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Aliases for CNA1 Gene

Aliases for CNA1 Gene

  • Cornea Plana 1 (Autosomal Dominant) 2 3

External Ids for CNA1 Gene

Summaries for CNA1 Gene

GeneCards Summary for CNA1 Gene

CNA1 (Cornea Plana 1 (Autosomal Dominant)) is a Genetic Locus. Diseases associated with CNA1 include Cornea Plana 1, Autosomal Dominant.

Additional gene information for CNA1 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 CNA1 Gene

Genomics for CNA1 Gene

Genomic Locations for CNA1 Gene

Genomic Locations for CNA1 Gene
Unknown strand

Genomic View for CNA1 Gene

Cytogenetic band:
GeneLoc Logo Gene Density

No data available for GeneHancer (GH) Regulatory Elements and RefSeq DNA sequence for CNA1 Gene

Function for CNA1 Gene

Animal Model 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 CNA1 Gene

Localization for CNA1 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 CNA1 Gene

Pathways & Interactions for CNA1 Gene

No Data Available

Interacting Proteins for CNA1 Gene

Gene Ontology (GO) - Biological Process for CNA1 Gene


No data available for Pathways by source and SIGNOR curated interactions for CNA1 Gene

Drugs & Compounds for CNA1 Gene

No Compound Related Data Available

Transcripts for CNA1 Gene

Alternative Splicing Database (ASD) splice patterns (SP) for CNA1 Gene

No ASD Table

Relevant External Links for CNA1 Gene

ECgene alternative splicing isoforms for

No data available for mRNA/cDNA for CNA1 Gene

Expression for CNA1 Gene

NURSA nuclear receptor signaling pathways regulating expression of CNA1 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 CNA1 Gene

Orthologs for CNA1 Gene

No data available for Orthologs and Evolution for CNA1 Gene

Paralogs for CNA1 Gene

No data available for Paralogs for CNA1 Gene

Variants for CNA1 Gene

Additional Variant Information for CNA1 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 CNA1 Gene

Disorders for CNA1 Gene

MalaCards: The human disease database

(1) MalaCards diseases for CNA1 Gene - From: OMIM and GeneCards

Disorder Aliases PubMed IDs
cornea plana 1, autosomal dominant
  • cna1
- elite association - COSMIC cancer census association via MalaCards
Search CNA1 in MalaCards View complete list of genes associated with diseases
genes like me logo Genes that share disorders with CNA1: view

No data available for UniProtKB/Swiss-Prot , Genatlas and External Links for CNA1 Gene

Publications for CNA1 Gene

  1. Clinical and molecular characterization of a patient with an interstitial deletion of chromosome 12q15-q23 and peripheral corneal abnormalities. (PMID: 16490510) Tocyap ML … Wiggs J (American journal of ophthalmology 2006) 3 58
  2. Dominantly and recessively inherited cornea plana congenita map to the same small region of chromosome 12. (PMID: 8723718) Tahvanainen E … de la Chapelle A (Genome research 1996) 3 58

Products for CNA1 Gene

Sources for CNA1 Gene

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