heterogeneous nuclear ribonucleoprotein H2

Summary
Gene Symbol
  • HNRNPH2
Organism
Homo sapiens (human)
NCBI Gene
3188
PubChem
3188
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Acetylation
  • Direct protein sequencing
  • Disease variant
  • Intellectual disability
  • Isopeptide bond
  • Methylation
  • Nucleus
  • Phosphoprotein
  • RNA-binding
  • Reference proteome
  • Repeat
  • Ribonucleoprotein
  • Ubl conjugation
Proteins
Displaying all 2 entries
UniProt Protein Name
A0A384MDT2
  • Heterogeneous nuclear ribonucleoprotein H'
P55795
  • FTP-3
  • Heterogeneous nuclear ribonucleoprotein H'
Gene Ontology (GO)
Displaying 1 entry
GO Term Evidence Code PMID
regulation of RNA splicing
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
heterogeneous nuclear ribonucleoprotein
Functional Category
  • J: Translation, ribosomal structure and biogenesis
  • K: Transcription
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying 1 entry
DO ID Disease Name Source
DOID:0070538 syndromic X-linked intellectual developmental disorder bain type

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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