Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: KLHL17 ENSBTAG00000013813

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Description

kelch like family member 17 [Source:VGNC Symbol;Acc:VGNC:30646]

Location

Primary_assembly 16: 51,498,246-51,513,194 reverse strand.

ARS-UCD2.0:CM008183.2

About this gene

This gene has 6 transcripts (splice variants), 202 orthologues and 54 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000125256.1	KLHL17-203	4541	1179aa	ENSBTAP00000089507.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SW09	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 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,
ENSBTAT00000115184.1	KLHL17-202	3123	640aa	ENSBTAP00000100796.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TUK3	-
ENSBTAT00000019320.5	KLHL17-201	3012	603aa	ENSBTAP00000019320.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1BMJ2	-
ENSBTAT00000018351.5	KLHL17-205	2755	643aa	ENSBTAP00000018351.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1B7Y3	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,
ENSBTAT00000117360.1	KLHL17-206	2642	602aa	ENSBTAP00000102124.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TZH4	-
ENSBTAT00000076507.2	KLHL17-204	2160	621aa	ENSBTAP00000064814.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1N4N7	-

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Summary

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