Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "S"
1091 to 1100 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1091
SRY-box transcription factor 10
DOM, PCWH, SOX-10, WS2E, WS4, WS4C
Charcot-marie-tooth disease, Deaf blind hypopigmentation syndrome, Schizophrenia, Hearing impairment, Hirschsprung disease, Hypogonadotropic hypogonadism, Hypopituitarism, Growth hormone deficiency, Kallmann syndrome, Panhypopituitarism, Pituitary dwarfism, Pituitary short stature, Sheehan syndrome, Waardenburg syndrome, Waardenburg-shah syndrome
View all (1 more)

1092
SRY-box transcription factor 11
CSS9, IDDMOH, MRD27
Adenoid cystic carcinoma, Kidney disease, Obstructive pulmonary disease, Coffin-siris syndrome, Craniosynostosis, Hearing loss, Hypogonadotropic hypogonadism, Intellectual developmental disorder microcephaly ocular, Pituitary stalk interruption syndrome, Salivary gland neoplasms, Diabetes mellitus type 2

1093
SRY-box transcription factor 12
SOX22
Neurodevelopmental disorder, Diabetes mellitus type 2

1094
SRY-box transcription factor 14
SOX28
Connective tissue disease, Mixed connective tissue disease

1095
SRY-box transcription factor 15
SOX20, SOX26, SOX27
Atrial fibrillation, Congenital disorder of glycosylation, Polycystic ovary syndrome

1096
SRY-box transcription factor 17
PPH7, VUR3
Kidney disease, Colorectal neoplasms, Digestive system disease, Pulmonary hypertension, Vesicoureteral reflux, Pulmonary arterial hypertension, Intracranial aneurysm, Patent ductus arteriosus

1097
SRY-box transcription factor 18
HLTRS, HLTS
Bladder exstrophy and epispadias complex, Basal cell carcinoma, Dermatologic disorder, Skin disease

1098
SRY-box transcription factor 2
ANOP3, MCOPS3
Aniridia, Anophthalmia/microphthalmia-esophageal atresia syndrome, Anophthalmia, Ataxia, Brain neoplasms, Squamous cell carcinoma, Colobomatous microphthalmia, Desbuquois syndrome, Developmental disability, Esophageal squamous cell carcinoma, Lung neoplasms, Microphthalmia, Microphthalmos, Nanophthalmos, Osteosarcoma
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1099
SRY-box transcription factor 3
GHDX, MRGH, PHP, PHPX, SOXB
46, xx ovotesticular disorder of sex development, 46, xx sex reversal, Desbuquois syndrome, Genetic panhypopituitarism, Hypertrichosis, Intellectual developmental disorder, x-linked, Panhypopituitarism, Septo-optic dysplasia, Teratozoospermia, X-linked congenital generalized hypertrichosis, X-linked intellectual disability

1100
SRY-box transcription factor 30
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Lung neoplasms, Male infertility