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
4391 to 4400 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4391
Family with sequence similarity 118 member A
C22orf8
Androgenetic alopecia, Ankylosing spondylitis, Atrial fibrillation, Colorectal cancer, Colonic neoplasms, Crohn disease, Dental caries, Diverticular disease, Osteoarthritis, Prostate cancer, Psoriasis, Sclerosing cholangitis, Ulcerative colitis

4392
Family with sequence similarity 120 member A
C9orf10, HBVPTPAP, OSSA
Anorexia nervosa, Dyslexia, Generalized anxiety disorder, Tourette syndrome, Insomnia, Irritable bowel syndrome, Major depressive disorder, Myocardial infarction, Neurotic disorder, Post-traumatic stress disorder, Schizophrenia

4393
Family with sequence similarity 120 member A opposite strand
C9orf10OS
Lung disease, Color vision deficiency, Cutis laxa, Esophageal squamous cell carcinoma, Insomnia, Irritable bowel syndrome, Neurotic disorder, Post-traumatic stress disorder, Schizophrenia, Scoliosis

4394
Family with sequence similarity 120 member B
CCPG, KIAA1838, PGCC1, SAN1, dJ894D12.1
Behcet disease, Dementia, Dilated cardiomyopathy, Insomnia, Schizophrenia, Scoliosis

4395
Family with sequence similarity 124 member A
-
Cerebral amyloid angiopathy, Non-small cell lung carcinoma, Oligodendroglioma, Pelvic organ prolapse

4396
Family with sequence similarity 124 member B
-
Alzheimer disease, Brain aneurysm, Dementia, Polycystic ovary syndrome, Squamous cell carcinoma

4397
Family with sequence similarity 131 member B
-
Becker generalized myotonia

4398
Family with sequence similarity 131 member C
C1orf117
Cardiovascular disease, Nonalcoholic fatty liver disease

4399
Family with sequence similarity 133 member B
-
Cardiovascular disease, Hypertension

4400
Family with sequence similarity 135 member A
KIAA1411
Color vision deficiency