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

Configure this page

Share this page

Bookmark this page

.

Gene: INSIG2 ENSBTAG00000002112

.

Description

insulin induced 2 [Source:VGNC Symbol;Acc:VGNC:30218]

Location

Primary_assembly 2: 69,756,859-69,800,152 forward strand.

ARS-UCD1.3:CM008169.2

About this gene

This gene has 4 transcripts (splice variants), 208 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000134058.1	INSIG2-201	2006	266aa	ENSBTAP00000091411.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSBTAT00000064251.3	INSIG2-204	1024	243aa	ENSBTAP00000053974.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G3MWS1	-
ENSBTAT00000082556.2	INSIG2-202	960	245aa	ENSBTAP00000056880.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LFF2	-
ENSBTAT00000002725.6	INSIG2-203	888	225aa	ENSBTAP00000002725.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1BP19	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,

.

Summary

.

.