Gene: Nol8 ENSRNOG00000046968

Description

nucleolar protein 8 [Source:RGD Symbol;Acc:1309551]

Gene Synonyms

LOC361221, NEWGENE_1309551

Location

GRCr8:CM070407.1

About this gene

This gene has 2 transcripts (splice variants), 231 orthologues and is associated with 4 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000093381.3	Nol8-202	3480	1159aa	ENSRNOP00000076111.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A1W2Q629	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 ALT2: 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 appear to be conserved in fewer than 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 ALT2,
ENSRNOT00000073035.3	Nol8-201	4575	1152aa	ENSRNOP00000067842.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	M0RDX9	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,

Summary