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

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Gene: olfcq8 ENSDARG00000056009

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Description

olfactory receptor C family, q8 [Source:ZFIN;Acc:ZDB-GENE-050419-176]

Gene Synonyms

Dr16-7, H09, si:ch211-127a20.4, v2rh9

Location

Chromosome 18: 33,464,345-33,473,581 forward strand.

GRCz11:CM002902.2

About this gene

This gene has 2 transcripts (splice variants), 470 orthologues and 63 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000059447.6	olfcq8-201	2658	885aa	ENSDARP00000059446.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1QSU5	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, APPRIS P5: Where the APPRIS core modules are unable to choose a clear principal variant and none of the candidate variants are annotated by CCDS, APPRIS selects the longest of the candidate isoforms 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 P5,
ENSDART00000131769.2	olfcq8-202	2355	784aa	ENSDARP00000122012.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A3KQH8	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, 5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,

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Summary

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