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

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Gene: Dner ENSRNOG00000016640

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Description

delta/notch-like EGF repeat containing [Source:RGD Symbol;Acc:1359385]

Gene Synonyms

LOC316573

Location

Primary_assembly 9: 93,035,108-93,350,568 reverse strand.

GRCr8:CM070399.1

About this gene

This gene has 2 transcripts (splice variants), 205 orthologues and 5 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000093357.3	Dner-202	3272	746aa	ENSRNOP00000076139.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A1W2Q656 A6JWC6	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,
ENSRNOT00000022564.8	Dner-201	1529	371aa	ENSRNOP00000088607.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A870	-

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Summary

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