Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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13961 to 13970 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

13961
Taperin
C9orf75, DFNB79
Isolated sensorineural deafness, Nonsyndromic intellectual disability, Obstructive pulmonary disease, Congenital ear anomaly, Deafness, Hearing impairment, Hearing loss, Obesity, Nonsyndromic hearing loss

13962
Tetrapeptide repeat homeobox 2
TPRX2P, TPRX2P1, TPRXP1
Leber congenital amaurosis

13963
Tryptase alpha/beta 1
TPS1, TPS2, TPSB1, TPSB2, Tryptase-2
Connective tissue disease, Contact dermatitis, Dysautonomia, Irritable bowel syndrome, Pruritus, Systemic mastocytosis, Urticaria

13964
Tryptase beta 2
TPS2, tryptaseB, tryptaseC
Urticaria

13965
Tryptase delta 1
MCP7-LIKE, MCP7L1, MMCP-7L
Bladder exstrophy and epispadias complex, Systemic mastocytosis, Urticaria

13966
Tyrosylprotein sulfotransferase 1
TANGO13A
Autism, Gout, Psychiatric disorders

13967
Tyrosylprotein sulfotransferase 2
TANGO13B, TPST-2
Autism, Ocular hypotension, Specific language disorder

13968
Tumor protein, translationally-controlled 1
HRF, TCTP, p02, p23
Kidney neoplasms, Prostatic neoplasms, Schizophrenia, Diabetes mellitus type 2

13969
Transmembrane phosphatase with tensin homology
CT44, PTEN2, TPTE1
Autism, Celiac disease

13970
TPTEP2-CSNK1E readthrough
LOC400927-CSNK1E
Cardiac arrhythmia, Cerebellar ataxia, Developmental and epileptic encephalopathy, Keratoconus, Mastocytosis