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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:
  • cartilage paired-class homeoprotein 1,
  • U31986,
  • OTTHUMG00000169820,
  • FND3,
  • HEL23,
  • uc001tae.5,
  • HGNC:1494,
  • NM_006982,
  • CART1,
  • CART1,
  • ALX1
  • identifiers:
  • 8092,
  • ENSG00000180318,
  • ALX1

Genome feature

Region: gene ? Length: 21527  
Location: 12:85280258-85301784 Cyto location: 12q21.31


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Gene Expression Atlas Tissues Displayer

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Publication Counts Displayer

Curated Proteins Displayer

Function

Gene Ontology Displayer

0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene Structure Displayer

Overlapping Features Displayer

Mouse Alleles Displayer

Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

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]

Homology

Homologue Displayer

Gene --> Orthologues

Interactions

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Gene --> Physical and Genetic Interactions

Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

0 Pathways

10 SN Ps

5 Cross References

17 Data Sets

28 Homologues

0 Located Features

90 Rna Seq Results