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

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Gene: PBX4 ENSG00000105717

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Description

pre-B-cell leukemia homeobox 4 [Source:HGNC Symbol;Acc:13403]

Location

Chromosome 19: 19,672,522-19,729,725 reverse strand.

GRCh37:CM000681.1

About this gene

This gene has 5 transcripts (splice variants), 199 orthologues and 13 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000251203.9	PBX4-001	1724	374aa	ENSP00000251203.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS12406	Q9BYU1	NM_025245.2	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, A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.GENCODE Basic,
ENST00000557978.2	PBX4-003	1130	116aa	ENSP00000453348.1	Nonsense mediated decay		H0YL59	-	-
ENST00000558222.1	PBX4-002	1034	116aa	ENSP00000453069.1	Nonsense mediated decay		H0YL59	-	-
ENST00000559735.1	PBX4-005	769	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-
ENST00000558276.3	PBX4-006	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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