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

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Gene: Aarsd1 ENSRNOG00000020658

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Description

alanyl-tRNA synthetase domain containing 1 [Source:RGD Symbol;Acc:1561650]

Gene Synonyms

LOC619440

Location

Primary_assembly 10: 86,840,874-86,849,734 reverse strand.

GRCr8:CM070400.1

About this gene

This gene has 1 transcript (splice variant), 201 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000028047.6	Aarsd1-201	3465	402aa	ENSRNOP00000028047.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5XI97	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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