Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Skint2 ENSRNOG00000042047

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Description

selection and upkeep of intraepithelial T cells 2 [Source:RGD Symbol;Acc:1566327]

Gene Synonyms

AABR07049648.1, LOC313485, RGD1566327, Skint4

Location

Primary_assembly 5: 132,112,328-132,138,084 forward strand.

GRCr8:CM070395.1

About this gene

This gene has 2 transcripts (splice variants), 46 orthologues and 22 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000116511.2	Skint2-202	1293	430aa	ENSRNOP00000081877.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZVY8	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,
ENSRNOT00000041421.7	Skint2-201	1188	395aa	ENSRNOP00000043233.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZBR5	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,

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Summary

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