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

Configure this page

Share this page

Bookmark this page

.

Gene: HHLA2 ENSSSCG00000027275

.

Description

HHLA2 member of B7 family [Source:VGNC Symbol;Acc:VGNC:88876]

Location

Primary_assembly 13: 151,156,800-151,298,330 reverse strand.

Sscrofa11.1:CM000824.5

About this gene

This gene has 3 transcripts (splice variants), 103 orthologues and 24 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000024843.4	HHLA2-203	4037	409aa	ENSSSCP00000020031.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1SPN2 I3L7M5	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,
ENSSSCT00000058172.2	HHLA2-202	3934	383aa	ENSSSCP00000042429.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287AF24 A0A8D1JAU2	-
ENSSSCT00000071915.2	HHLA2-201	2811	376aa	ENSSSCP00000072515.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2RDM5	-

.

Summary

.

.