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
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
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Molecular interactions
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ID History
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Gene: Timeless ENSRNOG00000031916

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Description

timeless circadian regulator [Source:RGD Symbol;Acc:620939]

Gene Synonyms

Tim, rTIM, rTLP

Location

Primary_assembly 7: 1,239,450-1,263,337 forward strand.

GRCr8:CM070397.1

About this gene

This gene has 2 transcripts (splice variants), 192 orthologues and is associated with 6 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000083899.3	Timeless-201	4508	1205aa	ENSRNOP00000070516.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JY47	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,
ENSRNOT00000116339.2	Timeless-202	4331	1146aa	ENSRNOP00000085093.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GBL8	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,

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Summary

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