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

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Gene: DISC1FP1 ENSG00000261645

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Description

DISC1 fusion partner 1 (non-protein coding) [Source:HGNC Symbol;Acc:33625]

Gene Synonyms

Boymaw

Location

Chromosome 11: 89,984,400-90,648,220 forward strand.

GRCh37:CM000673.1

About this gene

This gene has 5 transcripts (splice variants).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	RefSeq	Flags
ENST00000569513.1	DISC1FP1-002	1734	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	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,
ENST00000562678.1	DISC1FP1-004	796	No protein	-	lincRNA		-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000562245.1	DISC1FP1-003	774	No protein	-	lincRNA		-	-
ENST00000561596.1	DISC1FP1-001	545	No protein	-	lincRNA		-	-
ENST00000563681.1	DISC1FP1-005	466	No protein	-	lincRNA		-	-

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Summary

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