Gene: Swt1 ENSRNOG00000032258

Description

SWT1 RNA endoribonuclease homolog [Source:RGD Symbol;Acc:1308695]

Gene Synonyms

LOC289088, RGD1308695

Location

mRatBN7.2:CM026986.1

About this gene

This gene has 2 transcripts (splice variants), 185 orthologues and is associated with 4 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000044255.5	Swt1-201	3679	910aa	ENSRNOP00000049813.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZHR0	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,
ENSRNOT00000086460.2	Swt1-202	3726	865aa	ENSRNOP00000072271.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K2J8	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