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
Supporting evidence
ID History
- Gene history

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Gene: hng1 FBgn0034599

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Description

hinge1

Gene Synonyms

hng1

Location

Primary_assembly 2R: 21,168,930-21,170,010 forward strand.

BDGP6.46:AE013599.5

About this gene

This gene has 1 transcript (splice variant), 6 orthologues and 13 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
FBtr0071575	hng1-RA	1081	315aa	FBpp0071502	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AQF9 A0AQG0 A0AQG3 A0AQG5 A0AQG6 C0MK19 C0MK27 C0MK29 Q95R85 Q9W2K3	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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