Genes | GeDiPNet - Gene Disease Pathway & Associations

Dataset:

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 "D"

321 to 330 of 466 Genes

Show

	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
321	54567	DLL4	Delta like canonical Notch ligand 4	AOS6, delta4, hdelta2	Adams-oliver syndrome, Aplasia cutis congenita, Breast neoplasm, Desbuquois syndrome, Multiple sclerosis
322	54798	DCHS2	Dachsous cadherin-related 2	CDH27, CDHJ, CDHR7, PCDH23, PCDHJ	Alzheimer disease, Eczema, Auditory system disease, Bipolar disorder, Obstructive pulmonary disease, Coronary artery disease, Glioma, Graves disease, Hypertension, Major depressive disorder, Obesity, Oligodendroglioma, Schizophrenia, Sjogren syndrome, Thyrotoxic periodic paralysis View all (2 more)
323	54808	DYM	Dymeclin	DMC, SMC	Alzheimer disease, Congenital cartilage disorder, Connective tissue disease, Cutaneous leishmaniasis, Dental caries, Desbuquois syndrome, Osteoarthritis, Osteochondrodysplasias, Schizophrenia, Smith-mccort dysplasia
324	54849	DEF8	Differentially expressed in FDCP 8 homolog	-	Autism, Basal cell carcinoma, Keratinocyte carcinoma, Melanocytic nevus, Melanoma, Non-small cell lung carcinoma, Obsessive-compulsive disorder, Sebaceous gland disease, Seborrheic keratosis, Squamous cell carcinoma, Vitiligo
325	54919	DNAAF5	Dynein axonemal assembly factor 5	CILD18, HEATR2	Ciliary dyskinesia, Congenital nasopharyngeal atresia, Schizophrenia
326	54920	DUS2	Dihydrouridine synthase 2	DUS2L, SMM1, URLC8	Biliary cirrhosis, Interstitial lung disease, Biliary cholangitis
327	55112	DYNC2I1	Dynein 2 intermediate chain 1	CFAP163, DIC6, FAP163, SRPS6, SRTD8, WDR60	Jeune syndrome, Cutaneous mastocytosis, Desbuquois syndrome, Jeune thoracic dystrophy, Saldino-noonan syndrome, Scoliosis, Short rib dysplasia-polydactyly syndrome, Short-rib thoracic dysplasia
328	55152	DALRD3	DALR anticodon binding domain containing 3	DEE86, EIEE86	Developmental and epileptic encephalopathy, Myocardial infarction
329	55157	DARS2	Aspartyl-tRNA synthetase 2, mitochondrial	ASPRS, LBSL, MT-ASPRS, mtAspRS	Alzheimer disease, Central nervous system demyelinating disease, Cerebral cortical atrophy, Congenital clubfoot, Gout, Hypertension, Mitochondrial disease, Spastic ataxia
330	55172	DNAAF2	Dynein axonemal assembly factor 2	C14orf104, CILD10, KTU, PF13	Atherosclerosis, Autism, Ciliary dyskinesia, Congenital nasopharyngeal atresia

«««...31 323334 35...»»»