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: si:ch211-113g11.6 ENSDARG00000070442

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Description

si:ch211-113g11.6 [Source:NCBI gene (formerly Entrezgene);Acc:559008]

Location

Chromosome 16: 29,407,666-29,452,039 reverse strand.

GRCz11:CM002900.2

About this gene

This gene has 2 transcripts (splice variants), 80 orthologues and 36 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000148960.3	si:ch211-113g11.6-202	8240	474aa	ENSDARP00000124606.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A3KH15	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,
ENSDART00000148405.3	si:ch211-113g11.6-201	8611	608aa	ENSDARP00000124866.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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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