Homo sapiens (human): 894
Help
Entry
894 CDS
T01001
Symbol
CCND2, KIAK0002, MPPH3
Name
(RefSeq) cyclin D2
KO
K10151
G1/S-specific cyclin-D2
Organism
hsa
Homo sapiens (human)
Pathway
hsa04068
FoxO signaling pathway
hsa04110
Cell cycle
hsa04115
p53 signaling pathway
hsa04151
PI3K-Akt signaling pathway
hsa04218
Cellular senescence
hsa04310
Wnt signaling pathway
hsa04340
Hedgehog signaling pathway
hsa04390
Hippo signaling pathway
hsa04510
Focal adhesion
hsa04630
JAK-STAT signaling pathway
hsa04917
Prolactin signaling pathway
hsa05162
Measles
hsa05165
Human papillomavirus infection
hsa05166
Human T-cell leukemia virus 1 infection
hsa05169
Epstein-Barr virus infection
hsa05200
Pathways in cancer
hsa05202
Transcriptional misregulation in cancer
hsa05203
Viral carcinogenesis
hsa05206
MicroRNAs in cancer
Network
nt06160
Human T-cell leukemia virus 1 (HTLV-1)
nt06163
Hepatitis C virus (HCV)
nt06164
Kaposi sarcoma-associated herpesvirus (KSHV)
nt06165
Epstein-Barr virus (EBV)
nt06166
Human papillomavirus (HPV)
nt06167
Human cytomegalovirus (HCMV)
nt06170
Influenza A virus (IAV)
nt06230
Cell cycle (cancer)
nt06240
Transcription (cancer)
nt06262
Pancreatic cancer
nt06263
Hepatocellular carcinoma
nt06265
Bladder cancer
nt06266
Non-small cell lung cancer
nt06267
Small cell lung cancer
nt06268
Melanoma
nt06270
Breast cancer
nt06273
Glioma
nt06276
Chronic myeloid leukemia
Element
N00066
MDM2-p21-Cell cycle G1/S
N00067
Deleted p14(ARF) to p21-cell cycle G1/S
N00068
Amplified MDM2 to p21-cell cycle G1/S
N00069
p16-Cell cycle G1/S
N00070
Mutation-inactivated p16(INK4a) to p16-cell cycle G1/S
N00071
Deleted p16(INK4a) to p16-cell cycle G1/S
N00072
Amplified CDK4 to cell cycle G1/S
N00073
Mutation-activated CDK4 to cell cycle G1/S
N00076
Mutation-inactivated p14(ARF) to p21-cell cycle G1/S
N00088
Amplified MYC to p15-cell cycle G1/S
N00089
Amplified MYC to cell cycle G1/S
N00090
p15-Cell cycle G1/S
N00123
Amplified REL to transcription
N00124
IGH-MAF fusion to transcriptional activation
N00125
IGH-MMSET fusion to transcriptional activation
N00347
p300-p21-Cell cycle G1/S
N00483
EBV EBNA3C to cell cycle G1/S
N00489
HTLV-1 p30II to c-myc-mediated transcription
Disease
H00023
Testicular cancer
H01885
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
894 (CCND2)
04390 Hippo signaling pathway
894 (CCND2)
04630 JAK-STAT signaling pathway
894 (CCND2)
04068 FoxO signaling pathway
894 (CCND2)
04151 PI3K-Akt signaling pathway
894 (CCND2)
09150 Organismal Systems
09152 Endocrine system
04917 Prolactin signaling pathway
894 (CCND2)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
894 (CCND2)
05202 Transcriptional misregulation in cancer
894 (CCND2)
05206 MicroRNAs in cancer
894 (CCND2)
05203 Viral carcinogenesis
894 (CCND2)
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
894 (CCND2)
05162 Measles
894 (CCND2)
05169 Epstein-Barr virus infection
894 (CCND2)
05165 Human papillomavirus infection
894 (CCND2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Cyclin_N
Cyclin_C
K-cyclin_vir_C
Motif
Other DBs
NCBI-GeneID:
894
NCBI-ProteinID:
NP_001750
OMIM:
123833
HGNC:
1583
Ensembl:
ENSG00000118971
UniProt:
P30279
Structure
PDB
PDBj
LinkDB
All DBs
Position
12:4273762..4305353
Genome browser
AA seq
289 aa
AA seq
DB search
MELLCHEVDPVRRAVRDRNLLRDDRVLQNLLTIEERYLPQCSYFKCVQKDIQPYMRRMVA
TWMLEVCEEQKCEEEVFPLAMNYLDRFLAGVPTPKSHLQLLGAVCMFLASKLKETSPLTA
EKLCIYTDNSIKPQELLEWELVVLGKLKWNLAAVTPHDFIEHILRKLPQQREKLSLIRKH
AQTFIALCATDFKFAMYPPSMIATGSVGAAICGLQQDEEVSSLTCDALTELLAKITNTDV
DCLKACQEQIEAVLLNSLQQYRQDQRDGSKSEDELDQASTPTDVRDIDL
NT seq
870 nt
NT seq
+upstream
nt +downstream
nt
atggagctgctgtgccacgaggtggacccggtccgcagggccgtgcgggaccgcaacctg
ctccgagacgaccgcgtcctgcagaacctgctcaccatcgaggagcgctaccttccgcag
tgctcctacttcaagtgcgtgcagaaggacatccaaccctacatgcgcagaatggtggcc
acctggatgctggaggtctgtgaggaacagaagtgcgaagaagaggtcttccctctggcc
atgaattacctggaccgtttcttggctggggtcccgactccgaagtcccatctgcaactc
ctgggtgctgtctgcatgttcctggcctccaaactcaaagagaccagcccgctgaccgcg
gagaagctgtgcatttacaccgacaactccatcaagcctcaggagctgctggagtgggaa
ctggtggtgctggggaagttgaagtggaacctggcagctgtcactcctcatgacttcatt
gagcacatcttgcgcaagctgccccagcagcgggagaagctgtctctgatccgcaagcat
gctcagaccttcattgctctgtgtgccaccgactttaagtttgccatgtacccaccgtcg
atgatcgcaactggaagtgtgggagcagccatctgtgggctccagcaggatgaggaagtg
agctcgctcacttgtgatgccctgactgagctgctggctaagatcaccaacacagacgtg
gattgtctcaaagcttgccaggagcagattgaggcggtgctcctcaatagcctgcagcag
taccgtcaggaccaacgtgacggatccaagtcggaggatgaactggaccaagccagcacc
cctacagacgtgcgggatatcgacctgtga
DBGET
integrated database retrieval system