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Aliases for OED Gene

Aliases for OED Gene

  • Oregon Eye Disease 2 3

External Ids for OED Gene

Summaries for OED Gene

GeneCards Summary for OED Gene

OED (Oregon Eye Disease) is a Genetic Locus. Diseases associated with OED include Eye Disease and Aland Island Eye Disease.

No data available for Entrez Gene Summary , UniProtKB/Swiss-Prot , Tocris Summary , Gene Wiki entry , PharmGKB "VIP" Summary , fRNAdb sequence ontologies and piRNA Summary for OED Gene

Genomics for OED Gene

Genomic Location for OED Gene

Unknown strand

Genomic View for OED Gene

Cytogenetic band:
GeneLoc Logo Gene Density

No data available for Regulatory Elements and RefSeq DNA sequence for OED Gene

Proteins for OED Gene

Post-translational modifications for OED Gene

No Post-translational modifications

No data available for DME Specific Peptides for OED Gene

Domains & Families for OED Gene

Graphical View of Domain Structure for InterPro Entry

No data available for Gene Families , Protein Domains , Suggested Antigen Peptide Sequences and UniProtKB/Swiss-Prot for OED Gene

Function for OED Gene

Animal Model Products

No data available for Molecular function , Enzyme Numbers (IUBMB) , Gene Ontology (GO) - Molecular Function , Phenotypes , Human Phenotype Ontology , Animal Models , miRNA , Transcription Factor Targets and HOMER Transcription for OED Gene

Localization for OED Gene

No data available for Subcellular locations from UniProtKB/Swiss-Prot , Subcellular locations from COMPARTMENTS and Gene Ontology (GO) - Cellular Components for OED Gene

Pathways & Interactions for OED Gene

SuperPathways for OED Gene

No Data Available

Interacting Proteins for OED Gene

Gene Ontology (GO) - Biological Process for OED Gene


No data available for Pathways by source and SIGNOR curated interactions for OED Gene

Transcripts for OED Gene

Alternative Splicing Database (ASD) splice patterns (SP) for OED Gene

No ASD Table

Relevant External Links for OED Gene

ECgene alternative splicing isoforms for

No data available for mRNA/cDNA for OED Gene

Expression for OED Gene

NURSA nuclear receptor signaling pathways regulating expression of OED Gene:

No Expression Related Data Available

No data available for mRNA expression in normal human tissues , mRNA expression in embryonic tissues and stem cells from LifeMap Discovery , mRNA differential expression in normal tissues , Protein differential expression in normal tissues , Protein expression , Protein tissue co-expression partners and mRNA Expression by UniProt/SwissProt for OED Gene

Orthologs for OED Gene

No data available for Orthologs and Evolution for OED Gene

Paralogs for OED Gene

No data available for Paralogs for OED Gene

Variants for OED Gene

Relevant External Links for OED Gene

SNPedia medical, phenotypic, and genealogical associations of SNPs for

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot , Sequence variations from dbSNP and Humsavar , Structural Variations from Database of Genomic Variants (DGV) and Variation tolerance for OED Gene

Disorders for OED Gene

MalaCards: The human disease database

(3) MalaCards diseases for OED Gene - From: GeneCards

Disorder Aliases PubMed IDs
eye disease
  • eye diseases
aland island eye disease
  • forsius-eriksson syndrome
congenital stationary night blindness
  • congenital essential nyctalopia
- elite association - COSMIC cancer census association via MalaCards
Search OED in MalaCards View complete list of genes associated with diseases
genes like me logo Genes that share disorders with OED: view

No data available for UniProtKB/Swiss-Prot , Genatlas and External Links for OED Gene

Publications for OED Gene

  1. Negative-configuration electroretinogram in Oregon eye disease. Consistent phenotype in Xp21 deletion syndrome. (PMID: 8240114) Pillers D.A. … Weleber R.G. (Arch. Ophthalmol. 1993) 2 3 64
  2. Aland Island eye disease (Forsius-Eriksson ocular albinism) and an Xp21 deletion in a patient with Duchenne muscular dystrophy, glycerol kinase deficiency, and congenital adrenal hypoplasia. (PMID: 2159212) Pillers D.A. … Buist N.R. (Am. J. Med. Genet. 1990) 3 64
  3. Aland Island eye disease (Forsius-Eriksson syndrome) associated with contiguous deletion syndrome at Xp21. Similarity to incomplete congenital stationary night blindness. (PMID: 2667510) Weleber R.G. … Buist N.R. (Arch. Ophthalmol. 1989) 3 64

Products for OED Gene

Sources for OED Gene

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