Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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11871 to 11880 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11871
SH3 domain and tetratricopeptide repeats 2
CMT4C, MNMN
Arthrogryposis multiplex congenita, Breast cancer, Charcot-marie-tooth disease, Congenital hemihypertrophy, Congenital joint contractures, Congenital pes cavus, Dejerine-sottas disease, Distal spinal muscular atrophy, Hereditary motor and sensory neuropathies, Motor neuron disease, Hypertension, Hypertrophic neuropathy, Peripheral neuropathy, Peroneal muscle atrophy, Psoriasis
View all (4 more)

11872
SH3 and SYLF domain containing 1
RAY
Large artery stroke, Metabolic syndrome, Willis-ekbom disease, Diabetes mellitus type 2

11873
SH3 and multiple ankyrin repeat domains 1
SPANK-1, SSTRIP, synamon
Anxiety disorder, Autism, Breast cancer, Renal cell carcinoma, Neurodevelopmental disorder, Developmental coordination disorder, Insomnia, Intellectual developmental disorder, Motor skills disorder, Non-organic psychosis, Non-specific syndromic intellectual disability, Psychotic disorders, Schizophrenia

11874
SH3 and multiple ankyrin repeat domains 2
AUTS17, CORTBP1, CTTNBP1, ProSAP1, SHANK, SPANK-3
Alzheimer disease, Autism, Bipolar disorder, Colorectal cancer, Neurodevelopmental disorder, Bipolar depression, Eosinophilia, Global developmental delay, Hodgkin lymphoma, Intellectual developmental disorder, Major depressive disorder, Kawasaki disease, Non-specific syndromic intellectual disability, Obesity, Oligodendroglioma
View all (6 more)

11875
SH3 and multiple ankyrin repeat domains 3
DEL22q13.3, PROSAP2, PSAP2, SCZD15, SPANK-2
22q13.3 deletion syndrome, Arthritis, Autism, Developmental disability, Global developmental delay, Intellectual developmental disorder, Language development disorders, Neurodevelopmental disorder, Psychotic disorders, Schizophrenia, 22q13 monosomy syndrome, Venous thromboembolism

11876
SHANK associated RH domain interactor
AIFID, SIPL1
Alzheimer disease, Asthma, Atrial fibrillation, Autoinflammation with episodic fever and immune dysregulation, Dementia, Dermatitis, Eosinophilia, Respiratory system disease

11877
SH2 domain containing adaptor protein B
bA3J10.2
Androgenetic alopecia, Atrial fibrillation, Obstructive pulmonary disease, Sarcoidosis, Scoliosis, Diabetes mellitus type 2

11878
Sex hormone binding globulin
ABP, SBP, TEBG
Bone fracture, Dilated cardiomyopathy, Diabetes mellitus type 2, Erectile dysfunction, Hypogonadism, Mesothelioma, Metabolic syndrome, Osteoarthritis, Prostatic neoplasms

11879
SHC adaptor protein 1
SHC, SHCA
Amyotrophic lateral sclerosis, Cardiomegaly, Crohn disease, Inflammatory bowel disease, Liver cirrhosis, Motor neuron disease, Ulcerative colitis

11880
SHC adaptor protein 3
N-Shc, NSHC, RAI, SHCC
Attention deficit hyperactivity disorder, Pelvic organ prolapse, Substance abuse