Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Ccnl2 ENSRNOG00000018691

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Description

cyclin L2 [Source:RGD Symbol;Acc:1309149]

Gene Synonyms

LOC298686

Location

Primary_assembly 5: 171,699,689-171,711,231 forward strand.

GRCr8:CM070395.1

About this gene

This gene has 3 transcripts (splice variants), 152 orthologues, 6 paralogues and is associated with 12 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000089936.3	Ccnl2-202	2464	521aa	ENSRNOP00000068952.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QZY3	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, APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSRNOT00000096422.2	Ccnl2-203	2158	496aa	ENSRNOP00000077305.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5Y5M3	-
ENSRNOT00000025531.8	Ccnl2-201	879	224aa	ENSRNOP00000025531.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0H2UHQ5	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,

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Summary

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