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
3591 to 3600 of 15380 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

3591
Delta like canonical Notch ligand 1
DELTA1, DL1, Delta, NEDBAS
Nonsyndromic intellectual disability, Brain neoplasms, Breast neoplasms, Holoprosencephaly, Microform holoprosencephaly, Syntelencephaly, Neurodevelopmental disorder, Semilobar holoprosencephaly, Septopreoptic holoprosencephaly

3592
Delta like canonical Notch ligand 3
SCDO1
Astrocytoma, Spondylocostal dysostosis, Congenital abnormalities, Congenital cartilage disorder, Congenital fusion of ribs, Congenital hemivertebra, Craniofacial abnormalities, Desbuquois syndrome, Dysphoric mood, Jarcho-levin syndrome, Osteochondrodysplasias, Scoliosis, Syndactyly

3593
Delta like canonical Notch ligand 4
AOS6, delta4, hdelta2
Adams-oliver syndrome, Aplasia cutis congenita, Breast neoplasms, Desbuquois syndrome, Multiple sclerosis

3594
Dihydrolipoamide S-succinyltransferase
DLTS, KGD2, PGL7, PPGL7
Alzheimer disease, Migraine, Non-small cell lung carcinoma, Pheochromocytoma/paraganglioma syndrome

3595
Distal-less homeobox 1
-
Autism, Bipolar disorder, Craniofacial abnormalities, Non-organic psychosis, Psychotic disorders, Schizophrenia

3596
Distal-less homeobox 2
TES-1, TES1
Autism, Craniofacial abnormalities, Schizophrenia

3597
Distal-less homeobox 3
AI4, TDO
Amelogenesis imperfecta, Dentin dysplasia, Dentinogenesis imperfecta, Desbuquois syndrome, Peripheral pulmonary artery stenosis, Tricho-dento-osseous syndrome

3598
Distal-less homeobox 4
BP1, DLX7, DLX8, DLX9, OFC15
Cleft lip and palate, Orofacial cleft

3599
Distal-less homeobox 5
SHFM1, SHFM1D
Alzheimer disease, Bone disease, Congenital cleft hand, Congenital malformation syndromes predominantly involving limbs, Craniofacial abnormalities, Desbuquois syndrome, Ectrodactyly, Gastroesophageal reflux disease, Klippel-trenaunay syndrome, Osteoarthritis, Rubinstein-taybi syndrome, Split hand-foot malformation, Thrombocytopenia, Vacterl association

3600
Distal-less homeobox 6
-
Attention deficit hyperactivity disorder, Autism, Craniofacial abnormalities, Desbuquois syndrome, Ectrodactyly, Split hand-foot malformation, Substance abuse