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Protein Coding Gene : Rnpc3 RNA-binding region (RNP1, RRM) containing 3
Primary Identifier  MGI:1914475 Organism  mouse, laboratory
Chromosome  3 NCBI Gene Number  67225
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable U12 snRNA binding activity and pre-mRNA intronic binding activity. Predicted to be involved in mRNA splicing, via spliceosome. Predicted to be located in nucleoplasm. Predicted to be part of U12-type spliceosomal complex. Is expressed in central nervous system; dorsal root ganglion; nose; trigeminal nerve; and urinary system. Human ortholog(s) of this gene implicated in panhypopituitarism. Orthologous to human RNPC3 (RNA binding region (RNP1, RRM) containing 3).
PHENOTYPE: Embryos homozygous for a knock-out allele fail to develop beyond the morula stage and die before implantation. [provided by MGI curators]
  • synonyms:
  • RIKEN cDNA 2810441O16 gene,
  • Rnpc3,
  • AI447568,
  • RIKEN cDNA C030014B17 gene,
  • expressed sequence AI447568,
  • RNA-binding region (RNP1, RRM) containing 3,
  • C030014B17Rik,
  • MGI:1924629,
  • MGI:2139707,
  • 2810441O16Rik
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Features --> Cross References

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2 Involved In Mutations

Trail: ProteinCodingGene

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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

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Function

Mouse features --> Functions (GO terms)

Homology

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Interactions

4 Pathways

Trail: ProteinCodingGene

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Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

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