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Gene : ALX1 Homo sapiens

Name  ? ALX homeobox 1 Cytological Location  12q21.31
Brief Description  ALX homeobox 1
Description  The specific function of this gene has yet to be determined in humans; however, in rodents, it is necessary for survival of the forebrain mesenchyme and may also be involved in development of the cervix. Mutations in the mouse gene lead to neural tube defects such as acrania and meroanencephaly. [provided by RefSeq, Jul 2008]
  • synonyms:
  • FND3,
  • ALX1,
  • CART1,
  • U31986,
  • cartilage paired-class homeoprotein 1,
  • CART1,
  • OTTHUMG00000169820,
  • uc001tae.5,
  • NM_006982,
  • HGNC:1494,
  • HEL23
  • identifiers:
  • 8092,
  • ENSG00000180318,
  • ALX1

Genome feature

Region: gene ? Length: 21565  
Location: 12:85280220-85301784 Cyto location: 12q21.31

Uni Prot Comments Displayer

Protein Atlas Displayer

Gene Expression Atlas Tissues Displayer

Gene Expression Atlas Diseases Displayer

Publication Counts Displayer

Curated Proteins Displayer


Gene Ontology Displayer

0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


J Browse Displayer

Gene Structure Displayer

Overlapping Features Displayer

Mouse Alleles Displayer

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]


Homologue Displayer


Cytoscape Network Displayer

Gene --> Physical and Genetic Interactions


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

Gene Ontology

Gene --> GO terms.



0 Pathways

9 SNPs

5 Cross References

18 Data Sets

10 Homologues

0 Located Features

97 Rna Seq Results