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

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Gene: szrd1 ENSDARG00000056338

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Description

SUZ RNA binding domain containing 1 [Source:NCBI gene;Acc:554231]

Gene Synonyms

wu:fb15h05, wu:fk86c07, zgc:109926

Location

Chromosome 23: 24,501,918-24,508,821 forward strand.

GRCz11:CM002907.2

About this gene

This gene has 2 transcripts (splice variants) and 212 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000078824.5	szrd1-201	2131	161aa	ENSDARP00000073284.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q504E7	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,
ENSDART00000136948.2	szrd1-202	688	55aa	ENSDARP00000123839.1	Nonsense mediated decay	F8W4Y9	-

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Summary

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