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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 **1451 - 1475** of **1582** in total

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Gene ID	Gene Name ▲	Gene Symbol	Organism	Disease Ontology
54978	solute carrier family 35 member F6	SLC35F6 Aliases: ANT2-binding protein ANT2BP FLJ20555 TANGO9 transport and golgi organization 9 homolog (Drosophila)	Homo sapiens (human)	microphthalmia obsolete Matthew-Wood syndrome pancreatic cancer pancreatic carcinoma
159371	solute carrier family 35 member G1	SLC35G1 Aliases: C10orf60 FLJ33990 POST partner of STIM1	Homo sapiens (human)	Laron syndrome Werner syndrome acute myeloid leukemia agnosia arteriosclerotic cardiovascular disease atherosclerosis atopic dermatitis atrial fibrillation autistic disorder breast cancer breast carcinoma cancer colorectal cancer colorectal carcinoma coronary artery disease depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis dysthymic disorder embryoma epilepsy hemolytic-uremic syndrome hepatoblastoma hepatocellular carcinoma hyperglycemia intussusception kidney failure large intestine cancer leukemia major depressive disorder melancholic depression mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis myotonic disease myotonic dystrophy type 1 myotonic dystrophy type 2 neurotic disorder nutmeg liver obesity obsolete melancholia obsolete type 1 diabetes mellitus 9 occipital horn syndrome polycystic ovary syndrome progeria prostate cancer prostate carcinoma schizophrenia sensorineural hearing loss transient myeloproliferative syndrome type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus uremia
80723	solute carrier family 35 member G2	SLC35G2 Aliases: DKFZp564K2464 MGC3295	Homo sapiens (human)	chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma
146861	solute carrier family 35 member G3	SLC35G3 Aliases: FLJ40154	Homo sapiens (human)
646000	solute carrier family 35 member G4	SLC35G4	Homo sapiens (human)
83650	solute carrier family 35 member G5	SLC35G5	Homo sapiens (human)
643664	solute carrier family 35 member G6	SLC35G6	Homo sapiens (human)
2542	solute carrier family 37 member 4	SLC37A4 Aliases: G6PT GSD1b GSD1c GSD1d Glucose-6-phosphate exchanger SLC37A4 SPX4 glucose-6-phosphatase transporter sugar-phosphate exchange protein 4	Homo sapiens (human)	Gerstmann-Straussler-Scheinker syndrome Gorham's disease Laron syndrome achondroplasia acute pancreatitis agranulocytosis aphthous stomatitis autoimmune disease autoimmune lymphoproliferative syndrome brain cancer cancer central nervous system cancer congenital disorder of glycosylation type II cystinuria diabetes mellitus diabetic ketoacidosis disease of metabolism embryoma essential hypertension eyelid disease familial hyperlipidemia focal segmental glomerulosclerosis galactosemia giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease Ib glycogen storage disease Ic glycogen storage disease gout hepatoblastoma hepatocellular carcinoma high grade glioma hypertension hyperuricemia hypoglycemia immune system disease inherited metabolic disorder kidney disease kidney failure kwashiorkor lactic acidosis leukopenia liver cancer marasmus mixed glioma nephritis nephrolithiasis nephrosis neutropenia nutrition disease obesity obsolete type 1 diabetes mellitus 9 osteoporosis pancreatitis polycystic ovary syndrome primary pulmonary hypertension protein-energy malnutrition proteinuria pyoureter severe congenital neutropenia sudden infant death syndrome type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus uric acid nephrolithiasis xanthomatosis
23516	solute carrier family 39 member 14	SLC39A14	Homo sapiens (human)	hypermanganesemia with dystonia 2
64116	solute carrier family 39 member 8	SLC39A8 Aliases: BCG-induced integral membrane protein in monocyte clone 103 BIGM103 Metal cation symporter ZIP8 ZIP-8 ZIP8 ZRT/IRT-like protein 8 Zinc transporter ZIP8	Homo sapiens (human)	Crohn's colitis Crohn's disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Laron syndrome Leigh disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Wilson disease achondroplasia acute chest syndrome alcohol dependence alcohol use disorder alternating hemiplegia of childhood androgen insensitivity syndrome anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy astigmatism atherosclerosis atrial fibrillation attention deficit hyperactivity disorder autonomic neuropathy bacterial sepsis breast cancer breast carcinoma cancer central nervous system disease cerebral infarction cerebrovascular disease childhood leukemia colorectal cancer colorectal carcinoma congenital disorder of glycosylation Ii congenital disorder of glycosylation In congenital disorder of glycosylation type I congenital disorder of glycosylation type IIn congenital disorder of glycosylation congenital nystagmus congestive heart failure coronary artery disease craniosynostosis dermatitis diabetes mellitus diabetic ketoacidosis dissociated nystagmus dystonia epilepsy essential hypertension focal hand dystonia generalized dystonia hemochromatosis hydrocephalus hyperopia hypertension hypertropia idiopathic scoliosis inflammatory bowel disease 1 inflammatory bowel disease intellectual disability iron metabolism disease kwashiorkor large intestine cancer learning disability left ventricular noncompaction leukemia macrocytic anemia marasmus mechanical strabismus mitochondrial metabolism disease mitochondrial myopathy nervous system disease neuroblastoma nicotine dependence nutrition disease obsolete infantile epileptic encephalopathy ophthalmoplegia osteoarthritis pathologic nystagmus protein-energy malnutrition pulmonary tuberculosis schizophrenia sensorineural hearing loss spontaneous ocular nystagmus strabismus systemic lupus erythematosus tuberculosis tuberculous pneumothorax type 2 diabetes mellitus ulcerative colitis visual epilepsy
6523	solute carrier family 5 member 1	SLC5A1 Aliases: D22S675 NAGT SGLT-1 sodium/glucose cotransporter 1	Homo sapiens (human)	Bartter disease Conn's syndrome Fanconi syndrome Waterhouse-Friderichsen syndrome X-linked juvenile retinoschisis 1 abdominal obesity-metabolic syndrome 1 acute myocardial infarction adenocarcinoma adenoma arteriosclerotic cardiovascular disease atherosclerosis bacterial infectious disease bacterial sepsis brain stem infarction breast cancer breast carcinoma calcinosis calcium metabolism disease cancer cardiomyopathy cardiovascular system disease cerebral artery occlusion cerebral infarction cerebrovascular disease cholera colon adenocarcinoma congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma cutaneous leishmaniasis cystinosis diabetes mellitus diabetic ketoacidosis diarrhea dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism embryoma endomyocardial fibrosis essential hypertension familial hypertrophic cardiomyopathy galactosemia glomerulonephritis glucose intolerance granular cell carcinoma heart disease hepatocellular carcinoma hypercalcemia hyperglycemia hypertension hypertrophic cardiomyopathy hypoglycemia intestinal atresia kidney disease kidney failure kwashiorkor lactic acidosis listeriosis liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma marasmus middle cerebral artery infarction myocardial infarction nephritis nephrocalcinosis nephrosis nutmeg liver nutrition disease obesity obsolete type 1 diabetes mellitus 9 optic atrophy 1 optic atrophy pancreatic cancer pancreatic carcinoma phosphorus metabolism disease pneumonia prediabetes syndrome primary hyperaldosteronism protein-energy malnutrition pyoureter renal glycosuria silent myocardial infarction squamous cell carcinoma tongue squamous cell carcinoma toxic shock syndrome tropical sprue tubular adenocarcinoma type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus
6524	solute carrier family 5 member 2	SLC5A2	Homo sapiens (human)	hypertension renal glycosuria
6652	sorbitol dehydrogenase	SORD	Homo sapiens (human)	Alzheimer's disease Bannayan-Riley-Ruvalcaba syndrome Clouston syndrome Coffin-Siris syndrome 1 Coffin-Siris syndrome Cowden syndrome Leber congenital amaurosis 1 MELAS syndrome Peutz-Jeghers syndrome adenocarcinoma adenoma adrenal gland cancer autosomal recessive distal hereditary motor neuronopathy 8 background diabetic retinopathy bladder carcinoma breast cancer cancer cardiomyopathy cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types cataract childhood kidney cell carcinoma chromophobe renal cell carcinoma chronic obstructive pulmonary disease clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer dementia diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic neuropathy diabetic retinopathy disease of metabolism duodenum cancer eclampsia embryoma endomyocardial fibrosis essential hypertension exudative vitreoretinopathy follicular adenoma gastrointestinal stromal tumor glomerulonephritis heart cancer hepatocellular carcinoma hyperglycemia hypertension hypertrophic cardiomyopathy kidney cancer kidney disease kwashiorkor large intestine cancer leiomyoma leukodystrophy liver cancer liver carcinoma marasmus mesenchymal cell neoplasm microcystic adenoma mitochondrial complex II deficiency mitochondrial metabolism disease mitochondrial myopathy multiple endocrine neoplasia type 1 myofibrillar myopathy 1 myofibroma nephritis nephrosis neuroblastoma neurofibromatosis 1 neurofibromatosis nonpapillary renal cell carcinoma nutrition disease obsolete eye and adnexa disease obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy papillary adenoma papillary renal cell carcinoma paraganglioma perinatal necrotizing enterocolitis pheochromocytoma proliferative diabetic retinopathy prostate cancer prostate carcinoma protein-energy malnutrition pyoureter renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma skin benign neoplasm skin cancer small intestine cancer steatotic liver disease thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland medullary carcinoma tuberous sclerosis 1 tuberous sclerosis type 2 diabetes mellitus urinary bladder cancer uterine fibroid von Hippel-Lindau disease
124912	sperm acrosome associated 3	SPACA3 Aliases: ALLP17 CT54 LYC3 LYZL3 SLLP1 cancer/testis antigen 54 sperm lyzozyme-like acrosomal protein 1	Homo sapiens (human)	acute myeloid leukemia cancer hematologic cancer seminoma testicular cancer testis seminoma
171169	sperm acrosome associated 4	SPACA4 Aliases: SAMP14	Homo sapiens (human)
389852	sperm acrosome associated 5	SPACA5 Aliases: LYC5 LYZL5 PNPK6288 SLLP2 Sperm Lysozyme-Like Protein 2 UNQ6288 dJ54B20.3	Homo sapiens (human)
729201	sperm acrosome associated 5B	SPACA5B Aliases: LYZL5B	Homo sapiens (human)
6677	sperm adhesion molecule 1	SPAM1 Aliases: HYAL5 PH-20 PH-20 hyaluronidase SPAG15	Homo sapiens (human)	bladder carcinoma breast cancer breast carcinoma cancer carcinoma chronic obstructive pulmonary disease embryoma endocrine exophthalmos endometrial cancer endometrial carcinoma melanoma mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis osteochondrodysplasia ovarian carcinoma prostate cancer prostate carcinoma skin melanoma squamous cell carcinoma thromboangiitis obliterans tongue squamous cell carcinoma urinary bladder cancer uterine corpus cancer
64847	spermatogenesis associated 20	SPATA20	Homo sapiens (human)	oligoasthenoteratozoospermia
6609	sphingomyelin phosphodiesterase 1	SMPD1 Aliases: ASM Niemann-Pick type A/B acid sphingomyelinase	Homo sapiens (human)	Alzheimer's disease Chagas disease Evans' syndrome Fabry disease Gaucher's disease Laron syndrome Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease type C1 Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Wilson disease achondroplasia acute myocardial infarction acute promyelocytic leukemia adrenal gland cancer adult fibrosarcoma adult respiratory distress syndrome aggressive systemic mastocytosis alcohol dependence alcohol use disorder alcoholic hepatitis allergic asthma alternating hemiplegia of childhood amnestic disorder antithrombin III deficiency anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis atrial fibrillation attention deficit hyperactivity disorder autoimmune thrombocytopenic purpura autonomic neuropathy bacterial sepsis bipolar disorder botryoid rhabdomyosarcoma cancer cataract 32 multiple types central nervous system cancer central nervous system disease cerebral infarction cerebrovascular disease cholecystolithiasis choledocholithiasis cholelithiasis chronic fatigue syndrome chronic obstructive pulmonary disease chylomicron retention disease colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congenital nystagmus congestive heart failure coronary artery disease coronary thrombosis cystic fibrosis depressive disorder diabetes mellitus diabetic angiopathy diabetic autonomic neuropathy diabetic ketoacidosis diabetic neuropathy diabetic polyneuropathy disease of mental health disease of metabolism dissociated nystagmus duodenum cancer dysthymic disorder embryoma embryonal rhabdomyosarcoma encephalitis encephalomyelitis familial adenomatous polyposis 1 familial adenomatous polyposis fibrosarcoma gastroenteritis generalized anxiety disorder gliosarcoma head and neck squamous cell carcinoma heart cancer hemochromatosis hepatitis hepatocellular carcinoma herpes simplex high grade glioma hyperhomocysteinemia hypersplenism ileitis ileocolitis indolent systemic mastocytosis inflammatory bowel disease 1 inflammatory bowel disease interstitial lung disease intrinsic asthma iron metabolism disease islet cell tumor kwashiorkor large intestine cancer late onset Parkinson's disease lipid storage disease liver cancer liver carcinoma liver cirrhosis lung cancer lung non-small cell carcinoma lysosomal storage disease major depressive disorder marasmus mast-cell leukemia mastocytosis melancholic depression melanoma metachromatic leukodystrophy microcytic anemia mixed glioma multiple myeloma multiple sclerosis myelitis myocardial infarction nasopharynx carcinoma nervous system disease neuronal ceroid lipofuscinosis 6A neuropathy neurotic disorder newborn respiratory distress syndrome nutmeg liver nutrition disease obesity obsolete major affective disorder 1 obsolete major affective disorder 2 obsolete melancholia osteoporosis ovarian cancer ovarian carcinoma pathologic nystagmus periodontal disease peripheral nervous system disease pheochromocytoma pneumonia prostate cancer prostate carcinoma protein C deficiency protein S deficiency protein-energy malnutrition psychotic disorder respiratory syncytial virus infectious disease retrograde amnesia rheumatoid arthritis sea-blue histiocytosis sickle cell anemia silent myocardial infarction skin melanoma small intestine cancer sphingolipidosis splenic disease splenic infarction spontaneous ocular nystagmus steatotic liver disease systemic lupus erythematosus systemic mastocytosis thrombophilia trypanosomiasis tuberculosis type 2 diabetes mellitus ulcerative colitis urinary bladder cancer viral infectious disease xanthomatosis
6610	sphingomyelin phosphodiesterase 2	SMPD2 Aliases: ISC1 nSMase neutral sphingomyelinase	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Guillain-Barre syndrome Miller Fisher syndrome Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome acute myocardial infarction arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atopic dermatitis bone osteosarcoma breast cancer breast carcinoma cancer cerebral degeneration childhood leukemia childhood osteosarcoma congestive heart failure coronary artery disease coronary thrombosis embryoma hepatocellular carcinoma leprosy leukemia liver cancer myocardial infarction osteosarcoma patent ductus arteriosus pneumonia pulmonary emphysema silent myocardial infarction sphingolipidosis tuberculosis visceral leishmaniasis
55512	sphingomyelin phosphodiesterase 3	SMPD3 Aliases: NSMASE2 neutral sphingomyelinase II	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Ehlers-Danlos syndrome Guillain-Barre syndrome Kallmann syndrome Laron syndrome Miller Fisher syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Sheehan syndrome Zika fever achondroplasia acute myeloid leukemia acute pericementitis aggressive periodontitis alternating hemiplegia of childhood arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autonomic neuropathy breast cancer breast carcinoma cancer central nervous system disease cerebral degeneration chronic kidney disease chronic obstructive pulmonary disease coronary artery disease embryoma essential thrombocythemia hepatocellular carcinoma hyperphosphatemia hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency leprosy leukemia liver cancer lymphoid leukemia microcephaly myelodysplastic syndrome myeloid leukemia nervous system disease osteogenesis imperfecta type 10 osteogenesis imperfecta type 11 osteogenesis imperfecta type 12 osteogenesis imperfecta type 13 osteogenesis imperfecta type 14 osteogenesis imperfecta type 15 osteogenesis imperfecta type 16 osteogenesis imperfecta type 17 osteogenesis imperfecta type 1 osteogenesis imperfecta type 2 osteogenesis imperfecta type 3 osteogenesis imperfecta type 4 osteogenesis imperfecta type 5 osteogenesis imperfecta type 6 osteogenesis imperfecta type 7 osteogenesis imperfecta type 8 osteogenesis imperfecta type 9 osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures osteogenesis imperfecta panhypopituitarism periodontosis primary pulmonary hypertension pulmonary emphysema pulmonary hypertension schizophrenia thymus gland disease transient cerebral ischemia vertebrobasilar insufficiency
55627	sphingomyelin phosphodiesterase 4	SMPD4 Aliases: FLJ20297 FLJ20756 KIAA1418 NET13 NSMASE3 nSMase-3 neutral sphingomyelinase-3	Homo sapiens (human)	acute myocardial infarction coronary thrombosis microcephaly myocardial infarction silent myocardial infarction
10924	sphingomyelin phosphodiesterase acid like 3A	SMPDL3A Aliases: ASM3A ASML3a FLJ20177 acid sphingomyelinase-like phosphodiesterase 3a yR36GH4.1	Homo sapiens (human)	Niemann-Pick disease endometriosis of ovary endometriosis of uterus endometriosis sphingolipidosis urinary bladder cancer
27293	sphingomyelin phosphodiesterase acid like 3B	SMPDL3B Aliases: ASML3B	Homo sapiens (human)	Moyamoya disease focal segmental glomerulosclerosis glomerulonephritis kidney disease nephritis nephrosis pyoureter

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