Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
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: Sigirr ENSRNOG00000015593

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Description

single Ig and TIR domain containing [Source:RGD Symbol;Acc:1306732]

Gene Synonyms

LOC309106, MGC114558, RGD1306732, TIR8

Location

Primary_assembly 1: 205,627,708-205,637,802 reverse strand.

GRCr8:CM070391.1

About this gene

This gene has 4 transcripts (splice variants), 175 orthologues and 10 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000044393.6	Sigirr-201	1636	423aa	ENSRNOP00000039252.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LY14	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,
ENSRNOT00000163850.1	Sigirr-204	1781	387aa	ENSRNOP00000111127.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HXP4	-
ENSRNOT00000129370.1	Sigirr-203	1597	401aa	ENSRNOP00000099184.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000054874.4	Sigirr-202	1398	410aa	ENSRNOP00000051758.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QR48	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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