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

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Gene: mhc2d8.45b1 ENSDARG00000041705

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Description

major histocompatibility complex class II d8.45b1 [Source:NCBI gene (formerly Entrezgene);Acc:368846]

Location

Chromosome 8: 44,373,764-44,378,410 reverse strand.

GRCz11:CM002892.2

About this gene

This gene has 2 transcripts (splice variants), 413 orthologues and 21 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000098138.4	mhc2d8.45b1-201	1136	263aa	ENSDARP00000088910.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8M1NAM7	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 ALT2: 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 appear to be conserved in fewer than 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 ALT2,
ENSDART00000158784.2	mhc2d8.45b1-202	912	303aa	ENSDARP00000133249.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q95HJ4	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be 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 P2,

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Summary

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