heterogeneous nuclear ribonucleoprotein A1

Summary
Gene Symbol
  • HNRNPA1
Organism
Homo sapiens (human)
NCBI Gene
3178
PubChem
3178
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Acetylation
  • Alternative splicing
  • Amyotrophic lateral sclerosis
  • Cytoplasm
  • Direct protein sequencing
  • Disease variant
  • Host-virus interaction
  • Isopeptide bond
  • Methylation
  • Nucleus
  • Phosphoprotein
  • RNA-binding
  • Reference proteome
  • Repeat
  • Ribonucleoprotein
  • Spliceosome
  • Ubl conjugation
  • mRNA transport
Proteins
Displaying all 2 entries
UniProt Protein Name
A0A024RB53
P09651
  • Helix-destabilizing protein
  • Single-strand RNA-binding protein
  • hnRNP core protein A1
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
heterogeneous nuclear ribonucleoprotein A1
Functional Category
  • I: Lipid transport and metabolism
  • K: Transcription
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying all 10 entries
DO ID Disease Name Source
DOID:0060211 amyotrophic lateral sclerosis type 20
DOID:0110306 autosomal dominant limb-girdle muscular dystrophy type 3
DOID:0111189 distal myopathy 3
DOID:0111386 inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 3
DOID:10652 Alzheimer's disease
DOID:1289 neurodegenerative disease
DOID:321 tropical spastic paraparesis
DOID:3908 lung non-small cell carcinoma
DOID:423 myopathy
DOID:684 hepatocellular carcinoma

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024