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

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Gene: B9D1 ENSSSCG00000039681

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Description

B9 domain containing 1 [Source:VGNC Symbol;Acc:VGNC:85737]

Location

Primary_assembly 12: 60,162,713-60,171,961 forward strand.

Sscrofa11.1:CM000823.5

About this gene

This gene has 2 transcripts (splice variants), 188 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000055077.2	B9D1-202	1558	204aa	ENSSSCP00000056023.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287BIY2 A0A8D0W5H9	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,
ENSSSCT00000089213.2	B9D1-201	543	174aa	ENSSSCP00000071644.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2RIX8 A0A8D1YM65	-

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Summary

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