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Protein Coding Gene : Cyp24a1 cytochrome P450, family 24, subfamily a, polypeptide 1

Primary Identifier  MGI:88593 Organism  mouse, laboratory
Chromosome  2 NCBI Gene Number  13081
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables 25-hydroxycholecalciferol-24-hydroxylase activity. Acts upstream of or within vitamin D metabolic process. Located in mitochondrion. Is expressed in axial skeleton; cranium; ear; genitourinary system; and nervous system. Human ortholog(s) of this gene implicated in colorectal adenoma; gastrointestinal system cancer (multiple); hypercalcemia; lung cancer (multiple); and ulcerative colitis. Orthologous to human CYP24A1 (cytochrome P450 family 24 subfamily A member 1).
PHENOTYPE: Mice homozygous for disruption of this gene suffer a 50% mortality rate between birth and weaning. abnormalities are seen in the development of membranous bones. [provided by MGI curators]
  • synonyms:
  • CP24,
  • cytochrome P450, subfamily XXIV (vitamin D hydroxylase),
  • 25-hydroxyvitamin D-24-hydroxylase,
  • cytochrome P450, 24,
  • 24-OHase,
  • cytochrome P450, family 24, subfamily a, polypeptide 1,
  • Cyp24,
  • MGD-MRK-2310,
  • Cyp24a1

Features --> Cross References

Genome

Sequence Feature Displayer

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0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

0 Involved In Mutations

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

8 Pathways

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