Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
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: MHCY2B2 ENSGALG00010002386

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Description

major histocompatibility complex Y, class II beta 2 [Source:NCBI gene (formerly Entrezgene);Acc:425256]

Gene Synonyms

BLB3, RJF.Contig1.LOC12.MHCY2B2

Location

Primary_assembly 16: 1,658,326-1,668,339 forward strand.

bGalGal1.mat.broiler.GRCg7b:CM028497.1

About this gene

This gene has 3 transcripts (splice variants), 612 orthologues and 9 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	Flags
ENSGALT00010005471.1	MHCY2B2-203	3468	279aa	ENSGALP00010003310.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	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,
ENSGALT00010005473.1	MHCY2B2-201	2097	330aa	ENSGALP00010003312.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-
ENSGALT00010005469.1	MHCY2B2-202	1587	281aa	ENSGALP00010003308.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	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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