HCSGD entry for PROM1


1. General information

Official gene symbolPROM1
Entrez ID8842
Gene full nameprominin 1
Other gene symbolsAC133 CD133 CORD12 MCDR2 PROML1 RP41 STGD4
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

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3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0001750Photoreceptor outer segmentISScellular_component
GO:0005515Protein bindingIPImolecular_function
GO:0005615Extracellular spaceIEAcellular_component
GO:0005886Plasma membraneIDAcellular_component
GO:0005887Integral component of plasma membraneIEAcellular_component
GO:0005903Brush borderIEAcellular_component
GO:0009986Cell surfaceIDA IEAcellular_component
GO:0010842Retina layer formationISSbiological_process
GO:0016021Integral component of membraneIEAcellular_component
GO:0016324Apical plasma membraneIEAcellular_component
GO:0031528Microvillus membraneIEAcellular_component
GO:0032420StereociliumIEAcellular_component
GO:0042622Photoreceptor outer segment membraneIDAcellular_component
GO:0042805Actinin bindingIDAmolecular_function
GO:0045296Cadherin bindingIPImolecular_function
GO:0045494Photoreceptor cell maintenanceIMPbiological_process
GO:0060042Retina morphogenesis in camera-type eyeIMPbiological_process
GO:0060219Camera-type eye photoreceptor cell differentiationIMP ISSbiological_process
GO:0072112Glomerular visceral epithelial cell differentiationIMPbiological_process
GO:0072139Glomerular parietal epithelial cell differentiationIMPbiological_process
GO:2000768Positive regulation of nephron tubule epithelial cell differentiationIMPbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.57033939820.43477247450.99999024731.0000000000

  • Individual experiment result
    ( "-" represent NA in the specific microarray platform )

Data sourceUp or downLog fold change
GSE11954Up0.2066960247
GSE13712_SHEARDown-0.0654352177
GSE13712_STATICUp0.1144887486
GSE19018Down-0.3375614649
GSE19899_A1Up0.0260459684
GSE19899_A2Up0.3938854425
PubMed_21979375_A1Up0.0853341890
PubMed_21979375_A2Down-0.0328946089
GSE35957Up0.0923734903
GSE36640Up0.1992471788
GSE54402Up0.1743127819
GSE9593Up0.0949540748
GSE43922Up0.0216926083
GSE24585Down-1.3257288795
GSE37065Down-0.0423809892
GSE28863_A1Up0.0007968684
GSE28863_A2Up0.0975457024
GSE28863_A3Up0.0822605928
GSE28863_A4Up0.0468944639
GSE48662Down-0.0341206581

5. Regulation relationships with compounds/drugs/microRNAs

  • Compounds

Not regulated by compounds

  • Drugs

Not regulated by drugs

  • MicroRNAs

  • mirTarBase

MiRNA_name

mirBase ID

miRTarBase ID

Experiment

Support type

References (Pubmed ID)

hsa-miR-142-3pMIMAT0000434MIRT021645Reporter assayFunctional MTI21394831
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  • mirRecord
No target information from mirRecord

6. Text-mining results about the gene

Gene occurances in abstracts of cellular senescence-associated articles: 7 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

26097880We recently developed CAR T cells targeting the prototypic cancer stem cell marker AC133 and showed that these CAR T cells killed AC133+ glioblastoma stem cells (GBM-SCs) in vitro and inhibited the growth of brain tumors initiated from GBM-SCs in xenograft mouse models in vivo
25426558The AC133 epitope of CD133 is a cancer stem cell (CSC) marker for many tumor entities, including the highly malignant glioblastoma multiforme (GBM)
25426558We have developed an AC133-specific chimeric antigen receptor (CAR) and show that AC133-CAR T cells kill AC133+ GBM stem cells (GBM-SCs) both in vitro and in an orthotopic tumor model in vivo
25239491Successful CD133+ mobilizers expressed fewer senescence-associated genes compared with poor mobilizers
25239491However, poor mobilization efficiency combined with high CD133+ senescence suggests futility in this approach
22719071In this study, we used quantitative real-time-PCR to define miRNA expression patterns in various stem/progenitor cell populations in prostate cancer, including CD44+, CD133+, integrin alpha2beta1+, and side population cells
20424141Results of flow cytometry showed that EPCs after 7 days of culture expressed both stem cell markers CD34 and CD133 and endothelial cell markers VEGFR-2 (flk-1) and VE-cadherin
17545049The expressions of CD29, CD44, and CD34 were observed in ASCs by flow cytometry while HLA-DR or CD133 expression was not detected
16698211CD34+/CD133 senescence and in vivo application
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