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

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Gene: sipa1l2 ENSDARG00000061640

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Description

signal-induced proliferation-associated 1 like 2 [Source:NCBI gene (formerly Entrezgene);Acc:497350]

Location

Chromosome 11: 31,323,746-31,473,982 forward strand.

GRCz11:CM002895.2

About this gene

This gene has 4 transcripts (splice variants), 213 orthologues and 9 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000088093.6	sipa1l2-201	6697	1672aa	ENSDARP00000082526.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E7FE99	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 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,
ENSDART00000189937.1	sipa1l2-204	9875	1689aa	ENSDARP00000154714.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2R8QKB1	-
ENSDART00000180220.1	sipa1l2-202	9692	1628aa	ENSDARP00000152277.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSDART00000185073.1	sipa1l2-203	6342	1672aa	ENSDARP00000152133.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E7FE99	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,

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Summary

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