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
12211 to 12220 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12211
Solute carrier family 41 member 3
SLC41A1-L2
Bell's palsy

12212
Solute carrier family 43 member 1
LAT3, PB39, POV1, R00504
Lung cancer, Squamous cell carcinoma

12213
Solute carrier family 43 member 2
LAT4
Alzheimer disease, Asthma, Diabetes mellitus type 2

12214
Solute carrier family 43 member 3
EEG1, ENBT1, FOAP-13, PRO1659, SEEEG-1
Crohn disease, Gout, Hypothyroidism, Iga nephropathy, Inflammatory bowel disease

12215
Solute carrier family 44 member 1
CD92, CDW92, CHTL1, CONATOC, CTL1
Alzheimer disease, Dry eye syndrome, Hyperaldosteronism, Neurodevelopmental disorder

12216
Solute carrier family 44 member 2 (CTL2 blood group)
CTL2, PP1292
Bipolar disorder, Thromboembolic pulmonary hypertension, Congenital heart disease, Cor pulmonale, Hyperlipidemia, Heart disease, Multiple sclerosis, Osteoarthritis, Stroke, Systemic lupus erythematosus, Venous thromboembolism

12217
Solute carrier family 44 member 3
CTL3
Dementia

12218
Solute carrier family 44 member 4
C6orf29, CTL4, DFNA72, NG22, TPPT, hTPPT1
Asthma, Isolated sensorineural deafness, Nonsyndromic hearing loss, Deafness, Hearing loss, Hypertension, Lung cancer, Parkinson disease, Psoriasis, Sarcoidosis, Squamous cell carcinoma, Systemic lupus erythematosus, Diabetes mellitus type 2, Upper aerodigestive tract neoplasm, Vitiligo
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12219
Solute carrier family 44 member 5
CTL5
Alzheimer disease, Major depressive disorder, Mood disorder, Neurotic disorder

12220
Solute carrier family 45 member 1
DNB5, IDDNPF, PAST-A
Eczema, Nonsyndromic intellectual disability, Inflammatory skin disease, Intellectual developmental disorder neuropsychiatric, Migraine, Psoriasis, Schizophrenia, Diabetes mellitus type 1