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

Aliases for CNPY3-GNMT Gene

Aliases for CNPY3-GNMT Gene

  • CNPY3-GNMT Readthrough 3

External Ids for CNPY3-GNMT Gene

Summaries for CNPY3-GNMT Gene

Entrez Gene Summary for CNPY3-GNMT Gene

  • This locus represents naturally occurring readthrough transcription between the upstream CNPY3 (canopy FGF signaling regulator 3) and the downstream GNMT (glycine N-methyltransferase) genes. Readthrough transcripts may encode proteins that have amino acid similarity with proteins encoded by both individual genes. [provided by RefSeq, Jan 2016]

GeneCards Summary for CNPY3-GNMT Gene

CNPY3-GNMT (CNPY3-GNMT Readthrough) is a Protein Coding gene.

Additional gene information for CNPY3-GNMT 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 CNPY3-GNMT Gene

Genomics for CNPY3-GNMT Gene

Genomic Locations for CNPY3-GNMT Gene

Genomic Locations for CNPY3-GNMT Gene
chr6:-
(GRCh38/hg38)
Orientation:
Unknown strand

Genomic View for CNPY3-GNMT Gene


Cytogenetic band:
GeneLoc Logo Gene Density

RefSeq DNA sequence for CNPY3-GNMT Gene

No data available for GeneHancer (GH) Regulatory Elements for CNPY3-GNMT Gene

Proteins for CNPY3-GNMT Gene

Post-translational modifications for CNPY3-GNMT Gene

No Post-translational modifications

Other Protein References for CNPY3-GNMT Gene

No data available for DME Specific Peptides for CNPY3-GNMT Gene

Domains & Families for CNPY3-GNMT 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 CNPY3-GNMT Gene

Function for CNPY3-GNMT Gene

Phenotypes From GWAS Catalog for CNPY3-GNMT 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 CNPY3-GNMT Gene

Localization for CNPY3-GNMT 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 CNPY3-GNMT Gene

Pathways & Interactions for CNPY3-GNMT Gene

SuperPathways for CNPY3-GNMT Gene

No Data Available

Interacting Proteins for CNPY3-GNMT Gene

Gene Ontology (GO) - Biological Process for CNPY3-GNMT Gene

None

No data available for Pathways by source and SIGNOR curated interactions for CNPY3-GNMT Gene

Drugs & Compounds for CNPY3-GNMT Gene

No Compound Related Data Available

Transcripts for CNPY3-GNMT Gene

mRNA/cDNA for CNPY3-GNMT Gene

Alternative Splicing Database (ASD) splice patterns (SP) for CNPY3-GNMT Gene

No ASD Table

Expression for CNPY3-GNMT 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 CNPY3-GNMT Gene

Orthologs for CNPY3-GNMT Gene

No data available for Orthologs and Evolution for CNPY3-GNMT Gene

Paralogs for CNPY3-GNMT Gene

No data available for Paralogs for CNPY3-GNMT Gene

Variants for CNPY3-GNMT Gene

Sequence variations from dbSNP and Humsavar for CNPY3-GNMT Gene

SNP ID Clin Chr 06 pos Variation AA Info Type
rs1051218 uncertain-significance, Zellweger syndrome 42,964,123(+) G/A downstream_transcript_variant
rs115180949 benign, uncertain-significance, likely-benign, not specified, Zellweger syndrome, not provided 42,964,342(+) G/A downstream_transcript_variant
rs121907888 pathogenic, Glycine N-methyltransferase deficiency 42,960,916(+) T/C intron_variant
rs121907889 pathogenic, Glycine N-methyltransferase deficiency 42,963,149(+) C/A coding_sequence_variant, intron_variant, missense_variant
rs144286892 benign, Zellweger syndrome 42,963,890(+) TTTATTTAT/TTTAT downstream_transcript_variant

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot , Structural Variations from Database of Genomic Variants (DGV) , Variation tolerance and Additional Variant Information for CNPY3-GNMT Gene

Disorders for CNPY3-GNMT Gene

Additional Disease Information for CNPY3-GNMT

No disorders were found for CNPY3-GNMT Gene.

No data available for MalaCards , UniProtKB/Swiss-Prot and Genatlas for CNPY3-GNMT Gene

Publications for CNPY3-GNMT Gene

  1. Expression of conjoined genes: another mechanism for gene regulation in eukaryotes. (PMID: 20967262) Prakash T … Taylor TD (PloS one 2010) 3 58

Products for CNPY3-GNMT Gene

Sources for CNPY3-GNMT Gene

Content
Loading form....