Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
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: NHP2 ENSPTRG00000048185

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Description

NHP2 ribonucleoprotein [Source:VGNC Symbol;Acc:VGNC:12395]

Location

Chromosome 5: 178,626,539-178,631,051 reverse strand.

Pan_tro_3.0:CM000319.3

About this gene

This gene has 2 transcripts (splice variants), 188 orthologues and 18 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000081295.1	NHP2-202	863	153aa	ENSPTRP00000082980.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	K7CE31	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,
ENSPTRT00000091897.1	NHP2-201	747	90aa	ENSPTRP00000062067.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3RBM1	-

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Summary

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