Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Ifng ENSRNOG00000007468

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Description

interferon gamma [Source:RGD Symbol;Acc:2866]

Gene Synonyms

IFNG2, If2f

Location

Primary_assembly 7: 55,761,736-55,793,216 forward strand.

GRCr8:CM070397.1

About this gene

This gene has 5 transcripts (splice variants), 171 orthologues and is associated with 198 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000127886.1	Ifng-203	1021	191aa	ENSRNOP00000102323.1	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,
ENSRNOT00000173962.1	Ifng-205	859	170aa	ENSRNOP00000099410.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000121425.1	Ifng-202	765	191aa	ENSRNOP00000107688.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000146986.1	Ifng-204	756	157aa	ENSRNOP00000103290.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000009919.4	Ifng-201	510	156aa	ENSRNOP00000009917.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A7R8C3J6 P01581	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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Strains

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Genomic alignments

Gene tree

Orthologues

Paralogues (Not available)

Families (Not available)

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

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Personal Data