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

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Gene: saa ENSDARG00000045999

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Description

serum amyloid A [Source:ZFIN;Acc:ZDB-GENE-040927-15]

Gene Synonyms

zgc:103580

Location

Chromosome 7: 12,950,507-12,956,434 forward strand.

GRCz11:CM002891.2

About this gene

This gene has 2 transcripts (splice variants), 382 orthologues, 1 paralogue and is associated with 6 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000067629.5	saa-201	638	121aa	ENSDARP00000067628.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q642J9	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,
ENSDART00000158004.2	saa-202	378	121aa	ENSDARP00000138355.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q642J9	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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