Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "S"
1541 to 1550 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1541
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)

1542
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

1543
SPT20 homolog, SAGA complex component
C13, C13orf19, FAM48A, FP757, P38IP, SPT20
Insomnia, Rheumatoid arthritis

1544
SUPT20H like 2
FAM48B1, FAM48B2
Schizophrenia

1545
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)

1546
SPT4 homolog, DSIF elongation factor subunit
SPT4, SPT4H, SUPT4H, Supt4a
Major depressive disorder, Prostate cancer, Uterine fibroid

1547
SPT6 homolog, histone chaperone and transcription elongation factor
SPT6, SPT6H, emb-5
Gout

1548
SPT7 like, STAGA complex subunit gamma
FZPS, SPT7L, STAF65, STAF65(gamma), STAF65G, SUPT7H
Lipodystrophy

1549
Suv3 like RNA helicase
SUV3
Congenital skin anomaly, Ichthyosis, Sarcopenia, Skin abnormalities, Xeroderma

1550
SURF1 cytochrome c oxidase assembly factor
CMT4K, MC4DN1, SHY1
Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency, Cerebellar ataxia, Charcot-marie-tooth disease, Craniofacial abnormalities, Cytochrome c oxidase deficiency, Dejerine-sottas disease, Dysarthria, Hereditary motor and sensory neuropathies, Hypertrophic neuropathy, Intellectual developmental disorder, Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Peroneal muscle atrophy, Roussy-levy syndrome