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: Myo9b ENSRNOG00000016256

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Description

myosin IXb [Source:RGD Symbol;Acc:3146]

Gene Synonyms

myr 5

Location

Primary_assembly 16: 17,979,439-18,064,332 forward strand.

GRCr8:CM070406.1

About this gene

This gene has 6 transcripts (splice variants), 203 orthologues, 42 paralogues and is associated with 4 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000148219.1	Myo9b-206	7509	2120aa	ENSRNOP00000110699.1	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,
ENSRNOT00000083651.3	Myo9b-203	7479	2110aa	ENSRNOP00000071138.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JZQ4	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,
ENSRNOT00000087576.3	Myo9b-205	7461	2104aa	ENSRNOP00000074785.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K8Y6	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,
ENSRNOT00000086105.3	Myo9b-204	7341	2064aa	ENSRNOP00000070646.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JYG5	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,
ENSRNOT00000045099.7	Myo9b-201	7248	2015aa	ENSRNOP00000048368.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QNB6	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,
ENSRNOT00000081321.3	Myo9b-202	7239	2012aa	ENSRNOP00000073856.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2R806	-

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Summary

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