Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Cellular component
- GO: Molecular function
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: Lrrc29 ENSRNOG00000025231

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Description

leucine rich repeat containing 29 [Source:RGD Symbol;Acc:1593150]

Location

Primary_assembly 19: 50,098,275-50,113,437 reverse strand.

GRCr8:CM070409.1

About this gene

This gene has 2 transcripts (splice variants), 211 orthologues, 18 paralogues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000059663.4	Lrrc29-201	2335	621aa	ENSRNOP00000056415.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6IYN9 F7EKW8	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,
ENSRNOT00000111096.2	Lrrc29-202	1180	166aa	ENSRNOP00000096935.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AVS5	-

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Summary

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