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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: RP11-196G11.1 ENSG00000255439

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Description

Uncharacterized protein [Source:UniProtKB/TrEMBL;Acc:E9PLN8]

Location

Chromosome 16: 31,094,760-31,106,277 reverse strand.

GRCh37:CM000678.1

About this gene

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

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000529564.1	RP11-196G11.1-001	725	166aa	ENSP00000431371.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		E9PLN8	-	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,
ENST00000532364.1	RP11-196G11.1-003	499	104aa	ENSP00000460316.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		I3L3B4	-	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENST00000533518.1	RP11-196G11.1-002	2362	121aa	ENSP00000433035.1	Nonsense mediated decay		I3L1P9	-	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,

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Summary

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