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: Opn4 ENSRNOG00000053893

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Description

opsin 4 [Source:RGD Symbol;Acc:621701]

Location

Primary_assembly 16: 9,926,902-9,949,928 reverse strand.

GRCr8:CM070406.1

About this gene

This gene has 3 transcripts (splice variants), 304 orthologues and 6 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000120847.2	Opn4-203	1994	474aa	ENSRNOP00000098459.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6KFQ9	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,
ENSRNOT00000108205.3	Opn4-202	1804	446aa	ENSRNOP00000079898.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZNW1	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,
ENSRNOT00000091315.3	Opn4-201	1611	470aa	ENSRNOP00000069548.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q8R456	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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