Gene: RGD1310852 ENSRNOG00000006370

Description

similar to RIKEN cDNA 9130401M01 [Source:RGD Symbol;Acc:1310852]

Gene Synonyms

LOC314992, MGC108982

Location

mRatBN7.2:CM026980.1

About this gene

This gene has 2 transcripts (splice variants), 197 orthologues and is associated with 2 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000090270.2	RGD1310852-202	1351	377aa	ENSRNOP00000070309.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JXK6	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,
ENSRNOT00000008382.6	RGD1310852-201	1342	374aa	ENSRNOP00000008382.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5BK24	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