|  Help  |  About  |  Contact Us

Protein Coding Gene : Smg9 SMG9 nonsense mediated mRNA decay factor

Primary Identifier  MGI:1919247 Organism  mouse, laboratory
Chromosome  7 NCBI Gene Number  71997
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable identical protein binding activity. Involved in brain development; eye development; and heart development. Acts upstream of or within in utero embryonic development. Orthologous to human SMG9 (SMG9 nonsense mediated mRNA decay factor).
PHENOTYPE: Mice homozygous for a severe hypomorphic allele exhibit edema, hemorrhage, exencephaly, preaxial polydactyly, reduced size and growth, decreased mid- and hindrain size, microphthalmia, thin myocardium and atrioventricular septal defect. [provided by MGI curators]
  • synonyms:
  • 1500002O20Rik,
  • MGI:2141954,
  • AI429693,
  • expressed sequence N28092,
  • N28092,
  • SMG9 nonsense mediated mRNA decay factor,
  • RIKEN cDNA 1500002O20 gene,
  • smg-9 homolog, nonsense mediated mRNA decay factor (C. elegans),
  • expressed sequence AI429693,
  • Smg9,
  • MGI:2142378

Features --> Cross References

Genome

Sequence Feature Displayer

JG Browse Displayer

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

 

Other

0 Driver For