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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: CHURC1-FNTB ENSG00000125954

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Description

CHURC1-FNTB readthrough [Source:HGNC Symbol;Acc:42960]

Location

Chromosome 14: 65,381,203-65,528,521 forward strand.

GRCh37:CM000676.1

About this gene

This gene has 4 transcripts (splice variants) and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000549987.1	CHURC1-FNTB-001	1468	472aa	ENSP00000447121.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		B3KSC2 B4DJ86 B4DL54 H0YHI0	NM_001202559.1	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, 5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,
ENST00000553743.1	CHURC1-FNTB-004	207	69aa	ENSP00000450692.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		H0YJ25	-	5' and 3' truncations in transcript evidence prevent annotation of the start and the end of the CDS.CDS 5' and 3' incomplete,
ENST00000552941.1	CHURC1-FNTB-002	1847	107aa	ENSP00000449668.1	Nonsense mediated decay		-	-	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,
ENST00000551823.1	CHURC1-FNTB-003	517	85aa	ENSP00000449709.1	Nonsense mediated decay		H0YIM9	-	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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