GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (9988) Glycans (5831) Glycoproteins (15733) Lectins (298) Pathways (2074)

Displaying entries **2676 - 2700** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
79692	zinc finger protein 322	ZNF322
79691	queuine tRNA-ribosyltransferase accessory subunit 2	QTRT2 FLJ12960
79690	galactose-3-O-sulfotransferase 4	GAL3ST4 FLJ12116	leprosy
79689	STEAP4 metalloreductase	STEAP4
79684	Myb/SANT DNA binding domain containing 2	MSANTD2
79682	centromere protein U	CENPU
79680	retrotransposon Gag like 10	RTL10
79679	V-set domain containing T cell activation inhibitor 1	VTCN1 B7 family member, H4 B7 superfamily member 1 B7-H4 B7H4 B7S1 B7x FLJ22418	B-cell lymphoma IgA glomerulonephritis Langerhans-cell histiocytosis Sjogren's syndrome adenocarcinoma adenoma adult lymphoma arthritis arthropathy atrophic gastritis autoimmune disease autoimmune lymphoproliferative syndrome benign breast phyllodes tumor bile duct adenocarcinoma bile duct carcinoma bladder carcinoma bone osteosarcoma breast cancer breast carcinoma breast ductal carcinoma breast malignant phyllodes tumor bronchus cancer bronchus carcinoma cancer carcinoma celiac disease central nervous system lymphoma cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ childhood leukemia childhood lymphoma childhood osteosarcoma cholangiocarcinoma chromophobe renal cell carcinoma ciliary body disease clear cell renal cell carcinoma colitis collecting duct carcinoma colorectal cancer colorectal carcinoma common wart complement deficiency cribriform carcinoma cutaneous Paget's disease depressive disorder diabetes mellitus diabetic ketoacidosis diffuse large B-cell lymphoma dilated cardiomyopathy 1A dilated cardiomyopathy embryoma endometrial cancer endometrial carcinoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma gastric adenocarcinoma gastritis gastroenteritis giant cell glioblastoma glioblastoma glomerulonephritis granular cell carcinoma hepatitis B hepatocellular carcinoma high grade glioma ileitis ileocolitis immune system disease intrahepatic cholangiocarcinoma invasive ductal carcinoma iris disease juvenile rheumatoid arthritis keratoconjunctivitis sicca kidney disease large intestine cancer laryngeal carcinoma larynx cancer leukemia liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma lupus erythematosus lupus nephritis lymphoma melanoma membranous glomerulonephritis microphthalmia myeloproliferative disorder with eosinophilia nephritis nephrosis neurogenic arthropathy non-Hodgkin lymphoma nonpapillary renal cell carcinoma obsolete Matthew-Wood syndrome obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal carcinoma panuveitis papillary carcinoma papillary renal cell carcinoma placental insufficiency pleural tuberculosis primary biliary cholangitis primary immunodeficiency disease pyoureter renal carcinoma renal cell carcinoma reticulosarcoma rheumatoid arthritis sarcoidosis sarcomatoid carcinoma sarcomatoid renal cell carcinoma skin melanoma sporadic breast cancer squamous cell carcinoma stomach cancer stomach carcinoma synovial sarcoma systemic lupus erythematosus thyroid adenoma thyroid cancer thyroid gland carcinoma tongue squamous cell carcinoma tuberculosis 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 urinary bladder cancer uterine corpus cancer uveitis uveoparotid fever
79677	structural maintenance of chromosomes 6	SMC6
79671	NLR family member X1	NLRX1
79668	poly(ADP-ribose) polymerase family member 8	PARP8 ARTD16 FLJ21308 pART16	colorectal cancer colorectal carcinoma large intestine cancer
79664	interactor of little elongation complex ELL subunit 2	ICE2
79661	nei like DNA glycosylase 1	NEIL1 DNA endonuclease eight-like glycosylase 1 FLJ22402 FPG1 NEI1 hFPG1	Alzheimer's disease Behcet's disease Chandler syndrome Fanconi anemia complementation group A Fanconi anemia Fuchs' endothelial dystrophy Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Werner syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 abdominal obesity-metabolic syndrome acquired immunodeficiency syndrome bile duct adenocarcinoma bile duct carcinoma cancer carcinoma cerebral infarction cerebrovascular disease cholangiocarcinoma chromosome 15q24 deletion syndrome colorectal cancer common variable immunodeficiency corneal disease depressive disorder diabetes mellitus distal arthrogryposis dysthymic disorder embryoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma familial hyperlipidemia gallbladder disease glucose intolerance head and neck squamous cell carcinoma hepatitis C hepatocellular carcinoma human immunodeficiency virus infectious disease hyperinsulinism intrahepatic cholangiocarcinoma keratoconus large intestine cancer liver cancer liver disease lung cancer lung non-small cell carcinoma major depressive disorder melancholic depression multiple myeloma neurotic disorder obesity obsolete melancholia prediabetes syndrome primary sclerosing cholangitis progeria sarcomatoid carcinoma sclerosing cholangitis squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma tongue squamous cell carcinoma type 2 diabetes mellitus
79660	protein phosphatase 1 regulatory subunit 3B	PPP1R3B FLJ14005 GL PP1 subunit R4 PPP1R4 hepatic glycogen-targeting subunit, G(L)	Lafora disease alcohol use disorder antithrombin III deficiency arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis breast cancer breast carcinoma cancer coronary artery disease depressive disorder diabetes mellitus dysthymic disorder embryoma head and neck cancer major depressive disorder maturity-onset diabetes of the young melancholic depression melanoma neurotic disorder obesity obsolete melancholia post-traumatic stress disorder protein C deficiency protein S deficiency skin melanoma steatotic liver disease thrombophilia type 2 diabetes mellitus
79659	dynein cytoplasmic 2 heavy chain 1	DYNC2H1
79652	transmembrane protein 204	TMEM204
79651	rhomboid 5 homolog 2	RHBDF2
79646	pantothenate kinase 3	PANK3
79644	steroid 5 alpha-reductase 3	SRD5A3 3-oxo-5-alpha-steroid 4-dehydrogenase (NADP(+)) FLJ13352 SRD5A2L SRD5A2L1 polyprenol reductase	Creutzfeldt-Jakob disease Hailey-Hailey disease Kahrizi syndrome Marfan syndrome Rothmund-Thomson syndrome acquired hyperkeratosis agnosia angioma serpiginosum antithrombin III deficiency autistic disorder 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 bilateral optic nerve hypoplasia blindness capillary hemangioma cataract cavernous hemangioma cerebellar ataxia cerebellar disease coloboma congenital disorder of glycosylation Iq congenital disorder of glycosylation type I congenital disorder of glycosylation congenital hypothyroidism congenital nystagmus craniosynostosis cutis laxa dermatitis developmental coordination disorder dissociated nystagmus epilepsy eye disease fundus dystrophy glaucoma hypertrichosis hypothyroidism ichthyosis inguinal hernia intellectual disability isolated cleft palate isolated growth hormone deficiency learning disability mal de Meleda microcytic anemia microphthalmia myxedema nonepidermolytic palmoplantar keratoderma obsolete infantile epileptic encephalopathy optic atrophy palmoplantar keratosis pathologic nystagmus pituitary hypoplasia prostate cancer prostate carcinoma protein C deficiency protein S deficiency recurrent corneal erosion restrictive dermopathy situs inversus spontaneous ocular nystagmus syndromic X-linked intellectual disability 94 thrombophilia tuberous sclerosis visual epilepsy
79642	arylsulfatase family member J	ARSJ FLJ23548
79641	rogdi atypical leucine zipper	ROGDI
79633	FAT atypical cadherin 4	FAT4
79632	family with sequence similarity 184 member A	FAM184A
79631	elongation factor like GTPase 1	EFL1
79630	chromosome 1 open reading frame 54	C1orf54

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