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
12281 to 12290 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12281
Solute carrier family 7 member 1
ATRC1, CAT-1, ERR, HCAT1, REC1L
Atrial fibrillation, Breast cancer, Cardiovascular disease, Hypertension, Major depressive disorder, Prostatic neoplasms

12282
Solute carrier family 7 member 10
ASC1, HASC-1, asc-1
Alzheimer disease, Asthma, Eczema, B-cell acute lymphoblastic leukemia, Crohn disease, Hoarding disorder, Inflammatory bowel disease, Mastocytosis, Multiple sclerosis, Respiratory system disease, Schizophrenia, Seasonal allergic rhinitis, Ulcerative colitis

12283
Solute carrier family 7 member 11
CCBR1, xCT
Central nervous system cancer, Contact dermatitis, Glioblastoma, Glioma, Major depressive disorder

12284
Solute carrier family 7 member 14
PPP1R142
Alzheimer disease, Obesity, Optic atrophy, Retinitis pigmentosa

12285
Solute carrier family 7 member 2
ATRC2, CAT-2A, CAT-2B, CAT2, HCAT2, SLC7A2A, SLC7A2B
Alzheimer disease, Basal cell carcinoma, Cerebral amyloid angiopathy, Conduct disorder, Dementia, Orofacial cleft

12286
Solute carrier family 7 member 3
ATRC3, CAT-3, CAT3
Autism, Prostate cancer, Uterine fibroid

12287
Solute carrier family 7 member 4
CAT-4, CAT4, HCAT3, VH
Eosinophilia

12288
Solute carrier family 7 member 5
4F2LC, CD98, D16S469E, E16, LAT1, MPE16
Asthma, Autism, Central serous retinopathy, Neurodevelopmental disorder, Allergic contact dermatitis, Lung neoplasms, Non-specific syndromic intellectual disability

12289
Solute carrier family 7 member 6
LAT-2, LAT3, y+LAT-2
Otosclerosis, Schizophrenia

12290
Solute carrier family 7 member 6 opposite strand
EPM12, Iwr1
Epilepsy, Progressive myoclonic epilepsy, Schizophrenia