Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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14221 to 14230 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14221
Tumor suppressor 2, mitochondrial calcium regulator
C3orf11, FUS1, PAP, PDAP2
Alzheimer disease, Gastroesophageal reflux disease, Peptic ulcer disease

14222
Tumor suppressor candidate 3
D8S1992, M33, MRT22, MRT7, MagT2, N33, OST3A, SLC58A2
Alzheimer disease, Attention deficit hyperactivity disorder, Nonsyndromic intellectual disability, Biliary atresia, Congenital disorder of glycosylation, Congenital neurologic anomalies, Corneal astigmatism, Intellectual developmental disorder, Metabolic syndrome, Neurodevelopmental disorder, Obsessive-compulsive disorder, Paraplegia, Hypertension, Diabetes mellitus type 2

14223
Terminal uridylyl transferase 1, U6 snRNA-specific
PAPD2, RBM21, STARPAP, TENT1, TUTase, URLC6
Obstructive pulmonary disease

14224
Terminal uridylyl transferase 4
PAPD3, TENT3A, ZCCHC11
Colorectal cancer

14225
Terminal uridylyl transferase 7
PAPD6, TENT3B, ZCCHC6
Asthma, Atrial fibrillation, Metabolic syndrome, Ocular hypertension, Diabetes mellitus type 2

14226
Trans-golgi network vesicle protein 23 homolog A
FAM18A, YDR084C
Oligodendroglioma

14227
Twinfilin actin binding protein 1
A6, PTK9
Crohn disease, Inflammatory bowel disease, Lymphoma, Oligodendroglioma, Ulcerative colitis

14228
Twinfilin actin binding protein 2
A6RP, A6r, MSTP011, PTK9L
Autism, Bipolar disorder, Colorectal cancer, Colonic neoplasms, Diverticular disease, Osteoarthritis, Schizophrenia

14229
Twist family bHLH transcription factor 1
ACS3, BPES2, BPES3, CRS, CRS1, CSO, SCS, SWCOS, TWIST, bHLHa38
Androgenetic alopecia, Asthma, Atherosclerosis, Atrial fibrillation, Brachycephaly, Cardiovascular disease, Central nervous system cancer, Cerebrovascular disorder, Ischemic heart disease, Obstructive pulmonary disease, Colorectal cancer, Coronal craniosynostosis, Coronary artery disease, Craniosynostosis, Desbuquois syndrome
View all (16 more)

14230
Twist family bHLH transcription factor 2
AMS, BBRSAY, DERMO1, FFDD3, SETLSS, bHLHa39
Ablepharon macrostomia syndrome, Alzheimer disease, Androgenetic alopecia, Barber-say syndrome, Congenital ectodermal dysplasia of face, Dry eye syndrome, Focal facial dermal dysplasia, Peptic ulcer disease, Sjogren syndrome