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: INSIG1 ENSBTAG00000001592

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Description

insulin induced 1 [Source:VGNC Symbol;Acc:VGNC:30217]

Location

Primary_assembly 4: 117,125,433-117,138,560 forward strand.

ARS-UCD1.3:CM008171.2

About this gene

This gene has 3 transcripts (splice variants), 203 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000002084.7	INSIG1-201	3178	378aa	ENSBTAP00000002084.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0JNC3	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,
ENSBTAT00000069908.2	INSIG1-203	1932	280aa	ENSBTAP00000065040.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0JNC3	-
ENSBTAT00000124853.1	INSIG1-202	1917	275aa	ENSBTAP00000098812.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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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