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DNAJC19

DNAJC19

Protein-coding gene in the species Homo sapiens

translocase subunit TIM14 is an enzyme that in humans is encoded by the DNAJC19 gene on chromosome 3. TIM14 belongs to the DnaJ family, which has been

DNAJC19

PAM16

Protein-coding gene in the species Homo sapiens

ATP-dependent protein translocation into the mitochondrial matrix, inhibition of DNAJC19 stimulation of HSPA9/Mortalin ATPase activity, and granulocyte-macrophage

PAM16

3-Methylglutaconic aciduria

Medical condition

(so-called apoptosis).[citation needed] Type IV 250951 ? ? 3-Methylglutaconic aciduria type IV Type V 610198 DNAJC19 3q26.3 3-Methylglutaconic aciduria type V

3-Methylglutaconic aciduria

3-Methylglutaconic_aciduria

Dilated cardiomyopathy with ataxia syndrome

Medical condition

atrophy. This syndrome is caused by autosomal recessive mutations in the DNAJC19 gene, in chromosome 3q26.33 This disorder is very rare, with only between

Dilated cardiomyopathy with ataxia syndrome

Dilated_cardiomyopathy_with_ataxia_syndrome

List of human protein-coding genes 2

Q9Y2G8 4415 DNAJC17 HGNC:25556; Q9NVM6 4416 DNAJC18 HGNC:28429; Q9H819 4417 DNAJC19 HGNC:30528; Q96DA6 4418 DNAJC21 HGNC:27030; Q5F1R6 4419 DNAJC22 HGNC:25802;

List of human protein-coding genes 2

List_of_human_protein-coding_genes_2

List of OMIM disorder codes

aciduria type III; 258501; OPA3 3-Methylglutaconic aciduria type V; 610198; DNAJC19 46XX true hermaphroditism; 400045; SRY 46XY complete gonadal dysgenesis;

List of OMIM disorder codes

List_of_OMIM_disorder_codes