Genes?

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?All genes including those with curated and unreviewed disease associations.
Log in to save this view

Save This View

Selected (0) TSV CSV PDF
This Page (10) TSV CSV PDF
All Matching (3886) TSV CSV PDF
Chromosome:
Gene type:
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
Showing genes starting with "S"
1641 to 1650 of 3886 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

1641
Schlafen family member 13
SLFN10, hSLFN13

Curated: N/A

Unreviewed: Stomach neoplasms

1642
Schlafen family member 14
BDPLT20

Curated: Thrombocytopenia with platelet secretion defect, Platelet-type bleeding disorder, Breast cancer, Prostate cancer, Thrombocytopenia, platelet-type bleeding disorder 20

Unreviewed: Atrial Septal Defect, Blood coagulation disorder, Hemorrhage, Platelet disorder, Stomach neoplasms, Thrombocytopenia With Platelet Secretion Defect, Visceral leishmaniasis

1643
Schlafen family member 5
-

Curated: Alzheimer disease

Unreviewed: Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinogenesis, Colonic neoplasm, Diabetes mellitus, Fibrosarcoma, Gastritis, Glioblastoma, Glioma, Intestinal disease, Lung Cancer, Lung carcinoma, Malignant Neoplasm, Melanoma, Ovarian neoplasm, Pancreatic cancer, Pancreatic carcinoma, Pancreatic neoplasm, Renal Carcinoma, Renal cell carcinoma, Stomach Carcinoma, Stomach Neoplasms

1644
Schlafen like 1
-

Curated: N/A

Unreviewed: Chronic obstructive pulmonary disease

1645
SLFNL1 antisense RNA 1
-

Curated: N/A

Unreviewed: N/A

1646
-
-

Curated: N/A

Unreviewed: Specific language disorder, Specific Language Impairment

1647
-
-

Curated: N/A

Unreviewed: Specific language disorder, Specific Language Impairment

1648
-
-

Curated: N/A

Unreviewed: Language development disorders, Specific Language Impairment

1649
-
-

Curated: N/A

Unreviewed: N/A

1650
SRA stem-loop interacting RNA binding protein
C14orf156, DC50, PD04872

Curated: Mitochondrial encephalomyopathy

Unreviewed: Chronic disease, Cytochrome c oxidase deficiency, Leigh syndrome, Mitochondrial disease, Neoplasms, Sepsis