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Gene : ALX3 Homo sapiens

Name  ? ALX homeobox 3 Cytological Location  1p13.3
Brief Description  ALX homeobox 3
Description  This gene encodes a nuclear protein with a homeobox DNA-binding domain that functions as a transcriptional regulator involved in cell-type differentiation and development. Preferential methylation of this gene's promoter is associated with advanced-stage neuroblastoma tumors. [provided by RefSeq, Jul 2008]
  • synonyms:
  • ALX3,
  • HGNC:449,
  • AF008203,
  • aristaless-like homeobox 3,
  • OTTHUMG00000011650,
  • FND1,
  • frontonasal dysplasia,
  • NM_006492,
  • uc001dzb.4,
  • FND,
  • FND
  • identifiers:
  • 257,
  • ENSG00000156150,
  • ALX3

Genome feature

Region: gene ? Length: 10803  
Location: 1:110059870-110070672 reverse strand Cyto location: 1p13.3

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



0 Pathways

19 SNPs

5 Cross References

17 Data Sets

9 Homologues

0 Located Features

97 Rna Seq Results