View ALX4 gene homepage

General information
Gene symbol ALX4
Gene name ALX homeobox 4
Chromosome 11
Chromosomal band p11.2
Imprinted Unknown
Genomic reference NG_015809.1
Transcript reference NM_021926.3
Associated with diseases CRS-5, PFM-2, dysplasia, frontonasal, type 2
Citation reference(s) -
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 0
Unique public DNA variants reported 0
Individuals with public variants 0
Hidden variants 0
Date created May 03, 2013

Links to other resources
HGNC 450
Entrez Gene 60529
PubMed articles ALX4
OMIM - Gene 605420
OMIM - Diseases CRS-5 (craniosynostosis, type 5, susceptibility to (CRS-5))
PFM-2 (foramina, parietal, type 2 (PFM-2))
dysplasia, frontonasal, type 2

Active transcripts




NCBI ID     

NCBI Protein ID     

00002417 11 ALX homeobox 4 NM_021926.3 NP_068745.2 0