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: Notch4 ENSRNOG00000000442

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Description

notch receptor 4 [Source:RGD Symbol;Acc:1303282]

Location

Primary_assembly 20: 4,161,730-4,189,072 reverse strand.

GRCr8:CM070410.1

About this gene

This gene has 2 transcripts (splice variants), 571 orthologues, 5 paralogues and is associated with 23 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000000513.6	Notch4-202	6484	1959aa	ENSRNOP00000000513.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6KTE6	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,
ENSRNOT00000000510.8	Notch4-201	1228	158aa	ENSRNOP00000000510.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6KTF4 Q6MG88	-

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Summary

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