CCND2 (cyclin D2)

symbol:
CCND2
locus group:
protein-coding gene
location:
12p13.32
gene_family:
Cyclins
alias symbol:
None
alias name:
G1/S-specific cyclin D2
entrez id:
894
ensembl gene id:
ENSG00000118971
ucsc gene id:
uc001qmo.4
refseq accession:
NM_001759
hgnc_id:
HGNC:1583
approved reserved:
1991-12-10
12p13.32
基因染色体位置图

The protein encoded by this gene belongs to the highly conserved cyclin family, whose members are characterized by a dramatic periodicity in protein abundance through the cell cycle. Cyclins function as regulators of CDK kinases. Different cyclins exhibit distinct expression and degradation patterns which contribute to the temporal coordination of each mitotic event. This cyclin forms a complex with CDK4 or CDK6 and functions as a regulatory subunit of the complex, whose activity is required for cell cycle G1/S transition. This protein has been shown to interact with and be involved in the phosphorylation of tumor suppressor protein Rb. Knockout studies of the homologous gene in mouse suggest the essential roles of this gene in ovarian granulosa and germ cell proliferation. High level expression of this gene was observed in ovarian and testicular tumors. Mutations in this gene are associated with megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3 (MPPH3). [provided by RefSeq, Sep 2014]

由该基因编码的蛋白质属于高度保守的细胞周期蛋白家族,其成员通过细胞周期的特征是急剧周期性的蛋白质丰度。细胞周期蛋白作为CDK激酶的监管。不同细胞周期蛋白表现出不同的表达和降解模式这有助于每个有丝分裂事件的时间协调。这个周期蛋白形成具有CDK4或CDK6和功能的复杂的复合物,其活性所需的细胞周期G1 / S期过渡的调节亚基。这种蛋白已经显示出交互和参与肿瘤抑制Rb蛋白的磷酸化。在小鼠的同源基因的敲除研究显示该基因在卵巢颗粒和生殖细胞增殖的重要作用。在卵巢和睾丸肿瘤中观察到这种基因的高水平表达。在这种基因突变与巨脑-多小脑-趾-积水综合征3(MPPH3)相关联。 [由RefSeq的,2014年9月提供]

CCND1基因的碱基序列:[NCBI]
Loading Gene Browser...
CCND2基因的碱基突变:           仅显示部分snp
rs1049606       rs3217783       rs3217784       rs3217785       rs3217786       rs3217787       rs3217788       rs3217789       rs3217790       rs3217791       rs3217792       rs3217793       rs3217794       rs3217795       rs3217796       rs3217797       rs3217798      

CCND2基因在不同组织中的表达:    [UniProt]

基因在不同组织中的表达图
正向引物序列
正向Tm值
反向引物序列
反向Tm值
评分
CAGGATGAGGAAGTGAGCT
59
GAGACAATCCACGTCTGTG
58
CTCAGACCTTCATTGCTCTG
58
AGATGCTGGTGACTTCCTG
59
AGACCTTCATTGCTCTGTG
58
CATCCCTTACCCTTACCCTG
59
TCATTGAGCACATCTTGCG
59
CAAACTTAAAGTCGGTGGCA
59
TCATTGAGCACATCTTGCG
58
CAAACTTAAAGTCGGTGGCA
59
AGAAGCTGTCTCTGATCCG
58
CTTCCTGAGATCCTTCCTCC
59
AGACCTTCATTGCTCTGTG
58
CATCCCTTACCCTTACCCT
58
TGCTCAGACCTTCATTGCT
59
ATGCTGGTGACTTCCTGAG
59
TCATTGAGCACATCTTGCG
58
AAACTTAAAGTCGGTGGCAC
59
AGGATGAGGAAGTGAGCTC
59
GAGACAATCCACGTCTGTG
58
转录因子
影响基因
影响类型
参考文献链接(PubMed)
ABL1
CCND2
Activation
BCL6
CCND2
Repression
EGR1
CCND2
Unknown
ETV4
CCND2
Activation
FOXL2
CCND2
Repression
FOXO3
CCND2
Repression
GATA4
CCND2
Activation
HDAC1
CCND2
Repression
IRF9
CCND2
Repression
MAF
CCND2
Unknown

CCND2基因(以及对应的蛋白质)的细胞分布位置:

[UniProt]     [GenomeNet]

" d="M482.414,245.296c3.539,4.293,4.455,10.009,0.202,11 c-4.244,0.996-4.983-10.983-8.293-8.438c-5.271,4.08,9.834,12.271,5.144,17.287c-3.717,3.607-6.172-5.75-10.839-1.976 c-4.673,3.776,6.781,7.299,2.831,11.326c-4.354,4.045-6.979-1.449-9.837-5.517c-1.193-1.742-2.059-3.851-3.595-2.748 c-1.516,1.078-1.854,1.795-0.938,3.666c2.374,4.854,9.235,10.119,5.156,12.535c-5.636,3.346-5.044-8.871-9.426-7.574 c-4.388,1.291,2.557,10.66-1.245,11.141c-4.089,0.545-3.483-10.239-6.979-8.575c-2.522,1.206-0.929,3.071-0.938,4.899 c0.004,1.32-0.964,3.6-2.372,4.062c-3.593,1.171-8.544-1.065-10.251-3.59c-6.04-8.93,0.396-15.997,4.639-7.015 c3.023,4.642,5.182,0.834,2.839-2.219c-1.032-1.354-4.309-5.901-0.781-7.252c2.904-1.113,4.271,1.941,5.985,4.592 c2.61,4.016,5.485,0.117,3.031-3.414c-1.828-2.633-2.74-3.803,3.156-7.42c6.405-4.369,6.52,3.869,10.077,0.646 c2.309-1.832-4.783-5.149,0.06-8.995c2.896-2.293,5.18,6.207,7.961,3.516c3.523-2.737-7.717-7.369,0.117-11.736 C473.413,240.77,480.519,242.891,482.414,245.296z"/> Extracellular space Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi Apparatus Nucleus Mitochondrion 0 1 2 3 4 5 Confidence
  • 质膜
  • 细胞质
  • 细胞外
  • 高尔基体
  • 囊泡
  • 细胞骨架
  • 内质网
  • 细胞核
  • 内体
  • 溶酶体
  • 线粒体

CCND2基因的本体(GO)信息:

GO库代码
对应的蛋白质
来源代码
GO:0007049
H0YGD4 (UniProtKB)
IEA
GO:0000307
P30279 (UniProtKB)
IDA
GO:0000307
P30279 (UniProtKB)
IDA
GO:0000785
P30279 (UniProtKB)
IDA
GO:0001934
P30279 (UniProtKB)
IDA
GO:0005515
P30279 (UniProtKB)
IPI
GO:0005515
P30279 (UniProtKB)
IPI
GO:0005515
P30279 (UniProtKB)
IPI
GO:0005515
P30279 (UniProtKB)
IPI
GO:0005515
P30279 (UniProtKB)
IPI
GO:0005515
P30279 (UniProtKB)
IPI
GO:0005515
P30279 (UniProtKB)
IPI
GO:0005634
P30279 (UniProtKB)
IDA
GO:0005654
P30279 (UniProtKB)
IDA
GO:0005730
P30279 (UniProtKB)
IDA
GO:0005829
P30279 (UniProtKB)
IDA
GO:0007049
P30279 (UniProtKB)
IEA
GO:0019901
P30279 (UniProtKB)
IPI
GO:0031965
P30279 (UniProtKB)
IDA
GO:0045737
P30279 (UniProtKB)
IDA
GO:0051301
P30279 (UniProtKB)
IEA

可能调控 CCND2基因的相关microRNA:     

MINT

BioGrid

IntAct

mentha

String

基因与其他基因之间的相互作用关系图
序号 作用方式 资源库来源/分值 基因名称 基因名称
疾病名称 关系值 NofPmids NofSnps 来源
疾病名称 关系值 NofPmids NofSnps 来源
Colonic Neoplasms 0.2 1 0 CTD_human_RGD
Prostatic Neoplasms 0.122995792 2 0 BeFree_CTD_human_LHGDN
Diabetes Mellitus, Non-Insulin-Dependent 0.122909916 3 1 BeFree_CTD_human_GAD
Colorectal Cancer 0.120542884 2 4 BeFree_GWASCAT
Megalanecephaly Polymicrogyria-Polydactyly Hydrocephalus Syndrome 0.120271442 1 0 BeFree_CTD_human
Cardiomegaly 0.12 1 0 CTD_human
MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3 0.12 1 0 UNIPROT
Myocardial Ischemia 0.12 1 0 CTD_human
ovarian neoplasm 0.12 1 0 CTD_human
Fibrosis 0.12 1 0 CTD_human

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