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

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Gene: LHX8 ENSBTAG00000019192

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Description

LIM homeobox 8 [Source:VGNC Symbol;Acc:VGNC:30877]

Location

Primary_assembly 3: 69,636,164-69,662,292 reverse strand.

ARS-UCD2.0:CM008170.2

About this gene

This gene has 2 transcripts (splice variants), 265 orthologues and 21 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000025544.6	LHX8-201	1808	377aa	ENSBTAP00000025544.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1BBB7	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,
ENSBTAT00000079551.3	LHX8-202	1608	293aa	ENSBTAP00000063763.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1M1Y4	-

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Summary

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