Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: CDC42EP4 ENSSSCG00000017245

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Description

CDC42 effector protein 4 [Source:VGNC Symbol;Acc:VGNC:86458]

Location

Primary_assembly 12: 7,638,085-7,660,186 forward strand.

Sscrofa11.1:CM000823.5

About this gene

This gene has 2 transcripts (splice variants), 235 orthologues and 5 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000058168.3	CDC42EP4-201	3039	357aa	ENSSSCP00000052917.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1SKS7 F1RV35	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,
ENSSSCT00000018774.4	CDC42EP4-202	2958	357aa	ENSSSCP00000018272.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1SKS7 F1RV35	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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