Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Molecular function
- GO: Biological process
- GO: Cellular component
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

Gene: sinup ENSDARG00000017163

Description

siaz-interacting nuclear protein [Source:ZFIN;Acc:ZDB-GENE-050913-2]

Gene Synonyms

zgc:136513

Location

GRCz11:CM002888.2

About this gene

This gene has 2 transcripts (splice variants), 2 orthologues and is associated with 6 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000003621.9	sinup-201	578	145aa	ENSDARP00000019122.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5TYU1	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,
ENSDART00000132356.2	sinup-202	609	93aa	ENSDARP00000119585.1	Nonsense mediated decay	Q1RM31	-

Summary