Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Biological process
- 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: dnajc27 ENSDARG00000070916

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Description

DnaJ (Hsp40) homolog, subfamily C, member 27 [Source:NCBI gene;Acc:402784]

Gene Synonyms

rbj, zgc:194263, zgc:194279

Location

Chromosome 17: 33,296,436-33,309,689 forward strand.

GRCz11:CM002901.2

About this gene

This gene has 2 transcripts (splice variants), 201 orthologues and 88 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000154580.2	dnajc27-202	909	273aa	ENSDARP00000127972.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B3DHR2 Q6IMK3	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, APPRIS ALT1: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that is conserved in at least three tested species. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS ALT1,
ENSDART00000123114.3	dnajc27-201	5971	273aa	ENSDARP00000109834.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E7FCB8	APPRIS P5: Where the APPRIS core modules are unable to choose a clear principal variant and none of the candidate variants are annotated by CCDS, APPRIS selects the longest of the candidate isoforms as the principal variant. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P5,

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Summary

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