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

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Gene: KLHL12 ENSG00000117153

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Description

kelch-like family member 12 [Source:HGNC Symbol;Acc:19360]

Gene Synonyms

C3IP1, DKIR, hDKIR

Location

Chromosome 1: 202,860,228-202,897,764 reverse strand.

GRCh37:CM000663.1

About this gene

This gene has 4 transcripts (splice variants) and 12 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000367261.3	KLHL12-001	3359	568aa	ENSP00000356230.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS1429	Q53G59	NM_021633.2	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000367259.1	KLHL12-002	2257	204aa	ENSP00000356228.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		Q9H7R2	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000435533.3	KLHL12-201	1999	606aa	ENSP00000416886.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding		J3QSX3 Q53G59	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000367258.1	KLHL12-003	1033	315aa	ENSP00000356227.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		J3QSX3	-	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,

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Summary

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