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: B9D2 ENSBTAG00000023452

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Description

B9 domain containing 2 [Source:VGNC Symbol;Acc:VGNC:26397]

Location

Primary_assembly 18: 50,509,252-50,517,800 reverse strand.

ARS-UCD1.3:CM008185.2

About this gene

This gene has 4 transcripts (splice variants), 161 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000116927.1	B9D2-201	1233	236aa	ENSBTAP00000092825.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSBTAT00000117198.1	B9D2-204	1106	177aa	ENSBTAP00000097521.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	APPRIS ALT1: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that is conserved in at least three tested species. 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 ALT1,
ENSBTAT00000090791.1	B9D2-202	1010	182aa	ENSBTAP00000091986.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000031968.4	B9D2-203	951	175aa	ENSBTAP00000031913.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MT24	APPRIS P4: Where the APPRIS core modules are unable to choose a clear principal CDS and there is more than one variant with a distinct (but consecutive) CCDS identifiers, APPRIS selects the longest CCDS isoform as the principal variant. 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 P4,

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Summary

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