Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Gene families
Literature
Metazoan Compara
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Pan-taxonomic Compara
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- Orthologues
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
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External references
Supporting evidence
ID History
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DB built by FlyBase

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Gene: Try29F FBgn0015316

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Description

Trypsin 29F

Gene Synonyms

Location

Primary_assembly 2L: 8,998,537-8,999,816 forward strand.

BDGP6.32:AE014134.6

About this gene

This gene has 2 transcripts (splice variants), 46 orthologues and 28 paralogues.

Transcripts

Show transcript tableHide transcript table

Name	Transcript ID	bp	Protein	Translation ID	Biotype	UniProt	RefSeq	Flags
Try29F-RD	FBtr0345312	1280	267aa	FBpp0311472	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B3DMZ7 Q24091 Q9VLF5	NM_001298843 NM_001298843.1 NM_078794.3 NP_001285772 NP_001285772.1 NP_523518.2	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,
Try29F-RC	FBtr0301665	932	267aa	FBpp0290879	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q9VLF5	NM_001298843.1 NM_078794 NM_078794.3 NP_001285772.1 NP_523518 NP_523518.2	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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Gene-based displays