1391
|
|
|
Solute carrier family 35 member G5 |
AMAC, AMAC1L2 |
Curated: N/A
Unreviewed: N/A
|
1392
|
|
|
Solute carrier family 35 member G6 |
AMAC1L3, TMEM21B |
Curated: N/A
Unreviewed: N/A
|
1393
|
|
|
Solute carrier family 35 member H1 |
BA394O2.1, C20orf5, CGI-15, OVCOV1, SLC35C2 |
Curated: N/A
Unreviewed: N/A
|
1394
|
|
|
Solute carrier family 36 member 1 |
Dct1, LYAAT1, PAT1, TRAMD3 |
Curated: Autism, Cerebellar ataxia, Glycinuria with/without oxalate urolithiasis, Iminoglycinuria, Oligodendroglioma, Scoliosis, Spinocerebellar ataxia
Unreviewed: Breast Cancer, Breast Carcinoma, Breast neoplasm, Colorectal neoplasm, Congenital chloride diarrhea, Fragile X Syndrome, Hyperoxaluria, Hypertension, Inflammatory Bowel Disease, Kidney neoplasm, Kidney stone, Lung Diseases, Metabolic Diseases, Multiple myeloma, Myeloid leukemia, Neoplasms, Nephrolithiasis, Pancreatic neoplasm, Perry Syndrome, Prostate cancer, Prostatic Neoplasms, Vascular disease
|
1395
|
|
|
Solute carrier family 36 member 2 |
PAT2, TRAMD1 |
Curated: Cannabis abuse, Glycinuria with/without oxalate urolithiasis, Hyperglycinuria, Iminoglycinuria, Oligodendroglioma, Scoliosis, Substance abuse
Unreviewed: Ischemic stroke, Mental retardation, Nephronophthisis, Prolinuria
|
1396
|
|
|
Solute carrier family 36 member 3 |
PAT3, TRAMD2, tramdorin2 |
Curated: N/A
Unreviewed: N/A
|
1397
|
|
|
Solute carrier family 36 member 4 |
PAT4 |
Curated: Metabolic syndrome, Obesity, Osteoarthritis, Polycystic ovary syndrome, Diabetes mellitus type 2
Unreviewed: Colorectal Cancer
|
1398
|
|
|
Solute carrier family 37 member 1 |
G3PP, SPX1 |
Curated: Obsessive-compulsive disorder
Unreviewed: Breast Cancer, Breast Carcinoma, Colorectal Cancer, Malignant Neoplasm, Metabolic Diseases
|
1399
|
|
|
Solute carrier family 37 member 2 |
SPX2, pp11662 |
Curated: N/A
Unreviewed: Brain neoplasms, Breast Cancer, Breast Carcinoma, Breast neoplasm, Cortical Congenital Hyperostosis, Esophageal squamous cell carcinoma, Glioblastoma, Hepatocellular carcinoma, Hypoxia, Stomach neoplasms
|
1400
|
|
|
Solute carrier family 37 member 3 |
SPX3 |
Curated: Androgenetic alopecia, Eye disease, Meniere disease, Non-small cell lung carcinoma, Retinitis pigmentosa
Unreviewed: Congenital hyperinsulinism, Diabetes mellitus, type 1, Hepatocellular carcinoma, Retinitis Pigmentosa
|