Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
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: DEF8 ENSPTRG00000008497

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Description

differentially expressed in FDCP 8 homolog [Source:VGNC Symbol;Acc:VGNC:13825]

Location

Chromosome 16: 81,451,174-81,471,208 forward strand.

Pan_tro_3.0:CM000330.3

About this gene

This gene has 1 transcript (splice variant), 196 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000015676.4	DEF8-201	4252	451aa	ENSPTRP00000014503.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2J8J014 A0A6D2WMD2	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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