Free for academic non-profit institutions. Other users need a Commercial license

Aliases for CHED1 Gene

Aliases for CHED1 Gene

  • Corneal Endothelial Dystrophy 1 (Autosomal Dominant) 2 3
  • CHED2 3
  • CHED 3

External Ids for CHED1 Gene

Summaries for CHED1 Gene

GeneCards Summary for CHED1 Gene

CHED1 (Corneal Endothelial Dystrophy 1 (Autosomal Dominant)) is a Genetic Locus. Diseases associated with CHED1 include Corneal Endothelial Dystrophy 1, Autosomal Dominant.

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 CHED1 Gene

Genomics for CHED1 Gene

Genomic Location for CHED1 Gene

Unknown strand

Genomic View for CHED1 Gene

Cytogenetic band:
GeneLoc Logo Gene Density

No data available for Regulatory Elements and RefSeq DNA sequence for CHED1 Gene

Proteins for CHED1 Gene

Post-translational modifications for CHED1 Gene

No Post-translational modifications

No data available for DME Specific Peptides for CHED1 Gene

Domains & Families for CHED1 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 CHED1 Gene

Function for CHED1 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 CHED1 Gene

Localization for CHED1 Gene

No data available for Subcellular locations from UniProtKB/Swiss-Prot , Subcellular locations from COMPARTMENTS and Gene Ontology (GO) - Cellular Components for CHED1 Gene

Pathways & Interactions for CHED1 Gene

SuperPathways for CHED1 Gene

No Data Available

Interacting Proteins for CHED1 Gene

Gene Ontology (GO) - Biological Process for CHED1 Gene


No data available for Pathways by source and SIGNOR curated interactions for CHED1 Gene

Transcripts for CHED1 Gene

Alternative Splicing Database (ASD) splice patterns (SP) for CHED1 Gene

No ASD Table

Relevant External Links for CHED1 Gene

ECgene alternative splicing isoforms for

No data available for mRNA/cDNA for CHED1 Gene

Expression for CHED1 Gene

NURSA nuclear receptor signaling pathways regulating expression of CHED1 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 CHED1 Gene

Orthologs for CHED1 Gene

No data available for Orthologs and Evolution for CHED1 Gene

Paralogs for CHED1 Gene

No data available for Paralogs for CHED1 Gene

Variants for CHED1 Gene

Relevant External Links for CHED1 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 CHED1 Gene

Disorders for CHED1 Gene

MalaCards: The human disease database

(1) MalaCards diseases for CHED1 Gene - From: OMIM and GeneCards

Disorder Aliases PubMed IDs
corneal endothelial dystrophy 1, autosomal dominant
  • congenital hereditary endothelial dystrophy of cornea
- elite association - COSMIC cancer census association via MalaCards
Search CHED1 in MalaCards View complete list of genes associated with diseases
genes like me logo Genes that share disorders with CHED1: view

No data available for UniProtKB/Swiss-Prot , Genatlas and External Links for CHED1 Gene

Publications for CHED1 Gene

  1. Linkage of congenital hereditary endothelial dystrophy to chromosome 20. (PMID: 8634716) Toma N.M. … Bhattacharya S.S. (Hum. Mol. Genet. 1995) 2 3 64
  2. Exclusion of positional candidate gene coding region mutations in the common posterior polymorphous corneal dystrophy 1 candidate gene interval. (PMID: 19574904) Aldave A.J. … Papp J. (Cornea 2009) 3 64
  3. Clinicopathologic correlation and genetic analysis in a case of posterior polymorphous corneal dystrophy. (PMID: 12654361) Moroi S.E. … Richards J.E. (Am. J. Ophthalmol. 2003) 3 64
  4. Homozygosity mapping and linkage analysis demonstrate that autosomal recessive congenital hereditary endothelial dystrophy (CHED) and autosomal dominant CHED are genetically distinct. (PMID: 10209448) Callaghan M. … Parfrey N.A. (Br J Ophthalmol 1999) 3 64

Products for CHED1 Gene

Sources for CHED1 Gene

Loading form....