Gene: INTS2 ENSSSCG00000017673

Description

integrator complex subunit 2 [Source:VGNC Symbol;Acc:VGNC:89162]

Location

Sscrofa11.1:CM000823.5

About this gene

This gene has 2 transcripts (splice variants) and 196 orthologues.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000019237.5	INTS2-201	5802	1119aa	ENSSSCP00000018727.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1S221	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 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,
ENSSSCT00000047797.3	INTS2-202	5804	1113aa	ENSSSCP00000050167.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287B251	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,

Breeds

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