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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 **9476 - 9500** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
3081	homogentisate 1,2-dioxygenase	HGD	Homo sapiens (human)
100532736	MICOS10-NBL1 readthrough	MICOS10-NBL1	Homo sapiens (human)
10749	kinesin family member 1C	KIF1C	Homo sapiens (human)
285533	ring finger protein 175	RNF175	Homo sapiens (human)
403239	olfactory receptor family 2 subfamily T member 27	OR2T27	Homo sapiens (human)
54816	zinc finger protein 280D	ZNF280D	Homo sapiens (human)
8368	H4 clustered histone 13	H4C13	Homo sapiens (human)
6692	serine peptidase inhibitor, Kunitz type 1	SPINT1	Homo sapiens (human)
410	arylsulfatase A	ARSA Aliases: ASA metachromatic leucodystrophy	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 Behcet's 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 2 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 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 Clostridium difficile colitis Clouston syndrome Cockayne syndrome Cornelia de Lange syndrome Crohn's colitis Crohn's disease DiGeorge syndrome Down syndrome Dubowitz syndrome Fabry disease GM1 gangliosidosis type 1 GM1 gangliosidosis Gaucher's disease Klatskin's tumor Krabbe disease Landau-Kleffner syndrome Lynch syndrome Niemann-Pick disease Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Phelan-McDermid syndrome Pick's disease Prader-Willi syndrome Reye syndrome Robinow syndrome Sandhoff disease Seckel syndrome Silver-Russell syndrome Sneddon syndrome T-cell acute lymphoblastic leukemia T-cell adult acute lymphocytic leukemia Tay-Sachs disease Unverricht-Lundborg syndrome Wilson disease X-linked Aarskog syndrome X-linked ichthyosis X-linked nonsyndromic deafness abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 acoustic neuroma acute chest syndrome acute intermittent porphyria acute interstitial pneumonia acute kidney tubular necrosis acute myocardial infarction adenocarcinoma adenoma agenesis of the corpus callosum with peripheral neuropathy agnosia alcohol dependence alcohol use disorder allergic asthma alternating hemiplegia of childhood amnestic disorder amyloidosis anemia angioedema ankylosing spondylitis anterior spinal artery syndrome anxiety disorder argininosuccinic aciduria arteriosclerotic cardiovascular disease arthritis arthropathy asthma ataxia telangiectasia atherosclerosis 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 autism spectrum disorder autistic disorder autoimmune hepatitis autonomic neuropathy autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 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 dominant osteopetrosis 2 autosomal recessive Robinow syndrome 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 autosomal recessive osteopetrosis 7 bacterial sepsis benign epilepsy with centrotemporal spikes blood coagulation disease brain cancer brain disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiac arrest cardiovascular system disease carotid artery disease carotid artery thrombosis carotid stenosis cataract cellular schwannoma central nervous system disease cerebellar ataxia cerebellar disease cerebral degeneration cerebral infarction cerebral palsy cerebrovascular disease childhood T-cell acute lymphoblastic leukemia cholangiocarcinoma cholecystitis chondrodysplasia-pseudohermaphroditism syndrome choreatic disease chronic fatigue syndrome chronic kidney disease chronic obstructive pulmonary disease chylomicron retention disease colitis colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital hypothyroidism coronary artery disease coronary thrombosis craniosynostosis critical illness polyneuropathy dementia demyelinating disease demyelinating polyneuropathy dentatorubral-pallidoluysian atrophy depressive disorder diabetes mellitus diabetic ketoacidosis disease of mental health disease of metabolism diverticulitis dysthymic disorder dystonia early myoclonic encephalopathy embryoma encephalitis encephalomyelitis enterocele epilepsy esophageal cancer esophageal carcinoma esophagitis essential hypertension essential thrombocythemia familial hyperlipidemia female stress incontinence follicular adenoma gallbladder cancer gastroenteritis gastroesophageal reflux disease generalized anxiety disorder generalized atherosclerosis giant cell glioblastoma glioblastoma glomerulonephritis glycogen storage disease Ia heart disease hemiplegia hemochromatosis hepatitis B hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 herpes zoster high grade glioma hyperglycemia hypertension hypothyroidism ichthyosis idiopathic interstitial pneumonia ileitis ileocolitis inflammatory and toxic neuropathy inflammatory bowel disease 1 inflammatory bowel disease inguinal hernia intellectual disability intermediate coronary syndrome intrahepatic cholangiocarcinoma intrinsic asthma iron metabolism disease irritable bowel syndrome keratitis keratoconjunctivitis kidney disease kidney failure large intestine cancer late onset Parkinson's disease learning disability leukodystrophy lipid storage disease locked-in syndrome lung benign neoplasm lung cancer lung carcinoma lung disease lysosomal storage disease macrocytic anemia major depressive disorder malignant peripheral nerve sheath tumor malignant pleural mesothelioma mediastinitis medium chain acyl-CoA dehydrogenase deficiency melancholic depression melanotic neurilemmoma meningoencephalitis metachromatic leukodystrophy microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcystic adenoma microphthalmia mitochondrial metabolism disease mitochondrial myopathy motor peripheral neuropathy mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis mucosulfatidosis multiple sclerosis myelitis myelomeningocele myocardial infarction myxedema nasopharynx carcinoma nephritis nephrosis nervous system disease neurilemmoma neuroblastoma neurocirculatory asthenia neurodegenerative disease neuropathy neurotic disorder nutmeg liver obesity obsolete Matthew-Wood syndrome obsolete autosomal recessive nonsyndromic deafness 105 obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete inherited blood coagulation disease obsolete melancholia obstructive sleep apnea optic atrophy osteoarthritis osteopetrosis osteoporosis osteosclerosis pancreatic adenocarcinoma pancreatic ductal adenocarcinoma papillary adenoma patent foramen ovale peptic esophagitis peripheral artery disease peripheral nervous system disease phobic disorder plexiform schwannoma pneumonia polyneuropathy primary immunodeficiency disease primary pulmonary hypertension primary sclerosing cholangitis progressive bulbar palsy progressive myoclonus epilepsy 1A progressive myoclonus epilepsy psychotic disorder pyoureter quadriplegia rectal benign neoplasm rectum adenocarcinoma rectum cancer red-green color blindness retrograde amnesia sarcomatoid carcinoma schizoaffective disorder schizophrenia schizophreniform disorder sclerosing cholangitis silent myocardial infarction spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy sphingolipidosis spina bifida spinal cancer superior mesenteric artery syndrome syndromic X-linked intellectual disability type 10 systemic lupus erythematosus tethered spinal cord syndrome thyroid adenoma thyroid cancer thyroid gland carcinoma tuberculosis type 2 diabetes mellitus ulcerative colitis urethral stricture urticaria vascular dementia velocardiofacial syndrome ventricular septal defect visual epilepsy
3689	integrin subunit beta 2	ITGB2	Homo sapiens (human)
401145	coiled-coil serine rich protein 1	CCSER1	Homo sapiens (human)
4926	nuclear mitotic apparatus protein 1	NUMA1	Homo sapiens (human)
33	acyl-CoA dehydrogenase long chain	ACADL Aliases: ACAD4 LCAD long-chain acyl-CoA dehydrogenase	Homo sapiens (human)	Pearson syndrome atrial fibrillation cancer cardiomyopathy chronic kidney disease embryoma endomyocardial fibrosis esophagus squamous cell carcinoma familial hypertrophic cardiomyopathy fibromyalgia hepatocellular carcinoma hypertrophic cardiomyopathy hypoglycemia liver cancer liver carcinoma myositis nuclear type mitochondrial complex I deficiency 20 steatotic liver disease urea cycle disorder very long chain acyl-CoA dehydrogenase deficiency
9647	protein phosphatase, Mg2+/Mn2+ dependent 1F	PPM1F	Homo sapiens (human)
50508	NADPH oxidase 3	NOX3	Homo sapiens (human)
51208	claudin 18	CLDN18	Homo sapiens (human)
939	CD27 molecule	CD27	Homo sapiens (human)
9993	DiGeorge syndrome critical region gene 2	DGCR2 Aliases: DGS-C IDD KIAA0163 LAN SEZ-12 integral membrane protein DGCR2	Homo sapiens (human)	Bannayan-Riley-Ruvalcaba syndrome Baraitser-Winter syndrome Cowden syndrome DiGeorge syndrome Fraser syndrome Goldenhar syndrome Laron syndrome Moebius syndrome Muenke Syndrome Nance-Horan syndrome Nezelof syndrome Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome achondroplasia acromegaly acute myocardial infarction adrenal gland cancer amyloidosis autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome bipolar disorder blepharophimosis branchiootic syndrome cancer cervix disease chronic interstitial cystitis congenital heart disease coronary thrombosis craniosynostosis degenerative disc disease delusional disorder diabetes mellitus diabetic ketoacidosis double outlet right ventricle duodenum cancer embryoma epilepsy heart cancer hyperpituitarism hypoparathyroidism-deafness-renal disease syndrome hypoparathyroidism immune system disease intellectual disability interstitial cystitis learning disability microcephaly myocardial infarction myotonic dystrophy type 1 neuroblastoma obsolete type 1 diabetes mellitus 9 orofaciodigital syndrome I orofaciodigital syndrome X osteoporosis paranoid schizophrenia pheochromocytoma primary biliary cholangitis prune belly syndrome pseudohypoparathyroidism schizophrenia silent myocardial infarction small intestine cancer 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 velocardiofacial syndrome ventricular septal defect visual epilepsy
6625	small nuclear ribonucleoprotein U1 subunit 70	SNRNP70	Homo sapiens (human)
1514	cathepsin L	CTSL	Homo sapiens (human)
256764	WD repeat domain 72	WDR72	Homo sapiens (human)
26046	listerin E3 ubiquitin protein ligase 1	LTN1	Homo sapiens (human)
25976	TCDD inducible poly(ADP-ribose) polymerase	TIPARP Aliases: ARTD14 DDF1 DKFZP434J214 DKFZp686N0351 PARP-1 PARP-7 PARP7 RM1 pART14	Homo sapiens (human)	acoustic neuroma alcohol dependence alcohol use disorder angiomatous meningioma benign meningioma cancer cerebral convexity meningioma cervical cancer cervix carcinoma clear cell meningioma embryoma fibrous meningioma hepatitis A hepatitis intraorbital meningioma intraventricular meningioma meningioma meningothelial meningioma microcystic meningioma olfactory groove meningioma ovarian cancer parasagittal meningioma pituitary adenoma psammomatous meningioma secretory meningioma spinal meningioma transitional meningioma
48	aconitase 1	ACO1 Aliases: IREBP IRP1 aconitate hydratase, cytoplasmic cytosplasmic aconitase soluble aconitase	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 Down syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Wilson disease acquired polycythemia adrenal gland cancer age related macular degeneration anemia arthritis arthropathy bipolar disorder cancer cerebral degeneration deficiency anemia degeneration of macula and posterior pole duodenal ulcer duodenum cancer dysplastic nevus syndrome embryoma erythropoietin polycythemia essential hypertension familial erythrocytosis 2 heart cancer hemochromatosis type 1 hemochromatosis hepatocellular carcinoma hypertension hypochromic anemia iron metabolism disease leech infestation liver cancer macrocytic anemia macular degeneration melanoma metabolic dysfunction-associated steatotic liver disease microcytic anemia myiasis neuroblastoma osteoarthritis pancreatic cancer pancreatic carcinoma parapsoriasis pheochromocytoma polycythemia vera polycythemia porphyria prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole skin melanoma small intestine cancer stress polycythemia toxoplasmosis
7512	X-prolyl aminopeptidase 2	XPNPEP2	Homo sapiens (human)	acquired angioedema androgen insensitivity syndrome angioedema cancer cervical adenocarcinoma cervical cancer cervix carcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma hereditary angioedema nonpapillary renal cell carcinoma papillary renal cell carcinoma premature menopause primary cutaneous amyloidosis primary ovarian insufficiency prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma

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