Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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3881 to 3890 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3881
Dynein light chain Tctex-type 4
TCTEX1D4
Neurodevelopmental disorder

3882
Dynein light chain Tctex-type family member 5
TCTEX1D1
Amblyopia

3883
Dual specificity tyrosine phosphorylation regulated kinase 1A
DYRK, DYRK1, HP86, MNB, MNBH, MRD7
Autism, Cholecystitis, Cholecystolithiasis, Colonic neoplasms, Neurodevelopmental disorder, Intellectual disability syndrome, Epilepsy, Seizure, Global developmental delay, Intellectual developmental disorder, Major depressive disorder, Male infertility spermatogenesis disorder, Metabolic syndrome, Microphthalmos, Non-specific syndromic intellectual disability
View all (8 more)

3884
Dual specificity tyrosine phosphorylation regulated kinase 1B
AOMS3, MIRK
Metabolic syndrome, Ovarian neoplasms

3885
Dual specificity tyrosine phosphorylation regulated kinase 2
-
Androgenetic alopecia, Gastrointestinal stromal tumor

3886
Dual specificity tyrosine phosphorylation regulated kinase 3
DYRK5, RED, REDK, hYAK3-2
Migraine, Diabetes mellitus type 1, Diabetes mellitus type 2

3887
Dual specificity tyrosine phosphorylation regulated kinase 4
-
Seasonal allergic rhinitis, Diabetes mellitus type 2

3888
Dysferlin
FER1L1, LGMD2B, LGMDR2, MMD1
Juvenile arthritis, Asthma, Attention deficit hyperactivity disorder, Autism, Limb girdle muscular dystrophy, Dilated cardiomyopathy, Cerebral amyloid angiopathy, Congenital muscular dystrophy, Congenital myopathy, Digestive system neoplasms, Disorder of pharynx, Distal myopathy, Dysferlinopathy, Heart failure, Hepatocellular carcinoma
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3889
Dystrotelin
-
Spondylosis

3890
Double zinc ribbon and ankyrin repeat domains 1
ANKRD64, C20orf12, C20orf84
Asthma, Central nervous system cancer, Glioblastoma, Glioma