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 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14081
TSC22 domain family member 3
DIP, DSIPI, GILZ, TSC-22R
Hyperinsulinism, Male infertility, Testicular disease

14082
TRNA splicing endonuclease subunit 15
C1orf19, PCH2F, sen15
Color vision deficiency, Congenital microcephaly, Global developmental delay, Open angle glaucoma, Osteoarthritis, Pontocerebellar hypoplasia, Prostate cancer, Scoliosis, Diabetes mellitus type 2

14083
TRNA splicing endonuclease subunit 2
PCH2B, SEN2, SEN2L
Alzheimer disease, Coronary artery disease, Deglutition disorder, Hemolytic uremic syndrome, Hypertrophic cardiomyopathy, Osteonecrosis of the femoral head, Intellectual developmental disorder, Metabolic syndrome, Microcephaly, Movement disorder, Nonalcoholic fatty liver disease, Periodontal disease, Periodontitis, Pontocerebellar hypoplasia, Systemic lupus erythematosus
View all (3 more)

14084
TRNA splicing endonuclease subunit 34
LENG5, PCH2C, SEN34, SEN34L
Deglutition disorder, Intellectual developmental disorder, Microcephaly, Movement disorder, Obesity, Pontocerebellar hypoplasia, Visual disorder

14085
TRNA splicing endonuclease subunit 54
PCH2A, PCH4, PCH5, SEN54L, sen54
Amblyopia, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Obstructive pulmonary disease, Congenital neurologic anomalies, Deglutition disorder, Global developmental delay, Intellectual developmental disorder, Methylmalonic acidemia, Microcephaly, Movement disorder, Pontocerebellar hypoplasia, Visual disorder

14086
Ts translation elongation factor, mitochondrial
EFTS, EFTSMT
Dilated cardiomyopathy, Combined oxidative phosphorylation deficiency, Skeletal muscle disorder, Dyskinesia, Gout, Leigh syndrome, Mitochondrial disease, Multiple sclerosis, Nephrotic syndrome, Sarcoidosis, Steroid-resistant nephrotic syndrome

14087
Testis specific 10
CEP4L, CT79, SPGF26
Spermatogenic failure, Uterine fibroid

14088
Testis specific 10 interacting protein
FAM161C
Breast cancer, Gout, Multiple sclerosis, Non-melanoma skin carcinoma, Open angle glaucoma

14089
Testis specific 13
-
Osteonecrosis

14090
Thyroid stimulating hormone subunit beta
TSH-B, TSH-BETA
Bipolar disorder, Thyroid agenesis, Congenital thyroid atrophy, Congenital hypothyroidism, Congenital hypothyroidism without goiter, Bipolar depression, Graves disease, Hypothyroidism