Loading…

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

Configure this page

Share this page

Bookmark this page

.

Gene: CXXC11 ENSG00000188011

.

Description

CXXC finger protein 11 [Source:HGNC Symbol;Acc:26585]

Gene Synonyms

C2orf85, FLJ33590

Location

Chromosome 2: 242,811,752-242,815,975 forward strand.

GRCh37:CM000664.1

About this gene

This gene has 2 transcripts (splice variants) and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000343216.3	CXXC11-001	2296	572aa	ENSP00000345374.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS42843	Q14D33	NM_173821.2	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000419912.1	CXXC11-002	2602	55aa	ENSP00000397191.1	Nonsense mediated decay		F8WB75	-	-

.

Summary

.

.