ENSG00000144233


Homo sapiens

Features
Gene ID: ENSG00000144233
  
Biological name :AMMECR1L
  
Synonyms : AMMECR1L / AMMECR1 like / Q6DCA0
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 2
Strand: -1
Band: q14.3
Gene start: 127861630
Gene end: 127885922
  
Corresponding Affymetrix probe sets: 223297_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000376726
Ensembl peptide - ENSP00000272647
NCBI entrez gene - 83607     See in Manteia.
RefSeq - XM_011511955
RefSeq - NM_001199140
RefSeq - NM_031445
RefSeq - XM_005263806
RefSeq - XM_005263807
RefSeq - XM_011511952
RefSeq - XM_011511954
RefSeq - XM_005263804
RefSeq Peptide - NP_001186069
RefSeq Peptide - NP_113633
swissprot - Q6DCA0
swissprot - A0A024RAG1
Ensembl - ENSG00000144233
  
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
 AMMECR1LENSGALG00000026728Gallus gallus
 Q8JZZ6ENSMUSG00000041915Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Q9Y4X0 / AMMECR1 / Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1ENSG0000010193565


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
No match


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