Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: TLR7 ENSBTAG00000022161

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Description

toll like receptor 7 [Source:VGNC Symbol;Acc:VGNC:52836]

Location

Primary_assembly X: 130,767,590-130,787,736 reverse strand.

ARS-UCD1.3:CM008197.2

About this gene

This gene has 7 transcripts (splice variants), 197 orthologues and 23 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000029895.6	TLR7-204	4399	1055aa	ENSBTAP00000029890.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A1XC24	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,
ENSBTAT00000133396.1	TLR7-201	5502	1046aa	ENSBTAP00000091261.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000096664.1	TLR7-202	5182	1046aa	ENSBTAP00000077958.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000118401.1	TLR7-203	4795	1046aa	ENSBTAP00000093104.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000092060.1	TLR7-206	4775	1046aa	ENSBTAP00000076860.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000079344.2	TLR7-205	4380	1054aa	ENSBTAP00000071792.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MK24	-
ENSBTAT00000077162.2	TLR7-207	3788	1050aa	ENSBTAP00000061744.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A1XC24	APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1,

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Summary

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