ENSMUSG00000042225


Mus musculus

Features
Gene ID: ENSMUSG00000042225
  
Biological name :Ammecr1
  
Synonyms : Ammecr1 / AMME syndrome candidate 1 protein homolog / Q9JHT5
  
Possible biological names infered from orthology : Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 / Q9Y4X0
  
Species: Mus musculus
  
Chr. number: X
Strand: -1
Band: F2
Gene start: 142851146
Gene end: 142966728
  
Corresponding Affymetrix probe sets: 10607116 (MoGene1.0st)   1430697_at (Mouse Genome 430 2.0 Array)   1450546_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000036085
NCBI entrez gene - 56068     See in Manteia.
MGI - MGI:1860206
RefSeq - NM_019496
RefSeq Peptide - NP_062369
swissprot - Q9JHT5
Ensembl - ENSMUSG00000042225
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 ammecr1ENSDARG00000012892Danio rerio
 AMMECR1ENSGALG00000008074Gallus gallus
 Q9Y4X0ENSG00000101935Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Q8JZZ6 / Ammecr1l / AMMECR1-like protein / Q6DCA0* / AMMECR1 like*ENSMUSG0000004191558


Protein motifs (from Interpro)
Interpro ID Name
 IPR002733  AMMECR1 domain
 IPR023473  AMMECR1
 IPR027485  AMMECR1, N-terminal
 IPR036071  AMMECR1 domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0008150 biological_process ND
 cellular_componentGO:0005634 nucleus ISO
 molecular_functionGO:0003674 molecular_function ND


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
No match
  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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