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
11891 to 11900 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11891
Shugoshin 1
CAID, NY-BR-85, SGO, SGOL1
Cardiac arrhythmias, Cardiac arrhythmia, Atrial and intestinal dysrhythmia, Chronobiology disorder, Intestinal disease

11892
Shugoshin 2
SGOL2, TRIPIN
Gonadal dysgenesis, Premature ovarian failure, Perrault syndrome

11893
Sphingosine-1-phosphate lyase 1
NPHS14, RENI, S1PL, SPL
Eczema, Attention deficit hyperactivity disorder, Charcot-marie-tooth disease, Digestive system disease, Hyperopia, Multiple myeloma, Nephrotic syndrome, Obesity, Willis-ekbom disease, Scoliosis, Seborrheic dermatitis, Substance abuse, Diabetes mellitus type 2, Uveal melanoma

11894
Sphingosine-1-phosphate phosphatase 2
SPP2, SPPase2
Anorexia nervosa, Eating disorder, Major depressive disorder, Tourette syndrome

11895
N-sulfoglucosamine sulfohydrolase
HSS, MPS3A, SFMD
Autoinflammatory syndrome, Central nervous system cancer, Desbuquois syndrome, Developmental regression, Glioblastoma, Glioma, Global developmental delay, Intellectual developmental disorder, Mucopolysaccharidosis, Nystagmus, Psoriasis, Sanfilippo syndrome

11896
Small G protein signaling modulator 1
RUTBC2
Hypertension, Sclerosing cholangitis, Diabetes mellitus type 2

11897
Small G protein signaling modulator 2
RUTBC1
Attention deficit hyperactivity disorder, Autism, Hypertension, Insomnia, Migraine, Multiple sclerosis, Substance abuse

11898
Small G protein signaling modulator 3
CIP85, MAP, RABGAP5, RUSC3, RUTBC3, RabGAP-5, rabGAPLP
Autism, Breast cancer, Intellectual developmental disorder, Major depressive disorder, Neurodevelopmental disorder

11899
Small glutamine rich tetratricopeptide repeat co-chaperone alpha
SGT, SGT1, Vpu, alphaSGT, hSGT
Schizophrenia

11900
SH2B adaptor protein 1
PSM, SH2B
Chromosome 16p11.2 deletion syndrome, Crohn disease, Chromosome 16p11.2 microdeletion syndrome, Inflammatory bowel disease, Obesity, Premature ovarian failure, Schizophrenia, Ulcerative colitis