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

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Gene: Serpinb1a ENSRNOG00000016581

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Description

serpin family B member 1A [Source:RGD Symbol;Acc:1306203]

Gene Synonyms

LOC291091, MGC112650, Serpinb1

Location

Primary_assembly 17: 31,799,415-31,808,166 forward strand.

GRCr8:CM070407.1

About this gene

This gene has 1 transcript (splice variant), 276 orthologues and 48 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000059854.5	Serpinb1a-201	1610	379aa	ENSRNOP00000056600.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q4G075	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,

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Summary

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