|  Help  |  About  |  Contact Us

Protein Coding Gene : Trnt1 tRNA nucleotidyl transferase, CCA-adding, 1

Primary Identifier  MGI:1917297 Organism  mouse, laboratory
Chromosome  6 NCBI Gene Number  70047
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable CCACCA tRNA nucleotidyltransferase activity; protein homodimerization activity; and tRNA binding activity. Predicted to be involved in rescue of stalled ribosome and tRNA metabolic process. Predicted to act upstream of or within tRNA processing. Located in mitochondrion. Human ortholog(s) of this gene implicated in sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay. Orthologous to human TRNT1 (tRNA nucleotidyl transferase 1).
  • synonyms:
  • Trnt1,
  • tRNA nucleotidyl transferase, CCA-adding, 1,
  • 2410043H24Rik,
  • AA408384,
  • EST AA408384,
  • RIKEN cDNA 2410043H24 gene,
  • RIKEN cDNA 2610044E04 gene,
  • MGI:1353629,
  • MGI:1917240,
  • CGI-47,
  • 2610044E04Rik,
  • C76540,
  • MGI:1889337,
  • EST C76540

Features --> Cross References

Genome

Sequence Feature Displayer

JG Browse Displayer

0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

1 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

0 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