Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
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  - Gene tree
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Ontologies
Phenotypes
Genetic Variation
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- Structural variants
Gene expression
Pathway
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ID History
- Gene history

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Gene: LOC120093759 ENSRNOG00000046224

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Description

olfactory receptor 63-like [Source:RGD Symbol;Acc:41304589]

Location

Primary_assembly 7: 12,782,691-12,788,381 forward strand.

mRatBN7.2:CM026980.1

About this gene

This gene has 2 transcripts (splice variants), 140 orthologues, 232 paralogues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000113913.1	LOC120093759-202	1196	325aa	ENSRNOP00000081614.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZVD7	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 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,
ENSRNOT00000071599.2	LOC120093759-201	1095	314aa	ENSRNOP00000065476.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	M0R7P4	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,

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Summary

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