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Protein Coding Gene : Cyp2c65 cytochrome P450, family 2, subfamily c, polypeptide 65
Primary Identifier  MGI:1919553 Organism  mouse, laboratory
Chromosome  19 NCBI Gene Number  72303
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable caffeine oxidase activity; heme binding activity; and monooxygenase activity. Predicted to be involved in epoxygenase P450 pathway and xenobiotic metabolic process. Predicted to be located in plasma membrane. Predicted to be active in cytoplasm and intracellular membrane-bounded organelle. Human ortholog(s) of this gene implicated in several diseases, including end stage renal disease; glucose metabolism disease (multiple); head and neck squamous cell carcinoma; hypertension (multiple); and warfarin resistance. Orthologous to human CYP2C8 (cytochrome P450 family 2 subfamily C member 8) and CYP2C9 (cytochrome P450 family 2 subfamily C member 9).
  • synonyms:
  • 2210009K14Rik,
  • Cyp2c65,
  • RIKEN cDNA 2210009K14 gene,
  • cytochrome P450, family 2, subfamily c, polypeptide 65
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Features --> Cross References

Genome

Sequence Feature Displayer

JG Browse Displayer

0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

2 Involved In Mutations

Trail: ProteinCodingGene

0 Strain

0 Transcripts

0 Transgenic Expressors

0 UTRs

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

17 Pathways

Trail: ProteinCodingGene

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

Other

0 Driver For





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