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
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Lpin2 ENSRNOG00000014876

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Description

lipin 2 [Source:RGD Symbol;Acc:1304588]

Gene Synonyms

LOC316737

Location

Primary_assembly 9: 118,529,943-118,604,796 forward strand.

GRCr8:CM070399.1

About this gene

This gene has 4 transcripts (splice variants), 205 orthologues, 3 paralogues and is associated with 10 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000082005.3	Lpin2-202	5854	932aa	ENSRNOP00000070532.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JY62	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 ALT1: 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 is conserved in at least 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 ALT1,
ENSRNOT00000020476.9	Lpin2-201	5892	894aa	ENSRNOP00000020476.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6KF98 D3ZYB4	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,
ENSRNOT00000113074.2	Lpin2-204	5739	843aa	ENSRNOP00000092729.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AH46	-
ENSRNOT00000095983.2	Lpin2-203	3086	902aa	ENSRNOP00000078237.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZKH7	-

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Paralogues

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Personal Data