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: Biological process
- GO: Molecular function
- GO: Cellular component
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

Gene: Nrg1 ENSMUSG00000118541

Description

neuregulin 1 [Source:MGI Symbol;Acc:MGI:96083]

Gene Synonyms

6030402G23Rik, ARIA, D230005F13Rik, GGF, GGFII, HGL, HRG, HRGalpha, NDF, SMDF, heregulin

Location

GRCm39:CM001001.3

About this gene

This gene has 1 transcript (splice variant), 1 orthologue and is associated with 82 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000239000.2	Nrg1-234	186	61aa	ENSMUSP00000158957.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		A0A5F8MPU8	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, 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