heterogeneous nuclear ribonucleoprotein C

Summary
Gene Symbol
  • HNRNPC
Organism
Homo sapiens (human)
NCBI Gene
3183
PubChem
3183
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Acetylation
  • Alternative splicing
  • Coiled coil
  • Direct protein sequencing
  • Disease variant
  • Intellectual disability
  • Isopeptide bond
  • Nucleus
  • Phosphoprotein
  • RNA-binding
  • Reference proteome
  • Ribonucleoprotein
  • Spliceosome
  • Ubl conjugation
Proteins
Displaying 1 entry
UniProt Protein Name
P07910
Gene Ontology (GO)
GO Hierarchy
Displaying entries 1 - 5 of 16 in total
GO Term Evidence Code PMID
chromatin
extracellular region
nucleus
nucleus
nucleus
OrthoDB (Group)
Group level
Eukaryota
Group Name
heterogeneous nuclear ribonucleoprotein C-like
Functional Category
  • J: Translation, ribosomal structure and biogenesis
  • K: Transcription
  • T: Signal transduction mechanisms
Displaying 1 entry
Gene Ontology
mRNA processing
Disease
Disease Ontology
Displaying 1 entry
DO ID Disease Name Source
DOID:0060307 autosomal dominant intellectual developmental disorder

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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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