Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Anatomical entity
- PHI: Phibase identifier
- PHI: Phenotype
- PHI: Experiment specification
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

Gene: NAM9 YNL137C

Description

Mitochondrial ribosomal component of the small subunit [Source:SGD;Acc:S000005081]

Gene Synonyms

MNA6

Location

R64-1-1:BK006947.3

About this gene

This gene has 1 transcript (splice variant).

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
YNL137C_mRNA	NAM9	1461	486aa	YNL137C	Gene/transcipt that contains an open reading frame (ORF).Protein coding	P27929	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical,

Summary