Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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12981 to 12990 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12981
Sad1 and UNC84 domain containing 1
UNC84A
Atrial fibrillation, Atrial flutter, Insomnia

12982
Sad1 and UNC84 domain containing 2
UNC84B, rab5IP
Diverticular disease, Prostate cancer

12983
Sad1 and UNC84 domain containing 3
SUNC1
Alzheimer disease, Psoriasis

12984
Sad1 and UNC84 domain containing 5
SPAG4L, SPGF16, TSARG4, dJ726C3.1
Male infertility acephalic spermatozoa, Spermatogenic failure

12985
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)

12986
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

12987
SPT20 homolog, SAGA complex component
C13, C13orf19, FAM48A, FP757, P38IP, SPT20
Insomnia, Rheumatoid arthritis

12988
SUPT20H like 2
FAM48B1, FAM48B2
Schizophrenia

12989
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)

12990
SPT4 homolog, DSIF elongation factor subunit
SPT4, SPT4H, SUPT4H, Supt4a
Major depressive disorder, Prostate cancer, Uterine fibroid