Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
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: SLC25A22 ENSGALG00010022990

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Description

solute carrier family 25 member 22 [Source:NCBI gene (formerly Entrezgene);Acc:429678]

Location

Primary_assembly 5: 15,405,364-15,440,975 forward strand.

bGalGal1.mat.broiler.GRCg7b:CM028486.1

About this gene

This gene has 4 transcripts (splice variants), 119 orthologues and 37 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSGALT00010055978.1	SLC25A22-201	2621	445aa	ENSGALP00010033876.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8V0ZTQ5	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,
ENSGALT00010055973.1	SLC25A22-204	3126	364aa	ENSGALP00010033873.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8V0ZKH9	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,
ENSGALT00010055984.1	SLC25A22-202	3008	332aa	ENSGALP00010033881.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8V0ZTR1	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,
ENSGALT00010055962.1	SLC25A22-203	1397	93aa	ENSGALP00010033867.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8V0ZSQ5	-

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Summary

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