Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
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Comparative Genomics
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Gene: sordd2 FBgn0052581

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Description

suppression of retinal degeneration disease 1 upon overexpression 2

Gene Synonyms

sordd2

Location

Primary_assembly X: 15,796,908-15,799,162 reverse strand.

BDGP6.54:AE014298.5

About this gene

This gene has 2 transcripts (splice variants), 387 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
FBtr0074184	sordd2-RA	1428	283aa	FBpp0073969	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q8IR26	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,
FBtr0113439	sordd2-RB	1345	283aa	FBpp0112351	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q8IR26	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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