Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
  - Paralogues
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: LRRC71 ENSBTAG00000012348

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Description

leucine rich repeat containing 71 [Source:VGNC Symbol;Acc:VGNC:31025]

Location

Primary_assembly 3: 13,925,539-13,938,200 reverse strand.

ARS-UCD1.3:CM008170.2

About this gene

This gene has 5 transcripts (splice variants) and 163 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000107227.1	LRRC71-204	2261	652aa	ENSBTAP00000081378.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSBTAT00000113789.1	LRRC71-205	4242	515aa	ENSBTAP00000102946.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000112274.1	LRRC71-201	4062	466aa	ENSBTAP00000079459.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000112967.1	LRRC71-202	3903	402aa	ENSBTAP00000084929.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000016383.7	LRRC71-203	2046	559aa	ENSBTAP00000016383.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1BDU2	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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