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
12801 to 12810 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12801
Serglycin
PPG, PRG, PRG1
Color vision deficiency, Liver cirrhosis

12802
Sorcin
CP-22, CP22, SCN, V19
Hypertrophic cardiomyopathy, Liver cirrhosis

12803
Sarcalumenin
SAR
Diverticular disease, Hypertrophic cardiomyopathy, Obesity

12804
Src-related kinase lacking C-terminal regulatory tyrosine and N-terminal myristylation sites
C20orf148, PTK70, SRM, dJ697K14.1
Liver neoplasms

12805
Signal recognition particle 19
-
Severe congenital neutropenia, Neutropenia, Congenital neutropenia, Shwachman-diamond syndrome

12806
Signal recognition particle 54
SCN8
Severe congenital neutropenia, Ciliary dyskinesia, Desbuquois syndrome, Metabolic syndrome, Oligodendroglioma, Congenital neutropenia, Shwachman-diamond syndrome, Diabetes mellitus type 2

12807
Signal recognition particle 68
SCN10
Craniofacial abnormalities, Dermatologic disorder, Neutropenia, Severe congenital neutropenia, Congenital neutropenia, Skin disease

12808
Signal recognition particle 72
BMFF, BMFS1, HEL103
Myeloid leukemia, Aplasia and myelodysplasia, Bone marrow failure syndromes, Cholelithiasis, Congenital bone marrow failure syndrome

12809
Signal recognition particle 9
ALURBP
Endometrial cancer, Endometrial neoplasms, Osteoarthritis

12810
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