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
Regulation
External references
Supporting evidence
ID History
- Gene history

Configure this page

Export data

Share this page

Bookmark this page

.

Gene: Neurod1 ENSRNOG00000005609

.

Description

neuronal differentiation 1 [Source:RGD Symbol;Acc:3165]

Gene Synonyms

BHF-1

Location

Primary_assembly 3: 84,764,725-84,770,810 reverse strand.

GRCr8:CM070393.1

About this gene

This gene has 3 transcripts (splice variants), 203 orthologues, 15 paralogues and is associated with 16 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000162126.1	Neurod1-203	4408	357aa	ENSRNOP00000108550.1	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,
ENSRNOT00000159286.1	Neurod1-202	2969	357aa	ENSRNOP00000101657.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000007662.9	Neurod1-201	2714	357aa	ENSRNOP00000007662.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q64289	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,

.

Strains

.

Genomic alignments

Gene tree

Orthologues

Paralogues

Families (Not available)

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

.

Personal Data