Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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13951 to 13960 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

13951
Triggering receptor expressed on myeloid cells 1
CD354, TREM-1
Alzheimer disease, Liver disease, Schizophrenia, Sepsis

13952
Triggering receptor expressed on myeloid cells 2
AD17, PLOSL2, TREM-2, Trem2a, Trem2b, Trem2c
Alzheimer disease, Amyotrophic lateral sclerosis, Aortic stenosis, Aortic valve disease, Dementia, Desbuquois syndrome, Frontotemporal dementia, Nasopharyngeal neoplasms, Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy

13953
Triggering receptor expressed on myeloid cells like 1
GLTL1825, PRO3438, TLT-1, TLT1, dJ238O23.3
Juvenile arthritis, Juvenile idiopathic arthritis, Oligoarticular juvenile idiopathic arthritis

13954
Triggering receptor expressed on myeloid cells like 2
C6orf76, TLT-2, TLT2, dJ238O23.1
Alzheimer disease, Aortic stenosis, Aortic valve disease, Dementia, Lewy body disease, Diabetes mellitus type 2

13955
Transcriptional regulating factor 1
BCAR2, HSA277276, RAPA, TREP132, TReP-132, dJ139D8.5
Breast neoplasms, Neurodevelopmental disorder, Non-specific syndromic intellectual disability

13956
Three prime repair exonuclease 1
AGS1, CRV, DRN3, HERNS, RVCLS
Aicardi goutieres syndrome, Brain disease, Cadasil, Chilblain lupus erythematosus, Vascular dementia, Chilblain lupus, Systemic lupus erythematosus, Neurodevelopmental disorder, Obesity, Retinitis pigmentosa, Type i interferonopathy, Retinal vasculopathy with cerebral leukodystrophy

13957
Three prime repair exonuclease 2
-
Intellectual developmental disorder

13958
Thyrotropin releasing hormone
Pro-TRH, TRF
Alzheimer disease, Amnesia, Cardiac arrhythmias, Bradycardia, Cardiac arrhythmia, Catalepsy, Major depressive disorder, Endometriosis, Hypertension, Learning disorders, Myeloid leukemia, Narcolepsy, Seizures, Tremor, Depression

13959
Thyrotropin releasing hormone degrading enzyme
PAP-II, PGPEP2, TRH-DE
Anorexia nervosa, Attention deficit hyperactivity disorder, Esophageal disease, Esophageal ulcer, Major depressive disorder, Neurotic disorder, Obesity, Obsessive-compulsive disorder, Rheumatoid arthritis, Schizophrenia, Scoliosis, Substance abuse

13960
Thyrotropin releasing hormone receptor
CHNG7, TRH-R
Androgenetic alopecia, Brachycephaly, Congenital central hypothyroidism, Corneal neovascularization, Coronary artery disease, Female infertility, Global developmental delay, Hypertension, Hypothyroidism, Keratitis, Metabolic syndrome, Intellectual disability, Oligodendroglioma, Schizophrenia, Thyroid hormone resistance
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