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

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Gene: MYO1B ENSBTAG00000011256

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Description

myosin IB [Source:VGNC Symbol;Acc:VGNC:31817]

Location

Primary_assembly 2: 79,795,595-79,994,940 forward strand.

ARS-UCD2.0:CM008169.2

About this gene

This gene has 6 transcripts (splice variants), 208 orthologues and 42 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000152349.1	MYO1B-206	4731	1149aa	ENSBTAP00000107645.1	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,
ENSBTAT00000073370.3	MYO1B-204	4900	1111aa	ENSBTAP00000061301.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LV94	-
ENSBTAT00000072917.3	MYO1B-205	4875	1107aa	ENSBTAP00000056873.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MR81	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,
ENSBTAT00000014951.5	MYO1B-201	4825	1136aa	ENSBTAP00000014951.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6QLD6	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,
ENSBTAT00000076425.3	MYO1B-203	4811	1082aa	ENSBTAP00000074102.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MU95	-
ENSBTAT00000084166.2	MYO1B-202	4738	1107aa	ENSBTAP00000068263.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MBW7	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,

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Summary

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