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Gene : MNX1 Homo sapiens

Name  ? motor neuron and pancreas homeobox 1 Cytological Location  7q36.3
Brief Description  motor neuron and pancreas homeobox 1
Description  This gene encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in this gene result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]
  • synonyms:
  • MNX1,
  • NM_001165255,
  • SCRA1,
  • AF107457,
  • HB9,
  • HGNC:4979,
  • HLXB9,
  • HLXB9,
  • OTTHUMG00000157181,
  • uc064jri.1,
  • HB9,
  • homeo box HB9,
  • HOXHB9,
  • homeobox HB9,
  • HOXHB9,
  • SCRA1
  • identifiers:
  • 3110,
  • ENSG00000130675,
  • MNX1

Genome feature

Region: gene ? Length: 5811  
Location: 7:157004853-157010663 reverse strand Cyto location: 7q36.3


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Function

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> GO terms.

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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

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Interactions

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Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

90 SN Ps

5 Cross References

19 Data Sets

6 Homologues

0 Located Features

97 Rna Seq Results