Gene: Nme8 ENSRNOG00000058285

Description

NME/NM23 family member 8 [Source:RGD Symbol;Acc:735069]

Gene Synonyms

Sptrx2, Txndc3

Location

GRCr8:CM070407.1

About this gene

This gene has 2 transcripts (splice variants), 123 orthologues, 9 paralogues and is associated with 3 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000090021.3	Nme8-201	2687	596aa	ENSRNOP00000068777.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2R1L1	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,
ENSRNOT00000092051.3	Nme8-202	2026	572aa	ENSRNOP00000069890.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F7EU06	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,

Summary