Gene: Myh11 ENSMUSG00000018830

Description

myosin, heavy polypeptide 11, smooth muscle [Source:MGI Symbol;Acc:MGI:102643]

Gene Synonyms

SM1, SM2, smMHC

Location

Chromosome 16: 14,012,399-14,109,236 reverse strand.

GRCm39:CM001009.3

About this gene

This gene has 4 transcripts (splice variants), 293 orthologues, 42 paralogues and is associated with 32 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000231567.2	Myh11-204	6450	1979aa	ENSMUSP00000156021.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		A0A338P6K2	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 ALT1: 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 is conserved in at least 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 ALT1,
ENSMUST00000090287.5	Myh11-201	6549	1972aa	ENSMUSP00000087756.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding		E9QPE7	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, APPRIS P4: Where the APPRIS core modules are unable to choose a clear principal CDS and there is more than one variant with a distinct (but consecutive) CCDS identifiers, APPRIS selects the longest CCDS isoform as 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 P4, 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,
ENSMUST00000230397.2	Myh11-202	6214	1938aa	ENSMUSP00000155052.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS27972	A0A2R8VHF9	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENSMUST00000230643.2	Myh11-203	1730	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-

Gene: Myh11 ENSMUSG00000018830

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Gene: Myh11 ENSMUSG00000018830

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