Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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3691 to 3700 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3691
DnaJ heat shock protein family (Hsp40) member C3
ACPHD, ERdj6, HP58, P58, P58IPK, PRKRI, p58(IPK)
Ataxia with hearing loss and diabetes mellitus, Diabetes mellitus type 2, Diabetes mellitus-central and peripheral neurodegeneration syndrome, Prostatic neoplasms

3692
DnaJ heat shock protein family (Hsp40) member C30
LHONAR, LHONAR1, MC1DN38, WBSCR18
Leber hereditary optic neuropathy, Optic atrophy, Williams syndrome

3693
DnaJ heat shock protein family (Hsp40) member C5
CLN4, CLN4B, CSP, DNAJC5A, NCL, mir-941-2, mir-941-3, mir-941-4, mir-941-5
Neuronal ceroid lipofuscinosis, Hypertension, Metabolic syndrome, Diabetes mellitus type 2

3694
DnaJ heat shock protein family (Hsp40) member C5 beta
CSP-beta
Coronary artery disease, Epilepsy

3695
DnaJ heat shock protein family (Hsp40) member C5 gamma
CSP-gamma
Psoriasis

3696
DnaJ heat shock protein family (Hsp40) member C6
DJC6, PARK19
Juvenile parkinsonism, Autoimmune thrombocytopenic purpura, Hepatocellular carcinoma, Dementia, Hemiparkinsonism, Osteonecrosis of the femoral head, Parkinson disease, Diabetes mellitus-central and peripheral neurodegeneration syndrome

3697
DnaJ heat shock protein family (Hsp40) member C7
DJ11, DJC7, TPR2, TTC2
Amyotrophic lateral sclerosis, Bipolar disorder, Epilepsy, Major depressive disorder, Schizophrenia

3698
DnaJ heat shock protein family (Hsp40) member C9
HDJC9, JDD1, SB73
Joubert syndrome

3699
Dynein axonemal light chain 1
C14orf168, CILD16, LC1
Ciliary dyskinesia, Color vision deficiency, Congenital nasopharyngeal atresia

3700
Dynein axonemal light chain 4
MRMV3, PIG27
Breast cancer, Congenital mirror movements, Mirror movements, Polycystic ovary syndrome