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
12601 to 12610 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12601
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
View all (6 more)

12602
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

12603
SRY-box transcription factor 30
-
Lung neoplasms, Male infertility

12604
SRY-box transcription factor 4
CSS10, EVI16, IDDSDF
Atrial fibrillation, Adenoid cystic carcinoma, Basal cell carcinoma, Cardiomegaly, Coffin-siris syndrome, Congestive heart failure, Developmental delay, Heart failure, Intellectual developmental disorder speech dysmorphic, Intellectual developmental disorder, Liver cirrhosis, Liver neoplasms, Intellectual disability, Neurodevelopmental disorder, Salivary gland neoplasms

12605
SRY-box transcription factor 5
L-SOX5, L-SOX5B, L-SOX5F, LAMSHF
12p12.1 microdeletion syndrome, Anorexia nervosa, Anxiety disorder, Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Azoospermia, Bipolar disorder, Color vision deficiency, Colorectal cancer, Coronary artery disease, Crohn disease, Developmental and epileptic encephalopathy, Tourette syndrome, Hemorrhoid
View all (22 more)

12606
SRY-box transcription factor 6
HSSOX6, SOXD, TOLCAS
Atrial fibrillation, Basal cell carcinoma, Bipolar disorder, Bone fracture, Cardiovascular disease, Colorectal cancer, Neurodevelopmental disorder, Coronary artery disease, Melanoma, Generalized anxiety disorder, Hypertension, Intellectual developmental disorder, Major depressive disorder, Metabolic syndrome, Mood disorder
View all (8 more)

12607
SRY-box transcription factor 7
-
Autism, Brain aneurysm, Congenital heart disease, Neurotic disorder, Systemic lupus erythematosus, Tetralogy of fallot, Diabetes mellitus type 2

12608
SRY-box transcription factor 8
-
Multiple sclerosis, Neurodevelopmental disorder, Non-neoplastic peripheral nervous system disease, Peripheral nervous system disease, Peripheral neuropathy, Polycystic ovary syndrome

12609
SRY-box transcription factor 9
CMD1, CMPD1, ENH13, SRA1, SRXX2, SRXY10, TES, TESCO
46, xx ovotesticular disorder of sex development, 46, xx sex reversal, 46, xy complete gonadal dysgenesis, 46, xy partial gonadal dysgenesis, Anonychia, Autism, Bent bone dysplasia, Campomelic dysplasia, Camptomelic dysplasia, Carcinoma, Congenital hand deformities, Connective tissue disease, Cooks syndrome, Craniofacial abnormalities, Desbuquois syndrome
View all (5 more)

12610
Sp1 transcription factor
-
Schizophrenia, Colorectal neoplasms, Hyperglycemia, Hypospadias, Metabolic syndrome, Non-organic psychosis, Osteoporosis, Parkinson disease, Progressive supranuclear palsy, Psychotic disorders, Skin neoplasms, Diabetes mellitus type 2