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: Kctd10 ENSRNOG00000047896

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Description

potassium channel tetramerization domain containing 10 [Source:RGD Symbol;Acc:1591979]

Location

Primary_assembly 12: 47,890,819-47,909,390 forward strand.

GRCr8:CM070402.1

About this gene

This gene has 2 transcripts (splice variants), 253 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000073019.4	Kctd10-201	2966	316aa	ENSRNOP00000065635.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QWU8	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 ALT1: 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 is conserved in at least 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 ALT1,
ENSRNOT00000103729.2	Kctd10-202	3149	315aa	ENSRNOP00000086565.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GF35 A6J204 Q7TPL3	APPRIS P4: Where the APPRIS core modules are unable to choose a clear principal CDS and there is more than one variant with a distinct (but consecutive) CCDS identifiers, APPRIS selects the longest CCDS isoform as 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 P4,

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Summary

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