Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
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: Rinl ENSRNOG00000025354

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Description

Ras and Rab interactor-like [Source:RGD Symbol;Acc:1310133]

Gene Synonyms

LOC292760, RGD1310133

Location

Primary_assembly 1: 93,204,789-93,215,851 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 3 transcripts (splice variants), 106 orthologues and 6 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000036907.6	Rinl-201	3001	568aa	ENSRNOP00000034246.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6J9L1 D3ZP73	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 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,
ENSRNOT00000078156.3	Rinl-202	2869	524aa	ENSRNOP00000073226.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K4Y9	-
ENSRNOT00000139379.1	Rinl-203	2093	562aa	ENSRNOP00000106412.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,

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Summary

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