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

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Gene: Ndrg2 ENSRNOG00000010389

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Description

NDRG family member 2 [Source:RGD Symbol;Acc:621874]

Location

Primary_assembly 15: 27,074,481-27,083,125 reverse strand.

GRCr8:CM070405.1

About this gene

This gene has 4 transcripts (splice variants), 201 orthologues, 5 paralogues and is associated with 6 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000040540.4	Ndrg2-201	1995	385aa	ENSRNOP00000039619.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JSU4 A0A0G2K3T7	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 P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,
ENSRNOT00000042055.5	Ndrg2-202	2032	371aa	ENSRNOP00000042949.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JSV0 A6KEE6	APPRIS ALT1: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that is conserved in at least three tested species. 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 ALT1,
ENSRNOT00000094910.2	Ndrg2-203	1999	359aa	ENSRNOP00000081522.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZS65	-
ENSRNOT00000099063.2	Ndrg2-204	1183	367aa	ENSRNOP00000089946.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ACP0	-

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Summary

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