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

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Gene: lnx1 ENSDARG00000043323

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Description

ligand of numb-protein X 1 [Source:ZFIN;Acc:ZDB-GENE-030131-9439]

Gene Synonyms

fj78f06, lnx, si:dkey-12h2.1, wu:fj78f06, zgc:152906

Location

Chromosome 20: 22,666,548-22,740,675 forward strand.

GRCz11:CM002904.2

About this gene

This gene has 2 transcripts (splice variants), 207 orthologues and 7 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000147520.3	lnx1-202	3317	765aa	ENSDARP00000118247.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5RH21	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,
ENSDART00000143286.2	lnx1-201	492	164aa	ENSDARP00000119355.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5RH22	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,

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Summary

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