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

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Gene: RP11-529K1.3 ENSG00000260537

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Description

Uncharacterized protein [Source:UniProtKB/TrEMBL;Acc:H3BN59]

Location

Chromosome 16: 70,333,097-70,400,163 forward strand.

GRCh37:CM000678.1

About this gene

This gene has 2 transcripts (splice variants) and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000567706.1	RP11-529K1.3-002	867	261aa	ENSP00000454699.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		H3BN59	-	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, 3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENST00000565116.1	RP11-529K1.3-001	565	30aa	ENSP00000455483.1	Nonsense mediated decay		H3BPV3	-	-

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Summary

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