Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Trem3 ENSRNOG00000013748

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Description

triggering receptor expressed on myeloid cells 3 [Source:RGD Symbol;Acc:1305477]

Gene Synonyms

LOC367215, RGD1305477

Location

Primary_assembly 9: 12,749,852-12,760,779 reverse strand.

mRatBN7.2:CM026982.1

About this gene

This gene has 1 transcript (splice variant), 18 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000018500.5	Trem3-201	1647	238aa	ENSRNOP00000018500.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZJA7	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,

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Summary

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