Genes | GeDiPNet - Gene Disease Pathway & Associations

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3331 to 3340 of 12229 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
3331	22936	ELL2	Elongation factor for RNA polymerase II 2	MRCCAT1	Hodgkin disease, Lymphocytic leukemia, Monoclonal gammapathies, Multiple myeloma, Paraproteinemia
3332	22937	SCAP	SREBF chaperone	-	Liver carcinoma
3333	2294	FOXF1	Forkhead box F1	ACDMPV, FKHL5, FREAC1	Agenesis of gallbladder, Alveolar capillary dysplasia, Annular pancreas, Anomalous pulmonary venous return, Aortic valve sclerosis, Asplenia, Atrial septal defect, Bicuspid aortic valve, Congenital atresia of pulmonary valve, Congenital diaphragmatic hernia, Congenital malrotation of intestine, Duodenal atresia, Fetal megacystis, Gastrointestinal stromal tumor, Hirschsprung disease View all (18 more)
3334	22941	SHANK2	SH3 and multiple ankyrin repeat domains 2	AUTS17, CORTBP1, CTTNBP1, ProSAP1, SHANK, SPANK-3	Attention deficit hyperactivity disorder, Autism, Autism spectrum disorder, Bipolar disorder, Dysmorphic features, Glioma, Mental retardation, Leukemia, Manic disorder, Mental depression
3335	22943	DKK1	Dickkopf Wnt signaling pathway inhibitor 1	DKK-1, SK	Arnold-chiari malformation, Basilar invagination, Breast cancer, Mammary neoplasms, Breast carcinoma, Cerebellar ataxia, Cranial nerve compression, Cranial nerve paralysis, Distal peripheral sensory neuropathy, Dysphagia, Endometrioma, Endometriosis, Klippel feil syndrome, Marfan syndrome, Nystagmus View all (8 more)
3336	22947	DUX4L1	Double homeobox 4 like 1 (pseudogene)	DUX10, DUX4	Facioscapulohumeral dystrophy, Facioscapulohumeral muscular dystrophy
3337	22948	CCT5	Chaperonin containing TCP1 subunit 5	CCT-epsilon, CCTE, HEL-S-69, HSNSP, PNAS-102, TCP-1-epsilon	Atrophy of the spinal cord, Breast cancer, Mammary neoplasms, Breast carcinoma, Distal amyotrophy, Dysautonomia, Foot osteomyelitis, Hereditary sensory neuropathy with spastic paraplegia, Hypocholesterolemia, Lung adenocarcinoma, Marfan syndrome, Peripheral axonal neuropathy, Spastic paraplegia
3338	2295	FOXF2	Forkhead box F2	FKHL6, FREAC-2, FREAC2	Stroke
3339	22950	SLC4A1AP	Solute carrier family 4 member 1 adaptor protein	HLC3	Gout, Gouty arthritis
3340	22953	P2RX2	Purinergic receptor P2X 2	DFNA41, P2X2	Deafness, Epilepsy, Non-syndromic sensorineural deafness, Nonsyndromic deafness

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