Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
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  - Orthologues
  - Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
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ID History
- Gene history

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Gene: 2900052N01Rik ENSMUSG00000099696

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Description

RIKEN cDNA 2900052N01 gene [Source:MGI Symbol;Acc:MGI:1920290]

Location

Chromosome 9: 46,823,892-46,838,665 forward strand.

GRCm39:CM001002.3

About this gene

This gene has 15 transcripts (splice variants) and 3 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	Flags
ENSMUST00000191603.7	2900052N01Rik-203	2695	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, 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,
ENSMUST00000189828.4	2900052N01Rik-202	2608	No protein	-	lncRNA		A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.GENCODE Basic, 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,
ENSMUST00000185568.3	2900052N01Rik-201	2381	No protein	-	lncRNA		A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.GENCODE Basic, TSL 5: A transcript where no single transcript supports the model structure. 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:5,
ENSMUST00000246357.1	2900052N01Rik-207	2321	No protein	-	lncRNA		-
ENSMUST00000314714.1	2900052N01Rik-208	2314	No protein	-	lncRNA		-
ENSMUST00000314717.1	2900052N01Rik-211	2281	No protein	-	lncRNA		-
ENSMUST00000314718.1	2900052N01Rik-212	2205	No protein	-	lncRNA		-
ENSMUST00000314715.1	2900052N01Rik-209	2127	No protein	-	lncRNA		-
ENSMUST00000242591.1	2900052N01Rik-205	2069	No protein	-	lncRNA		-
ENSMUST00000244520.2	2900052N01Rik-206	1751	No protein	-	lncRNA		-
ENSMUST00000314716.1	2900052N01Rik-210	1573	No protein	-	lncRNA		-
ENSMUST00000241563.1	2900052N01Rik-204	1165	No protein	-	lncRNA		-
ENSMUST00000314719.1	2900052N01Rik-213	576	No protein	-	lncRNA		A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.GENCODE Basic,
ENSMUST00000314721.1	2900052N01Rik-215	404	No protein	-	lncRNA		-
ENSMUST00000314720.1	2900052N01Rik-214	274	No protein	-	lncRNA		-

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Strains

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Genomic alignments

Gene tree

Orthologues

Paralogues (Not available)

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data