Gene: Aimp1 ENSRNOG00000011384

Description

aminoacyl tRNA synthetase complex-interacting multifunctional protein 1 [Source:RGD Symbol;Acc:620466]

Gene Synonyms

Emap2, MGC112632, Scye1

Location

Primary_assembly 2: 223,825,931-223,849,994 reverse strand.

GRCr8:CM070392.1

About this gene

This gene has 2 transcripts (splice variants), 304 orthologues and is associated with 5 phenotypes.

Transcripts

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Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000112244.2	Aimp1-202	1335	321aa	ENSRNOP00000077517.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A263 Q4G079	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 P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,
ENSRNOT00000015213.8	Aimp1-201	1052	315aa	ENSRNOP00000015213.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5Y7U7 Q4G079	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,