Gene: sim1a ENSDARG00000023316

Description

SIM bHLH transcription factor 1a [Source:NCBI gene (formerly Entrezgene);Acc:260351]

Location

GRCz11:CM002900.2

About this gene

This gene has 2 transcripts (splice variants), 198 orthologues, 13 paralogues and is associated with 35 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000036348.6	sim1a-201	2655	745aa	ENSDARP00000033085.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1QMF7	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,
ENSDART00000187189.1	sim1a-202	7344	745aa	ENSDARP00000151913.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1QMF7	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,

Summary