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Protein Coding Gene : Pitpnm3 PITPNM family member 3
Primary Identifier  MGI:2685726 Organism  mouse, laboratory
Chromosome  11 NCBI Gene Number  327958
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable calcium ion binding activity; phospholipase activity; and receptor tyrosine kinase binding activity. Predicted to be involved in phospholipid transport. Predicted to be located in cell body and cell projection. Predicted to be active in cytoplasm. Is expressed in retina outer nuclear layer. Human ortholog(s) of this gene implicated in cone-rod dystrophy 5. Orthologous to human PITPNM3 (PITPNM family member 3).
  • synonyms:
  • expressed sequence AI848332,
  • MGI:2144294,
  • Ackr6,
  • gene model 880, (NCBI),
  • RIKEN cDNA A330068P14 gene,
  • PITPNM family member 3,
  • Pitpnm3,
  • AI848332,
  • Gm880,
  • A330068P14Rik
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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

5 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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