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Aliases for MDC1B Gene

Aliases for MDC1B Gene

  • Muscular Dystrophy, Congenital, 1B 3

External Ids for MDC1B Gene

Summaries for MDC1B Gene

GeneCards Summary for MDC1B Gene

MDC1B (Muscular Dystrophy, Congenital, 1B) is a Genetic Locus. Diseases associated with MDC1B include Muscular Dystrophy, Congenital, 1B.

Additional gene information for MDC1B 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 MDC1B Gene

Genomics for MDC1B Gene

Genomic Locations for MDC1B Gene

Genomic Locations for MDC1B Gene
Unknown strand

Genomic View for MDC1B Gene

Cytogenetic band:
GeneLoc Logo Gene Density

No data available for GeneHancer (GH) Regulatory Elements and RefSeq DNA sequence for MDC1B Gene

Proteins for MDC1B Gene

Post-translational modifications for MDC1B Gene

No Post-translational modifications

No data available for DME Specific Peptides for MDC1B Gene

Domains & Families for MDC1B 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 MDC1B Gene

Function for MDC1B 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 MDC1B Gene

Localization for MDC1B 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 MDC1B Gene

Pathways & Interactions for MDC1B Gene

SuperPathways for MDC1B Gene

No Data Available

Interacting Proteins for MDC1B Gene

Gene Ontology (GO) - Biological Process for MDC1B Gene


No data available for Pathways by source and SIGNOR curated interactions for MDC1B Gene

Drugs & Compounds for MDC1B Gene

No Compound Related Data Available

Transcripts for MDC1B Gene

Alternative Splicing Database (ASD) splice patterns (SP) for MDC1B Gene

No ASD Table

No data available for mRNA/cDNA for MDC1B Gene

Expression for MDC1B 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 MDC1B Gene

Orthologs for MDC1B Gene

No data available for Orthologs and Evolution for MDC1B Gene

Paralogs for MDC1B Gene

No data available for Paralogs for MDC1B Gene

Variants for MDC1B 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 MDC1B Gene

Disorders for MDC1B Gene

MalaCards: The human disease database

(1) MalaCards diseases for MDC1B Gene - From: OMIM and GeneCards

Disorder Aliases PubMed IDs
muscular dystrophy, congenital, 1b
  • mdc1b
- elite association - COSMIC cancer census association via MalaCards
Search MDC1B in MalaCards View complete list of genes associated with diseases
genes like me logo Genes that share disorders with MDC1B: view

No data available for UniProtKB/Swiss-Prot , Genatlas and External Links for MDC1B Gene

Publications for MDC1B Gene

  1. Assignment of a form of congenital muscular dystrophy with secondary merosin deficiency to chromosome 1q42. (PMID: 10677302) Brockington M … Muntoni F (American journal of human genetics 2000) 3 58

Products for MDC1B Gene

Sources for MDC1B Gene

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