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: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

Configure this page

Export data

Share this page

Bookmark this page

.

Gene: LRRC51 ENSSSCG00000014803

.

Description

leucine rich repeat containing 51 [Source:NCBI gene (formerly Entrezgene);Acc:100520208]

Location

Primary_assembly 9: 6,663,134-6,673,271 forward strand.

Sscrofa11.1:CM000820.5

About this gene

This gene has 2 transcripts (splice variants) and 204 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000016154.4	LRRC51-201	886	193aa	ENSSSCP00000015722.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1V2T3 F1SUX3	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,
ENSSSCT00000088385.1	LRRC51-202	605	175aa	ENSSSCP00000067467.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1V2A4 A0A8D1FK33	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,

.

Breeds

.

Genomic alignments

Gene tree

Orthologues

Paralogues (Not available)

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

.

Personal Data