Gene: Rsf1 ENSRNOG00000024194

Description

remodeling and spacing factor 1 [Source:RGD Symbol;Acc:1311245]

Gene Synonyms

Hbxap, LOC308839

Location

GRCr8:CM070391.1

About this gene

This gene has 2 transcripts (splice variants), 257 orthologues, 9 paralogues and is associated with 1 phenotype.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000037050.7	Rsf1-201	4971	1448aa	ENSRNOP00000031549.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZGQ8	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,
ENSRNOT00000098705.2	Rsf1-202	5025	1402aa	ENSRNOP00000092847.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GKD6	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,

Paralogues