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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 **801 - 825** of **393515** in total

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Gene ID	Gene Name	Gene Symbol	Organism	Disease Ontology ▲
44058	UDP-glycosyltransferase family 36 member A1	Ugt36A1	Drosophila melanogaster (fruit fly)	Crigler-Najjar syndrome bilirubin metabolic disorder hyperthyroidism type 1 diabetes mellitus type 2 diabetes mellitus
41573	UDP-glycosyltransferase family 37 member A2	Ugt37A2	Drosophila melanogaster (fruit fly)	Crigler-Najjar syndrome bilirubin metabolic disorder hyperthyroidism type 1 diabetes mellitus type 2 diabetes mellitus
37420	UDP-glycosyltransferase family 49 member B1	Ugt49B1	Drosophila melanogaster (fruit fly)	Crigler-Najjar syndrome bilirubin metabolic disorder hyperthyroidism type 1 diabetes mellitus type 2 diabetes mellitus
23545	ATPase H+ transporting V0 subunit a2	ATP6V0A2 Aliases: ATP6N1D ATP6a2 J6B7 RTF Stv1 TJ6 TJ6M TJ6s V-ATPase subunit a2 V-type proton ATPase 116 kDa subunit a2 Vph1 a2 a2V infantile malignant osteopetrosis regeneration and tolerance factor	Homo sapiens (human)	Crohn's colitis Crohn's disease Dandy-Walker syndrome Ehlers-Danlos syndrome Hailey-Hailey disease Joubert syndrome Laron syndrome Miller-Dieker lissencephaly syndrome Rothmund-Thomson syndrome achondroplasia agnosia alopecia aortic valve disease 1 aortic valve disease 2 aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis 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 autosomal recessive osteopetrosis 1 autosomal recessive osteopetrosis 7 bacterial sepsis bicuspid aortic valve disease bone disease breast cancer breast carcinoma cancer cartilage disease clubfoot complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital disorder of glycosylation Il congenital disorder of glycosylation type I congenital disorder of glycosylation congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 connective tissue disease coronary artery disease cortical dysplasia-focal epilepsy syndrome cryptococcosis cryptorchidism cutis laxa dementia dental caries dentin caries developmental coordination disorder diabetic cataract diabetic retinopathy encephalitis encephalomyelitis epilepsy essential hypertension generalized atherosclerosis geroderma osteodysplasticum giant cell glioblastoma glioblastoma gliosarcoma high grade glioma hydranencephaly hypertension hypertropia inflammatory bowel disease 1 inflammatory bowel disease inguinal hernia intellectual disability intracranial aneurysm learning disability lipoatrophic diabetes mellitus lipodystrophy lissencephaly lung disease mal de Meleda male infertility mechanical strabismus microcephaly mixed glioma myelitis myopia omphalocele ophthalmoplegia osteogenesis imperfecta osteopetrosis osteosclerosis placental insufficiency platelet-type bleeding disorder 11 platelet-type bleeding disorder 3 platelet-type bleeding disorder 8 platelet-type bleeding disorder 9 pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 pulmonary emphysema renal tubular acidosis restrictive dermopathy scoliosis septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly status epilepticus strabismus syndromic X-linked intellectual disability Najm type ulcerative colitis umbilical hernia visual epilepsy von Willebrand's disease wrinkly skin syndrome
873	carbonyl reductase 1	CBR1 Aliases: SDR21C1 short chain dehydrogenase/reductase family 21C, member 1	Homo sapiens (human)	Crohn's colitis Crohn's disease Down syndrome Marfan syndrome acute myeloid leukemia acute promyelocytic leukemia adenocarcinoma adenoma amyotrophic lateral sclerosis bile duct adenocarcinoma bile duct carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cannabis abuse cannabis dependence carcinoma cardiomyopathy cervical cancer cholangiocarcinoma chordoma chorioamnionitis chronic kidney disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cribriform carcinoma decubitus ulcer diabetes mellitus diabetic ketoacidosis embryoma endomyocardial fibrosis familial adenomatous polyposis 1 familial adenomatous polyposis gastric tubular adenocarcinoma gastrointestinal system cancer giant cell glioblastoma glioblastoma glucocorticoid-remediable aldosteronism glucose intolerance granular cell carcinoma head and neck squamous cell carcinoma hepatocellular carcinoma high grade glioma hypertrophic cardiomyopathy inflammatory bowel disease 1 inflammatory bowel disease intracranial aneurysm intrahepatic cholangiocarcinoma irritant dermatitis islet cell tumor large intestine cancer leukemia liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung oat cell carcinoma lung small cell carcinoma lung squamous cell carcinoma obesity obsolete type 1 diabetes mellitus 9 ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma prediabetes syndrome primary hypertrophic osteoarthropathy progressive muscular atrophy prostate cancer prostate carcinoma sarcomatoid carcinoma secondary hypertrophic osteoarthropathy situs inversus steatotic liver disease stomach cancer stomach carcinoma thyroid gland medullary carcinoma tongue squamous cell carcinoma trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberous sclerosis 1 tuberous sclerosis 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 ulcerative colitis ureteral obstruction uterus leiomyosarcoma vitiligo
2813	glycoprotein 2	GP2 Aliases: ZAP75	Homo sapiens (human)	Crohn's colitis Crohn's disease Ebola hemorrhagic fever acute myeloid leukemia classic galactosemia galactokinase deficiency galactosemia gallbladder disease gastroenteritis gastrointestinal system disease hepatitis C herpes zoster inflammatory bowel disease 1 inflammatory bowel disease intestinal disease liver disease microphthalmia obsolete Matthew-Wood syndrome pancreatic cancer pancreatic carcinoma proctitis ulcerative colitis
3161	hyaluronan mediated motility receptor	HMMR Aliases: CD168 RHAMM	Homo sapiens (human)	Crohn's colitis Crohn's disease Ewing sarcoma Richter's syndrome acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia adult lymphoma agranulocytosis anaplastic astrocytoma arthritis arthropathy atrophy of testis autoimmune hemolytic anemia autoimmune lymphoproliferative syndrome bladder carcinoma brain cancer breast cancer breast carcinoma cancer carcinoma central nervous system cancer central nervous system lymphoma cerebral primitive neuroectodermal tumor cervical adenocarcinoma cervical cancer cervix carcinoma childhood cerebral astrocytoma childhood leukemia childhood lymphoma choriocarcinoma chromophobe renal cell carcinoma chromosome 5q deletion syndrome chronic leukemia chronic lymphocytic leukemia chronic myeloid leukemia clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma diffuse large B-cell lymphoma embryoma endometrial cancer endometrial carcinoma epithelioid leiomyosarcoma epithelioid malignant peripheral nerve sheath tumor fibrillary astrocytoma gemistocytic astrocytoma gestational trophoblastic neoplasm giant cell glioblastoma glioblastoma gliosarcoma hepatitis B hepatocellular carcinoma high grade glioma inflammatory bowel disease 1 inflammatory bowel disease invasive ductal carcinoma juvenile pilocytic astrocytoma large intestine cancer leiomyosarcoma leukemia leukopenia liver cancer luminal breast carcinoma A lung adenocarcinoma lung benign neoplasm lung cancer lung disease lung non-small cell carcinoma lymphoblastic lymphoma lymphoma lymphoplasmacytic lymphoma macroglobulinemia malignant astrocytoma malignant peripheral nerve sheath tumor medulloblastoma medulloepithelioma microphthalmia mixed glioma multiple myeloma myxoid leiomyosarcoma neurilemmoma neuroectodermal tumor neurofibrosarcoma neutropenia nodular prostate nonpapillary renal cell carcinoma obsolete Matthew-Wood syndrome obsolete embryonal Tumor with Multilayered Rosettes, C19MC-Altered obsolete lymphoplasmacytic lymphoma obsolete ymphosarcoma ossifying fibroma osteoarthritis ovarian cancer ovarian carcinoma oxyphilic adenoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma pilocytic astrocytoma placenta cancer polycystic ovary syndrome prostate cancer prostate carcinoma prostatic adenoma protoplasmic astrocytoma renal carcinoma renal cell carcinoma renal oncocytoma rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma seminoma severe congenital neutropenia sporadic breast cancer squamous cell carcinoma stomach cancer stomach carcinoma subependymal giant cell astrocytoma supratentorial primitive neuroectodermal tumor testicular cancer testicular germ cell cancer testis seminoma tongue squamous cell carcinoma transitional cell carcinoma ulcerative colitis urinary bladder cancer uterine corpus cancer
9415	fatty acid desaturase 2	FADS2 Aliases: D6D DES6 FADSD6 SLL0262 TU13 delta-6-desaturase	Homo sapiens (human)	Crohn's colitis Crohn's disease Fabry disease Wolman disease abdominal obesity-metabolic syndrome 1 acquired immunodeficiency syndrome acute myocardial infarction age related macular degeneration alcohol use disorder allergic asthma alopecia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis atopic dermatitis atrial fibrillation attention deficit hyperactivity disorder autism spectrum disorder autistic disorder bipolar I disorder bipolar disorder breast cancer breast carcinoma cancer cardiovascular system disease cerebral infarction cerebrovascular disease chronic kidney disease chylomicron retention disease colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma congenital hypothyroidism congestive heart failure coronary artery disease coronary thrombosis degeneration of macula and posterior pole depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy discrete subaortic stenosis embryoma giant cell glioblastoma glioblastoma glomerulonephritis heart disease hemochromatosis type 1 hemochromatosis hepatitis hepatocellular carcinoma high grade glioma human immunodeficiency virus infectious disease hypothyroidism inflammatory bowel disease 1 inflammatory bowel disease intrinsic asthma kidney disease kwashiorkor large intestine cancer laryngeal squamous cell carcinoma lipid metabolism disorder lipid storage disease liver cancer lung benign neoplasm lung carcinoma macular degeneration major depressive disorder marasmus melancholic depression myocardial infarction myxedema nephritis nephrosis neurotic disorder nutmeg liver nutrition disease obesity obsolete melancholia polycystic ovary syndrome progressive pseudorheumatoid arthropathy of childhood protein-energy malnutrition psoriatic arthritis pyoureter rheumatoid arthritis schizophrenia silent myocardial infarction skin disease steatotic liver disease stomach cancer stomach carcinoma type 1 diabetes mellitus type 2 diabetes mellitus ulcerative colitis vitiligo
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
140733	mono-ADP ribosylhydrolase 2	MACROD2 Aliases: O-acetyl-ADP-ribose deacetylase MACROD2 dJ631M13.5	Homo sapiens (human)	Crohn's colitis Crohn's disease Kabuki syndrome acquired immunodeficiency syndrome acute myeloid leukemia autism spectrum disorder autistic disorder bipolar I disorder bipolar disorder cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma disease of mental health embryoma essential hypertension hepatocellular carcinoma human immunodeficiency virus infectious disease hypertension hypogonadotropic hypogonadism 21 with or without anosmia inflammatory bowel disease 1 inflammatory bowel disease intellectual disability large intestine cancer learning disability liver cancer malignant fibrous histiocytoma obesity psychotic disorder substance abuse substance-related disorder ulcerative colitis
80329	UL16 binding protein 1	ULBP1 Aliases: RAET1I	Homo sapiens (human)	Crohn's colitis Crohn's disease Kawasaki disease adult lymphoma bone osteosarcoma bronchus cancer bronchus carcinoma cancer embryoma giant cell glioblastoma glioblastoma head and neck squamous cell carcinoma hepatitis C hepatocellular carcinoma inflammatory bowel disease 1 inflammatory bowel disease liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma osteosarcoma stomach cancer stomach carcinoma ulcerative colitis
91869	RFT1 homolog	RFT1 Aliases: CDG1N congenital disorder of glycosylation 1N	Homo sapiens (human)	Crohn's colitis Crohn's disease Laron syndrome Unverricht-Lundborg syndrome West syndrome achondroplasia blepharospasm blindness blood coagulation disease cancer clubfoot congenital disorder of glycosylation In congenital disorder of glycosylation type I congenital disorder of glycosylation developmental and epileptic encephalopathy 36 diabetes mellitus diabetic ketoacidosis early myoclonic encephalopathy epilepsy focal hand dystonia hypertropia inflammatory bowel disease 1 inflammatory bowel disease mechanical strabismus microcephaly obsolete infantile epileptic encephalopathy obsolete inherited blood coagulation disease ophthalmoplegia schizophrenia sensorineural hearing loss strabismus syndromic X-linked intellectual disability 94 type 2 diabetes mellitus ulcerative colitis visual epilepsy
92579	glucose-6-phosphatase catalytic subunit 3	G6PC3 Aliases: UGRP	Homo sapiens (human)	Crohn's colitis Crohn's disease Marfan syndrome Wiskott-Aldrich syndrome acute myeloid leukemia agranulocytosis androgen insensitivity syndrome anemia 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 bacterial sepsis bronchiectasis cancer cleft palate colitis congenital heart disease cryptorchidism cyclic hematopoiesis cystinuria embryoma essential thrombocythemia eunuchism galactosemia gastroenteritis 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 hydronephrosis hypogonadism ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease intellectual disability isolated cleft palate learning disability leukopenia lymphopenia macrocytic anemia microcephaly mitral valve insufficiency mitral valve prolapse myelodysplastic syndrome neutropenia oculocutaneous albinism pancytopenia patent ductus arteriosus patent foramen ovale premature menopause primary immunodeficiency disease primary pulmonary hypertension pulmonary valve stenosis sensorineural hearing loss severe congenital neutropenia 4 severe congenital neutropenia situs inversus thrombocytopenia tuberous sclerosis ulcerative colitis varicose veins
8399	phospholipase A2 group X	PLA2G10 Aliases: GXPLA2	Homo sapiens (human)	Crohn's colitis Crohn's disease Norum disease Tangier disease abdominal aortic aneurysm abetalipoproteinemia adenocarcinoma adenoma adult respiratory distress syndrome allergic asthma alternating hemiplegia of childhood anaplastic astrocytoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy ascending cholangitis asthma atherosclerosis autonomic neuropathy bacterial infectious disease bacterial sepsis bipolar disorder breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiovascular system disease central nervous system disease childhood cerebral astrocytoma cholangitis cholecystolithiasis choledocholithiasis cholelithiasis choreaacanthocytosis chronic kidney disease chronic obstructive pulmonary disease colitis colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary artery disease craniosynostosis cribriform carcinoma diabetes mellitus diabetic ketoacidosis embryoma epilepsy familial adenomatous polyposis 1 familial adenomatous polyposis familial hyperlipidemia fibrillary astrocytoma gastroenteritis gemistocytic astrocytoma granular cell carcinoma heart disease hepatocellular carcinoma high grade glioma hypolipoproteinemia ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease intrinsic asthma islet cell tumor juvenile pilocytic astrocytoma large intestine cancer liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphopenia malignant astrocytoma nervous system disease newborn respiratory distress syndrome nutmeg liver obsolete major affective disorder 1 obsolete major affective disorder 2 parapsoriasis pilocytic astrocytoma pleurisy primary sclerosing cholangitis prostate cancer prostate carcinoma protoplasmic astrocytoma psoriasis pulmonary coin lesion pustulosis of palm and sole rheumatoid arthritis schizophrenia sclerosing cholangitis subependymal giant cell astrocytoma suppurative cholangitis tuberculosis tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis visual epilepsy
7915	aldehyde dehydrogenase 5 family member A1	ALDH5A1 Aliases: SSADH SSDH succinate-semialdehyde dehydrogenase	Homo sapiens (human)	Crohn's colitis Crohn's disease Rett syndrome X-linked dystonia-parkinsonism Zika fever age related macular degeneration agnosia anxiety disorder autistic disorder carcinoma degeneration of macula and posterior pole developmental coordination disorder dystonia 12 dystonia 16 dystonia 21 dystonia 25 dystonia 27 dystonia 5 dystonia epilepsy focal dystonia focal hand dystonia generalized anxiety disorder generalized dystonia generalized epilepsy with febrile seizures plus hypertropia idiopathic generalized epilepsy inflammatory bowel disease 1 inflammatory bowel disease intellectual disability juvenile myoclonic epilepsy learning disability lingual-facial-buccal dyskinesia macular degeneration mechanical strabismus movement disease myoclonic dystonia 11 ophthalmoplegia ovarian cancer ovarian carcinoma psychotic disorder schizoaffective disorder schizophreniform disorder status epilepticus strabismus succinic semialdehyde dehydrogenase deficiency syndromic X-linked intellectual disability 94 torsion dystonia 13 torsion dystonia 17 torsion dystonia 1 torsion dystonia 2 torsion dystonia 4 torsion dystonia 6 torsion dystonia with onset in infancy tuberculosis ulcerative colitis visual epilepsy
160364	C-type lectin domain family 12 member A	CLEC12A Aliases: CD371 CLL-1 DCAL-2 MICL dendritic cell-associated lectin 2 myeloid inhibitory C-type lectin-like receptor	Homo sapiens (human)	Crohn's colitis Crohn's disease Richter's syndrome acute leukemia acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia arthritis arthropathy cancer childhood leukemia chronic fatigue syndrome chronic lymphocytic leukemia chronic myeloid leukemia dermatophytosis embryoma encephalitis encephalomyelitis essential thrombocythemia fungal infectious disease immune system disease inflammatory bowel disease 1 inflammatory bowel disease leukemia lymphoblastic lymphoma lymphocytic choriomeningitis lymphoplasmacytic lymphoma macroglobulinemia monoclonal gammopathy of uncertain significance multiple myeloma multiple sclerosis myelitis myelodysplastic syndrome obsolete lymphoplasmacytic lymphoma rheumatoid arthritis ulcerative colitis
8547	ficolin 3	FCN3 Aliases: FCNH HAKA1 Hakata antigen	Homo sapiens (human)	Crohn's colitis Crohn's disease abdominal aortic aneurysm acute myocardial infarction amyotrophic lateral sclerosis anogenital venereal wart arteriosclerotic cardiovascular disease atherosclerosis bacterial infectious disease cancer common wart complement component 2 deficiency complement component 4a deficiency complement component 4b deficiency complement component 6 deficiency complement component 7 deficiency complement component 9 deficiency complement deficiency coronary artery disease coronary thrombosis diabetes mellitus essential hypertension gestational diabetes hepatocellular carcinoma hypertension inflammatory bowel disease 1 inflammatory bowel disease interstitial lung disease leprosy liver cancer lupus nephritis myocardial infarction ovarian cancer ovarian carcinoma placental insufficiency primary immunodeficiency disease progressive muscular atrophy sarcoidosis scleroderma silent myocardial infarction systemic lupus erythematosus systemic scleroderma tuberculosis type 2 diabetes mellitus type I complement component 8 deficiency type II complement component 8 deficiency ulcerative colitis
2590	polypeptide N-acetylgalactosaminyltransferase 2	GALNT2 Aliases: GalNAc-T2 polypeptide GalNAc transferase 2	Homo sapiens (human)	Crohn's colitis Crohn's disease abdominal obesity-metabolic syndrome 1 achondroplasia acute myeloid leukemia arteriosclerotic cardiovascular disease atherosclerosis cancer central nervous system cancer cerebral infarction cerebrovascular disease cholesterol-ester transfer protein deficiency chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma congenital disorder of glycosylation type II coronary artery disease diabetes mellitus embryoma essential hypertension familial hyperlipidemia gastric adenocarcinoma gliosarcoma hepatocellular carcinoma high grade glioma hyperalphalipoproteinemia 1 hyperglycemia hypertension hypochondroplasia inflammatory bowel disease 1 inflammatory bowel disease liver cancer mixed glioma nutmeg liver obesity papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia squamous cell carcinoma stomach cancer stomach carcinoma temporal arteritis tongue squamous cell carcinoma type 2 diabetes mellitus ulcerative colitis
3992	fatty acid desaturase 1	FADS1 Aliases: D5D FADS6 FADSD5 TU12 acyl-CoA (8-3)-desaturase delta-5 desaturase	Homo sapiens (human)	Crohn's colitis Crohn's disease abdominal obesity-metabolic syndrome 1 acute chest syndrome acute lymphoblastic leukemia adult acute lymphocytic leukemia age related macular degeneration alcohol use disorder allergic asthma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis atrial fibrillation attention deficit hyperactivity disorder autism spectrum disorder autistic disorder bipolar I disorder bipolar disorder bone osteosarcoma borderline personality disorder breast cancer breast carcinoma cancer cardiovascular system disease cerebral infarction cerebrovascular disease childhood acute lymphocytic leukemia childhood osteosarcoma chronic kidney disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease degeneration of macula and posterior pole depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis embryoma essential hypertension gestational diabetes heart disease hepatocellular carcinoma hypertension inflammatory bowel disease 1 inflammatory bowel disease intermittent explosive disorder intrinsic asthma kwashiorkor large intestine cancer laryngeal squamous cell carcinoma liver cancer liver cirrhosis lung benign neoplasm lung carcinoma macular degeneration major depressive disorder marasmus melancholic depression neurotic disorder nutmeg liver nutrition disease obesity obsolete melancholia osteosarcoma pancreatic cancer pancreatic carcinoma polycystic ovary syndrome progressive pseudorheumatoid arthropathy of childhood protein-energy malnutrition rheumatoid arthritis schizophrenia steatotic liver disease stomach cancer stomach carcinoma type 2 diabetes mellitus ulcerative colitis vitiligo
8529	cytochrome P450 family 4 subfamily F member 2	CYP4F2	Homo sapiens (human)	Crohn's colitis Crohn's disease abdominal obesity-metabolic syndrome 1 acute myocardial infarction adrenal carcinoma adrenal cortex cancer adrenocortical carcinoma adrenoleukodystrophy arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation brain stem infarction cancer cardiovascular system disease cerebral artery occlusion cerebral infarction cerebrovascular disease coronary artery disease coronary thrombosis embryoma essential hypertension heart disease hepatocellular carcinoma hypertension inflammatory bowel disease 1 inflammatory bowel disease liver cancer myocardial infarction nutmeg liver obesity pancreatic ductal adenocarcinoma patent ductus arteriosus silent myocardial infarction steatotic liver disease thrombophilia ulcerative colitis varicose veins vascular disease
2525	fucosyltransferase 3 (Lewis blood group)	FUT3 Aliases: CD174 galactoside 3(4)-L-fucosyltransferase	Homo sapiens (human)	Crohn's colitis Crohn's disease achalasia adult respiratory distress syndrome alopecia anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis bile duct adenocarcinoma bile duct carcinoma bipolar disorder bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer candidiasis carcinoma childhood leukemia childhood osteosarcoma cholangiocarcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma colitis collecting duct carcinoma colon adenocarcinoma colon carcinoma colorectal cancer colorectal carcinoma congenital diaphragmatic hernia coronary artery disease cystic fibrosis depressive disorder dilated cardiomyopathy 1A dilated cardiomyopathy embryoma esophagitis gastroenteritis gastroesophageal reflux disease herpes simplex hiatus hernia ileitis ileocolitis immunoglobulin alpha deficiency inflammatory bowel disease 1 inflammatory bowel disease intrahepatic cholangiocarcinoma invasive ductal carcinoma large intestine cancer leech infestation leukemia lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease macrocytic anemia major depressive disorder megaesophagus melancholic depression microphthalmia myiasis nonpapillary renal cell carcinoma nutmeg liver obsolete Matthew-Wood syndrome obsolete melancholia osteosarcoma pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma peptic esophagitis primary sclerosing cholangitis prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma rumination disorder sarcomatoid carcinoma sarcomatoid renal cell carcinoma sclerosing cholangitis selective IgA deficiency disease stomach cancer stomach carcinoma toxoplasmosis ulcerative colitis
593	branched chain keto acid dehydrogenase E1 subunit alpha	BCKDHA Aliases: MSU maple syrup urine disease	Homo sapiens (human)	Crohn's colitis Crohn's disease acute pancreatitis arthritis arthropathy bacterial sepsis brain edema cerebral infarction cerebrovascular disease epilepsy gout hypoglycemia inflammatory bowel disease 1 inflammatory bowel disease intellectual disability lactic acidosis learning disability maple syrup urine disease pancreatitis placental insufficiency shigellosis trichohepatoenteric syndrome 1 trichohepatoenteric syndrome ulcerative colitis visual epilepsy
5968	regenerating family member 1 beta	REG1B Aliases: PSPS2 REGH REGI-BETA REGL lithostathine 1 beta secretory pancreatic stone protein 2	Homo sapiens (human)	Crohn's colitis Crohn's disease acute pancreatitis bronchus cancer bronchus carcinoma cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma diabetes mellitus diabetic ketoacidosis gastrointestinal system disease inflammatory bowel disease 1 inflammatory bowel disease intestinal disease kwashiorkor large intestine cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma marasmus microphthalmia myocardial infarction nutrition disease obsolete Matthew-Wood syndrome obsolete type 1 diabetes mellitus 9 pancreatitis protein-energy malnutrition squamous cell carcinoma tongue squamous cell carcinoma 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 ulcerative colitis
55600	intelectin 1	ITLN1 Aliases: FLJ20022 HL-1 ITLN LFR hIntL omentin	Homo sapiens (human)	Crohn's colitis Crohn's disease adenocarcinoma adenoma allergic asthma arteriosclerotic cardiovascular disease asthma atherosclerosis atopic dermatitis bacterial infectious disease benign mesothelioma cancer carcinoma coronary artery disease cribriform carcinoma dermatitis diabetes mellitus diabetic ketoacidosis granular cell carcinoma inflammatory bowel disease 1 inflammatory bowel disease intrinsic asthma malignant epithelial mesothelioma malignant mesothelioma multiple sclerosis neuroblastoma nutmeg liver obesity osteoporosis parapsoriasis pneumonia polycystic ovary syndrome primary biliary cholangitis psoriasis pustulosis of palm and sole sarcomatoid carcinoma stomach cancer stomach carcinoma tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis
51363	carbohydrate sulfotransferase 15	CHST15 Aliases: B cell RAG associated protein BRAG GALNAC4S-6ST KIAA0598 N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase	Homo sapiens (human)	Crohn's colitis Crohn's disease adult astrocytic tumor anaplastic astrocytoma breast cancer breast carcinoma cancer childhood astrocytic tumor childhood cerebral astrocytoma colitis embryoma endometrial cancer endometrial carcinoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma fibrillary astrocytoma gastroenteritis gemistocytic astrocytoma giant cell glioblastoma glioblastoma high grade glioma idiopathic interstitial pneumonia ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease juvenile pilocytic astrocytoma lung benign neoplasm malignant astrocytoma microphthalmia obsolete Matthew-Wood syndrome ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma patent ductus arteriosus pilocytic astrocytoma postinflammatory pulmonary fibrosis protoplasmic astrocytoma pulmonary fibrosis subependymal giant cell astrocytoma ulcerative colitis uterine corpus cancer

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