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
14131 to 14140 of 15448 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

14131
Transient receptor potential cation channel subfamily V member 2
VRL, VRL-1, VRL1
Endometrial neoplasms

14132
Transient receptor potential cation channel subfamily V member 3
FNEPPK2, OLMS, OLMS1, VRL3
Congenital palmoplantar and perioral keratoderma of olmsted, Gestational diabetes, Hyperplasia, Migraine, Oguchi disease, Olmsted syndrome, Schizophrenia

14133
Transient receptor potential cation channel subfamily V member 4
BCYM3, CMT2C, HMSN2C, OTRPC4, SMAL, SPSMA, SSQTL1, TRP12, VRL2, VROAC
Alzheimer disease, Osteonecrosis of the femoral head, Auditory neuropathy, Brachyolmia, Charcot-marie-tooth disease, Congenital benign spinal muscular atrophy, Distal hereditary motor neuropathy, Avascular necrosis of bone, Avascular necrosis of femoral head, Bone disease, Brachyrachia, Obstructive airway disease, Congenital cartilage disorder, Congenital clubfoot, Connective tissue disease
View all (26 more)

14134
Transient receptor potential cation channel subfamily V member 5
CAT2, ECAC1, OTRPC3
Bladder calculus, Hypercalciuria, Nephrolithiasis, Neurotic disorder, Diabetes mellitus type 2, Urolithiasis

14135
Transient receptor potential cation channel subfamily V member 6
ABP/ZF, CAT1, CATL, ECAC2, HRPTTN, HSA277909, LP6728, ZFAB
Hereditary chronic pancreatitis, Bladder calculus, Desbuquois syndrome, Hyperparathyroidism, Intestinal hypomagnesemia, Mastocytosis, Nephrolithiasis, Neurotic disorder, Pancreatitis, Polycystic ovary syndrome, Urolithiasis

14136
Transformation/transcription domain associated protein
DEDDFA, DFNA75, PAF350/400, PAF400, STAF40, TR-AP, Tra1
Isolated sensorineural deafness, Nonsyndromic hearing loss, Neurodevelopmental disorder, Deafness, Developmental delay with or without intellectual or behavioral abnormalities, Global developmental delay, Hearing loss, Melanoma, Schizophrenia

14137
TruB pseudouridine synthase family member 1
PUS4
Attention deficit hyperactivity disorder, Bipolar disorder, Diverticular disease

14138
TruB pseudouridine synthase family member 2
CLONE24922
Obesity, Spastic ataxia

14139
Testis expressed basic protein 1
C6orf10, TSBP
Asthma, Eczema, Autism, Autoimmune disease, Autoimmune hepatitis, Bipolar disorder, Celiac disease, Lymphocytic leukemia, Obstructive pulmonary disease, Liver cirrhosis, Coronary artery disease, Crohn disease, Graves disease, Hearing loss, Hepatitis c induced liver cirrhosis
View all (21 more)

14140
TSC complex subunit 1
LAM, TSC
Autism, Brain disease, Hepatocellular carcinoma, Renal cell carcinoma, Squamous cell carcinoma, Cognition disorder, Cortical dysplasia, Cryptogenic west syndrome, Delirium, dementia, and cognitive disorders, Epilepsy, Focal cortical dysplasia, Keratoconus, Intellectual developmental disorder, Mouth neoplasms, Psoriasis
View all (5 more)