HCSGD entry for SCGB2A2


1. General information

Official gene symbolSCGB2A2
Entrez ID4250
Gene full namesecretoglobin, family 2A, member 2
Other gene symbolsMGB1 UGB2
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

color bar
This gene isn't in Literature mining network.

3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0003674Molecular_functionNDmolecular_function
GO:0005496Steroid bindingIEAmolecular_function
GO:0005575Cellular_componentNDcellular_component
GO:0008150Biological_processNDbiological_process
Entries Per Page
Displaying Page of

4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.31332521560.89936031310.99999024731.0000000000

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

Data sourceUp or downLog fold change
GSE11954Up0.2057793091
GSE13712_SHEARUp0.1686466506
GSE13712_STATICDown-0.2245617851
GSE19018Down-0.1592829187
GSE19899_A1Down-0.0047071724
GSE19899_A2Up0.1980681138
PubMed_21979375_A1Up1.1390991560
PubMed_21979375_A2Up0.1441696037
GSE35957Up0.1630527185
GSE36640Up0.1094467045
GSE54402Up0.0498783338
GSE9593Down-0.0848097210
GSE43922Up0.0069805863
GSE24585Down-0.0303201712
GSE37065Up0.0732903793
GSE28863_A1Up0.1297416868
GSE28863_A2Down-0.0281130805
GSE28863_A3Up0.1892562271
GSE28863_A4Up0.0042328736
GSE48662Up0.0047150601

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-335-5pMIMAT0000765MIRT019036MicroarrayFunctional MTI (Weak)18185580
Entries Per Page
Displaying Page of
  • mirRecord
No target information from mirRecord

6. Text-mining results about the gene

Gene occurances in abstracts of cellular senescence-associated articles: 1 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

25964555MATERIALS AND METHODS: Multiplex Ligation-dependent Probe Amplification, TP53 sequencing, real-time polymerase chain reaction (PCR) for MUC1 and SCGB2A2 and immunocytochemistry, together with senescence detection assay and real-time microscopic observations were used to analyze primary neoplastic cells isolated from prostate, breast and colorectal tumors, as well as stable cancer cell lines (MCF7, MDA-MB-468, SW962, SK-MEL28, NCI-H1975 and NCI-H469)
Entries Per Page
Displaying Page of