Gene: Samsn1 ENSRNOG00000030930

Description

SAM domain, SH3 domain and nuclear localization signals, 1 [Source:RGD Symbol;Acc:620926]

Gene Synonyms

Nash

Location

GRCr8:CM070401.1

About this gene

This gene has 1 transcript (splice variant), 267 orthologues, 2 paralogues and is associated with 2 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000082143.3	Samsn1-201	2202	372aa	ENSRNOP00000074870.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K960 A6JL18	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 P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1,

Strains

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.