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
12151 to 12160 of 15380 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

12151
Solute carrier family 31 member 1
COPT1, CTR1, NSCT
Congenital abnormalities, Pulmonary hypertension, Intellectual developmental disorder, Necrosis, Prostatic neoplasms

12152
Solute carrier family 31 member 2
COPT2, CTR2, hCTR2
Breast cancer

12153
Solute carrier family 32 member 1
DEE114, GEFSP12, VGAT, VIAAT, VIAAT GEFSP12
Anorexia nervosa, Developmental and epileptic encephalopathy, Generalized epilepsy with febrile seizures plus, Seizure, Intellectual developmental disorder, Obesity, Obsessive-compulsive disorder, Willis-ekbom disease, Schizophrenia

12154
Solute carrier family 33 member 1
ACATN, AT-1, AT1, CCHLND, HPBDS, SPG42
Spastic paraplegia, Cataract, Colorectal cancer, Congenital cataract hearing loss developmental delay syndrome, Dementia, Developmental disability, Global developmental delay, Hearing impairment, Hearing loss, Hypothyroidism, Insomnia, Neurotic disorder, Partial epilepsy, Hereditary spastic paraplegia

12155
Solute carrier family 34 member 1
FRTS2, HCINF2, NAPI-3, NPHLOP1, NPT2, NPTIIa, SLC11, SLC17A2
Asthma, Bladder calculus, Bone disease, Kidney and ureter calculus, Kidney disease, Crohn disease, De toni-debre-fanconi syndrome, Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis, Dominant hypophosphatemia with nephrolithiasis or osteoporosis, Fanconi renotubular syndrome, Fanconi syndrome, Hypercalcemia, Idiopathic infantile hypercalcemia, Hypercalciuria, Hypophosphatemic rickets
View all (6 more)

12156
Solute carrier family 34 member 2
NAPI-3B, NAPI-IIb, NPTIIb, NaPi2b, PULAM
Non-small-cell lung carcinoma

12157
Solute carrier family 34 member 3
HHRH, NPT2C, NPTIIc
Hypophosphatemic rickets, Desbuquois syndrome, Nephrolithiasis

12158
Solute carrier family 35 member A1
CDG2F, CMPST, CST, hCST
Congenital disorder of glycosylation

12159
Solute carrier family 35 member A2
CDG2M, CDGX, UDP-Gal-Tr, UGALT, UGAT, UGT, UGT1, UGT2, UGTL
Autism, Congenital disorder of glycosylation, Developmental and epileptic encephalopathy, X-linked complex neurodevelopmental disorder

12160
Solute carrier family 35 member A3
AMRS
Arthrogryposis multiplex congenita, Arthrogryposis with neurodevelopmental impairment and seizures, Autism, Kidney disease