Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

Configure this page

Share this page

Bookmark this page

.

Gene: PLCG2 ENSBTAG00000002103

.

Description

phospholipase C gamma 2 [Source:VGNC Symbol;Acc:VGNC:32989]

Location

Primary_assembly 18: 8,303,201-8,467,942 forward strand.

ARS-UCD2.0:CM008185.2

About this gene

This gene has 5 transcripts (splice variants), 225 orthologues and 13 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000131694.2	PLCG2-202	4299	1320aa	ENSBTAP00000078749.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9S613	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,
ENSBTAT00000074574.3	PLCG2-204	4565	1189aa	ENSBTAP00000072956.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MMD9	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,
ENSBTAT00000106611.2	PLCG2-201	4352	1297aa	ENSBTAP00000094275.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9T8I8	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,
ENSBTAT00000068519.3	PLCG2-205	4141	1227aa	ENSBTAP00000056752.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MQS5	-
ENSBTAT00000002717.8	PLCG2-203	3951	1227aa	ENSBTAP00000002717.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1N4C7	-

.

Summary

.

.