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
13891 to 13900 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

13891
Tripeptidyl peptidase 2
IMD78, TPP-2, TPP-II, TPPII
Autoimmune hemolytic anemia, Color vision deficiency, Cutis marmorata, Global developmental delay, Immunodeficiency, Thrombocytopenia

13892
Tubulin polymerization promoting protein
TPPP/p25, TPPP1, p24, p25, p25alpha
Barrett esophagus, Brugada syndrome, Kidney disease, Depression, Esophageal adenocarcinoma, Hemorrhoid, Hypothyroidism, Kidney failure, Osteoarthritis, Peptic ulcer disease

13893
Tubulin polymerization promoting protein family member 2
C14orf8, CT152, P18, p25beta
Exostoses

13894
Translocated promoter region, nuclear basket protein
MRT79
Nonsyndromic intellectual disability, Camptodactyly-arthropathy-coxa vara-pericarditis syndrome, Differentiated thyroid carcinoma, Intellectual developmental disorder, Thyroid neoplasms

13895
Transmembrane protein adipocyte associated 1
GPR175, TMEM227, TPRA40
Parkinson disease, Rheumatoid arthritis

13896
Tumor protein p63 regulated 1
FAM79B
Color vision deficiency, Cutaneous squamous cell carcinoma, Lung cancer, Non-small cell lung carcinoma, Pancreatic neoplasms, Psoriasis, Psychiatric disorders, Rheumatoid arthritis, Seborrheic keratosis, Skin disease, Squamous cell carcinoma, Hypertension

13897
Tumor protein p63 regulated 1 like
FAM79A, SVAP30, TPRGL, h-mover, mover
Breast cancer

13898
TP53RK binding protein
CGI-121, CGI121, GAMOS5
Galloway-mowat syndrome, Nephrotic syndrome, Thyroiditis

13899
Taperin
C9orf75, DFNB79
Isolated sensorineural deafness, Nonsyndromic intellectual disability, Obstructive pulmonary disease, Congenital ear anomaly, Deafness, Hearing impairment, Hearing loss, Obesity, Nonsyndromic hearing loss

13900
Tetrapeptide repeat homeobox 2
TPRX2P, TPRX2P1, TPRXP1
Leber congenital amaurosis