DNAJC19


Summary: The protein encoded by this gene is thought to be part of a complex involved in the ATP-dependent transport of transit peptide-containing proteins from the inner cell membrane to the mitochondrial matrix. Defects in this gene are a cause of 3-methylglutaconic aciduria type 5 (MGA5), also known as dilated cardiomyopathy with ataxia (DCMA). Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 1, 2, 6, 10, 14 and 19. [provided by RefSeq, Jan 2012].

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GO terms in DNAJC19


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Term Type
Evidence Type
GO Term ID
GO Des.
MF IBA GO:0001671 ATPase activator activity
MF IPI GO:0005515 protein binding
MF IBA GO:0008565 protein transporter activity
CC IBA GO:0001405 presequence translocase-associated import motor
CC IDA GO:0005739 mitochondrion
CC IDA GO:0005743 mitochondrial inner membrane
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Gene expression in normal tissue: DNAJC19

Gene-model tissue-cancer distribution: Bubble Plot

undefinetissue: undefine cancer: undefined model num: 0undefinedtissue: undefined cancer: PANCAN model num: 1

Gene-drug pathway distribution

Pathways in DNAJC19


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Database
Pathway ID
Pathway Des.
reactome R-HSA-1268020 Mitochondrial protein import
reactome R-HSA-392499 Metabolism of proteins
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Gene-Drug: Aster Plot


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Drug ID
Drug Name
Model Num.
iGMDRD190 Nilotinib 1
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Gene in drug-gene network: Network Plot

Gene-drug targets distribution

Gene Structure: PDB

Models in DNAJC19

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Level
Reference ID
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Cancer
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