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
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Tle7 ENSRNOG00000038741

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Description

TLE family member 7 [Source:RGD Symbol;Acc:6498598]

Gene Synonyms

AABR07043818.1, LOC100910419, LOC292014, RGD1564655

Location

Primary_assembly 19: 54,982,049-54,994,085 forward strand.

GRCr8:CM070409.1

About this gene

This gene has 1 transcript (splice variant), 249 orthologues and 6 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000098556.2	Tle7-201	2070	437aa	ENSRNOP00000092662.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AID4	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 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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Paralogues

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