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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	October 29, 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 **6701 - 6725** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▲	Organism	Disease Ontology
151056	phospholipase B1	PLB1 Aliases: FLJ30866 PLB	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 Balo concentric sclerosis Barrett's esophagus Crohn's colitis Crohn's disease Guillain-Barre syndrome IgA glomerulonephritis IgG4-related disease Krabbe disease Kufor-Rakeb syndrome Marfan syndrome Miller Fisher syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Werner syndrome West Nile fever X-linked chronic granulomatous disease acoustic neuroma acute chest syndrome acute myeloid leukemia acute myocardial infarction adrenoleukodystrophy adult respiratory distress syndrome allergic asthma allergic rhinitis alternating hemiplegia of childhood anaplastic astrocytoma angiomatous meningioma anthrax disease arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma ataxia telangiectasia atherosclerosis atopic dermatitis autoimmune disease autoimmune lymphoproliferative syndrome autonomic neuropathy autosomal dominant cerebellar ataxia autosomal dominant distal hereditary motor neuronopathy 2 bacterial infectious disease bacterial sepsis basal ganglia disease benign meningioma benign mesothelioma bipolar disorder blepharospasm blood coagulation disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer candidiasis cardiac arrest cardiovascular system disease cataract central nervous system disease cerebral convexity meningioma cerebral degeneration childhood cerebral astrocytoma chronic ethmoiditis chronic fatigue syndrome chronic granulomatous disease chronic interstitial cystitis chronic kidney disease chronic obstructive pulmonary disease chronic sphenoidal sinusitis clear cell meningioma clonorchiasis colitis colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma complement deficiency coronary artery disease coronary thrombosis cryptococcosis cryptosporidiosis cystic fibrosis depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1A dilated cardiomyopathy dysthymic disorder embryoma encephalitis encephalomyelitis endometrial cancer endometrial carcinoma esophagitis esophagus adenocarcinoma familial adenomatous polyposis 1 familial adenomatous polyposis familial hyperlipidemia familial nephrotic syndrome fibrillary astrocytoma fibrous meningioma focal hand dystonia focal segmental glomerulosclerosis fragile X-associated tremor/ataxia syndrome gastroduodenal Crohn's disease gastroenteritis gastroesophageal reflux disease gemistocytic astrocytoma glaucoma glomerulonephritis glucose intolerance heart disease hepatitis C hepatocellular carcinoma hereditary spastic paraplegia 35 high grade glioma hyperglycemia ileitis ileocolitis immune system disease inflammatory bowel disease 1 inflammatory bowel disease intermediate coronary syndrome interstitial cystitis intraorbital meningioma intraventricular meningioma intrinsic asthma islet cell tumor isovaleric acidemia jejunoileitis juvenile pilocytic astrocytoma keratitis keratoconjunctivitis kidney disease large intestine cancer leukemia leukodystrophy lingual-facial-buccal dyskinesia lipoid nephrosis liver cancer liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphangioleiomyomatosis lymphoplasmacyte-rich meningioma macular corneal dystrophy major depressive disorder malignant astrocytoma malignant mesothelioma mastitis melancholic depression membranous glomerulonephritis meningioma meningothelial meningioma microcystic meningioma mood disorder movement disease multiple sclerosis myelitis myocardial infarction narcolepsy nasopharynx carcinoma nephritis nephrosis nephrotic syndrome nervous system disease neuroaxonal dystrophy neuroblastoma neurodegeneration with brain iron accumulation 2a neurodegeneration with brain iron accumulation 2b neurodegeneration with brain iron accumulation 3 neurodegeneration with brain iron accumulation 4 neurodegeneration with brain iron accumulation 5 neurodegeneration with brain iron accumulation 6 neurodegeneration with brain iron accumulation neurodegenerative disease neurotic disorder newborn respiratory distress syndrome nutmeg liver obesity obsolete inherited blood coagulation disease obsolete major affective disorder 1 obsolete major affective disorder 2 obsolete melancholia olfactory groove meningioma oral candidiasis osteoarthritis ovarian cancer ovarian carcinoma pantothenate kinase-associated neurodegeneration parapsoriasis parasagittal meningioma patent ductus arteriosus peptic esophagitis pilocytic astrocytoma pituitary adenoma pre-eclampsia prediabetes syndrome primary open angle glaucoma progeria prostate cancer prostate carcinoma protoplasmic astrocytoma psammomatous meningioma psoriasis pulmonary coin lesion pustulosis of palm and sole pyoureter rheumatoid arthritis sarcoidosis schizophrenia secondary Parkinson disease secretory meningioma sick sinus syndrome silent myocardial infarction situs inversus spinal meningioma spinocerebellar ataxia type 2 subependymal giant cell astrocytoma systemic lupus erythematosus thrombophilia transitional meningioma tuberous sclerosis 1 tuberous sclerosis type 2 diabetes mellitus ulcerative colitis uterine corpus cancer uveoparotid fever vascular disease vasculitis vasomotor rhinitis vulvovaginitis
79887	phospholipase B domain containing 1	PLBD1 Aliases: FLJ22662 PLB homolog 1 (Dictyostelium)	Homo sapiens (human)
196463	phospholipase B domain containing 2	PLBD2 Aliases: PLB homolog 2 (Dictyostelium) mannose-6-phosphate protein associated protein p76 p76	Homo sapiens (human)
23236	phospholipase C beta 1	PLCB1 Aliases: KIAA0581 PLC-I PLC154 phosphoinositide phospholipase C	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 Chagas disease Hirschsprung's disease Kawasaki disease Meier-Gorlin syndrome 1 Meier-Gorlin syndrome Miller-Dieker lissencephaly syndrome Pick's disease Reye syndrome Unverricht-Lundborg syndrome West syndrome abdominal obesity-metabolic syndrome 1 acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adult oligodendroglioma amyotrophic lateral sclerosis anaplastic astrocytoma autism spectrum disorder autistic disorder benign epilepsy with centrotemporal spikes bipolar disorder blepharospasm brain disease breast cancer breast carcinoma cancer cardiovascular system disease central nervous system cancer cerebral degeneration childhood cerebral astrocytoma childhood oligodendroglioma chromosome 17p13.1 deletion syndrome colon adenocarcinoma colon cancer colonic benign neoplasm colorectal cancer coronary aneurysm coronary thrombosis cribriform carcinoma depressive disorder developmental and epileptic encephalopathy 12 developmental and epileptic encephalopathy 1 diabetes mellitus diabetic ketoacidosis early infantile epileptic encephalopathy early myoclonic encephalopathy endometriosis of uterus endometriosis epilepsy essential thrombocythemia fibrillary astrocytoma focal epilepsy focal hand dystonia gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma glucose intolerance granular cell carcinoma heart disease hepatocellular carcinoma high grade glioma infertility juvenile pilocytic astrocytoma large intestine cancer lissencephaly liver cancer major depressive disorder malignant astrocytoma melancholic depression mixed glioma mixed oligodendroglioma-astrocytoma mood disorder myelodysplastic syndrome myocardial infarction myotonic disease myotonic dystrophy type 1 myotonic dystrophy type 2 neuroblastoma neurotic disorder nicotine dependence obesity obsolete infantile epileptic encephalopathy obsolete melancholia obstructive sleep apnea oligodendroglioma partial motor epilepsy pilocytic astrocytoma poikiloderma with neutropenia prediabetes syndrome primary biliary cholangitis progressive muscular atrophy protoplasmic astrocytoma schizophrenia silent myocardial infarction subependymal giant cell astrocytoma substance abuse substance-related disorder trypanosomiasis tubular adenocarcinoma visual epilepsy
5330	phospholipase C beta 2	PLCB2 Aliases: FLJ38135	Homo sapiens (human)	acute myocardial infarction adenocarcinoma adenoma breast cancer breast carcinoma cancer congenital heart disease coronary thrombosis cribriform carcinoma embryoma granular cell carcinoma hepatocellular carcinoma invasive ductal carcinoma liver cancer melanoma myocardial infarction obesity silent myocardial infarction skin melanoma tubular adenocarcinoma viral infectious disease
5331	phospholipase C beta 3	PLCB3	Homo sapiens (human)	acrodermatitis acute myocardial infarction adenocarcinoma adenoma adrenal carcinoma adrenal cortex cancer adrenocortical carcinoma cancer coronary thrombosis cribriform carcinoma cystic fibrosis dermatitis diabetes mellitus diabetic ketoacidosis essential hypertension extragonadal germ cell cancer granular cell carcinoma hyperparathyroidism hypertension lung cancer lung disease lung non-small cell carcinoma multiple endocrine neoplasia type 1 myocardial infarction neuroendocrine carcinoma neuroendocrine tumor obesity osteitis fibrosa silent myocardial infarction spondylometaphyseal dysplasia with corneal dystrophy tubular adenocarcinoma type 2 diabetes mellitus vitiligo
5332	phospholipase C beta 4	PLCB4	Homo sapiens (human)	46,XY sex reversal Chagas disease Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 3 Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Kawasaki disease abdominal obesity-metabolic syndrome 1 absence epilepsy acute chest syndrome acute myeloid leukemia adenocarcinoma adenoma agenesis of the corpus callosum with peripheral neuropathy agnosia ankylosis bipolar disorder breast cancer breast carcinoma cancer central sleep apnea childhood absence epilepsy childhood acute myeloid leukemia cleft palate congenital ptosis coronary aneurysm cribriform carcinoma cutaneous fibrous histiocytoma dengue hemorrhagic fever depressive disorder embryoma endometriosis of uterus endometriosis essential thrombocythemia gastrointestinal stromal tumor granular cell carcinoma hereditary neuropathy with liability to pressure palsies hidradenoma isolated cleft palate lung cancer lung non-small cell carcinoma major depressive disorder melancholic depression melanoma mood disorder motor peripheral neuropathy myelodysplastic syndrome neurotic disorder nicotine dependence obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete melancholia obstructive sleep apnea ptosis retinal degeneration retinal disease schizoaffective disorder schizophrenia schizophreniform disorder sensorineural hearing loss skin melanoma skin papilloma skin tag syringoma tongue disease trypanosomiasis tubular adenocarcinoma uveal melanoma
5333	phospholipase C delta 1	PLCD1 Aliases: 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-1 Phospholipase C δ1	Homo sapiens (human)	Alzheimer's disease Marfan syndrome actinic keratosis alopecia amyotrophic lateral sclerosis arthritis arthropathy blepharitis breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma chronic myeloid leukemia colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease coronary artery vasospasm cystic fibrosis diabetes mellitus embryoma esophagus squamous cell carcinoma essential hypertension glycoproteinosis hypertension impulse control disorder intermittent explosive disorder irritant dermatitis kleptomania large intestine cancer lung benign neoplasm lung cancer lung carcinoma microphthalmia mucolipidosis II alpha/beta nephrolithiasis nonsyndromic congenital nail disorder 3 obsolete Matthew-Wood syndrome obsolete asthenopia osteoarthritis parapsoriasis progressive muscular atrophy psoriasis pustulosis of palm and sole sarcomatoid carcinoma seborrheic keratosis situs inversus skin disease squamous cell carcinoma stomach cancer stomach carcinoma tongue squamous cell carcinoma tuberous sclerosis 1 tuberous sclerosis type 2 diabetes mellitus uric acid nephrolithiasis
113026	phospholipase C delta 3	PLCD3	Homo sapiens (human)	Goldenhar syndrome acquired immunodeficiency syndrome alcohol dependence alcohol use disorder arteriosclerotic cardiovascular disease atherosclerosis coronary artery disease human immunodeficiency virus infectious disease microphthalmia nasopharynx carcinoma obsolete Matthew-Wood syndrome senile cataract
84812	phospholipase C delta 4	PLCD4	Homo sapiens (human)	breast cancer breast carcinoma primary pulmonary hypertension
51196	phospholipase C epsilon 1	PLCE1 Aliases: KIAA1516 NPHS3 PLCE nephrosis type 3 phosphoinositide phospholipase C	Homo sapiens (human)	46,XY sex reversal Alzheimer's disease Barrett's esophagus Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 3 Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Japanese encephalitis Miller-Dieker lissencephaly syndrome West Nile fever acute myeloid leukemia adenocarcinoma adenoma adenosarcoma agenesis of the corpus callosum with peripheral neuropathy atrophic gastritis bladder carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiovascular system disease chromosome 17p13.1 deletion syndrome chronic kidney disease chronic obstructive pulmonary disease colorectal cancer colorectal carcinoma common wart congestive heart failure cribriform carcinoma cytochrome-c oxidase deficiency disease dengue disease dengue hemorrhagic fever embryoma esophageal cancer esophageal carcinoma esophagitis esophagus adenocarcinoma esophagus squamous cell carcinoma essential hypertension essential thrombocythemia familial nephrotic syndrome focal segmental glomerulosclerosis gallbladder cancer gallbladder carcinoma gastric adenocarcinoma gastric cardia adenocarcinoma gastric cardia carcinoma gastritis gastroesophageal reflux disease gastrointestinal system cancer glomerulonephritis granular cell carcinoma head and neck squamous cell carcinoma heart disease hepatitis B hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies hypertension large intestine cancer lipoid nephrosis lissencephaly liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma migraine mitochondrial metabolism disease motor peripheral neuropathy myelodysplastic syndrome nephritis nephroblastoma nephrotic syndrome type 1 nephrotic syndrome type 2 nephrotic syndrome type 3 nephrotic syndrome obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum open-angle glaucoma peptic esophagitis primary open angle glaucoma proteinuria sarcomatoid carcinoma squamous cell carcinoma squamous cell neoplasm stomach cancer stomach carcinoma temporal arteritis tongue squamous cell carcinoma tubular adenocarcinoma urinary bladder cancer viral infectious disease yellow fever
5335	phospholipase C gamma 1	PLCG1 Aliases: NCKAP3 PLC-II PLC148 PLCgamma1	Homo sapiens (human)	Alzheimer's disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Kaposi's sarcoma Meckel syndrome Miller-Dieker lissencephaly syndrome Richter's syndrome SADDAN Sezary's disease T-cell acute lymphoblastic leukemia X-linked lymphoproliferative syndrome 1 X-linked lymphoproliferative syndrome 2 abdominal obesity-metabolic syndrome 1 achondroplasia acute monocytic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adult T-cell leukemia/lymphoma allergic asthma angioedema angioimmunoblastic T-cell lymphoma angiosarcoma arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis atrial fibrillation autosomal dominant polycystic kidney disease bacterial sepsis bipolar disorder bone osteosarcoma borderline personality disorder breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer candidiasis carcinoma central nervous system cancer cerebral infarction cerebrovascular disease childhood angiosarcoma childhood osteosarcoma chromosome 17p13.1 deletion syndrome chronic lymphocytic leukemia colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease cribriform carcinoma depressive disorder diabetes mellitus diabetic ketoacidosis embryoma epilepsy essential hypertension essential thrombocythemia familial adenomatous polyposis focal segmental glomerulosclerosis fragile X syndrome gastric adenocarcinoma gastroenteritis giant cell glioblastoma glioblastoma gliosarcoma glycoproteinosis granular cell carcinoma hepatocellular carcinoma high grade glioma hypertension ileitis ileocolitis immune system disease impulse control disorder intermittent explosive disorder intrinsic asthma irritant dermatitis kleptomania large intestine cancer laryngeal squamous cell carcinoma leukemia lissencephaly liver angiosarcoma liver cancer luminal breast carcinoma A lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma major depressive disorder maturity-onset diabetes of the young melancholic depression mixed glioma mucolipidosis II alpha/beta myelodysplastic syndrome obsolete melancholia oral candidiasis oral squamous cell carcinoma osteoarthritis osteosarcoma ovarian cancer ovarian carcinoma placental insufficiency primary cutaneous T-cell non-Hodgkin lymphoma prostate cancer prostate carcinoma sarcomatoid carcinoma schizophrenia squamous cell carcinoma steatotic liver disease tongue squamous cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus urticaria visual epilepsy
5336	phospholipase C gamma 2	PLCG2	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 Burkitt lymphoma CINCA Syndrome Creutzfeldt-Jakob disease Crohn's colitis Crohn's disease Hailey-Hailey disease Lewy body dementia Muckle-Wells syndrome Pick's disease Reye syndrome Richter's syndrome Rothmund-Thomson syndrome acute lymphoblastic leukemia acute myeloid leukemia adenosarcoma age related macular degeneration allergic rhinitis angioedema autoimmune disease autoimmune lymphoproliferative syndrome autoimmune thyroiditis autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB bone osteosarcoma breast cancer breast carcinoma bronchiolitis cancer candidiasis cellulitis central nervous system lymphoma cerebral degeneration cherubism childhood osteosarcoma childhood type dermatomyositis chronic lymphocytic leukemia coronary artery disease cutis laxa degeneration of macula and posterior pole dermatomyositis diffuse large B-cell lymphoma embryoma exostosis familial adenomatous polyposis 1 familial adenomatous polyposis familial cold autoinflammatory syndrome 1 familial cold autoinflammatory syndrome 3 familial cold autoinflammatory syndrome 4 familial cold autoinflammatory syndrome granuloma annulare hepatocellular carcinoma immune system disease inflammatory bowel disease 1 inflammatory bowel disease interstitial lung disease islet cell tumor kidney cancer leukemia lipoid nephrosis liver cancer lymphoma lymphoplasmacytic lymphoma macroglobulinemia macular degeneration mal de Meleda nephroblastoma neurodegenerative disease obsolete lymphoplasmacytic lymphoma obsolete ymphosarcoma oral candidiasis osteoporosis osteosarcoma progressive supranuclear palsy restrictive dermopathy rheumatoid arthritis stomach cancer thrombophilia ulcerative colitis urticaria vasomotor rhinitis vitiligo
23007	phospholipase C eta 1	PLCH1 Aliases: 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase eta-1 DKFZp434C1372 KIAA1069 MGC117152 PLCeta1	Homo sapiens (human)	bronchus cancer bronchus carcinoma colon cancer colonic benign neoplasm colorectal cancer holoprosencephaly idiopathic scoliosis large intestine cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma squamous cell carcinoma tongue squamous cell carcinoma
9651	phospholipase C eta 2	PLCH2 Aliases: 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase eta-2 KIAA0450 PLC-eta2 PLCeta2 RP3-395M20.1	Homo sapiens (human)	azoospermia intellectual disability learning disability schizophrenia
5334	phospholipase C like 1 (inactive)	PLCL1	Homo sapiens (human)
23228	phospholipase C like 2	PLCL2	Homo sapiens (human)
345557	phosphatidylinositol specific phospholipase C X domain containing 3	PLCXD3	Homo sapiens (human)
89869	phospholipase C zeta 1	PLCZ1 Aliases: NYD-SP27 PLCzeta	Homo sapiens (human)	cystic fibrosis infertility ovarian cancer ovarian carcinoma spermatogenic failure 17
5337	phospholipase D1	PLD1 Aliases: choline phosphatase 1	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 Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome acral lentiginous melanoma acute myocardial infarction adult respiratory distress syndrome allergic asthma amnestic disorder anaplastic astrocytoma arthritis arthropathy asthma atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect autoimmune disease autoimmune lymphoproliferative syndrome bacterial sepsis bone osteosarcoma brain infarction breast cancer breast carcinoma cancer candidiasis carcinoma central nervous system cancer cerebral degeneration childhood cerebral astrocytoma childhood osteosarcoma chromophobe renal cell carcinoma chronic kidney disease clear cell renal cell carcinoma colitis collecting duct carcinoma colorectal cancer colorectal carcinoma complex partial epilepsy congestive heart failure coronary thrombosis dementia developmental cardiac valvular defect diabetes mellitus disseminated intravascular coagulation embryoma epilepsy fibrillary astrocytoma gastroenteritis gemistocytic astrocytoma gliosarcoma high grade glioma hydronephrosis ileitis ileocolitis immune system disease inguinal hernia intrinsic asthma juvenile pilocytic astrocytoma large intestine cancer malignant astrocytoma melanoma microphthalmia middle cerebral artery infarction mitral valve insufficiency mitral valve prolapse mitral valve stenosis mixed glioma multiple sclerosis myocardial infarction newborn respiratory distress syndrome nodular prostate nonpapillary renal cell carcinoma obesity obsolete Matthew-Wood syndrome oral candidiasis osteosarcoma pancreatic ductal adenocarcinoma papillary renal cell carcinoma patent foramen ovale pilocytic astrocytoma pneumonia postural orthostatic tachycardia syndrome primary immunodeficiency disease prostate cancer prostate carcinoma prostatic adenoma protoplasmic astrocytoma pterygium purpura fulminans relapsing-remitting multiple sclerosis renal carcinoma renal cell carcinoma retrograde amnesia rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction skin melanoma stomach cancer stomach carcinoma subependymal giant cell astrocytoma temporal lobe epilepsy tricuspid atresia tricuspid valve insufficiency tricuspid valve prolapse type 2 diabetes mellitus urethral diverticulum visual epilepsy
5338	phospholipase D2	PLD2 Aliases: choline phosphatase 2	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 Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome abdominal obesity-metabolic syndrome 1 actinic keratosis amnestic disorder anaplastic astrocytoma anodontia basal cell carcinoma brain infarction breast cancer breast carcinoma cancer carcinoma central nervous system cancer central nervous system lymphoma cerebral degeneration childhood cerebral astrocytoma chromophobe renal cell carcinoma chronic kidney disease clear cell renal cell carcinoma colitis collecting duct carcinoma colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma complex partial epilepsy congestive heart failure developmental cardiac valvular defect embryoma epilepsy epithelioid sarcoma essential hypertension fibrillary astrocytoma gastroenteritis gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma high grade glioma hypertension ileitis ileocolitis in situ carcinoma inverted follicular keratosis juvenile pilocytic astrocytoma keratoacanthoma kwashiorkor large intestine cancer lymphoid leukemia lymphoma malignant astrocytoma marasmus melanoacanthoma mixed glioma myeloid leukemia nonpapillary renal cell carcinoma nutrition disease obsolete ymphosarcoma papillary adenocarcinoma papillary renal cell carcinoma penis carcinoma in situ pilocytic astrocytoma pneumonia prostate cancer prostate carcinoma protein-energy malnutrition protoplasmic astrocytoma renal carcinoma renal cell carcinoma retinal disease retinitis retrograde amnesia sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma seborrheic keratosis skin disease spindle cell sarcoma squamous cell carcinoma subependymal giant cell astrocytoma systemic lupus erythematosus temporal lobe epilepsy thyroid gland papillary carcinoma tongue squamous cell carcinoma tooth agenesis vascular cancer visual epilepsy
23646	phospholipase D family member 3	PLD3 Aliases: HU-K4	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 Henoch-Schoenlein purpura Pick's disease Reye syndrome amyloidosis atopic dermatitis cerebral degeneration congenital nystagmus conjunctival folliculosis conjunctivitis dermatitis dissociated nystagmus hypersensitivity vasculitis keratitis keratoconjunctivitis pathologic nystagmus rheumatoid arthritis scleroderma shipyard eye spinocerebellar ataxia 46 spontaneous ocular nystagmus systemic scleroderma
122618	phospholipase D family member 4	PLD4	Homo sapiens (human)	Usher syndrome type 2 Usher syndrome type 3 Usher syndrome colon cancer colon carcinoma colonic benign neoplasm colorectal cancer hepatitis large intestine cancer retinitis pigmentosa-deafness syndrome rheumatoid arthritis scleroderma systemic lupus erythematosus systemic scleroderma
200150	phospholipase D family member 5	PLD5	Homo sapiens (human)
201164	phospholipase D family member 6	PLD6	Homo sapiens (human)

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