HCSGD entry for BMF


1. General information

Official gene symbolBMF
Entrez ID90427
Gene full nameBcl2 modifying factor
Other gene symbols
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

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This gene isn't in Literature mining network.

3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0001669Acrosomal vesicleIEAcellular_component
GO:0005515Protein bindingIPImolecular_function
GO:0005741Mitochondrial outer membraneTAScellular_component
GO:0005829CytosolTAScellular_component
GO:0005886Plasma membraneTAScellular_component
GO:0006915Apoptotic processIEA TASbiological_process
GO:0016459Myosin complexIEA ISScellular_component
GO:0032464Positive regulation of protein homooligomerizationIEA ISSbiological_process
GO:0043276AnoikisIDAbiological_process
GO:0090200Positive regulation of release of cytochrome c from mitochondriaIEA ISSbiological_process
GO:0097193Intrinsic apoptotic signaling pathwayTASbiological_process
GO:1900740Positive regulation of protein insertion into mitochondrial membrane involved in apoptotic signaling pathwayTASbiological_process
GO:2001234Negative regulation of apoptotic signaling pathwayIEAbiological_process
GO:2001235Positive regulation of apoptotic signaling pathwayIEAbiological_process
GO:2001244Positive regulation of intrinsic apoptotic signaling pathwayTASbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.04288213210.65174746400.46162833201.0000000000

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

Data sourceUp or downLog fold change
GSE11954Up0.1290292740
GSE13712_SHEARDown-1.4884025632
GSE13712_STATICDown-0.5291785315
GSE19018Up0.1646056716
GSE19899_A1Up0.2108983661
GSE19899_A2Up0.6928337686
PubMed_21979375_A1Down-0.2545666256
PubMed_21979375_A2Up0.9035163302
GSE35957Up0.1036323167
GSE36640Down-0.1793386001
GSE54402Up0.6082074767
GSE9593Down-0.2628425319
GSE43922Up0.2455435169
GSE24585Up1.0125345349
GSE37065Up0.1741159968
GSE28863_A1Up0.1380683178
GSE28863_A2Up0.0223941065
GSE28863_A3Up0.3134310582
GSE28863_A4Up0.0483751829
GSE48662Down-0.1900406831

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-221-3pMIMAT0000278MIRT000141Luciferase reporter assay//qRT-PCR//Western blotFunctional MTI19671867
hsa-miR-125b-5pMIMAT0000423MIRT003394immunoblot//Luciferase reporter assay//qRT-PCRFunctional MTI19471102
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  • mirRecord

MicroRNA name

mirBase ID

Target site number

MiRNA mature ID

Test method inter

MiRNA regulation site

Reporter target site

Pubmed ID

hsa-miR-221-3pMIMAT0000278NAhsa-miR-221{Western blot}{overexpression}19671867
hsa-miR-125b-5pMIMAT00004232hsa-miR-125b{Western blot}{overexpression}19471102
hsa-miR-125b-5pMIMAT00004231hsa-miR-125b{Western blot}{overexpression}19471102
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6. Text-mining results about the gene

Gene occurances in abstracts of cellular senescence-associated articles: 2 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

22932806Dyskeratosis congenita is characterized by a mucocutaneous triad, bone marrow failure (BMF), and presence of short telomeres because of mutations in telomerase
22932806Allelic variations in TRF1 have been found associated with BMF
22932806To address a possible role for TRF1 dysfunction in BMF, here we generated a mouse model with conditional TRF1 deletion in the hematopoietic system
22932806Together, these results represent proof of principle that mutations in TRF1 lead to the main clinical features of BMF
19572808During childhood, most FA patients display progressive bone marrow failure (BMF), the mechanism of which has not been clarified to date
19572808However, FA MSCs showed reduced long-term proliferation ability, higher stem cell factor and interleukin-6 levels, and increased expression of senescent-associated beta-galactosidase compared to normal MSCs, suggesting a potential role of the BM microenvironment in long-term BMF
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