Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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6541 to 6550 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

6541
Junctional cadherin 5 associated
KIAA1462
Alzheimer disease, Attention deficit hyperactivity disorder, Ischemic heart disease, Obstructive pulmonary disease, Liver cirrhosis, Coronary artery disease, Diverticulitis, Heart disease, Insomnia, Large artery stroke, Major depressive disorder, Migraine, Myocardial infarction, Myocardial ischemia, Nonalcoholic fatty liver disease
View all (4 more)

6542
Jun dimerization protein 2
JUNDM2
Asthma, Eczema, Basal cell carcinoma, Hepatocellular carcinoma, Keratinocyte carcinoma, Multiple sclerosis, Non-melanoma skin carcinoma, Obesity, Rheumatoid arthritis, Skin cancer, Skin neoplasms

6543
Junctional cadherin complex regulator
C11orf63
Alzheimer disease

6544
JNK1/MAPK8 associated membrane protein
C14orf100, C24orf100, CDA06, HSPC213, HSPC327, JAMP
Schizophrenia

6545
Jumonji domain containing 1C
KDM3C, TRIP-8, TRIP8
22q11.2 deletion syndrome, Alzheimer disease, Juvenile arthritis, Asthma, Atrial fibrillation, Atrial flutter, Attention deficit hyperactivity disorder, Autism, Breast cancer, Adenoid cystic carcinoma, Cholecystolithiasis, Neurodevelopmental disorder, Coronary artery disease, Digeorge syndrome, Myoclonic encephalopathy
View all (14 more)

6546
Jumonji domain containing 6, arginine demethylase and lysine hydroxylase
PSR, PTDSR, PTDSR1
Breast neoplasms, Melanoma, Mesothelioma, Ovarian neoplasms, Prostatic neoplasms, Schizophrenia, Uveal melanoma

6547
JMJD7-PLA2G4B readthrough
HsT16992, cPLA2-beta
Neurodevelopmental disorder

6548
Jumonji domain containing 8
C16orf20, PP14397
Cerebellar ataxia, Spinocerebellar ataxia

6549
Junction mediating and regulatory protein, p53 cofactor
WHAMM2, WHDC1L3
Hearing loss, Diabetes mellitus type 2

6550
Junctophilin 1
CMT2K, CMYO25, JP-1, JP1
Central nervous system cancer, Charcot-marie-tooth disease, Congenital myopathy, Dejerine-sottas disease, Glioblastoma, Glioma, Hereditary motor and sensory neuropathies, Hypertrophic neuropathy, Peroneal muscle atrophy, Roussy-levy syndrome, Scoliosis, Diabetes mellitus type 2, Uterine fibroid