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Gene Symbol |
PDCD4 |
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Aliases |
H731 |
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Entrez Gene ID |
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Gene Name |
Programmed cell death 4 |
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Chromosomal Location |
10q25.2 |
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HGNC ID |
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Summary |
This gene is a tumor suppressor and encodes a protein that binds to the eukaryotic translation initiation factor 4A1 and inhibits its function by preventing RNA binding. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2010]
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e!Ensembl
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Protein Information |
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Protein Name |
Programmed cell death protein 4, neoplastic transformation inhibitor protein, nuclear antigen H731, programmed cell death 4 (neoplastic transformation inhibitor), protein 197/15a |
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Function |
Inhibits translation initiation and cap-dependent translation. May excert its function by hindering the interaction between EIF4A1 and EIF4G. Inhibits the helicase activity of EIF4A. Modulates the activation of JUN kinase. Down-regulates the expression of MAP4K1, thus inhibiting events important in driving invasion, namely, MAPK85 activation and consequent JUN-dependent transcription. May play a role in apoptosis. Tumor suppressor. Inhibits tumor promoter-induced neoplastic transformation. Binds RNA (By similarity). |
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UniProt |
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PDB |
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Interactions |
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STRING |
MINT |
IntAct |
ENSP00000298472 |
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Q05940 |
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View interactions
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Associated Diseases
Disease group | Disease Name | References |
Endocrine System Diseases |
PCOS |
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Neoplasms |
Lung Cancer |
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References |
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PubMed ID |
Associated gene/s |
Associated condition |
Genetic Mutation |
Diagnostic Criteria |
Association with PCOS |
Ethnicity |
Conclusion |
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BAX, BCL2 |
PCOS, hyperandrogenism, menstrual irregularities (oligomenorrhea and amenorrhea), signs of androgen excess (hirsutism, acne, and androgenic alopecia), ovulation disorders (oligoovulation or anovulation), abdominal adiposity, insulin resistance, glucose in |
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Rotterdam European Society of Human Reproduction and Embryology/American Society for Reproductive Medicine |
Related
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77 PCOS women and 67 control women |
Our study suggests for the first time that higher PDCD4 expression might play an important role in PCOS pathogenesis by affecting obesity, insulin resistance, lipid metabolism disorders, and GC apoptosis. |
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