ENSGALG00000008074


Gallus gallus

Features
Gene ID: ENSGALG00000008074
  
Biological name :AMMECR1
  
Synonyms : Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 / AMMECR1
  
Possible biological names infered from orthology : AMME syndrome candidate 1 protein homolog / Q9JHT5 / Q9Y4X0
  
Species: Gallus gallus
  
Chr. number: 4
Strand: 1
Band:
Gene start: 13672485
Gene end: 13738312
  
Corresponding Affymetrix probe sets: GgaAffx.5069.1.S1_at (Chicken Array)   
  
Cross references: Ensembl peptide - ENSGALP00000013092
NCBI entrez gene - 422343     See in Manteia.
RefSeq - XM_015278601
RefSeq - XM_015278602
swissprot - E1C1I5
Ensembl - ENSGALG00000008074
  
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
 Q9Y4X0ENSG00000101935Homo sapiens
 Q9JHT5ENSMUSG00000042225Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
AMMECR1L / AMMECR1 like / Q6DCA0* / Q8JZZ6* / AMMECR1-like protein *ENSGALG0000002672866


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


Gene Ontology (GO)
TypeGO IDTermEv.Code
 cellular_componentGO:0005634 nucleus IEA


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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contact: otassy@igbmc.fr