Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
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: Klhdc8a ENSRNOG00000000036

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Description

kelch domain containing 8A [Source:RGD Symbol;Acc:1305132]

Gene Synonyms

LOC305096, RGD1305132

Location

Primary_assembly 13: 46,288,344-46,296,429 forward strand.

GRCr8:CM070403.1

About this gene

This gene has 1 transcript (splice variant), 126 orthologues and 52 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000000041.8	Klhdc8a-201	3199	350aa	ENSRNOP00000000041.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F2Z3R0	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 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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