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
External references
Supporting evidence
ID History
- Gene history

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Gene: Rp1l1 ENSRNOG00000046326

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Description

RP1 like 1 [Source:RGD Symbol;Acc:1586886]

Gene Synonyms

LOC683404

Location

Primary_assembly 15: 42,435,803-42,447,165 forward strand.

GRCr8:CM070405.1

About this gene

This gene has 1 transcript (splice variant), 212 orthologues, 1 paralogue and is associated with 11 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000070815.4	Rp1l1-201	6557	1860aa	ENSRNOP00000064085.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6K6H0 M0R410	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 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,

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Summary

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