Free for academic non-profit institutions. Other users need a Commercial license

Aliases for CUP2Q35 Gene

Aliases for CUP2Q35 Gene

  • Syndactyly, Type I 3
  • C2DUPq35 3
  • SDTY1 3
  • SD1 3

External Ids for CUP2Q35 Gene

Summaries for CUP2Q35 Gene

GeneCards Summary for CUP2Q35 Gene

CUP2Q35 (Syndactyly, Type I) is an Uncategorized gene. Diseases associated with CUP2Q35 include Craniosynostosis, Philadelphia Type.

No data available for Entrez Gene Summary , UniProtKB/Swiss-Prot , Tocris Summary , Gene Wiki entry , PharmGKB "VIP" Summary , fRNAdb sequence ontologies and piRNA Summary for CUP2Q35 Gene

Genomics for CUP2Q35 Gene

Genomic Location for CUP2Q35 Gene

Unknown strand

Genomic View for CUP2Q35 Gene

Cytogenetic band:
GeneLoc Logo Gene Density

No data available for Regulatory Elements and RefSeq DNA sequence for CUP2Q35 Gene

Proteins for CUP2Q35 Gene

Post-translational modifications for CUP2Q35 Gene

No Post-translational modifications

No data available for DME Specific Peptides for CUP2Q35 Gene

Domains & Families for CUP2Q35 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 CUP2Q35 Gene

Function for CUP2Q35 Gene

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 CUP2Q35 Gene

Localization for CUP2Q35 Gene

No data available for Subcellular locations from UniProtKB/Swiss-Prot , Subcellular locations from COMPARTMENTS and Gene Ontology (GO) - Cellular Components for CUP2Q35 Gene

Pathways & Interactions for CUP2Q35 Gene

SuperPathways for CUP2Q35 Gene

No Data Available

Interacting Proteins for CUP2Q35 Gene

Gene Ontology (GO) - Biological Process for CUP2Q35 Gene


No data available for Pathways by source and SIGNOR curated interactions for CUP2Q35 Gene

Drugs & Compounds for CUP2Q35 Gene

No Compound Related Data Available

Expression for CUP2Q35 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 , mRNA Expression by UniProt/SwissProt and Protein tissue co-expression partners for CUP2Q35 Gene

Orthologs for CUP2Q35 Gene

No data available for Orthologs and Evolution for CUP2Q35 Gene

Paralogs for CUP2Q35 Gene

No data available for Paralogs for CUP2Q35 Gene

Variants for CUP2Q35 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 Relevant External Links for CUP2Q35 Gene

Disorders for CUP2Q35 Gene

MalaCards: The human disease database

(1) MalaCards diseases for CUP2Q35 Gene - From: OMIM

Disorder Aliases PubMed IDs
craniosynostosis, philadelphia type
  • syndactyly, type i
- elite association - COSMIC cancer census association via MalaCards
genes like me logo Genes that share disorders with CUP2Q35: view

No data available for UniProtKB/Swiss-Prot , Genatlas and External Links for CUP2Q35 Gene

Publications for CUP2Q35 Gene

  1. Confirmation of genetic homogeneity of syndactyly type 1 in an Iranian family. (PMID: 11746046) Ghadami M. … Niikawa N. (Am. J. Med. Genet. 2001) 3 67
  2. Localization of a gene for syndactyly type 1 to chromosome 2q34-q36. (PMID: 10877983) Bosse K. … NAPthen M.M. (Am. J. Hum. Genet. 2000) 3

Products for CUP2Q35 Gene

Sources for CUP2Q35 Gene