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
14081 to 14090 of 15448 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

14081
Tripartite motif containing 69
HSD-34, HSD34, RNF36, Trif
Alzheimer disease, Depression

14082
Tripartite motif containing 71
HYC4, HYDCC1, LIN-41, LIN41
Attention deficit hyperactivity disorder, Colorectal cancer, Congenital communicating hydrocephalus, Congenital hydrocephalus, Cryptospermia, Hydrocephalus, Major depressive disorder, Multiple sclerosis, Open angle glaucoma, Preeclampsia, Testicular azoospermia, Venous thromboembolism

14083
Tripartite motif containing 77
TRIM77P
Non-melanoma skin carcinoma

14084
Tripartite motif containing 8
FSGSNEDS, GERP, RNF27
Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Developmental and epileptic encephalopathy, Focal glomerulosclerosis, Focal segmental glomerulosclerosis, Major depressive disorder, Obsessive-compulsive disorder, Prostate cancer, Schizophrenia, Tourette syndrome

14085
Tripartite motif containing 9
RNF91, SPRING
Alzheimer disease, Gastroesophageal reflux disease, Orofacial cleft, Psychotic disorders, Schizophrenia, Scoliosis

14086
Tripartite motif family like 2
SPRYD6
Prostate cancer, Systemic lupus erythematosus

14087
Trio Rho guanine nucleotide exchange factor
ARHGEF23, MEBAS, MRD44, MRD63, tgat
Anaphylaxis, Angioedema, Asthma, Color vision deficiency, Deafness, Developmental delay, Essential tremor, Gout, Intellectual developmental disorder, Myeloid leukemia, Liver neoplasms, Major depressive disorder, Neuroblastoma, Neurodevelopmental disorder, Neuropathy
View all (2 more)

14088
TRIO and F-actin binding protein
DFNB28, HRIHFB2122, TAP68, TARA, dJ37E16.4
Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Isolated sensorineural deafness, Nonsyndromic hearing loss, Deafness, Glaucoma, Hearing impairment, Hearing loss, Hereditary hearing loss, Meniere disease, Nephrolithiasis, Open angle glaucoma, Osteoarthritis

14089
Thyroid hormone receptor interactor 11
ACG1A, CEV14, GMAP-210, GMAP210, ODCD, ODCD1, TRIP-11, TRIP230
Achondrogenesis, Connective tissue disease, Desbuquois syndrome, Major depressive disorder, Spondylometaphyseal dysplasia

14090
Thyroid hormone receptor interactor 12
MRD49, TRIP-12, TRIPC, ULF
Clark-baraitser syndrome, Color vision deficiency, Neurodevelopmental disorder, Intellectual developmental disorder, Metabolic syndrome, Non-specific syndromic intellectual disability, Diabetes mellitus type 2