Gene: PLEKHG2 ENSSSCG00000030048

Description

pleckstrin homology and RhoGEF domain containing G2 [Source:VGNC Symbol;Acc:VGNC:91543]

Location

Sscrofa11.1:CM000817.5

About this gene

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000031206.3	PLEKHG2-201	4528	1357aa	ENSSSCP00000021184.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1SEG8	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSSSCT00000084456.1	PLEKHG2-202	2185	576aa	ENSSSCP00000062922.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2QXI9	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,

Breeds

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.