Summary
- Splice variants
- Transcript comparison
- Gene alleles
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- Secondary Structure
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Metazoan Compara
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- GO: Cellular component
- GO: Biological process
- GO: Molecular function
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Gene: CG6191 FBgn0027581

Gene Synonyms

Location

Primary_assembly 2R: 13,580,313-13,593,339 reverse strand.

BDGP6.46:AE013599.5

About this gene

This gene has 3 transcripts (splice variants) and 70 orthologues.

Transcripts

Show transcript tableHide transcript table

Name	Transcript ID	bp	Protein	Translation ID	Biotype	UniProt	RefSeq	Flags
CG6191-RC	FBtr0330618	3439	746aa	FBpp0303468	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0B4KF19 Q9Y138	-	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,
CG6191-RB	FBtr0330617	3745	728aa	FBpp0303467	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0B4KEN8	-	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,
CG6191-RA	FBtr0087678	3439	717aa	FBpp0086798	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A1Z9G1	-	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,

Gene: CG6191 FBgn0027581

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Gene: CG6191 FBgn0027581

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