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
13991 to 14000 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

13991
Translocation associated membrane protein 1 like 1
-
Bronchopulmonary dysplasia, Obesity, Ulcerative colitis

13992
Translocation associated membrane protein 2
-
Peripheral arterial disease, Scoliosis

13993
Tetratricopeptide repeat and ankyrin repeat containing 1
LBA1
Alzheimer disease, Autism, Bilirubin metabolism disease, Bipolar disorder, Bipolar depression, Hypothyroidism, Kleine-levin syndrome, Metabolic syndrome, Schizophrenia, Diabetes mellitus type 2, Ulcerative colitis

13994
TNF receptor associated protein 1
HSP 75, HSP75, HSP90L, TRAP-1
Asthma, Atrial fibrillation, Congenital anomalies of the kidney and urinary tract, Gout, Osteoarthritis, Sclerosing cholangitis, Stomach neoplasms, Diabetes mellitus type 2, Vacterl association

13995
Trafficking protein particle complex subunit 10
EHOC-1, EHOC1, GT334, NEDMISS, TMEM1, TRS130, TRS30
Primary microcephaly, Crohn disease, Dermatologic disorder, Inflammatory bowel disease, Intellectual developmental disorder, Neurodevelopmental disorder, Skin disease, Ulcerative colitis

13996
Trafficking protein particle complex subunit 11
C4orf41, FOIGR, GRY, LGMD2S, LGMDR18
Androgenetic alopecia, Limb girdle muscular dystrophy, Glucocorticoid deficiency with achalasia, Intellectual developmental disorder movement cerebellar, Limb-girdle muscular dystrophy, Muscular dystrophy, Myopathy, Obesity, Sarcoidosis, Systemic lupus erythematosus, Triple a syndrome

13997
Trafficking protein particle complex subunit 12
CGI-87, PEBAS, TTC-15, TTC15
Cerebral amyloid angiopathy, Dementia, Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome, Obesity

13998
Trafficking protein particle complex subunit 14
C7orf43, MAP11, MCPH25
Primary microcephaly, Microcephaly

13999
Trafficking protein particle complex subunit 2
MIP2A, SEDL, SEDT, TRAPPC2P1, TRS20, ZNF547L, hYP38334
Connective tissue disease, Desbuquois syndrome, Osteochondrodysplasias, Spastic paraplegia, Spondyloepiphyseal dysplasia

14000
Trafficking protein particle complex subunit 2L
HSPC176, PERRB
Intellectual developmental disorder, Mucopolysaccharidosis, Parkinson disease