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Aliases for DYX9 Gene

Aliases for DYX9 Gene

  • Dyslexia Susceptibility 9 2 3
  • DXY9 3

External Ids for DYX9 Gene

Previous HGNC Symbols for DYX9 Gene

  • DXY9

Summaries for DYX9 Gene

GeneCards Summary for DYX9 Gene

DYX9 (Dyslexia Susceptibility 9) is a Genetic Locus. Diseases associated with DYX9 include Dyslexia 9 and Dyslexia.

Additional gene information for DYX9 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 DYX9 Gene

Genomics for DYX9 Gene

Genomic Locations for DYX9 Gene

Genomic Locations for DYX9 Gene
Unknown strand

Genomic View for DYX9 Gene

Cytogenetic band:
GeneLoc Logo Gene Density

No data available for GeneHancer (GH) Regulatory Elements and RefSeq DNA sequence for DYX9 Gene

Function for DYX9 Gene

Animal Model Products

Clone 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 DYX9 Gene

Localization for DYX9 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 DYX9 Gene

Pathways & Interactions for DYX9 Gene

No Data Available

Interacting Proteins for DYX9 Gene

Gene Ontology (GO) - Biological Process for DYX9 Gene


No data available for Pathways by source and SIGNOR curated interactions for DYX9 Gene

Drugs & Compounds for DYX9 Gene

No Compound Related Data Available

Transcripts for DYX9 Gene

Clone Products

Alternative Splicing Database (ASD) splice patterns (SP) for DYX9 Gene

No ASD Table

Relevant External Links for DYX9 Gene

ECgene alternative splicing isoforms for

No data available for mRNA/cDNA for DYX9 Gene

Expression for DYX9 Gene

NURSA nuclear receptor signaling pathways regulating expression of DYX9 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 DYX9 Gene

Orthologs for DYX9 Gene

No data available for Orthologs and Evolution for DYX9 Gene

Paralogs for DYX9 Gene

No data available for Paralogs for DYX9 Gene

Variants for DYX9 Gene

Additional Variant Information for DYX9 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 DYX9 Gene

Disorders for DYX9 Gene

MalaCards: The human disease database

(2) MalaCards diseases for DYX9 Gene - From: OMIM and GeneCards

Disorder Aliases PubMed IDs
dyslexia 9
  • dyslexia, susceptibility to, 9
- elite association - COSMIC cancer census association via MalaCards
Search DYX9 in MalaCards View complete list of genes associated with diseases
genes like me logo Genes that share disorders with DYX9: view

No data available for UniProtKB/Swiss-Prot , Genatlas and External Links for DYX9 Gene

Publications for DYX9 Gene

  1. Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family. (PMID: 15342694) de Kovel CG … Padberg GW (Journal of medical genetics 2004) 2 3 58
  2. Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia. (PMID: 11743577) Fisher SE … Monaco AP (Nature genetics 2002) 3 58

Products for DYX9 Gene

Sources for DYX9 Gene

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