ENSG00000227729


Homo sapiens

Features
Gene ID: ENSG00000227729
  
Biological name :RD3L
  
Synonyms : P0DJH9 / RD3L / retinal degeneration 3-like
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 14
Strand: -1
Band: q32.33
Gene start: 103940426
Gene end: 103942308
  
Corresponding Affymetrix probe sets:
  
Cross references: Ensembl peptide - ENSP00000455434
NCBI entrez gene - 647286     See in Manteia.
RefSeq - NM_001257268
RefSeq Peptide - NP_001244197
swissprot - P0DJH9
Ensembl - ENSG00000227729
  
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
 si:ch211-253p18.5ENSDARG00000091135Danio rerio
 RD3LENSGALG00000027643Gallus gallus
 Rd3lENSMUSG00000091402Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
RD3 / Q7Z3Z2 / retinal degeneration 3ENSG0000019857027


Protein motifs (from Interpro)
Interpro ID Name
 IPR028092  Retinal degeneration protein 3


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