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Aliases for MRX26 Gene

Aliases for MRX26 Gene

  • Mental Retardation, X-Linked 26 2 3

External Ids for MRX26 Gene

Summaries for MRX26 Gene

GeneCards Summary for MRX26 Gene

MRX26 (Mental Retardation, X-Linked 26) is a Genetic Locus. Diseases associated with MRX26 include Renpenning Syndrome.

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 MRX26 Gene

Genomics for MRX26 Gene

Genomic Location for MRX26 Gene

Unknown strand

Genomic View for MRX26 Gene

Cytogenetic band:
GeneLoc Logo Gene Density

No data available for Regulatory Elements and RefSeq DNA sequence for MRX26 Gene

Proteins for MRX26 Gene

Post-translational modifications for MRX26 Gene

No Post-translational modifications

No data available for DME Specific Peptides for MRX26 Gene

Domains & Families for MRX26 Gene

Gene Families for MRX26 Gene

Graphical View of Domain Structure for InterPro Entry

genes like me logo Genes that share domains with MRX26: view

No data available for Protein Domains , Suggested Antigen Peptide Sequences and UniProtKB/Swiss-Prot for MRX26 Gene

Function for MRX26 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 MRX26 Gene

Localization for MRX26 Gene

No data available for Subcellular locations from UniProtKB/Swiss-Prot , Subcellular locations from COMPARTMENTS and Gene Ontology (GO) - Cellular Components for MRX26 Gene

Pathways & Interactions for MRX26 Gene

SuperPathways for MRX26 Gene

No Data Available

Interacting Proteins for MRX26 Gene

Gene Ontology (GO) - Biological Process for MRX26 Gene


No data available for Pathways by source and SIGNOR curated interactions for MRX26 Gene

Drugs & Compounds for MRX26 Gene

No Compound Related Data Available

Transcripts for MRX26 Gene

Alternative Splicing Database (ASD) splice patterns (SP) for MRX26 Gene

No ASD Table

Relevant External Links for MRX26 Gene

ECgene alternative splicing isoforms for

No data available for mRNA/cDNA for MRX26 Gene

Expression for MRX26 Gene

NURSA nuclear receptor signaling pathways regulating expression of MRX26 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 MRX26 Gene

Orthologs for MRX26 Gene

No data available for Orthologs and Evolution for MRX26 Gene

Paralogs for MRX26 Gene

No data available for Paralogs for MRX26 Gene

Variants for MRX26 Gene

Relevant External Links for MRX26 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 MRX26 Gene

Disorders for MRX26 Gene

MalaCards: The human disease database

(1) MalaCards diseases for MRX26 Gene - From: GeneCards

Disorder Aliases PubMed IDs
renpenning syndrome
  • renpenning syndrome 1
- elite association - COSMIC cancer census association via MalaCards
Search MRX26 in MalaCards View complete list of genes associated with diseases
genes like me logo Genes that share disorders with MRX26: view

No data available for UniProtKB/Swiss-Prot , Genatlas and External Links for MRX26 Gene

Publications for MRX26 Gene

  1. Mutation frequencies of X-linked mental retardation genes in families from the EuroMRX consortium. (PMID: 17221867) de Brouwer A.P. … Hamel B.C. (Hum. Mutat. 2007) 2 3 64
  2. Further linkage evidence for localization of mutational sites for nonsyndromic types of X-linked mental retardation at the pericentromeric region. (PMID: 8826459) Robledo R. … Filippi G. (Am. J. Med. Genet. 1996) 2 3 64
  3. X-linked mental retardation. I. Martin-Bell syndrome (report of 18 families). (PMID: 3437265) Rocchi M. … Filippi G. (J Genet Hum 1987) 3 64
  4. X-linked mental retardation. II. Renpenning syndrome and other types (report of 14 families). (PMID: 3437266) Archidiacono N. … Filippi G. (J Genet Hum 1987) 3 64

Products for MRX26 Gene

Sources for MRX26 Gene

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