Genes | GeDiPNet - Gene Disease Pathway & Associations

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3561 to 3570 of 12229 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
3561	23302	WSCD1	WSC domain containing 1	-	Liver neoplasms, Liver cancer
3562	23305	ACSL6	Acyl-CoA synthetase long chain family member 6	ACS2, FACL6, LACS 6, LACS2, LACS5	Alzheimer disease, Leukemia, Myelodysplastic syndrome, Schizophrenia
3563	23306	NEMP1	Nuclear envelope integral membrane protein 1	TMEM194, TMEM194A	Leukemia
3564	23308	ICOSLG	Inducible T cell costimulator ligand	B7-H2, B7H2, B7RP-1, B7RP1, B7h, CD275, GL50, ICOS-L, ICOSL, IMD119, LICOS	Asthma, Autoimmune diseases, Celiac disease, Immune system diseases, Multiple sclerosis, Rheumatoid arthritis, Ulcerative colitis
3565	23310	NCAPD3	Non-SMC condensin II complex subunit D3	CAP-D3, CAPD3, MCPH22, hCAP-D3, hHCP-6, hcp-6	Agenesis of corpus callosum, Developmental delay, Dwarfism, Mental retardation, Microcephaly, Neuronal heterotopia, Pachygyria, Renal aplasia, Vesicoureteral reflux
3566	23312	DMXL2	Dmx like 2	DEE81, DFNA71, EIEE81, PEPNS, RC3	Central hypothyroidism, Deafness, Dwarfism, Dysarthria, Epileptic encephalopathy, Hearing loss, Hypoglycemia, Hypogonadism, Mental retardation, Motor delay, Non-syndromic sensorineural deafness, Polyendocrine-polyneuropathy syndrome, Polyneuropathy
3567	23313	KIAA0930	KIAA0930	C22orf9, LSC3	Leukemia
3568	23314	SATB2	SATB homeobox 2	C2DELq32q33, DEL2Q32Q33, GLSS	2q32-q33 deletion syndrome, 2q33.1 microdeletion syndrome, Anxiety disorder, Arachnodactyly, Attention deficit hyperactivity disorder, Autism, Brachycephaly, Camptodactyly of fingers, Clinodactyly, Colorectal cancer, Colorectal neoplasms, Congenital camptodactyly, Congenital clubfoot, Developmental delay, Dolichocephaly View all (22 more)
3569	23315	SLC9A8	Solute carrier family 9 member A8	NHE-8, NHE8	Ankylosing spondylitis, Cholangitis, Crohn disease, Dementia, Multiple sclerosis, Psoriasis, Senile paranoid dementia, Ulcerative colitis
3570	23316	CUX2	Cut like homeobox 2	CDP2, CUTL2, DEE67, EIEE67	Absence seizure, Autism, Bipolar disorder, Coronary heart disease, Developmental delay, Diabetes mellitus, Dyskinetic syndrome, Epileptic encephalopathy, Gout, Gouty arthritis, Hypertension, Hypotonic seizures, Lennox-gastaut syndrome, Major affective disorder, Mental retardation View all (4 more)

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