421
|
|
|
SH3 and PX domains 2B |
FAD49, FTHS, HOFI, KIAA1295, TKS4, TSK4 |
Androgenetic alopecia, Bone disease, Craniofacial abnormalities, Desbuquois syndrome, Eye abnormalities, Glaucoma, Growth disorder, Hearing loss, Ocular hypertension, Oligodendroglioma, Preeclampsia, Prostate cancer |
422
|
|
|
SH3 domain containing ring finger 1 |
POSH, RNF142, SH3MD2 |
|
423
|
|
|
SH3 domain containing ring finger 3 |
POSH2, SH3MD4 |
|
424
|
|
|
SH3 domain and tetratricopeptide repeats 1 |
- |
|
425
|
|
|
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, Roussy-levy syndrome, Schizophrenia, Scoliosis, Hereditary spastic paraplegiaView all (4 more) |
426
|
|
|
SH3 and SYLF domain containing 1 |
RAY |
|
427
|
|
|
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 |
428
|
|
|
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, Oropharyngeal cancer, Sarcoidosis, Scoliosis, Skin cancer, Skin neoplasms, Tonsil cancerView all (6 more) |
429
|
|
|
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 |
430
|
|
|
SHANK associated RH domain interactor |
AIFID, SIPL1 |
|