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Protein Coding Gene : P3h2 prolyl 3-hydroxylase 2

Primary Identifier  MGI:2146663 Organism  mouse, laboratory
Chromosome  16 NCBI Gene Number  210530
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable procollagen-proline 3-dioxygenase activity. Predicted to be involved in collagen metabolic process and negative regulation of cell population proliferation. Located in basement membrane. Is expressed in several structures, including central nervous system; limb bud; musculoskeletal system; renal cortex; and sensory organ. Orthologous to human P3H2 (prolyl 3-hydroxylase 2).
PHENOTYPE: Mice homozygous for a knock-out allele of exon 2 exhibit embryonic lethality between E8.5 and E12.5 with maternal platelets aggregate around the ectoplacental cone. Exon 3 knockouts are viable but mice exhibit reduced hydroxylation of collagen chains, especially in the sclera, leading to eye tissue dysmorphology and progressive myopia. [provided by MGI curators]
  • synonyms:
  • Leprel1,
  • P3h2,
  • prolyl 3-hydroxylase 2,
  • leprecan-like 1,
  • expressed sequence AW553532,
  • AW553532

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

3 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

 

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0 Driver For