Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

Configure this page

Share this page

Bookmark this page

.

Gene: IFNGR1 ENSGALG00010005291

.

Description

interferon gamma receptor 1 [Source:NCBI gene (formerly Entrezgene);Acc:421685]

Location

Primary_assembly 3: 54,493,042-54,515,567 forward strand.

bGalGal1.mat.broiler.GRCg7b:CM028484.1

About this gene

This gene has 1 transcript (splice variant), 296 orthologues and 12 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSGALT00010012544.1	IFNGR1-201	3059	437aa	ENSGALP00010007108.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8V0XK86	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,

.

Summary

.

.