Gene: Smc1b ENSMUSG00000022432

Description

structural maintenance of chromosomes 1B [Source:MGI Symbol;Acc:MGI:2154049]

Gene Synonyms

SMC1beta, Smc1l2

Location

GRCm39:CM001008.3

About this gene

This gene has 2 transcripts (splice variants), 205 orthologues, 7 paralogues and is associated with 12 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000023068.8	Smc1b-201	4047	1248aa	ENSMUSP00000023068.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS27718	A1L2Z0 Q920F6	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, 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, TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:1,
ENSMUST00000227591.2	Smc1b-202	336	15aa	ENSMUSP00000154461.2	Nonsense mediated decay		A0A2I3BR69	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,