Summary
- Splice variants
- Transcript comparison
- Gene alleles
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- GO: Anatomical entity
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Gene: Gm4668 ENSMUSG00000111243

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Description

predicted gene 4668 [Source:MGI Symbol;Acc:MGI:3782849]

Location

Chromosome 9: 116,004,358-116,024,114 forward strand.

GRCm39:CM001002.3

About this gene

This gene has 14 transcripts (splice variants).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	Flags
ENSMUST00000369693.1	Gm4668-204	1613	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,
ENSMUST00000369701.1	Gm4668-212	1855	No protein	-	lncRNA		A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.GENCODE Basic,
ENSMUST00000369695.1	Gm4668-206	1687	No protein	-	lncRNA		A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.GENCODE Basic,
ENSMUST00000369694.1	Gm4668-205	1424	No protein	-	lncRNA		-
ENSMUST00000369696.1	Gm4668-207	1216	No protein	-	lncRNA		-
ENSMUST00000369702.1	Gm4668-213	1177	No protein	-	lncRNA		-
ENSMUST00000214742.4	Gm4668-201	1101	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,
ENSMUST00000369697.1	Gm4668-208	1008	No protein	-	lncRNA		-
ENSMUST00000243138.2	Gm4668-203	973	No protein	-	lncRNA		-
ENSMUST00000369699.1	Gm4668-210	949	No protein	-	lncRNA		-
ENSMUST00000369698.1	Gm4668-209	924	No protein	-	lncRNA		-
ENSMUST00000242963.2	Gm4668-202	778	No protein	-	lncRNA		-
ENSMUST00000369700.1	Gm4668-211	445	No protein	-	lncRNA		-
ENSMUST00000369703.1	Gm4668-214	304	No protein	-	lncRNA		-

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Summary

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