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:cabz01090165.1 ENSDARG00000039500

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Description

si:cabz01090165.1 [Source:NCBI gene (formerly Entrezgene);Acc:100333421]

Location

Chromosome 18: 49,411,417-49,447,042 forward strand.

GRCz11:CM002902.2

About this gene

This gene has 2 transcripts (splice variants), 111 orthologues and 34 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000028944.9	si:cabz01090165.1-201	2054	639aa	ENSDARP00000038014.8	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E7FB24	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,
ENSDART00000174171.2	si:cabz01090165.1-202	3104	639aa	ENSDARP00000143052.1	Nonsense mediated decay	E7FB24	-

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Summary

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