Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: NSD2 ENSSSCG00000008682

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Description

nuclear receptor binding SET domain protein 2 [Source:VGNC Symbol;Acc:VGNC:90905]

Location

Primary_assembly 8: 964,893-1,018,028 forward strand.

Sscrofa11.1:CM000819.5

About this gene

This gene has 2 transcripts (splice variants), 245 orthologues and 19 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000009499.5	NSD2-202	6538	1069aa	ENSSSCP00000009255.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1S8S0	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,
ENSSSCT00000066342.3	NSD2-201	1934	608aa	ENSSSCP00000040233.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287A8W1 A0A4X1T0U1	-

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Summary

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