Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 664709
Gene Symbol: HNRNPA1P10
HNRNPA1P10
0.040 Biomarker disease BEFREE Mutations in RNA-binding proteins (RBPs) localized in ribonucleoprotein (RNP) granules, such as hnRNP A1 and TDP-43, promote aberrant protein aggregation, which is a pathological hallmark of various neurodegenerative diseases, such as amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). 30728452 2019
Entrez Id: 664709
Gene Symbol: HNRNPA1P10
HNRNPA1P10
0.040 GeneticVariation disease BEFREE TDP-43 regulates the alternative splicing of hnRNP A1 to yield an aggregation-prone variant in amyotrophic lateral sclerosis. 29562314 2018
Entrez Id: 664709
Gene Symbol: HNRNPA1P10
HNRNPA1P10
0.040 Biomarker disease BEFREE Immunohistochemistry in central nervous system tissue from C9orf72+ patients with amyotrophic lateral sclerosis demonstrated co-localization of RNA foci with SRSF2, hnRNP H1/F, ALYREF and hnRNP A1 in cerebellar granule cells and with SRSF2, hnRNP H1/F and ALYREF in motor neurons, the primary target of pathology in amyotrophic lateral sclerosis. 24866055 2014
Entrez Id: 664709
Gene Symbol: HNRNPA1P10
HNRNPA1P10
0.040 Biomarker disease BEFREE Consequently, hnRNP A1 decline contributes to the severity of symptoms in several neurodegenerative diseases, including Alzheimer's disease (AD), spinal muscular atrophy (SMA), fronto-temporal lobar degeneration (FTLD), amyotrophic lateral sclerosis (ALS), multiple sclerosis (MS), hereditary spastic paraparesis (HSP) and HTLV-I associated myelopathy/tropical spastic paraparesis (HAM/TSP). 23247072 2013