GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **3676 - 3700** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▲	Disease Ontology
23593	heme binding protein 2	HEBP2
51696	hdc homolog, cell cycle regulator	HECA
25831	HECT domain E3 ubiquitin protein ligase 1	HECTD1
23072	HECT, C2 and WW domain containing E3 ubiquitin protein ligase 1	HECW1
57493	heart development protein with EGF like domains 1	HEG1
3070	helicase, lymphoid specific	HELLS
113510	helicase, POLQ like	HELQ
9931	helicase with zinc finger	HELZ
220296	hepatic and glial cell adhesion molecule	HEPACAM
253012	HEPACAM family member 2	HEPACAM2
9843	hephaestin	HEPH
341208	hephaestin like 1	HEPHL1
8925	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	HERC1
8924	HECT and RLD domain containing E3 ubiquitin protein ligase 2	HERC2
51191	HECT and RLD domain containing E3 ubiquitin protein ligase 5	HERC5
55008	HECT and RLD domain containing E3 ubiquitin protein ligase family member 6	HERC6
3280	hes family bHLH transcription factor 1	HES1
3073	hexosaminidase subunit alpha	HEXA GM2 gangliosidosis Tay Sachs disease beta-hexosaminidase subunit alpha	GM2 gangliosidosis, AB variant GM2 gangliosidosis Gaucher's disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Sandhoff disease Tay-Sachs disease Werdnig-Hoffmann disease acquired immunodeficiency syndrome adult lymphoma amyotrophic lateral sclerosis blindness cancer central nervous system cancer central nervous system lymphoma childhood lymphoma childhood spinal muscular atrophy cystic fibrosis dementia diffuse scleroderma embryoma epilepsy gangliosidosis gliosarcoma glycoproteinosis high grade glioma human immunodeficiency virus infectious disease inherited metabolic disorder intellectual disability juvenile spinal muscular atrophy learning disability lingual-facial-buccal dyskinesia lymphoma lysosomal storage disease mixed glioma movement disease mucolipidosis type IV neurodegenerative disease obesity obsolete ymphosarcoma progressive muscular atrophy rheumatoid arthritis sensorineural hearing loss sickle cell anemia spinal muscular atrophy visual epilepsy
3074	hexosaminidase subunit beta	HEXB beta-hexosaminidase subunit beta	GM2 gangliosidosis, AB variant GM2 gangliosidosis HCL-V Sandhoff disease Schimke immuno-osseous dysplasia Tay-Sachs disease Unverricht-Lundborg syndrome acquired immunodeficiency syndrome acute kidney failure allergic asthma amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 anhidrosis anterior horn cell disease asthma autosomal recessive distal hereditary motor neuronopathy 1 blindness central nervous system cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congenital nystagmus dissociated nystagmus early myoclonic encephalopathy epilepsy gangliosidosis gliosarcoma hairy cell leukemia high grade glioma human immunodeficiency virus infectious disease hypohidrosis impotence inherited metabolic disorder intrinsic asthma kidney disease large intestine cancer lateral sclerosis liver cirrhosis lysosomal storage disease mixed glioma motor neuron disease multiple system atrophy neurodegenerative disease pathologic nystagmus postural orthostatic tachycardia syndrome premature ejaculation psychologic dyspareunia retinal disease retinitis rheumatoid arthritis spinal muscular atrophy spontaneous ocular nystagmus visual epilepsy
284004	hexosaminidase D	HEXD FLJ23825 hexosaminidase D, cytosolic	GM2 gangliosidosis Gilles de la Tourette syndrome Marfan syndrome Sandhoff disease Tay-Sachs disease Timothy syndrome dystonia lingual-facial-buccal dyskinesia long QT syndrome 8 situs inversus tricuspid valve stenosis tuberous sclerosis 1 tuberous sclerosis
10614	HEXIM P-TEFb complex subunit 1	HEXIM1
3077	homeostatic iron regulator	HFE
164045	helicase for meiosis 1	HFM1
3081	homogentisate 1,2-dioxygenase	HGD
3082	hepatocyte growth factor	HGF

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