Summary
- Splice variants
- Transcript comparison
- Gene alleles
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Comparative Genomics
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Gene: wgn FBgn0030941

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Description

wengen

Gene Synonyms

wgn

Location

Primary_assembly X: 18,624,042-18,634,908 reverse strand.

BDGP6.46:AE014298.5

About this gene

This gene has 2 transcripts (splice variants).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
FBtr0074617	wgn-RA	2415	343aa	FBpp0074388	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q9VWS4	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,
FBtr0342843	wgn-RB	2594	267aa	FBpp0309667	Gene/transcipt that contains an open reading frame (ORF).Protein coding	X2JCG6	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,

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Summary

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