ENSG00000169184


Homo sapiens

Features
Gene ID: ENSG00000169184
  
Biological name :MN1
  
Synonyms : MN1 / MN1 proto-oncogene, transcriptional regulator / Q10571
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 22
Strand: -1
Band: q12.1
Gene start: 27748277
Gene end: 27801498
  
Corresponding Affymetrix probe sets: 205330_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000304956
Ensembl peptide - ENSP00000397805
NCBI entrez gene - 4330     See in Manteia.
OMIM - 156100
RefSeq - NM_002430
RefSeq Peptide - NP_002421
swissprot - A0A024R1C3
swissprot - H7C105
swissprot - Q10571
Ensembl - ENSG00000169184
  
Related genetic diseases (OMIM): 607174 - Meningioma, 607174
See expression report in BioGPS
See gene description in Wikigenes
See gene description in GeneCards
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 mn1aENSDARG00000076529Danio rerio
 mn1bENSDARG00000079248Danio rerio
 MN1ENSGALG00000026119Gallus gallus
 Mn1ENSMUSG00000070576Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
No match


Protein motifs (from Interpro)
Interpro ID Name
 IPR015943  WD40/YVTN repeat-like-containing domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0001957 intramembranous ossification IEA
 biological_processGO:0006351 transcription, DNA-templated IEA
 biological_processGO:0006355 regulation of transcription, DNA-templated IEA
 biological_processGO:0007275 multicellular organism development IEA
 biological_processGO:0008150 biological_process ND
 cellular_componentGO:0005575 cellular_component ND
 molecular_functionGO:0003674 molecular_function ND
 molecular_functionGO:0005515 protein binding IEA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000006 Autosomal dominant inheritance "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele." [HPO:curators]
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 HP:0002858 Meningioma 
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 HP:0003581 Onset in adulthood 
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 HP:0003829 Incomplete penetrance 
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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