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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: LHX4 ENSG00000121454

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Description

LIM homeobox 4 [Source:HGNC Symbol;Acc:21734]

Gene Synonyms

CPHD4, Gsh4

Location

Chromosome 1: 180,199,421-180,249,380 forward strand.

GRCh37:CM000663.1

About this gene

This gene has 3 transcripts (splice variants), 11 paralogues and is associated with 6 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000263726.2	LHX4-001	7083	390aa	ENSP00000263726.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS1338	Q5RLJ1 Q5RLJ2 Q5RLJ3 Q969G2 Q96JP7	NM_033343.3	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000561113.1	LHX4-002	603	151aa	ENSP00000452783.1	Nonsense mediated decay		-	-	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,
ENST00000558139.1	LHX4-003	721	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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