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: Klhl12 ENSRNOG00000004193

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Description

kelch-like family member 12 [Source:RGD Symbol;Acc:628717]

Gene Synonyms

C3ip1, MGC93127

Location

Primary_assembly 13: 48,455,227-48,485,641 forward strand.

GRCr8:CM070403.1

About this gene

This gene has 2 transcripts (splice variants), 197 orthologues and 52 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000119533.2	Klhl12-202	1855	575aa	ENSRNOP00000086049.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A1G7	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,
ENSRNOT00000005832.8	Klhl12-201	3168	568aa	ENSRNOP00000005832.8	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A140TA97 A6ICC3	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,

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Summary

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