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
Showing genes starting with "Y"
31 to 40 of 41 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

31
YTH N6-methyladenosine RNA binding protein F2
CAHL, DF2, HGRG8, NY-REN-2
Hepatocellular carcinoma, Diabetes mellitus type 2

32
YTH N6-methyladenosine RNA binding protein F3
DF3
Myocardial infarction

33
Tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein beta
GW128, HEL-S-1, HS1, KCIP-1, YWHAA
Schizophrenia

34
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

35
Tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein gamma
14-3-3GAMMA, DEE56, EIEE56, PPP1R170
Developmental and epileptic encephalopathy, Intellectual developmental disorder, Multiple sclerosis, Schizophrenia, Specific learning disability

36
Tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein eta
YWHA1
Bipolar disorder, Cardiomyopathy, Diabetes mellitus type 2

37
Tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta
14-3-3, 1C5, HS1
Alzheimer disease, Oligodendroglioma, Osteoarthritis, Colorectal cancer

38
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, Non-specific syndromic intellectual disability, Schizophrenia

39
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

40
YY1 associated protein 1
GRNG, HCCA1, HCCA2, YY1AP
Progressive arterial occlusive disease with hypertension, Intellectual developmental disorder, Marfan syndrome