Gene: Tlr7 ENSRNOG00000004249

Description

toll-like receptor 7 [Source:RGD Symbol;Acc:1563357]

Gene Synonyms

LOC317468, RGD1563357

Location

Primary_assembly X: 27,027,425-27,054,754 forward strand.

mRatBN7.2:CM026994.1

About this gene

This gene has 3 transcripts (splice variants), 197 orthologues, 26 paralogues and is associated with 18 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000118923.1	Tlr7-203	3875	1068aa	ENSRNOP00000094649.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AM21	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,
ENSRNOT00000104011.1	Tlr7-202	5585	1046aa	ENSRNOP00000089883.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GHR4	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,
ENSRNOT00000005620.7	Tlr7-201	4871	1046aa	ENSRNOP00000005620.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GHR4	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,