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GlyCosmos Genes

Integrated list of glycan-related genes extracted KEGG GENES Database, UniProt, GlycoGene Database (GGDB), Plant GARDEN and FlyGlycoDB. Glycan-related genes including glycosyltransferase, hydrolase activity (acting on glycosyl bonds), carbohydrate metabolic process, etc .

Source	Last Updated
FlyGlycoDB	March 25, 2024
GlycoGene Database (GGDB)	January 26, 2018
KEGG GENES Database	September 20, 2023
Plant GARDEN	May 28, 2020
UniProt	July 8, 2024

Selecting the function you want to look up from the categories displays a list narrowed down to glycan-related genes with that function (Gene Ontology).

Catalytic activity

glycosyltransferase activity

hydrolase activity, acting on glycosyl bonds

Binding

carbohydrate binding

Response to carbohydrate

Primary metabolic process

Displaying entries **1176 - 1200** of **393515** in total

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Gene ID	Gene Name	Gene Symbol	Organism	Disease Ontology ▲
22845	dolichol kinase	DOLK Aliases: DK1 KIAA1094 dolichol kinase 1	Homo sapiens (human)	Marfan syndrome X-linked dilated cardiomyopathy autosomal recessive polycystic kidney disease congenital disorder of glycosylation Im congenital disorder of glycosylation Iq congenital disorder of glycosylation type I congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 dilated cardiomyopathy 1A dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy ichthyosis isolated elevated serum creatine phosphokinase levels lipoatrophic diabetes mellitus lipodystrophy nonepidermolytic palmoplantar keratoderma palmoplantar keratosis polycystic kidney disease 4 sensorineural hearing loss situs inversus tuberous sclerosis
139189	diacylglycerol kinase kappa	DGKK	Homo sapiens (human)	Marfan syndrome agnosia arteriosclerotic cardiovascular disease atherosclerosis conduct disorder coronary artery disease developmental coordination disorder disease of mental health fragile X syndrome hepatocellular carcinoma hypospadias liver cancer prostate cancer prostate carcinoma situs inversus syndromic X-linked intellectual disability 94 tuberous sclerosis
9524	trans-2,3-enoyl-CoA reductase	TECR Aliases: MRT14 TER very-long-chain enoyl-CoA reductase	Homo sapiens (human)	Marfan syndrome agnosia autosomal recessive intellectual developmental disorder 14 autosomal recessive intellectual developmental disorder cardiovascular system disease cerebral degeneration choreatic disease depressive disorder developmental coordination disorder dyskeratosis congenita dysthymic disorder dystonia endometriosis of uterus endometriosis epilepsy focal epilepsy heart disease influenza intellectual disability learning disability lingual-facial-buccal dyskinesia major depressive disorder melancholic depression microcephaly neurotic disorder non-syndromic intellectual disability obsolete infantile epileptic encephalopathy obsolete melancholia partial motor epilepsy pneumothorax situs inversus stereotypic movement disorder syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 tuberous sclerosis visual epilepsy
51604	phosphatidylinositol glycan anchor biosynthesis class T	PIGT Aliases: GPI transamidase component PIG-T GPI transamidase subunit PIG-T	Homo sapiens (human)	Marfan syndrome angioedema blindness brain disease breast cancer breast carcinoma calcinosis calcium metabolism disease cerebral degeneration congenital nystagmus craniosynostosis cystic kidney disease dermatographia diarrhea dissociated nystagmus epilepsy esotropia fibromyalgia hemolytic anemia hypercalcemia hyperopia hypertropia hypophosphatasia mechanical strabismus monocular esotropia multiple congenital anomalies-hypotonia-seizures syndrome 3 myositis nephrocalcinosis non-congenital cyst of kidney ophthalmoplegia osteoporosis paroxysmal nocturnal hemoglobinuria patent ductus arteriosus pathologic nystagmus phosphorus metabolism disease restrictive cardiomyopathy scoliosis situs inversus spontaneous ocular nystagmus strabismus tuberous sclerosis urticaria visual epilepsy
23443	solute carrier family 35 member A3	SLC35A3 Aliases: UDP-N-acetylglucosamine transporter	Homo sapiens (human)	Marfan syndrome autism spectrum disorder autistic disorder central nervous system cancer congenital disorder of glycosylation epilepsy gliosarcoma high grade glioma intellectual disability learning disability microcephaly mixed glioma mucopolysaccharidosis IV multiple epiphyseal dysplasia osteochondrodysplasia scoliosis situs inversus spondylocostal dysostosis syndromic X-linked intellectual disability 94 tuberous sclerosis visual epilepsy
5161	pyruvate dehydrogenase E1 subunit alpha 2	PDHA2	Homo sapiens (human)	Marfan syndrome azoospermia disease of metabolism male infertility pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency retinal degeneration situs inversus spermatogenic failure 1 spermatogenic failure tuberous sclerosis
23213	sulfatase 1	SULF1 Aliases: Extracellular sulfatase Sulf-1 KIAA1077 SULF-1 hSulf-1	Homo sapiens (human)	Marinesco-Sjogren syndrome acute pancreatitis adult hepatocellular carcinoma anal carcinoma in situ arthritis arthropathy bacterial sepsis bladder urothelial carcinoma brain cancer breast cancer breast carcinoma breast ductal carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cervix uteri carcinoma in situ childhood hepatocellular carcinoma colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma degenerative disc disease disease of metabolism embryoma giant cell glioblastoma glioblastoma head and neck squamous cell carcinoma hepatitis hepatocellular carcinoma high grade glioma idiopathic interstitial pneumonia large intestine cancer liver cancer liver carcinoma liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma melanoma nodular prostate osteoarthritis ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatitis pneumonia postinflammatory pulmonary fibrosis primary cerebellar degeneration prostatic adenoma pulmonary fibrosis seminoma skin melanoma steatotic liver disease stomach cancer stomach carcinoma testicular cancer testis seminoma transitional cell carcinoma
276	amylase alpha 1A	AMY1A	Homo sapiens (human)	McCune Albright syndrome Sjogren's syndrome Zollinger-Ellison syndrome adenocarcinoma adenoma allergic rhinitis anorexia nervosa anxiety disorder autism spectrum disorder autistic disorder cancer cribriform carcinoma depressive disorder diabetes mellitus dysthymic disorder embryoma essential hypertension generalized anxiety disorder granular cell carcinoma hepatocellular carcinoma hyperinsulinism hypertension hypothalamic disease inflammatory bowel disease 1 inflammatory bowel disease intellectual disability keratoconjunctivitis sicca kwashiorkor learning disability liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma major depressive disorder marasmus meconium aspiration syndrome melancholic depression multiple myeloma neurotic disorder nutrition disease obesity obsolete melancholia obstructive sleep apnea parathyroid gland disease periodontal disease phobic disorder post-traumatic stress disorder protein-energy malnutrition schizophrenia seasonal affective disorder substance abuse substance-related disorder tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis vasomotor rhinitis
277	amylase alpha 1B	AMY1B	Homo sapiens (human)	McCune Albright syndrome Sjogren's syndrome Zollinger-Ellison syndrome adenocarcinoma adenoma allergic rhinitis anorexia nervosa anxiety disorder autism spectrum disorder autistic disorder cancer cribriform carcinoma depressive disorder diabetes mellitus dysthymic disorder embryoma essential hypertension generalized anxiety disorder granular cell carcinoma hepatocellular carcinoma hyperinsulinism hypertension hypothalamic disease inflammatory bowel disease 1 inflammatory bowel disease intellectual disability keratoconjunctivitis sicca kwashiorkor learning disability liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma major depressive disorder marasmus meconium aspiration syndrome melancholic depression multiple myeloma neurotic disorder nutrition disease obesity obsolete melancholia obstructive sleep apnea parathyroid gland disease periodontal disease phobic disorder post-traumatic stress disorder protein-energy malnutrition seasonal affective disorder substance abuse substance-related disorder tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis vasomotor rhinitis
278	amylase alpha 1C	AMY1C	Homo sapiens (human)	McCune Albright syndrome Sjogren's syndrome Zollinger-Ellison syndrome adenocarcinoma adenoma allergic rhinitis anorexia nervosa anxiety disorder autism spectrum disorder autistic disorder cancer cribriform carcinoma depressive disorder diabetes mellitus dysthymic disorder embryoma essential hypertension generalized anxiety disorder granular cell carcinoma hepatocellular carcinoma hyperinsulinism hypertension hypothalamic disease inflammatory bowel disease 1 inflammatory bowel disease intellectual disability keratoconjunctivitis sicca kwashiorkor learning disability liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma major depressive disorder marasmus meconium aspiration syndrome melancholic depression multiple myeloma neurotic disorder nutrition disease obesity obsolete melancholia obstructive sleep apnea parathyroid gland disease periodontal disease phobic disorder post-traumatic stress disorder protein-energy malnutrition seasonal affective disorder substance abuse substance-related disorder tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis vasomotor rhinitis
378	ADP ribosylation factor 4	ARF4	Homo sapiens (human)	Meckel syndrome 1 Meckel syndrome 2 Meckel syndrome 3 Meckel syndrome 4 Meckel syndrome 5 Meckel syndrome 6 Meckel syndrome 8 Meckel syndrome autosomal dominant polycystic kidney disease breast cancer cystic kidney disease giant cell glioblastoma glioblastoma hepatitis C high grade glioma ovarian cancer ovarian carcinoma
79053	ALG8 alpha-1,3-glucosyltransferase	ALG8 Aliases: MGC2840 dolichyl-P-Glc:Glc(1)Man(9)GlcNAc(2)-PP-dolichol alpha- 1->3-glucosyltransferase	Homo sapiens (human)	Meckel syndrome 1 Meckel syndrome 2 Meckel syndrome 3 Meckel syndrome 4 Meckel syndrome 5 Meckel syndrome 6 Meckel syndrome 8 anemia asphyxia neonatorum autosomal dominant polycystic kidney disease cataract cholestasis clubfoot congenital disorder of glycosylation Ih congenital disorder of glycosylation type I congenital disorder of glycosylation congenital hypothyroidism cryptorchidism cystic kidney disease depressive disorder developmental and epileptic encephalopathy 36 diarrhea dysthymic disorder elephantiasis gastrointestinal system disease heart septal defect hypothyroidism intestinal disease lymphedema macrocytic anemia major depressive disorder melancholic depression myxedema neurotic disorder non-congenital cyst of kidney obsolete melancholia oligohydramnios patent ductus arteriosus placental insufficiency polycystic liver disease polyhydramnios protein-losing enteropathy thrombocytopenia
1579	cytochrome P450 family 4 subfamily A member 11	CYP4A11 Aliases: CYP4AII	Homo sapiens (human)	Meckel syndrome acute myocardial infarction alcoholic liver cirrhosis arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant polycystic kidney disease autosomal recessive polycystic kidney disease brain stem infarction cancer cerebral artery occlusion cerebral infarction cerebrovascular disease coronary artery disease coronary thrombosis diabetes mellitus diabetic ketoacidosis embryoma essential hypertension hepatocellular carcinoma hypertension liver cancer liver cirrhosis myocardial infarction nephrosclerosis nutmeg liver renal artery disease renal hypertension silent myocardial infarction steatotic liver disease varicose veins
23193	glucosidase II alpha subunit	GANAB Aliases: G2AN GIIA GluII KIAA0088 neutral alpha-glucosidase AB	Homo sapiens (human)	Meckel syndrome arthritis arthropathy autosomal dominant polycystic kidney disease chronic fatigue syndrome encephalitis encephalomyelitis gallbladder disease liver disease multiple sclerosis myelitis osteoarthritis polycystic kidney disease 1 polycystic kidney disease 2 polycystic kidney disease 3 polycystic kidney disease polycystic liver disease
342372	polycystin 1 like 3, transient receptor potential channel interacting	PKD1L3	Homo sapiens (human)	Meckel syndrome autosomal dominant polycystic kidney disease cerebral infarction cerebrovascular disease episodic kinesigenic dyskinesia 1 prostate cancer prostate carcinoma
114780	polycystin 1 like 2 (gene/pseudogene)	PKD1L2 Aliases: KIAA1879	Homo sapiens (human)	Meckel syndrome autosomal dominant polycystic kidney disease colorectal cancer colorectal carcinoma familial periodic paralysis hypoplastic left heart syndrome large intestine cancer myopathy neuromuscular disease
56953	5',3'-nucleotidase, mitochondrial	NT5M Aliases: dNT-2 dNT2 mdN	Homo sapiens (human)	Miller-Dieker lissencephaly syndrome Smith-Magenis syndrome
51	acyl-CoA oxidase 1	ACOX1 Aliases: PALMCOX palmitoyl-CoA oxidase	Homo sapiens (human)	Mitchell syndrome X-linked nonsyndromic deafness abdominal obesity-metabolic syndrome 1 adult lymphoma anodontia autosomal dominant auditory neuropathy 1 autosomal dominant nonsyndromic deafness 10 autosomal dominant nonsyndromic deafness 11 autosomal dominant nonsyndromic deafness 12 autosomal dominant nonsyndromic deafness 13 autosomal dominant nonsyndromic deafness 15 autosomal dominant nonsyndromic deafness 16 autosomal dominant nonsyndromic deafness 17 autosomal dominant nonsyndromic deafness 18 autosomal dominant nonsyndromic deafness 1 autosomal dominant nonsyndromic deafness 20 autosomal dominant nonsyndromic deafness 21 autosomal dominant nonsyndromic deafness 22 autosomal dominant nonsyndromic deafness 23 autosomal dominant nonsyndromic deafness 24 autosomal dominant nonsyndromic deafness 25 autosomal dominant nonsyndromic deafness 27 autosomal dominant nonsyndromic deafness 28 autosomal dominant nonsyndromic deafness 2A autosomal dominant nonsyndromic deafness 2B autosomal dominant nonsyndromic deafness 30 autosomal dominant nonsyndromic deafness 31 autosomal dominant nonsyndromic deafness 33 autosomal dominant nonsyndromic deafness 36 autosomal dominant nonsyndromic deafness 3A autosomal dominant nonsyndromic deafness 3B autosomal dominant nonsyndromic deafness 40 autosomal dominant nonsyndromic deafness 41 autosomal dominant nonsyndromic deafness 43 autosomal dominant nonsyndromic deafness 44 autosomal dominant nonsyndromic deafness 47 autosomal dominant nonsyndromic deafness 48 autosomal dominant nonsyndromic deafness 49 autosomal dominant nonsyndromic deafness 4A autosomal dominant nonsyndromic deafness 4B autosomal dominant nonsyndromic deafness 50 autosomal dominant nonsyndromic deafness 51 autosomal dominant nonsyndromic deafness 52 autosomal dominant nonsyndromic deafness 53 autosomal dominant nonsyndromic deafness 54 autosomal dominant nonsyndromic deafness 56 autosomal dominant nonsyndromic deafness 58 autosomal dominant nonsyndromic deafness 59 autosomal dominant nonsyndromic deafness 5 autosomal dominant nonsyndromic deafness 64 autosomal dominant nonsyndromic deafness 65 autosomal dominant nonsyndromic deafness 66 autosomal dominant nonsyndromic deafness 67 autosomal dominant nonsyndromic deafness 68 autosomal dominant nonsyndromic deafness 69 autosomal dominant nonsyndromic deafness 6 autosomal dominant nonsyndromic deafness 70 autosomal dominant nonsyndromic deafness 7 autosomal dominant nonsyndromic deafness 9 autosomal dominant nonsyndromic deafness autosomal recessive nonsyndromic deafness 101 autosomal recessive nonsyndromic deafness 102 autosomal recessive nonsyndromic deafness 103 autosomal recessive nonsyndromic deafness 104 autosomal recessive nonsyndromic deafness 12 autosomal recessive nonsyndromic deafness 13 autosomal recessive nonsyndromic deafness 14 autosomal recessive nonsyndromic deafness 15 autosomal recessive nonsyndromic deafness 16 autosomal recessive nonsyndromic deafness 17 autosomal recessive nonsyndromic deafness 18A autosomal recessive nonsyndromic deafness 18B autosomal recessive nonsyndromic deafness 1A autosomal recessive nonsyndromic deafness 1B autosomal recessive nonsyndromic deafness 20 autosomal recessive nonsyndromic deafness 21 autosomal recessive nonsyndromic deafness 22 autosomal recessive nonsyndromic deafness 23 autosomal recessive nonsyndromic deafness 24 autosomal recessive nonsyndromic deafness 25 autosomal recessive nonsyndromic deafness 26 autosomal recessive nonsyndromic deafness 27 autosomal recessive nonsyndromic deafness 28 autosomal recessive nonsyndromic deafness 29 autosomal recessive nonsyndromic deafness 2 autosomal recessive nonsyndromic deafness 30 autosomal recessive nonsyndromic deafness 31 autosomal recessive nonsyndromic deafness 32 autosomal recessive nonsyndromic deafness 33 autosomal recessive nonsyndromic deafness 35 autosomal recessive nonsyndromic deafness 36 autosomal recessive nonsyndromic deafness 37 autosomal recessive nonsyndromic deafness 38 autosomal recessive nonsyndromic deafness 39 autosomal recessive nonsyndromic deafness 3 autosomal recessive nonsyndromic deafness 40 autosomal recessive nonsyndromic deafness 42 autosomal recessive nonsyndromic deafness 44 autosomal recessive nonsyndromic deafness 45 autosomal recessive nonsyndromic deafness 46 autosomal recessive nonsyndromic deafness 47 autosomal recessive nonsyndromic deafness 48 autosomal recessive nonsyndromic deafness 49 autosomal recessive nonsyndromic deafness 4 autosomal recessive nonsyndromic deafness 51 autosomal recessive nonsyndromic deafness 53 autosomal recessive nonsyndromic deafness 55 autosomal recessive nonsyndromic deafness 59 autosomal recessive nonsyndromic deafness 5 autosomal recessive nonsyndromic deafness 61 autosomal recessive nonsyndromic deafness 62 autosomal recessive nonsyndromic deafness 63 autosomal recessive nonsyndromic deafness 65 autosomal recessive nonsyndromic deafness 66 autosomal recessive nonsyndromic deafness 67 autosomal recessive nonsyndromic deafness 68 autosomal recessive nonsyndromic deafness 6 autosomal recessive nonsyndromic deafness 70 autosomal recessive nonsyndromic deafness 71 autosomal recessive nonsyndromic deafness 74 autosomal recessive nonsyndromic deafness 76 autosomal recessive nonsyndromic deafness 77 autosomal recessive nonsyndromic deafness 79 autosomal recessive nonsyndromic deafness 7 autosomal recessive nonsyndromic deafness 83 autosomal recessive nonsyndromic deafness 84A autosomal recessive nonsyndromic deafness 84B autosomal recessive nonsyndromic deafness 85 autosomal recessive nonsyndromic deafness 86 autosomal recessive nonsyndromic deafness 88 autosomal recessive nonsyndromic deafness 89 autosomal recessive nonsyndromic deafness 8 autosomal recessive nonsyndromic deafness 91 autosomal recessive nonsyndromic deafness 93 autosomal recessive nonsyndromic deafness 96 autosomal recessive nonsyndromic deafness 97 autosomal recessive nonsyndromic deafness 98 autosomal recessive nonsyndromic deafness 9 autosomal recessive nonsyndromic deafness cancer central nervous system lymphoma cerebral infarction cerebrovascular disease childhood lymphoma citrullinemia colorectal cancer colorectal carcinoma cone-rod dystrophy congenital nystagmus craniosynostosis depressive disorder disease of metabolism dissociated nystagmus dysthymic disorder dystonia epilepsy familial hyperlipidemia fundus albipunctatus hepatocellular carcinoma hypertropia large intestine cancer leukodystrophy liver cancer liver carcinoma lymphoma major depressive disorder mechanical strabismus melancholic depression mitochondrial metabolism disease mitochondrial myopathy myopia neurodegenerative disease neurotic disorder obesity obsolete autosomal recessive nonsyndromic deafness 105 obsolete melancholia obsolete ymphosarcoma ophthalmoplegia optic atrophy pathologic nystagmus peroxisomal acyl-CoA oxidase deficiency peroxisomal disease retinitis pigmentosa sensorineural hearing loss speech disorder spontaneous ocular nystagmus steatotic liver disease strabismus syndromic X-linked intellectual disability 94 tooth agenesis visual epilepsy
37028	acyl-CoA oxidase 1	ACOX1	Drosophila melanogaster (fruit fly)	Mitchell syndrome obesity peroxisomal acyl-CoA oxidase deficiency peroxisomal disease steatotic liver disease
26903	dysferlin	Dysf	Mus musculus (house mouse)	Miyoshi muscular dystrophy 1 autosomal recessive limb-girdle muscular dystrophy type 2B distal myopathy with anterior tibial onset distal myopathy limb-girdle muscular dystrophy muscular dystrophy
27293	sphingomyelin phosphodiesterase acid like 3B	SMPDL3B Aliases: ASML3B	Homo sapiens (human)	Moyamoya disease focal segmental glomerulosclerosis glomerulonephritis kidney disease nephritis nephrosis pyoureter
56963	repulsive guidance molecule BMP co-receptor a	RGMA Aliases: RGM	Homo sapiens (human)	Mycobacterium avium complex disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease basal cell carcinoma breast cancer bronchiectasis cancer chronic fatigue syndrome chronic kidney disease complex partial epilepsy cone-rod dystrophy 2 cone-rod dystrophy cystic fibrosis disease of mental health embryoma encephalitis encephalomyelitis epilepsy hemochromatosis type 2 hemochromatosis type 2A hemochromatosis heroin dependence lesion of sciatic nerve lung disease middle cerebral artery infarction morphine dependence multiple sclerosis myelitis neuromyelitis optica obesity opiate dependence primary progressive multiple sclerosis progressive relapsing multiple sclerosis prostate cancer prostate carcinoma psychotic disorder sciatic neuropathy secondary progressive multiple sclerosis temporal lobe epilepsy visual epilepsy
64772	endo-beta-N-acetylglucosaminidase	ENGASE Aliases: Di-N-acetylchitobiosyl beta-N-acetylglucosaminidase FLJ21865 Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase	Homo sapiens (human)	NGLY1-deficiency breast cancer breast carcinoma rheumatoid arthritis
20597	sphingomyelin phosphodiesterase 1, acid lysosomal	Smpd1	Mus musculus (house mouse)	Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease Wilson disease
174131	Sphingomyelin phosphodiesterase 1	asm-1	Caenorhabditis elegans	Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease Wilson disease

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