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Gene : MN1 Homo sapiens

Name  ? MN1 proto-oncogene, transcriptional regulator Cytological Location  22q12.1
Brief Description  MN1 proto-oncogene, transcriptional regulator
Description  Meningioma 1 (MN1) contains two sets of CAG repeats. It is disrupted by a balanced translocation (4;22) in a meningioma, and its inactivation may contribute to meningioma 32 pathogenesis. [provided by RefSeq, Jul 2008]
  • synonyms:
  • meningioma chromosome region,
  • MGCR1-PEN,
  • MGCR1,
  • MGCR1,
  • meningioma (disrupted in balanced translocation) 1,
  • HGNC:7180,
  • dJ353E16.2,
  • X82209,
  • MN1,
  • CEBALID,
  • MGCR,
  • MGCR,
  • MGCR1-PEN,
  • probable tumor suppressor protein MN1,
  • OTTHUMG00000150975,
  • uc003adj.3,
  • NM_002430
  • identifiers:
  • 4330,
  • ENSG00000169184,
  • MN1

Genome feature

Region: gene ? Length: 53480  
Location: 22:27748277-27801756 reverse strand Cyto location: 22q12.1


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Function

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

2 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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Gene --> Physical and Genetic Interactions

Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

0 Pathways

205 SN Ps

5 Cross References

19 Data Sets

4 Homologues

0 Located Features

97 Rna Seq Results