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
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: SERPINB13 ENSPTRG00000024181

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Description

serpin family B member 13 [Source:VGNC Symbol;Acc:VGNC:9951]

Location

Chromosome 18: 61,066,906-61,078,770 forward strand.

Pan_tro_3.0:CM000332.3

About this gene

This gene has 2 transcripts (splice variants), 81 orthologues and 43 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000018498.6	SERPINB13-201	3203	400aa	ENSPTRP00000017136.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2XL05 H2QEN3	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,
ENSPTRT00000083946.1	SERPINB13-202	498	165aa	ENSPTRP00000091549.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3TQM5 A0A6D2XM29	-

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Summary

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