Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
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: Nlrp1b ENSRNOG00000048125

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Description

NLR family, pyrin domain containing 1B [Source:RGD Symbol;Acc:1593294]

Gene Synonyms

AABR07029890.1, LOC691998

Location

Primary_assembly 10: 55,843,001-55,912,774 reverse strand.

mRatBN7.2:CM026983.1

About this gene

This gene has 1 transcript (splice variant), 91 orthologues and 21 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000075185.3	Nlrp1b-201	3549	1182aa	ENSRNOP00000064378.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	M0R4T2	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 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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