Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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: spint2 ENSDARG00000069476

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Description

serine peptidase inhibitor, Kunitz type, 2 [Source:ZFIN;Acc:ZDB-GENE-061013-323]

Gene Synonyms

fb52h04, fe24a06, wu:fb52h04, wu:fe24a06, zgc:153795

Location

Chromosome 15: 20,239,141-20,250,516 forward strand.

GRCz11:CM002899.2

About this gene

This gene has 2 transcripts (splice variants), 200 orthologues and 13 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000101152.5	spint2-201	2024	431aa	ENSDARP00000091926.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1QEV7	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,
ENSDART00000152473.2	spint2-202	836	265aa	ENSDARP00000126920.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	R4GEK7	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,

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Summary

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