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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 Aland Island Eye Disease and Congenital Stationary Night Blindness.

Additional gene information for OED Gene

No data available for Entrez Gene Summary , CIViC 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 Locations for OED Gene

Genomic Locations for OED Gene
Unknown strand

Genomic View for OED Gene

Cytogenetic band:
GeneLoc Logo Gene Density

No data available for GeneHancer (GH) Regulatory Elements and RefSeq DNA sequence for OED Gene

Proteins for OED Gene

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

CRISPR Products

No data available for Molecular function , Enzyme Numbers (IUBMB) , Phenotypes From GWAS Catalog , 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 , Subcellular locations from the Human Protein Atlas (HPA) and Gene Ontology (GO) - Cellular Components for OED Gene

Pathways & Interactions for OED Gene

PathCards logo

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

Drugs & Compounds for OED Gene

No Compound Related Data Available

Transcripts for OED Gene

CRISPR Products

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 , mRNA Expression by UniProt/SwissProt , Evidence on tissue expression from TISSUES and Phenotype-based relationships between genes and organs from Gene ORGANizer 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

Additional Variant Information 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

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

Disorder Aliases PubMed IDs
aland island eye disease
  • aied
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 DA … Weleber RG (Archives of ophthalmology (Chicago, Ill. : 1960) 1993) 2 3 58
  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 DA … Buist NR (American journal of medical genetics 1990) 3 58
  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 RG … Buist NR (Archives of ophthalmology (Chicago, Ill. : 1960) 1989) 3 58

Products for OED Gene

Sources for OED Gene

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