Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
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Ontologies
- GO: Anatomical entity
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: Nlrp4al1 ENSRNOG00000059733

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Description

NLR family, pyrin domain containing 4A like 1 [Source:RGD Symbol;Acc:1560291]

Gene Synonyms

LOC299656, LOC691086, RGD1560291

Location

Primary_assembly 7: 14,114,807-14,147,898 reverse strand.

GRCr8:CM070397.1

About this gene

This gene has 1 transcript (splice variant), 51 orthologues and 20 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000029672.7	Nlrp4al1-201	3108	939aa	ENSRNOP00000031864.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZE70	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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