Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Myo5b ENSRNOG00000014104

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Description

myosin Vb [Source:RGD Symbol;Acc:621347]

Gene Synonyms

Myr6

Location

Primary_assembly 18: 70,311,990-70,613,918 forward strand.

GRCr8:CM070408.1

About this gene

This gene has 8 transcripts (splice variants), 232 orthologues, 42 paralogues and is associated with 11 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000154755.1	Myo5b-208	6419	2006aa	ENSRNOP00000105443.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000019512.8	Myo5b-201	6081	1846aa	ENSRNOP00000019512.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1M3R4	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,
ENSRNOT00000096247.2	Myo5b-205	5985	1850aa	ENSRNOP00000079126.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6G4V2	-
ENSRNOT00000087959.3	Myo5b-203	5958	1805aa	ENSRNOP00000072468.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K318	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,
ENSRNOT00000094389.2	Myo5b-204	5917	1828aa	ENSRNOP00000081367.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZST3	-
ENSRNOT00000117025.2	Myo5b-206	5863	1831aa	ENSRNOP00000091793.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ACS1	-
ENSRNOT00000085318.3	Myo5b-202	5415	1804aa	ENSRNOP00000069482.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JVH1	-
ENSRNOT00000138842.1	Myo5b-207	5412	1803aa	ENSRNOP00000110049.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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