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Protein Coding Gene : Gemin2 gem nuclear organelle associated protein 2
Primary Identifier  MGI:1913853 Organism  mouse, laboratory
Chromosome  12 NCBI Gene Number  66603
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Predicted to be involved in spliceosomal snRNP assembly. Located in cytoplasm and nucleus. Is expressed in several structures, including central nervous system; early embryo; genitourinary system; sensory organ; and tongue. Orthologous to human GEMIN2 (gem nuclear organelle associated protein 2).
PHENOTYPE: Mice homozygous for disruptions in this gene die as embryos. [provided by MGI curators]
  • synonyms:
  • survival of motor neuron protein interacting protein 1,
  • Sip1,
  • gem nuclear organelle associated protein 2,
  • RIKEN cDNA 1700012N19 gene,
  • Gemin2,
  • 1700012N19Rik
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Features --> Cross References

Genome

Sequence Feature Displayer

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0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

1 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

3 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

 

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0 Driver For





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