GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **7276 - 7300** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
79595	Sin3A associated protein 130	SAP130
79596	ORC ubiquitin ligase 1	OBI1
79600	tectonic family member 1	TCTN1
79603	ceramide synthase 4	CERS4 FLJ12089 Trh1	atopic dermatitis breast cancer breast carcinoma cancer chronic kidney disease colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma dermatitis embryoma hepatocellular carcinoma large intestine cancer liver cancer liver carcinoma rectal benign neoplasm rectum adenocarcinoma rectum cancer
79605	piggyBac transposable element derived 5	PGBD5
79609	valosin containing protein lysine methyltransferase	VCPKMT
79611	acyl-CoA synthetase short chain family member 3	ACSS3 FLJ21963	cancer embryoma stomach cancer stomach carcinoma
79612	N-alpha-acetyltransferase 16, NatA auxiliary subunit	NAA16
79616	cyclin J like	CCNJL
79623	polypeptide N-acetylgalactosaminyltransferase 14	GALNT14 FLJ12691 GalNac-T10 GalNac-T14 polypeptide GalNAc transferase 14	Balo concentric sclerosis Cockayne syndrome Cornelia de Lange syndrome 1 Cornelia de Lange syndrome Dubowitz syndrome 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 Prader-Willi syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome X-linked Aarskog syndrome acute myeloid leukemia adrenoleukodystrophy autistic disorder autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome basal cell carcinoma breast cancer breast carcinoma cancer central nervous system disease chondrodysplasia-pseudohermaphroditism syndrome colorectal cancer colorectal carcinoma corneal disease embryoma esophagus squamous cell carcinoma giant cell glioblastoma glioblastoma hepatocellular carcinoma high grade glioma keratoconus large intestine cancer liver cancer liver carcinoma lung adenocarcinoma lung cancer lung non-small cell carcinoma melanoma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II narcolepsy neuroblastoma otitis media ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma signet ring cell adenocarcinoma skin melanoma
79624	acidic residue methyltransferase 1	ARMT1 FLJ12910 Protein-glutamate O-methyltransferase
79625	neuron derived neurotrophic factor	NDNF
79627	opioid growth factor receptor like 1	OGFRL1
79630	chromosome 1 open reading frame 54	C1orf54
79631	elongation factor like GTPase 1	EFL1
79632	family with sequence similarity 184 member A	FAM184A
79633	FAT atypical cadherin 4	FAT4
79641	rogdi atypical leucine zipper	ROGDI
79642	arylsulfatase family member J	ARSJ FLJ23548
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
79646	pantothenate kinase 3	PANK3
79651	rhomboid 5 homolog 2	RHBDF2
79652	transmembrane protein 204	TMEM204
79659	dynein cytoplasmic 2 heavy chain 1	DYNC2H1
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

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