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: LRRC39 ENSPTRG00000001002

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Description

leucine rich repeat containing 39 [Source:VGNC Symbol;Acc:VGNC:11761]

Location

Chromosome 1: 100,778,998-100,814,737 reverse strand.

Pan_tro_3.0:CM000314.3

About this gene

This gene has 2 transcripts (splice variants), 194 orthologues and 34 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000001877.5	LRRC39-201	2013	339aa	ENSPTRP00000001720.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2J8MHM5 A0A6D2XM25	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,
ENSPTRT00000058970.4	LRRC39-202	1826	335aa	ENSPTRP00000052032.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2J8MHM4 A0A6D2WMQ4	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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