Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
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: Pilrb1l2 ENSRNOG00000049331

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Description

paired immunoglobin-like type 2 receptor beta 1 like 2 [Source:RGD Symbol;Acc:7556717]

Gene Synonyms

LOC102546903, LOC685048

Location

Primary_assembly 12: 22,512,532-22,518,517 forward strand.

GRCr8:CM070402.1

About this gene

This gene has 2 transcripts (splice variants), 111 orthologues and 29 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000072303.4	Pilrb1l2-202	1209	289aa	ENSRNOP00000066310.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	M0R9X6	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSRNOT00000064787.4	Pilrb1l2-201	854	238aa	ENSRNOP00000061816.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F7FGP9	APPRIS P4: Where the APPRIS core modules are unable to choose a clear principal CDS and there is more than one variant with a distinct (but consecutive) CCDS identifiers, APPRIS selects the longest CCDS isoform as 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 P4,

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Summary

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