Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: TRMT10C ENSSSCG00000011956

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Description

tRNA methyltransferase 10C, mitochondrial RNase P subunit [Source:UniProtKB Gene Name;Acc:F1SL15]

Location

Primary_assembly 13: 157,496,170-157,504,418 reverse strand.

Sscrofa11.1:CM000824.5

About this gene

This gene has 2 transcripts (splice variants), 184 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000040020.3	TRMT10C-202	5713	415aa	ENSSSCP00000055430.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D0ZCZ0 F1SL15	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, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,
ENSSSCT00000013082.4	TRMT10C-201	1542	415aa	ENSSSCP00000012737.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D0ZCZ0 F1SL15	APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,

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Summary

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