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Protein Coding Gene : Rbm14 RNA binding motif protein 14

Primary Identifier  MGI:1929092 Organism  mouse, laboratory
Chromosome  19 NCBI Gene Number  56275
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables mRNA binding activity and splicing factor binding activity. Involved in centriole assembly and mRNA splicing, via spliceosome. Acts upstream of or within apoptotic process; gastrulation; and regulation of response to DNA integrity checkpoint signaling. Predicted to be located in cytoplasm and nucleus. Predicted to be part of transcription regulator complex. Predicted to be active in nuclear speck. Is expressed in central nervous system; limb; liver; sensory organ; and stomach epithelium. Orthologous to several human genes including RBM14 (RNA binding motif protein 14).
PHENOTYPE: Mice homozygous for a null allele exhibit embryonic lethality with impaired gastrulation, reduced cell density in the epiblast and mesoderm, and absent allantois, chorion, amnion, and primitive streak. [provided by MGI curators]
  • synonyms:
  • PSP2,
  • Rbm14,
  • RNA binding motif protein 14,
  • 1300007E16Rik,
  • p16,
  • RIKEN cDNA 1300007E16 gene,
  • MGI:1919021

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

5 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