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
12691 to 12700 of 15448 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

12691
SPG7 matrix AAA peptidase subunit, paraplegin
CAR, CMAR, PGN, SPG5C
Attention deficit hyperactivity disorder, Optic atrophy, Breast cancer, Cancer, Cerebral cortical atrophy, Colorectal cancer, Melanoma, Distal spinal muscular atrophy, Dysarthria, Estrogen-receptor negative breast cancer, Frontotemporal dementia with or without amyotrophic lateral sclerosis, Intellectual developmental disorder, Lung cancer, Memory disorders, Mitochondrial disease
View all (14 more)

12692
Sphingosine kinase 1
SPHK
Ulcerative colitis, Diabetes mellitus type 2, Leukemia, Myelodysplastic syndrome

12693
Sphingosine kinase 2
SK 2, SK-2, SPK 2, SPK-2
Memory disorders, Psoriasis

12694
SPHK1 interactor, AKAP domain containing
SKIP
Anorexia nervosa, Attention deficit hyperactivity disorder, Congestive heart failure, Heart failure, Iga nephropathy, Metabolic syndrome, Osteoarthritis, Peripheral neuropathy, Schizophrenia, Diabetes mellitus type 2

12695
Spi-1 proto-oncogene
AGM10, OF, PU.1, SFPI1, SPI-1, SPI-A
Agammaglobulinemia, Alzheimer disease, Kidney disease, Gout, Hypertension, Insomnia, Myeloid leukemia, Myocardial infarction, Neurotic disorder, Open angle glaucoma, Prostate cancer, Schizophrenia, Squamous cell carcinoma, Venous thromboembolism

12696
Spi-B transcription factor
SPI-B
Biliary cirrhosis, Liver cirrhosis, Biliary cholangitis

12697
Spi-C transcription factor
SPI-C
Breast cancer

12698
Scaffold protein involved in DNA repair
KIAA0146, ODG9
46, xx gonadal dysgenesis, Gonadal dysgenesis, Ovarian dysgenesis

12699
Spindlin 1
SPIN, TDRD24
Gout

12700
Spindlin family member 2A
DXF34, SPIN2, TDRD25, dJ323P24.1
Liver cirrhosis, Neurotic disorder, Diabetes mellitus type 2