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
Showing genes starting with "S"
1531 to 1540 of 1624 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

1531
Sad1 and UNC84 domain containing 1
UNC84A
Atrial fibrillation, Atrial flutter, Insomnia

1532
Sad1 and UNC84 domain containing 2
UNC84B, rab5IP
Diverticular disease, Prostate cancer

1533
Sad1 and UNC84 domain containing 3
SUNC1
Alzheimer disease, Psoriasis

1534
Sad1 and UNC84 domain containing 5
SPAG4L, SPGF16, TSARG4, dJ726C3.1
Male infertility acephalic spermatozoa, Spermatogenic failure

1535
Sulfite oxidase
-
Ankylosing spondylitis, Asthma, Autism, Autoimmune disease, Autoimmune thyroid disease, Basal cell carcinoma, Celiac disease, Common variable immunodeficiency, Crohn disease, Gastroesophageal reflux disease, Juvenile idiopathic arthritis, Nasal polyp, Polycystic ovary syndrome, Psoriasis, Respiratory system disease
View all (7 more)

1536
SPT16 homolog, facilitates chromatin remodeling subunit
CDC68, FACTP140, NEDDFAC, SPT16, SPT16/CDC68
14q11.2 microduplication syndrome, Neurodevelopmental disorder, Conotruncal cardiac defect, Dextrocardia, Non-specific syndromic intellectual disability

1537
SPT20 homolog, SAGA complex component
C13, C13orf19, FAM48A, FP757, P38IP, SPT20
Insomnia, Rheumatoid arthritis

1538
SUPT20H like 2
FAM48B1, FAM48B2
Schizophrenia

1539
SPT3 homolog, SAGA and STAGA complex component
SPT3, SPT3L
Alzheimer disease, Androgenetic alopecia, Asthma, Attention deficit hyperactivity disorder, Bell's palsy, Bone disease, Bone fracture, Cleidocranial dysplasia, Color vision deficiency, Diffuse idiopathic skeletal hyperostosis, Essential tremor, Facial nerve disorder, Glaucoma, Large artery stroke, Migraine
View all (6 more)

1540
SPT4 homolog, DSIF elongation factor subunit
SPT4, SPT4H, SUPT4H, Supt4a
Major depressive disorder, Prostate cancer, Uterine fibroid