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

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Gene: LRRC46 ENSG00000141294

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Description

leucine rich repeat containing 46 [Source:HGNC Symbol;Acc:25047]

Gene Synonyms

MGC16309

Location

Chromosome 17: 45,908,993-45,915,079 forward strand.

GRCh37:CM000679.1

About this gene

This gene has 5 transcripts (splice variants) and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000269025.4	LRRC46-001	1922	321aa	ENSP00000269025.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS11518	A8K9Q0 Q96FV0	NM_033413.3	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000584580.1	LRRC46-002	2239	47aa	ENSP00000463232.1	Nonsense mediated decay		J3QQW4	-	-
ENST00000579971.1	LRRC46-004	872	98aa	ENSP00000462585.1	Nonsense mediated decay		J3KSP7	-	-
ENST00000579742.1	LRRC46-003	847	47aa	ENSP00000463930.1	Nonsense mediated decay		J3QQW4	-	-
ENST00000584809.1	LRRC46-005	859	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-

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Summary

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