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"
431 to 440 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

431
SH2 domain containing adaptor protein B
bA3J10.2
Androgenetic alopecia, Atrial fibrillation, Obstructive pulmonary disease, Sarcoidosis, Scoliosis, Diabetes mellitus type 2

432
Sex hormone binding globulin
ABP, SBP, TEBG
Bone fracture, Dilated cardiomyopathy, Diabetes mellitus type 2, Erectile dysfunction, Hypogonadism, Mesothelioma, Metabolic syndrome, Osteoarthritis, Prostatic neoplasms

433
SHC adaptor protein 1
SHC, SHCA
Amyotrophic lateral sclerosis, Cardiomegaly, Crohn disease, Inflammatory bowel disease, Liver cirrhosis, Motor neuron disease, Ulcerative colitis

434
SHC adaptor protein 3
N-Shc, NSHC, RAI, SHCC
Attention deficit hyperactivity disorder, Pelvic organ prolapse, Substance abuse

435
SHC adaptor protein 4
RaLP, SHCD
Bipolar disorder, Eating disorder, Major depressive disorder, Nonalcoholic fatty liver disease, Schizophrenia, Diabetes mellitus type 2

436
SHC binding and spindle associated 1
PAL
Liver cirrhosis, Sarcoma

437
Src homology 2 domain containing E
-
Major depressive disorder, Psychotic disorders

438
Src homology 2 domain containing F
-
Atypical femoral fracture

439
Shiftless antiviral inhibitor of ribosomal frameshifting
C19orf66, IRAV, RyDEN, SFL
Hereditary sensory and autonomic neuropathy

440
Sonic hedgehog signaling molecule
HHG1, HLP3, HPE3, MCOPCB5, SMMCI, ShhNC, TPT, TPTPS
Anemia, Asthma, Autism, Preaxial polydactyly with upper back hypertrichosis, Byzanthine arch palate, Hepatocellular carcinoma, Obstructive pulmonary disease, Colobomatous microphthalmia, Color vision deficiency, Corneal astigmatism, Desbuquois syndrome, Disorder of skeletal system, Dry eye syndrome, Eye abnormalities, Facial dysmorphism syndrome
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