Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
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Molecular interactions
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ID History
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Gene: 1700047L14Rik ENSMUSG00000101762

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Description

RIKEN cDNA 1700047L14 gene [Source:MGI Symbol;Acc:MGI:1920545]

Location

Chromosome 5: 108,911,689-108,916,784 forward strand.

GRCm39:CM000998.3

About this gene

This gene has 9 transcripts (splice variants).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	Flags
ENSMUST00000329956.1	1700047L14Rik-202	596	No protein	-	lncRNA		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,
ENSMUST00000329958.1	1700047L14Rik-204	590	No protein	-	lncRNA		-
ENSMUST00000329959.1	1700047L14Rik-205	559	No protein	-	lncRNA		-
ENSMUST00000329957.1	1700047L14Rik-203	529	No protein	-	lncRNA		-
ENSMUST00000189659.3	1700047L14Rik-201	515	No protein	-	lncRNA		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,
ENSMUST00000329960.1	1700047L14Rik-206	512	No protein	-	lncRNA		-
ENSMUST00000329961.1	1700047L14Rik-207	511	No protein	-	lncRNA		-
ENSMUST00000329962.1	1700047L14Rik-208	502	No protein	-	lncRNA		-
ENSMUST00000329963.1	1700047L14Rik-209	447	No protein	-	lncRNA		-

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Summary

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