Summary
- Splice variants
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- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
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- GO: Anatomical entity
Phenotypes
Genetic Variation
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Gene: Lypd9 ENSRNOG00000002845

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Description

LY6/PLAUR domain containing 9 [Source:RGD Symbol;Acc:1586225]

Gene Synonyms

LOC691286

Location

Primary_assembly 10: 43,128,696-43,136,825 reverse strand.

GRCr8:CM070400.1

About this gene

This gene has 1 transcript (splice variant) and 50 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000003801.5	Lypd9-201	546	145aa	ENSRNOP00000003801.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HEU0 D3Z8U4	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 P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,

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Strains

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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.

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Personal Data