Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
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ID History
- Gene history

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Gene: baz FBgn0000163

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Description

bazooka

Gene Synonyms

baz

Location

Primary_assembly X: 17,160,006-17,200,728 forward strand.

BDGP6.46:AE014298.5

About this gene

This gene has 4 transcripts (splice variants) and 550 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
FBtr0111000	baz-RB	10439	1520aa	FBpp0110299	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q0KHR3	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,
FBtr0343764	baz-RD	10334	1485aa	FBpp0310323	Gene/transcipt that contains an open reading frame (ORF).Protein coding	X2JCB3	-
FBtr0074388	baz-RA	6762	1464aa	FBpp0074162	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q9VX75	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,
FBtr0343763	baz-RC	6485	1499aa	FBpp0310322	Gene/transcipt that contains an open reading frame (ORF).Protein coding	O96782 Q86NX9 X2JFU8	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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