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
14921 to 14930 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14921
YTH N6-methyladenosine RNA binding protein F3
DF3
Myocardial infarction

14922
Tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein beta
GW128, HEL-S-1, HS1, KCIP-1, YWHAA
Schizophrenia

14923
Tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon
14-3-3E, HEL2, KCIP-1, MDCR, MDS
17p13.3 microduplication syndrome, Atrial fibrillation, Bipolar disorder, Clear cell sarcoma of kidney, Neurodevelopmental disorder, Connective tissue disease, Chromosome 17p13.3 microdeletion syndrome, Endometrial stromal sarcoma, Essential tremor, Heart failure, Hirschsprung disease, Hypertension, Miller-dieker syndrome, Non-specific syndromic intellectual disability, Schizophrenia

14924
Tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein gamma
14-3-3GAMMA, DEE56, EIEE56, PPP1R170
Developmental and epileptic encephalopathy, Intellectual developmental disorder, Liver cirrhosis, Multiple sclerosis, Schizophrenia, Specific learning disability

14925
Tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein eta
YWHA1
Bipolar disorder, Cardiomyopathy, Experimental diabetes, Diabetes mellitus type 2

14926
Tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta
14-3-3, 1C5, HS1
Alzheimer disease, Oligodendroglioma, Osteoarthritis, Colorectal cancer

14927
Tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta
14-3-3-zeta, HEL-S-3, HEL-S-93, HEL4, KCIP-1, POPCHAS, YWHAD
Attention deficit hyperactivity disorder, Nonsyndromic intellectual disability, Bipolar disorder, Carcinoma, Neurodevelopmental disorder, Conduct disorder, Liver cirrhosis, Non-specific syndromic intellectual disability, Schizophrenia

14928
YY1 transcription factor
DELTA, GADEVS, INO80S, NF-E1, UCRBP, YIN-YANG-1
Neurodevelopmental disorder, Congestive heart failure, Developmental and epileptic encephalopathy, Diabetic neuropathy, Heart failure, Intellectual developmental disorder, Multiple myeloma, Scoliosis, Uterine neoplasms

14929
YY1 associated protein 1
GRNG, HCCA1, HCCA2, YY1AP
Progressive arterial occlusive disease with hypertension, Intellectual developmental disorder, Marfan syndrome

14930
YY2 transcription factor
ZNF631
Keratosis follicularis spinulosa decalvans, x-linked, Olmsted syndrome, x-linked, Osteogenesis imperfecta