Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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12831 to 12840 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12831
SH3 and cysteine rich domain 3
CMYO13, CMYP13, MYPBB, NAM
Congenital myopathy, Hepatomegaly, Liver neoplasms, Native american myopathy

12832
STAG1 cohesin complex component
MRD47, SA1, SCC3A
Alzheimer disease, Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Carpal tunnel syndrome, Neurodevelopmental disorder, Coronary artery disease, Dental caries, Global developmental delay, Intellectual developmental disorder, Major depressive disorder, Metabolic syndrome, Myocardial infarction, Myocardial ischemia
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12833
STAG2 cohesin complex component
HPE13, MKMS, NEDXCF, SA-2, SA2, SCC3B, bA517O1.1
Transitional cell carcinoma, Chromosome xq25 duplication syndrome, Holoprosencephaly, Myeloid leukemia, Myelodysplastic syndrome, Neurodevelopmental disorder, Semilobar holoprosencephaly, Urinary bladder neoplasms, Xq25 microduplication syndrome

12834
STAG3 cohesin complex component
SA3, SPGF61
Alzheimer disease, Major depressive disorder, Male infertility single gene azoospermia, Premature ovarian failure, Spermatogenic failure, Testicular azoospermia

12835
Signal transducing adaptor molecule
STAM-1, STAM1
Asthma

12836
Signal transducing adaptor molecule 2
Hbp, STAM2A, STAM2B
Metabolic syndrome, Diabetes mellitus type 2

12837
STAM binding protein
AMSH, MICCAP
Bell's palsy, Brain disease, Capillary malformation-arteriovenous malformation, Developmental disability, Epilepsy, Microcephaly

12838
STAM binding protein like 1
ALMalpha, AMSH-FP, AMSH-LP, bA399O19.2
Lung cancer, Squamous cell carcinoma

12839
Signal transducing adaptor family member 1
BRDG1, STAP-1
Color vision deficiency, Hyperlipoproteinemia, Oligodendroglioma, Parkinson disease, Uveal melanoma

12840
Signal transducing adaptor family member 2
BKS
Nephrolithiasis, Psoriasis