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

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Gene: dnah9l ENSDARG00000062630

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Description

dynein, axonemal, heavy polypeptide 9 like [Source:ZFIN;Acc:ZDB-GENE-050506-1]

Gene Synonyms

dhc9

Location

Chromosome 6: 10,586,019-10,698,125 reverse strand.

GRCz11:CM002890.2

About this gene

This gene has 5 transcripts (splice variants), 101 orthologues and 16 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000187206.1	dnah9l-204	12807	4268aa	ENSDARP00000150502.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2R8RQB1	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,
ENSDART00000192319.1	dnah9l-205	12660	4219aa	ENSDARP00000157433.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2R8QP75	-
ENSDART00000150908.2	dnah9l-201	11802	3933aa	ENSDARP00000126195.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	I3ITD2	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,
ENSDART00000151376.2	dnah9l-202	792	41aa	ENSDARP00000126066.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	I3IT15	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENSDART00000151636.2	dnah9l-203	772	258aa	ENSDARP00000126155.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	I3IT93	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, 5' and 3' truncations in transcript evidence prevent annotation of the start and the end of the CDS.CDS 5' and 3' incomplete,

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Summary

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