3 Homo sapiens P25205
GMS
16899510
Intra
MCM2 P49736 MCM3 Homo sapiens P25205
SLC
31467278
Intra
MCM2 P49736 MCM3 Homo sapiens P25205
TAP
17296731
Intra
MCM2 P49736 MCM3 Homo sapiens P25205 22540012
Intra
MCM2 P49736 MCM3 Homo sapiens P25205 15232106
Intra
MCM2 P49736 MCM3 Homo sapiens P25205 26167883
Intra
MCM2 P49736 MCM7 Homo sapiens P33993
TAP
17296731
Intra
MCM2 P49736 MCM7 Homo sapiens P33993 17296731
Intra
MCM2 P49736 MCM7 Homo sapiens P33993 33961781
Intra
MCM2 P49736 MCM7 Homo sapiens P33993
GMS
16899510
Intra
MCM2 P49736 MCM7 Homo sapiens P33993 22540012
Intra
MCM2 P49736 MCM7 Homo sapiens P33993 15232106
Intra
MCM2 P49736 MCM5 Homo sapiens P33992
TAP
17296731
Intra
MCM2 P49736 MCM5 Homo sapiens P33992 22540012
Intra
MCM2 P49736 MCM5 Homo sapiens P33992 15232106
Intra
MCM2 P49736 MCM5 Homo sapiens P33992
GMS
16899510
Intra
MCM2 P49736 MCM5 Homo sapiens P33992 17296731
Intra
MCM2 P49736 MCM6 Homo sapiens Q14566 17296731
Intra
MCM2 P49736 MCM6 Homo sapiens Q14566 33961781
Intra
MCM2 P49736 MCM6 Homo sapiens Q14566 25416956
Intra
MCM2 P49736 MCM6 Homo sapiens Q14566 25416956
Intra
MCM2 P49736 MCM6 Homo sapiens Q14566
TAP
17296731
Intra
MCM2 P49736 MCM6 Homo sapiens Q14566 22540012
Intra
MCM2 P49736 MCM6 Homo sapiens Q14566
GMS
16899510
Intra
MCM2 P49736 MCM6 Homo sapiens Q14566 26167883
Intra
MCM2 P49736 MCM6 Homo sapiens Q14566 17296731
Intra
MCM2 P49736 MCM6 Homo sapiens Q14566 16189514
Intra
MCM2 P49736 MCM6 Homo sapiens Q14566 20211142
Intra
MCM2 P49736 CDC45 Homo sapiens O75419 26167883
Intra
MCM2 P49736 CDC45 Homo sapiens O75419 19805216
Intra
MCM2 P49736 FANCM Homo sapiens Q8IYD8
PLA
32769987
Intra
MCM2 P49736 PLK1 Homo sapiens P53350 15654075
Intra
MCM2 P49736 SNF8 Homo sapiens Q96H20 19819239
Intra
MCM2 P49736 SNF8 Homo sapiens Q96H20
Y2H
19819239
Intra
MCM2 P49736 SNF8 Homo sapiens Q96H20 19819239
Intra
MCM2 P49736 MCMBP Homo sapiens Q9BTE3 22540012
Intra
MCM2 P49736 MCMBP Homo sapiens Q9BTE3 33961781
Intra
MCM2 P49736 ASF1A Homo sapiens Q9Y294 26167883
Intra
MCM2 P49736 ASF1A Homo sapiens Q9Y294 26167883
Intra
MCM2 P49736 ASF1A Homo sapiens Q9Y294 32296183
Intra
MCM2 P49736 ASF1A Homo sapiens Q9Y294 32296183
Intra
MCM2 P49736 ASF1A Homo sapiens Q9Y294 33961781
Intra
MCM2 P49736 ASF1A Homo sapiens Q9Y294 32296183
Intra
MCM2 P49736 TERF2IP Homo sapiens Q9NYB0 21044950
Intra
MCM2 P49736 TERF2IP Homo sapiens Q9NYB0 21044950
Intra
MCM2 P49736 H3C1 Homo sapiens P68431 33961781
Cross: Cross-species interaction Intra: Intraspecies interaction

MCM2 Antibodies

Cat. No. 상품명 신청 Reactivity
HY-P80215 MCM2 Antibody (YA302) WB, IHC-P, ICC/IF, FC Human
HY-P80749 MCM2 Antibody (YA705) WB, IHC-F, IHC-P, ICC/IF, FC, IP Human, Mouse
HY-P810586 Phospho-MCM2 (Ser41) Antibody (YA9850) WB, ICC/IF, IHC-P, FC, IP Human, Mouse, Rat
HY-P810587 Phospho-MCM2 (Ser108) Antibody (YA9851) WB, IHC-P Human, Mouse, Rat
HY-P810588 Phospho-MCM2 (Ser27) Antibody (YA9852) WB, ICC/IF, IHC-P, IP Human, Mouse, Rat
HY-P810589 Phospho-MCM2 (Ser40) Antibody (YA9853) WB, ICC/IF, IHC-P, FC, IF-Tissue Human, Mouse, Rat
HY-P85058 MCM2 Antibody (YA4750) WB, IHC-P, ICC/IF, FC, ELISA Human, Mouse, Rat, Monkey
HY-P85959 MCM2 Antibody (YA5651) IHC-P, WB, ICC/IF, ELISA Human, Mouse,

Related Diseases

Diseases Alias
Deafness, Autosomal Dominant 70
  • DFNA70

  • Autosomal Dominant Nonsyndromic Deafness 70

  • Autosomal Dominant Deafness 70

  • Deafness, Autosomal Dominant, 70

Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna
  • Autosomal Dominant Isolated Neurosensory Deafness Type Dfna

  • Autosomal Dominant Isolated Neurosensory Hearing Loss Type Dfna

  • Autosomal Dominant Isolated Sensorineural Deafness Type Dfna

  • Autosomal Dominant Isolated Sensorineural Hearing Loss Type Dfna

  • Autosomal Dominant Non-Syndromic Neurosensory Deafness Type Dfna

  • Autosomal Dominant Non-Syndromic Neurosensory Hearing Loss Type Dfna

  • Autosomal Dominant Non-Syndromic Sensorineural Hearing Loss Type Dfna

Follicular Adenoma
  • Follicular Adenoma Of The Thyroid Gland

  • Thyroid Follicular Adenoma

  • Adenoma Follicular

  • Follicular Thyroid Adenoma

  • Thyroid Gland Follicular Adenoma

Laryngeal Squamous Cell Carcinoma
  • Epidermoid Carcinoma Of The Larynx

  • Squamous Cell Carcinoma Of Larynx

  • Squamous Cell Carcinoma Of The Larynx

  • Squamous Cell Carcinoma Of Head And Neck

Cervix Endometriosis
  • Endometriosis Of Cervix

  • Cervical Endometriosis

Transitional Cell Carcinoma
  • Transitional Cell Neoplasm

  • Carcinoma, Transitional Cell

  • Transitional Carcinoma

  • Transitional Cell Tumor

  • Urothelial Cell Carcinoma

  • Carcinoma Transitional Cell

  • Transitional Cell Carcinoma Of Bladder

Cardiomyopathy, Familial Hypertrophic, 6
  • Hypertrophic Cardiomyopathy 6

  • CMH6

  • Familial Hypertrophic Cardiomyopathy With Wolff-Parkinson-White Syndrome

  • Cardiomyopathy, Familial Hypertrophic 6

  • Cardiomyopathy, Hypertrophic 6

  • Cardiomyopathy, Hypertrophic, Familial, Type 6

Immunodeficiency 7
  • Tcr-Alpha-Beta-Positive T-Cell Deficiency

  • IMD7

  • T-Cell Receptor-Alpha/Beta Deficiency

  • Immunodeficiency 7, Tcr-Alpha/Beta Deficient

  • Tcr-Alpha/Beta Deficiency

  • Tcr-Alpha-Beta+ T-Cell Deficiency

  • T-Cell Receptor Alpha/Beta Deficiency

Barrett Esophagus
  • Barrett'S Esophagus

  • Barrett Esophagus/Esophageal Adenocarcinoma

  • Barrett Metaplasia

  • Barrett'S Ulcer Of Esophagus

  • Ulcerative Esophagitis

  • Barrett'S Esophagus With Esophagitis

  • Barrett'S Oesophagus

  • Barretts Syndrome

  • Barrett Syndrome

  • BE

  • Peptic Ulcer Of Esophagus

  • Adenocarcinoma Of Esophagus

Breast Cancer
  • Breast Carcinoma

  • Male Breast Cancer

  • Breast Cancer, Familial

  • Malignant Neoplasm Of Breast

  • Breast Cancer, Susceptibility To

  • Breast Cancer, Early-Onset

  • Malignant Tumor Of Breast

  • Carcinoma Of Male Breast

  • Breast Cancer, Invasive Ductal

  • Breast Cancer, Protection Against

  • Breast Cancer, Somatic

  • Breast Cancer, Male

  • Breast Cancer, Lobular, Somatic

  • Breast Tumor

  • Mammary Cancer

  • Mammary Tumor

  • Malignant Neoplasm Of Male Breast

  • Mammary Carcinoma

  • Male Breast Carcinoma

  • Familial Cancer Of Breast

  • Invasive Ductal Breast Carcinoma

  • Breast Cancer Susceptibility

  • Breast Cancer, Male, Susceptibility To

  • Breast Cancer, Early-Onset, Susceptibility To

  • Malignant Tumor Of The Breast

  • Mammary Neoplasm

  • Primary Breast Cancer

  • Neoplasm Of Male Breast

  • Carcinoma Of Breast

  • Breast Cancer In Men

  • Familial Breast Cancer

  • Cancer Of Breast

  • BC

  • Breast Cancer Familial

  • Breast Cancer Familial Male

  • Breast Cancer, Familial Male

  • Breast Male Carcinoma

  • Breast Neoplasms

  • Breast Neoplasms, Male

  • Mammary Tumors

  • Mammary Carcinomas

  • Cancer, Breast

  • Cancer, Breast, Susceptibility

  • Invasive Breast Ductal Carcinoma

  • Breast Neoplasm

  • Susceptibility To Breast Cancer

  • Mammary Neoplasms

  • Animal Mammary Neoplasms

  • Primary Malignant Neoplasm Of Breast

  • Infiltrating Ductal Carcinoma Of Breast

  • Infiltrating Duct Carcinoma Of Unspecified Site

  • Infiltrating Ductular Carcinoma Of Unspecified Site

  • Invasive Breast Carcinoma Of No Special Type

  • Microinvasive Carcinoma Of Breast

  • Carcinoma With Apocrine Differentiation

Familial Glucocorticoid Deficiency
  • Glucocorticoid Deficiency

  • Acth Resistance

  • Adrenal Unresponsiveness To Acth

  • Hereditary Unresponsiveness To Adrenocorticotropic Hormone

  • Isolated Glucocorticoid Deficiency

  • Glucocorticoid Deficiency, Familial

  • Glucocorticoid Deficiency 1

Lung Cancer
  • Lung Carcinoma

  • Non-Small Cell Lung Carcinoma

  • Lung Cancer, Susceptibility To

  • Lung Cancer, Protection Against

  • Adenocarcinoma Of Lung, Somatic

  • Adenocarcinoma Of Lung, Response To Tyrosine Kinase Inhibitor In

  • Nonsmall Cell Lung Cancer

  • Lung Neoplasm

  • Carcinoma Of Lung

  • Lung Non-Small Cell Carcinoma

  • Non-Small Cell Lung Cancer

  • Nsclc

  • Lung Neoplasms

  • Malignant Neoplasm Of Lung

  • Alveolar Cell Carcinoma

  • Nonsmall Cell Lung Cancer, Somatic

  • Nonsmall Cell Lung Cancer, Response To Tyrosine Kinase Inhibitor In

  • Nonsmall Cell Lung Cancer, Susceptibility To

  • Lung Cancer, Somatic

  • Lung Cancer, Resistance To

  • Cancer Of Lung

  • Cancer Of Bronchus

  • Cancer Of The Lung

  • Lung Malignancies

  • Lung Malignant Tumors

  • Malignant Lung Tumor

  • Malignant Tumor Of Lung

  • Pulmonary Cancer

  • Pulmonary Carcinoma

  • Pulmonary Neoplasms

  • Respiratory Carcinoma

  • LNCR

  • Adenocarcinoma Of Lung

  • Neoplasm Of Lung

  • Cancer Lung

  • Carcinoma Non-Small Cell Lung

  • Carcinoma, Non-Small-Cell Lung

  • Lung Cancers

  • Lung Carcinomas

  • Cancer, Lung

  • Cancer, Lung, Non-Small Cell

  • Primary Malignant Neoplasm Of Lung

  • Bronchioloalveolar Adenocarcinoma

Meier-Gorlin Syndrome 1
  • Meier-Gorlin Syndrome

  • Ear, Patella, Short Stature Syndrome

  • Microtia, Absent Patellae, Micrognathia Syndrome

  • MGORS1

  • Eps

  • Ear-Patella-Short Stature Syndrome

  • Ear Patella Short Stature Syndrome

  • Microtia Absent Patellae Micrognathia Syndrome

  • Meier-Gorlin Syndrome, Type 1

Prostate Cancer
  • Prostate Carcinoma

  • Prostate Cancer, Familial

  • Prostate Neoplasm

  • Prostate Cancer, Somatic

  • Prostate Cancer, Susceptibility To

  • Prostatic Cancer

  • Prostatic Neoplasms

  • Hereditary Prostate Cancer

  • Prostatic Neoplasm

  • Cancer Of Prostate

  • Carcinoma Of Prostate

  • Familial Prostate Cancer

  • Familial Prostate Carcinoma

  • Malignant Tumor Of Prostate

  • Malignant Neoplasm Of Prostate

  • Prostate Cancer, Familial, Susceptibility To

  • Malignant Tumor Of The Prostate

  • Ngp - New Growth Of Prostate

  • Tumor Of The Prostate

  • Prostate Cancer, Hereditary

  • Cancer Of The Prostate

  • Malignant Neoplasm Of The Prostate

  • Prostatic Carcinoma

  • PC

  • Prca

  • Cancer, Prostate

  • Malignant Prostatic Tumour

  • Malignant Tumour Of Prostate

  • Primary Prostate Cancer

  • Primary Malignant Neoplasm Of Prostate

  • Prostate Gland Cancer

Medulloblastoma
  • MDB

  • Cpnet

  • Localized Primitive Neuroectodermal Tumor

  • Classic Medulloblastoma

  • Medulloblastoma Predisposition Syndrome

  • Medulloblastoma, Somatic

  • Brain Medulloblastoma

  • Cns Pnet

  • Infratentorial Primitive Neuroectodermal Tumor

  • Neuroectodermal Tumors, Primitive

  • Medulloblastomas

  • Desmoplastic Medulloblastoma

  • Medulloblastoma, With Extensive Nodularity

  • Medulloblastoma Of Unspecified Site

  • Medullomyoblastoma Of Unspecified Site

Sensorineural Hearing Loss
  • Sensory Hearing Loss

  • Sensorineural Deafness

  • Sensorineural Hearing Loss Disorder

  • Hearing Loss, Sensorineural

  • Central Hearing Loss

  • High Frequency Deafness

  • High Frequency Hearing Loss

  • High-Frequency Hearing Loss

  • Perceptive Deafness

  • Perceptive Hearing Loss

  • Perceptive Hearing Loss Or Deafness

  • Hearing Loss Sensorineural

  • Deafness Sensorineural

  • Hearing Loss High-Frequency

  • Hearing Loss, Central

  • Hearing Loss, High-Frequency

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Rattus norvegicus MCM2 RGD RGD:1305577
Mus musculus MCM2 MGD MGI:105380
Canis familiaris MCM2 VGNC VGNC:43081
Bos taurus MCM2 VGNC VGNC:31308
Felis catus MCM2 VGNC VGNC:68212
Macaca mulatta MCM2 VGNC VGNC:74680
Others MCM2 NCBI