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
13411 to 13420 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

13411
Testis expressed 48
-
Asthma, Crohn disease, Inflammatory bowel disease, Major depressive disorder, Psychiatric disorders

13412
Testis expressed 51
-
Alzheimer disease, Color vision deficiency, Heart failure, Lung cancer, Pelvic organ prolapse, Periodontitis, Scoliosis, Systemic lupus erythematosus

13413
Testis expressed 55
C3orf30, TSCPA
Hodgkin lymphoma

13414
Testis expressed 9
-
Color vision deficiency, Heterotaxy syndrome, Situs inversus

13415
Transferrin
HEL-S-71p, PRO1557, PRO2086, TFQTL1
Alzheimer disease, Anemia, Hypochromic microcytic anemia, Autism, Carcinoma, Persistent hepatitis, Congenital atransferrinemia, Diabetes mellitus type 1, Digestive system disease, Fatty liver, Fatty liver, alcoholic, Hepatitis, Hereditary hemochromatosis, Hyperglycemia, Iron overload
View all (8 more)

13416
Transcription factor A, mitochondrial
MTDPS15, MTTF1, MTTFA, TCF6, TCF6L1, TCF6L2, TCF6L3
Alzheimer disease, Amyotrophic lateral sclerosis, , Neuronal ceroid lipofuscinosis, Gout, Huntington disease, Liver cirrhosis, Migraine, Mitochondrial dna depletion syndrome, Parkinson disease, Secondary parkinson disease, Hearing loss

13417
Transcription factor AP-2 alpha
AP-2, AP-2alpha, AP2TF, BOFS, TFAP2
Amblyopia, Anophthalmia/microphthalmia-esophageal atresia syndrome, Branchiooculofacial syndrome, Branchiootorenal syndrome, Breast neoplasms, Byzanthine arch palate, Congenital epicanthus, Craniofacial abnormalities, Esotropia, Eye abnormalities, Kidney disease, Microphthalmos, Nystagmus, Oral cavity carcinoma, Oropharyngeal cancer
View all (3 more)

13418
Transcription factor AP-2 beta
AP-2B, AP-2beta, AP2-B, PDA2
Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Bladder calculus, Body weight, Intestinal pseudo-obstruction, Clinodactyly, Congenital hand deformities, Coronary artery disease, Craniofacial abnormalities, Craniosynostosis, Melanoma, Diabetes mellitus, Diabetic neuropathy
View all (17 more)

13419
Transcription factor AP-2 gamma
AP2-GAMMA, ERF1, TFAP2G, hAP-2g
Ovarian cancer, Stomach neoplasms

13420
Transcription factor AP-2 delta
AP-2delta, TFAP2BL1
Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Bladder calculus, Cardiovascular disease, Diabetes mellitus, Diabetic neuropathy, Endometrial cancer, Endometriosis, Hypertension, Major depressive disorder, Metabolic syndrome, Nephrolithiasis, Psychiatric disorders, Willis-ekbom disease
View all (3 more)