Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "S"
901 to 910 of 1203 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

901
Serum response factor
MCM1
Cardiomyopathy, Congenital hereditary endothelial dystrophy, Human immunodeficiency virus infection

902
Spermidine synthase
PAPT, SPDSY, SPS1, SRML1

903
Src-related kinase lacking C-terminal regulatory tyrosine and N-terminal myristylation sites
C20orf148, PTK70, SRM, dJ697K14.1
Liver neoplasm

904
Signal recognition particle 9
ALURBP
Endometrial cancer, Endometrial neoplasm, Osteoarthritis

905
Signal recognition particle 54
SCN8
Severe congenital neutropenia, Ciliary dyskinesia, Desbuquois syndrome, Metabolic syndrome, Oligodendroglioma, Congenital neutropenia, Shwachman syndrome, Shwachman-diamond syndrome, Diabetes mellitus, type 2

906
Signal recognition particle 68
SCN10
Craniofacial abnormalities, Dermatologic disorder, Neutropenia, Severe congenital neutropenia, Congenital neutropenia, Skin disease

907
Signal recognition particle 72
BMFF, BMFS1, HEL103
Myeloid leukemia, Aplasia and myelodysplasia, Bone marrow failure syndromes, Cholelithiasis, Congenital bone marrow failure syndrome

908
SRSF protein kinase 2
SFRSK2
Anorexia nervosa, Atrophic macular degeneration, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Bipolar depression, Major depressive disorder, Melanoma, Obesity, Obsessive-compulsive disorder, Oligodendroglioma, Schizophrenia, Tourette syndrome, Diabetes mellitus, type 2, Age-related macular degeneration

909
Sex determining region Y
SRXX1, SRXY1, TDF, TDY
46,xx ovotesticular disorder of sex development, 46,xx sex reversal, 46,xy complete gonadal dysgenesis, 46,xy partial gonadal dysgenesis, 46,xy sex reversal, Gonadal dysgenesis

910
Single stranded DNA binding protein 1
Mt-SSB, OPA13, SOSS-B1, SSBP, mtSSB
Isolated sensorineural deafness, Cone-rod dystrophy, Dermatologic disorder, Leigh syndrome, Optic atrophy, Skin disease