Gene: Rilpl1 ENSMUSG00000029392

Description

Rab interacting lysosomal protein-like 1 [Source:MGI Symbol;Acc:MGI:1922945]

Gene Synonyms

2900002H16Rik, 6330559I19Rik, GOSPEL

Location

Chromosome 5: 124,631,143-124,669,454 reverse strand.

GRCm39:CM000998.3

About this gene

This gene has 4 transcripts (splice variants), 257 orthologues, 4 paralogues and is associated with 4 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000062153.12	Rilpl1-201	2249	406aa	ENSMUSP00000050014.8	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS19678	Q9JJC6	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, GENCODE Primary represents a minimal set that contains MANE Select, MANE Plus Clinical and Ensembl Canonical transcripts and transcripts containing any conserved exons and common alternative splicing events (including exons skips) that are absent from the MANE and Ensembl Canonical transcripts for protein-coding genes. Other biotypes will have the GENCODE Primary flag added to the Ensembl Canonical transcript and for lncRNA genes only this will be the transcripts with the longest genomic span.GENCODE Primary, A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.GENCODE Basic, 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, TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:1,
ENSMUST00000199125.2	Rilpl1-202	766	196aa	ENSMUSP00000142887.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		A0A0G2JES6	TSL 3: A transcript where the only support is from a single EST The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:3, 5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,
ENSMUST00000199766.5	Rilpl1-203	630	193aa	ENSMUSP00000143250.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		A0A0G2JFP1	TSL 2: A transcript where the best supporting mRNA is flagged as suspect or the support is from multiple ESTs The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:2, 5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,
ENSMUST00000200202.2	Rilpl1-204	682	97aa	ENSMUSP00000142757.2	Nonsense mediated decay		A0A0G2JEF9	TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:1, 5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,

Gene: Rilpl1 ENSMUSG00000029392

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Gene: Rilpl1 ENSMUSG00000029392

Summary

About Us

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