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Summary
- Splice variants
- Transcript comparison
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Sequence
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DB built by FlyBase

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Gene: Eaat2 FBgn0026438

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Description

Excitatory amino acid transporter 2

Gene Synonyms

Location

Primary_assembly 2L: 737,212-744,395 reverse strand.

BDGP6.54:AE014134.6

About this gene

This gene has 3 transcripts (splice variants), 89 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Name	Transcript ID	bp	Protein	Translation ID	Biotype	UniProt	RefSeq	Flags
Eaat2-RC	FBtr0301316	3398	579aa	FBpp0290531	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1JHQ6 Q8T0S9 Q9U9K1	-	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
Eaat2-RD	FBtr0301317	3169	563aa	FBpp0290532	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q9VPS6	-	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,
Eaat2-RA	FBtr0078043	3057	563aa	FBpp0077707	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q9VPS6	-	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,

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Summary

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