Summary
- Splice variants
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Sequence
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Pan-taxonomic Compara
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DB built by FlyBase

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Gene: Fatp2 FBgn0265187

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Description

Fatty acid transport protein 2

Gene Synonyms

Location

Primary_assembly 2R: 23,055,474-23,061,549 forward strand.

BDGP6.46:AE013599.5

About this gene

This gene has 3 transcripts (splice variants), 199 orthologues and 21 paralogues.

Transcripts

Show transcript tableHide transcript table

Name	Transcript ID	bp	Protein	Translation ID	Biotype	UniProt	RefSeq	Flags
Fatp2-RE	FBtr0339108	2745	714aa	FBpp0308253	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q7KVJ6 Q8SXT7	-	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 ALT1: 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 is conserved in at least 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 ALT1,
Fatp2-RD	FBtr0339109	2651	714aa	FBpp0308254	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q7KVJ6	-	APPRIS ALT1: 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 is conserved in at least 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 ALT1,
Fatp2-RB	FBtr0339110	2538	703aa	FBpp0308255	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q9W1W0	-	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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