Gene: Sf3b4 ENSRNOG00000021181

Description

splicing factor 3B subunit 4 [Source:RGD Symbol;Acc:1309667]

Gene Synonyms

LOC295270

Location

mRatBN7.2:CM026975.1

About this gene

This gene has 2 transcripts (splice variants), 221 orthologues, 27 paralogues and is associated with 14 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000028758.6	Sf3b4-201	1866	429aa	ENSRNOP00000028758.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QI40	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,
ENSRNOT00000113402.1	Sf3b4-202	3436	397aa	ENSRNOP00000079825.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZNJ0	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