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Aliases for CNE8 Gene

Aliases for CNE8 Gene

  • CNE8 Enhancer Downstream Of SHOX 3
  • Evolutionarily Conserved Region 7 3
  • Conserved Non-Coding Element 8 3
  • ECR7 3

External Ids for CNE8 Gene

Summaries for CNE8 Gene

Entrez Gene Summary for CNE8 Gene

  • This genomic element is found within the pseudoautosomal region 1 (PAR1) of chromosomes X and Y, where each chromosome contains the same DNA region. It is located approximately 191 kb downstream of the SHOX (short stature homeobox) gene, and is one of several conserved elements that surround that gene. It can function as an enhancer in various tissues in transgenic zebrafish embryos. Mutations that include this element, including deletions and microduplications, are associated with Leri-Weill dyschondrosteosis (LWD) and idiopathic short stature (ISS), and they have also been implicated in autism spectrum disorders (ASDs) and related neurodevelopmental conditions. [provided by RefSeq, Jul 2016]

GeneCards Summary for CNE8 Gene

CNE8 (CNE8 Enhancer Downstream Of SHOX) is an Uncategorized gene. Diseases associated with CNE8 include Leri-Weill Dyschondrosteosis and Langer Mesomelic Dysplasia.

Additional gene information for CNE8 Gene

No data available for CIViC summary , UniProtKB/Swiss-Prot , Tocris Summary , Gene Wiki entry , PharmGKB "VIP" Summary , fRNAdb sequence ontologies and piRNA Summary for CNE8 Gene

Genomics for CNE8 Gene

Genomic Locations for CNE8 Gene

No location information available

Genomic View for CNE8 Gene

Cytogenetic band:

No data available for GeneHancer (GH) Regulatory Elements and RefSeq DNA sequence for CNE8 Gene

Function for CNE8 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 CNE8 Gene

Localization for CNE8 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 CNE8 Gene

Pathways & Interactions for CNE8 Gene

No Data Available

Interacting Proteins for CNE8 Gene

Gene Ontology (GO) - Biological Process for CNE8 Gene


No data available for Pathways by source and SIGNOR curated interactions for CNE8 Gene

Drugs & Compounds for CNE8 Gene

No Compound Related Data Available

Transcripts for CNE8 Gene

Alternative Splicing Database (ASD) splice patterns (SP) for CNE8 Gene

No ASD Table

No data available for mRNA/cDNA for CNE8 Gene

Expression for CNE8 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 CNE8 Gene

Orthologs for CNE8 Gene

No data available for Orthologs and Evolution for CNE8 Gene

Paralogs for CNE8 Gene

No data available for Paralogs for CNE8 Gene

Variants for CNE8 Gene

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot , Sequence variations from dbSNP and Humsavar , Structural Variations from Database of Genomic Variants (DGV) , Variation tolerance and Additional Variant Information for CNE8 Gene

Disorders for CNE8 Gene

MalaCards: The human disease database

(3) MalaCards diseases for CNE8 Gene - From: GeneCards

Disorder Aliases PubMed IDs
leri-weill dyschondrosteosis
  • lwd
langer mesomelic dysplasia
  • lmd
  • autistic disorder
- elite association - COSMIC cancer census association via MalaCards
Search CNE8 in MalaCards View complete list of genes associated with diseases
genes like me logo Genes that share disorders with CNE8: view

No data available for UniProtKB/Swiss-Prot , Genatlas and External Links for CNE8 Gene

Publications for CNE8 Gene

  1. Microduplications at the pseudoautosomal SHOX locus in autism spectrum disorders and related neurodevelopmental conditions. (PMID: 27073233) Tropeano M … Murphy DG (Journal of medical genetics 2016) 3 58
  2. Duplications upstream and downstream of SHOX identified as novel causes of Leri-Weill dyschondrosteosis or idiopathic short stature. (PMID: 26698168) Bunyan DJ … Coviello DA (American journal of medical genetics. Part A 2016) 3 58
  3. Profiling of conserved non-coding elements upstream of SHOX and functional characterisation of the SHOX cis-regulatory landscape. (PMID: 26631348) Verdin H … De Baere E (Scientific reports 2015) 3 58
  4. The growth response to GH treatment is greater in patients with SHOX enhancer deletions compared to SHOX defects. (PMID: 26264720) Donze SH … Oostdijk W (European journal of endocrinology 2015) 3 58
  5. Compound heterozygous deletions in pseudoautosomal region 1 in an infant with mild manifestations of langer mesomelic dysplasia. (PMID: 24311385) Tsuchiya T … Fukami M (American journal of medical genetics. Part A 2014) 3 58

Products for CNE8 Gene

Sources for CNE8 Gene

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