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
4451 to 4460 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4451
Family with sequence similarity 186 member B
C12orf25
Attention deficit hyperactivity disorder, Nephronophthisis, Substance abuse

4452
Family with sequence similarity 187 member A
-
Ciliary dyskinesia

4453
Family with sequence similarity 187 member B
TMEM162
Color vision deficiency

4454
Family with sequence similarity 193 member A
C4orf8, RES4-22
Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Colorectal adenoma, Colorectal cancer, Connective tissue disease, Rheumatoid arthritis, Systemic lupus erythematosus

4455
Family with sequence similarity 209 member A
C20orf106, dJ1153D9.3
Alzheimer disease, Gastroesophageal reflux disease

4456
Family with sequence similarity 209 member B
C20orf107, dJ1153D9.4
Colorectal cancer, Obesity

4457
FAM20A golgi associated secretory pathway pseudokinase
AI1G, AIGFS, FP2747
Amelogenesis imperfecta, Juvenile arthritis, Breast cancer, Carney complex, Central nervous system cancer, Dentin dysplasia, Dentinogenesis imperfecta, Enamel-renal syndrome, Glioblastoma, Glioma, Juvenile idiopathic arthritis, Oligoarticular juvenile idiopathic arthritis

4458
FAM20B glycosaminoglycan xylosylkinase
gxk1
Alzheimer disease, Congenital disorder of glycosylation, Desbuquois dysplasia, Desbuquois syndrome, Squamous cell carcinoma, Systemic lupus erythematosus

4459
FAM20C golgi associated secretory pathway kinase
DMP-4, DMP4, G-CK, GEF-CK, RNS
Alzheimer disease, Amelogenesis imperfecta, Color vision deficiency, Cortical dysplasia, Desbuquois syndrome, Glioma

4460
Family with sequence similarity 210 member A
C18orf19, HsT2329
Aortic stenosis, Aortic valve disease, Bone fracture