Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Cellular component
- GO: Biological process
- GO: Molecular function
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: His3:CG33839 FBgn0053839

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Description

His3:CG33839

Gene Synonyms

H3-615, H3f2, His3:CG33839, Hist2h3c1, Hist2h3ca1

Location

Primary_assembly 2L: 21,494,875-21,495,403 forward strand.

BDGP6.54:AE014134.6

About this gene

This gene has 1 transcript (splice variant), 13 orthologues and 24 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
FBtr0091843	His3:CG33839-RA	529	136aa	FBpp0091085	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A1W2P768 B9EI85 P02299 P84228	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,

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Summary

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