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
External references
Supporting evidence
ID History
- Gene history

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Gene: Nop16 ENSRNOG00000017284

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Description

NOP16 nucleolar protein [Source:RGD Symbol;Acc:1305727]

Gene Synonyms

LOC306768, RGD1305727

Location

Primary_assembly 17: 10,028,034-10,033,038 forward strand.

GRCr8:CM070407.1

About this gene

This gene has 3 transcripts (splice variants), 188 orthologues and is associated with 4 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000023320.9	Nop16-201	1083	178aa	ENSRNOP00000023320.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B0BMU2 Q1RP77	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,
ENSRNOT00000145585.1	Nop16-203	1591	165aa	ENSRNOP00000107191.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000115861.2	Nop16-202	1053	168aa	ENSRNOP00000076503.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5Y0C6	-

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Summary

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