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
12191 to 12200 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12191
Solute carrier family 38 member 5
JM24, SN2, SNAT5, pp7194
Cortical development malformation

12192
Solute carrier family 38 member 6
NAT-1, SNAT6
Color vision deficiency

12193
Solute carrier family 38 member 7
SNAT7
Autism, Insomnia, Obesity, Schizophrenia

12194
Solute carrier family 38 member 8
FHASD, FVH2, SNAT8
Liver cirrhosis, Leber congenital amaurosis, Nonalcoholic fatty liver disease, Schizophrenia

12195
Solute carrier family 38 member 9
SNAT9, URLC11
Alzheimer disease, Astrocytoma, Liver neoplasms, Diabetes mellitus type 2

12196
Solute carrier family 39 member 1
ZIP1, ZIRTL
Prostate cancer, Prostatic neoplasms

12197
Solute carrier family 39 member 11
C17orf26, ZIP-11, ZIP11
Alzheimer disease, Amyotrophic lateral sclerosis, Ankylosing spondylitis, Breast cancer, Crohn disease, Diverticular disease, Inflammatory bowel disease, Prostate cancer, Psoriasis, Sclerosing cholangitis, Diabetes mellitus type 2, Ulcerative colitis

12198
Solute carrier family 39 member 12
LZT-Hs8, ZIP-12, ZIP12, bA570F3.1
Bipolar disorder, Hypertension, Melanoma, Major depressive disorder, Peripheral arterial disease, Psychiatric disorders, Retinitis pigmentosa, Schizophrenia

12199
Solute carrier family 39 member 13
EDSSPD3, LZT-Hs9, SCDEDS, ZIP13
Bone disease, Connective tissue disease, Cutis laxa, Desbuquois syndrome, Ehlers-danlos syndrome, Mitral valve prolapse, Myopia, Scleroderma, Spondyloepimetaphyseal dysplasia, Stroke, Tooth abnormalities

12200
Solute carrier family 39 member 14
HCIN, HMNDYT2, LZT-Hs4, NET34, ZIP14, cig19
Adult-onset dystonia-parkinsonism, Dystonia-parkinsonism-hypermanganesemia syndrome, Parkinson disease