ALX homeobox 4

Summary
Gene Symbol
  • ALX4
Organism
Homo sapiens (human)
NCBI Gene
60529
PubChem
60529
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Activator
  • Craniosynostosis
  • DNA-binding
  • Developmental protein
  • Disease variant
  • Homeobox
  • Nucleus
  • Phosphoprotein
  • Reference proteome
  • Transcription regulation
Proteins
Displaying 1 entry
UniProt Protein Name
Q9H161
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
homeobox
Functional Category
  • J: Translation, ribosomal structure and biogenesis
  • K: Transcription
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying entries 1 - 10 of 11 in total
DO ID Disease Name Source
DOID:0050776 non-syndromic X-linked intellectual disability
DOID:0060285 parietal foramina
DOID:0081046 frontonasal dysplasia 2
DOID:0112038 non-syndromic X-linked intellectual disability 1
DOID:1324 lung cancer
DOID:2340 craniosynostosis
DOID:3717 gastric adenocarcinoma
DOID:3910 lung adenocarcinoma
DOID:4926 bronchiolo-alveolar adenocarcinoma
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