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

Configure this page

Export data

Share this page

Bookmark this page

.

Gene: Gm15015 ENSMUSG00000086685

.

Description

predicted gene 15015 [Source:MGI Symbol;Acc:MGI:3709319]

Location

Chromosome X: 134,363,261-134,453,133 forward strand.

GRCm39:CM001013.3

About this gene

This gene has 12 transcripts (splice variants).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	Flags
ENSMUST00000322981.1	Gm15015-202	679	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,
ENSMUST00000135491.3	Gm15015-201	2084	No protein	-	lncRNA		A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.GENCODE Basic, 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,
ENSMUST00000322982.1	Gm15015-203	1558	No protein	-	lncRNA		-
ENSMUST00000322983.1	Gm15015-204	1028	No protein	-	lncRNA		-
ENSMUST00000322986.1	Gm15015-207	1019	No protein	-	lncRNA		A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.GENCODE Basic,
ENSMUST00000322985.1	Gm15015-206	1013	No protein	-	lncRNA		-
ENSMUST00000322990.1	Gm15015-211	995	No protein	-	lncRNA		-
ENSMUST00000322987.1	Gm15015-208	878	No protein	-	lncRNA		-
ENSMUST00000322984.1	Gm15015-205	809	No protein	-	lncRNA		-
ENSMUST00000322988.1	Gm15015-209	700	No protein	-	lncRNA		-
ENSMUST00000322989.1	Gm15015-210	597	No protein	-	lncRNA		-
ENSMUST00000322991.1	Gm15015-212	387	No protein	-	lncRNA		-

.

Strains

.

Genomic alignments

Gene tree (Not available)

Orthologues (Not available)

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.

.

Personal Data