Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
  - Paralogues
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

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Gene: ENSSSCG00000003080

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Description

immunoglobulin superfamily member 23 [Source:VGNC Symbol;Acc:VGNC:89066]

Location

Primary_assembly 6: 51,131,773-51,150,585 forward strand.

Sscrofa11.1:CM000817.5

About this gene

This gene has 3 transcripts (splice variants) and 51 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000091924.1	-	4458	253aa	ENSSSCP00000079270.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D0UUD9 A0A8W4FK48	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,
ENSSSCT00000003418.5	-	2375	278aa	ENSSSCP00000003335.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1RMS9	-
ENSSSCT00000102953.1	-	977	279aa	ENSSSCP00000076614.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D1K2B9 A0A8W4FBB6	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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