Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
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Comparative Genomics
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Gene: Eip78C FBgn0004865

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Description

Ecdysone-induced protein 78C

Gene Synonyms

Eip78C

Location

Primary_assembly 3L: 21,226,609-21,266,503 forward strand.

BDGP6.54:AE014296.5

About this gene

This gene has 4 transcripts (splice variants).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
FBtr0078306	Eip78C-RA	5223	862aa	FBpp0077963	Gene/transcipt that contains an open reading frame (ORF).Protein coding	M9NDE9 P45447	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,
FBtr0306157	Eip78C-RD	4192	862aa	FBpp0297287	Gene/transcipt that contains an open reading frame (ORF).Protein coding	M9NDE9 P45447	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,
FBtr0078307	Eip78C-RB	3832	392aa	FBpp0077964	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E3CTQ0	-
FBtr0306158	Eip78C-RE	3541	862aa	FBpp0297288	Gene/transcipt that contains an open reading frame (ORF).Protein coding	M9NDE9 P45447	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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