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
External references
Supporting evidence
ID History
- Gene history

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Gene: KLHL15 ENSPTRG00000021744

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Description

kelch like family member 15 [Source:VGNC Symbol;Acc:VGNC:2749]

Location

Chromosome X: 24,137,035-24,183,957 reverse strand.

Pan_tro_3.0:CM000336.3

About this gene

This gene has 2 transcripts (splice variants), 198 orthologues and 60 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000100016.1	KLHL15-202	6549	604aa	ENSPTRP00000070451.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2W5E1 K7BHE3	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,
ENSPTRT00000051043.4	KLHL15-201	6238	604aa	ENSPTRP00000044260.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2W5E1 K7BHE3	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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