Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
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  - Gene tree
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Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
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Genetic Variation
- Variant table
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- Structural variants
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Gene: Skint10 ENSRNOG00000022988

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Description

selection and upkeep of intraepithelial T cells 10 [Source:RGD Symbol;Acc:1587504]

Gene Synonyms

LOC689876

Location

Primary_assembly 5: 133,005,833-133,124,926 reverse strand.

GRCr8:CM070395.1

About this gene

This gene has 2 transcripts (splice variants), 8 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000106746.2	Skint10-202	1059	352aa	ENSRNOP00000094776.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AIF0	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 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,
ENSRNOT00000033163.5	Skint10-201	1334	326aa	ENSRNOP00000034344.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6JZ19 F1LX26	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,

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Summary

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