# ALX homeobox 4

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21111356](https://www.wikidata.org/wiki/Q21111356)  
**Source**: https://4ort.xyz/entity/alx-homeobox-4-q21111356


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/Q9H161)
3. Q20641742
4. [Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9H161)
5. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9H161)
6. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9H161&geneProductId=UniProtKB:Q9H161)
7. [A census of human transcription factors: function, expression and evolution](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9H161&geneProductId=UniProtKB:Q9H161)
8. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9H161)
9. [A census of human transcription factors: function, expression and evolution](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9H161)
10. [Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9H161&geneProductId=UniProtKB:Q9H161)
11. [ALX4 dysfunction disrupts craniofacial and epidermal development](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9H161&geneProductId=UniProtKB:Q9H161)
12. [ALX4 dysfunction disrupts craniofacial and epidermal development](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9H161)
13. [The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500)](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9H161)
14. Ensembl Release 99