Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
6521 to 6530 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

6521
Interacts with SUPT6H, CTD assembly factor 1
-
Developmental disorder, Heart disease, Upper aerodigestive tract neoplasm

6522
Iodotyrosine deiodinase
C6orf71, DEHAL1, IYD-1, TDH4
Alzheimer disease, Congenital hypothyroidism, Thyroid dyshormonogenesis, Panic disorder, Diabetes mellitus type 2

6523
IZUMO1 receptor, JUNO
FOLR4, FR-delta, Folbp3, JUNO
Astrocytoma, Central nervous system cancer, Chagas cardiomyopathy, Colorectal cancer, Glioblastoma, Glioma, Obstructive sleep apnea syndrome

6524
IZUMO family member 3
C9orf134, bA20A20.1
Attention deficit hyperactivity disorder, Auditory system disease, Autism, Carotid artery disease, Central nervous system cancer, Color vision deficiency, Glioblastoma, Glioma, Insomnia, Scoliosis, Substance abuse

6525
Jade family PHD finger 2
JADE-2, PHF15
Attention deficit hyperactivity disorder, Bipolar disorder, Central nervous system cancer, Diabetes mellitus type 2, Endometriosis, Glioblastoma, Glioma, Hypertension, Lung cancer, Multiple sclerosis, Prostatic neoplasms, Squamous cell carcinoma, Substance abuse

6526
Jade family PHD finger 3
JADE-3, PHF16
Uterine fibroid

6527
Jagged canonical Notch ligand 1
AGS, AGS1, AHD, AWS, CD339, CMT2HH, DCHE, HJ1, JAGL1
Alagille syndrome, Autism, Bone disease, Breast neoplasms, Congenital anomalies of the kidney and urinary tract, Adenoid cystic carcinoma, Pancreatic ductal carcinoma, Cataract, Charcot-marie-tooth disease, Congenital heart defects, Corneal opacity, Deafness, Deafness with congenital heart defects and posterior embryotoxon, Dupuytren contracture, Eye abnormalities
View all (14 more)

6528
Jagged canonical Notch ligand 2
HJ2, LGMDR27, SER2
Limb girdle muscular dystrophy, Breast neoplasms, Pancreatic ductal carcinoma, Craniofacial abnormalities, Glioblastoma, Limb-girdle muscular dystrophy, Muscular dystrophy, Orofacial cleft, Schizophrenia, Syndactyly

6529
Jagunal vesicle mediated transporter 1
GL009, SCN6
Severe congenital neutropenia, Neutropenia, Congenital neutropenia

6530
Janus kinase 1
AIIDE, JAK1A, JAK1B, JTK3
Autoimmune disease, Autoimmune thyroid disease, Autoinflammation, immune dysregulation, and eosinophilia, Breast implant-associated anaplastic large cell lymphoma, Diabetic neuropathy, Hypothyroidism, Lupus nephritis, Multiple sclerosis, Prostatic neoplasms