Entry Detail


General Information

Database ID: LDA0000787
Species: Homo sapiens
Confidence Score: 0.731059
Contents: >> ncRNA Information
>> ncRNA Association Statistics
>> Disease Information
>> Disease Association Statistics
>> Evidence Support
>> Reference
Causality: Yes
Clinical Significance: Unknown

 


ncRNA Information

Reference Genome Note: GRCh38 for human lncRNAs; GRCm39 for mouse lncRNAs; mRatBN7.2 for rat lncRNAs; hg19 for human circRNAs; mm9 for mouse circRNAs.

ncRNA Symbol:FER1L4
Full Name:fer-1 like family member 4 (pseudogene)
Category:LncRNA
Species:Homo sapiens
Synonyms:C20orf124
Chromosome:20
Strand:-
Coordinate:
Start Site(bp):35558737End Site(bp):35607562
External Links:
Ensembl ID:ENSG00000088340
Ensembl Transcript ID:N/A
Entrez Gene:80307.0
NONCODE ID:N/A
RefSeq Accession:N/A

 

ncRNA Association Statistics

Total Associated Disease Number:32   
More Information
Causal Disease Number:22
Network:
Top Causal Diseases:
Osteosarcoma  (Score: 0.999893)
Osteosarcoma  (Score: 0.999893)
Squamous Cell Carcinoma of Head and Neck  (Score: 0.985791)
Lung Neoplasms  (Score: 0.985791)
Carcinoma, Hepatocellular  (Score: 0.985791)
Squamous Cell Carcinoma of Head and Neck  (Score: 0.985791)
Lung Neoplasms  (Score: 0.985791)
Carcinoma, Hepatocellular  (Score: 0.985791)
Colorectal Neoplasms  (Score: 0.959542)
Colorectal Neoplasms  (Score: 0.959542)
More Information

 

 

Disease Information

 Disease OntologyMeSH
Disease ID:DOID:14330D010300
Disease Name:Parkinson's diseaseParkinson Disease
Category:Disease OntologyMeSH
Type:Nervous System Diseases
Define:A synucleinopathy that has_material_basis_in degeneration of the central nervous system that often impairs motor skills, speech, and other functions.A progressive, degenerative neurologic disease characterized by a TREMOR that is maximal at rest, retropulsion (i.e. a tendency to fall backwards), rigidity, stooped posture, slowness of voluntary movements, and a masklike facial expression. Pathologic features include loss of melanin containing neurons in the substantia nigra and other pigmented nuclei of the brainstem. LEWY BODIES are present in the substantia nigra and locus coeruleus but may also be found in a related condition (LEWY BODY DISEASE, DIFFUSE) characterized by dementia in combination with varying degrees of parkinsonism. (Adams et al., Principles of Neurology, 6th ed, p1059, pp1067-75)
Alias:Parkinson disease//paralysis agitansParkinson Disease//Idiopathic Parkinson's Disease//Lewy Body Parkinson's Disease//Parkinson's Disease, Idiopathic//Parkinson's Disease, Lewy Body//Parkinson Disease, Idiopathic//Parkinson's Disease//Idiopathic Parkinson Disease//Lewy Body Parkinson Disease//Primary Parkinsonism//Parkinsonism, Primary//Paralysis Agitans

 

Disease Association Statistics

Total Associated ncRNA Number:84   
More Information
Causal ncRNA Number:74
Network:
Top Causal ncRNAs:
NEAT1  (Score: 1)
NEAT1  (Score: 1)
Neat1  (Score: 0.999893)
Neat1  (Score: 0.999893)
Snhg14  (Score: 0.985791)
SNHG1  (Score: 0.985791)
hsa_circ_0004381  (Score: 0.985791)
Snhg14  (Score: 0.985791)
MEG3  (Score: 0.985791)
SNHG1  (Score: 0.985791)
More Information

 

Evidence Support

Strong Evidence:qRT-PCR//Western Blot
Weak Evidence:

 

Reference

[1] PubMed ID:35559379
Disease Name:Parkinson Disease
Sample:Neural stem cells
Dysfunction Pattern:Interaction( miR-874-3p/Ascl2)
Validated Method:qRT-PCR//Western Blot
Description:In the present research, we noted that FER1L4 is upregulated in NSCs induced with TNFα. Using Starbase online software, we identified that FER1L4 is one potential target gene of miR-874-3p. Ectopic expression of FER1L4 decreases miR-874-3p expression in NSCs. We identified Ascl2 is one target gene for miR-874-3p. Overexpression of FER1L4 enhances Ascl2 expression in NSCs. Furthermore, we proved that FER1L4 modulates the proliferation and differentiation of NSCs via regulating Ascl2.
Causality:Yes
Causal Description:Ectopic expression of FER1L4 suppresses NSCs proliferation and induces NSCs differentiated into neurons and astrocytes.
Clinical-realted Application: