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
Showing genes starting with "T"
821 to 830 of 1188 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

821
Tubulin polymerization promoting protein family member 2
C14orf8, CT152, P18, p25beta
Exostoses

822
Translocated promoter region, nuclear basket protein
MRT79
Nonsyndromic intellectual disability, Camptodactyly-arthropathy-coxa vara-pericarditis syndrome, Differentiated thyroid carcinoma, Intellectual developmental disorder, Thyroid neoplasms

823
Transmembrane protein adipocyte associated 1
GPR175, TMEM227, TPRA40
Parkinson disease, Rheumatoid arthritis

824
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

825
Tumor protein p63 regulated 1 like
FAM79A, SVAP30, TPRGL, h-mover, mover
Breast cancer

826
TP53RK binding protein
CGI-121, CGI121, GAMOS5
Galloway-mowat syndrome, Nephrotic syndrome, Thyroiditis

827
Taperin
C9orf75, DFNB79
Isolated sensorineural deafness, Nonsyndromic intellectual disability, Obstructive pulmonary disease, Congenital ear anomaly, Deafness, Hearing impairment, Hearing loss, Obesity, Nonsyndromic hearing loss

828
Tetrapeptide repeat homeobox 2
TPRX2P, TPRX2P1, TPRXP1
Leber congenital amaurosis

829
Tryptase alpha/beta 1
TPS1, TPS2, TPSB1, TPSB2, Tryptase-2
Connective tissue disease, Contact dermatitis, Dysautonomia, Irritable bowel syndrome, Pruritus, Systemic mastocytosis, Urticaria

830
Tryptase beta 2
TPS2, tryptaseB, tryptaseC
Urticaria