GlyCosmos Portal

Displaying entries **13201 - 13225** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol ▼	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q93099	Homogentisate 1,2-dioxygenase	HGD HGO	1	1
A2PYH4	Probable ATP-dependent DNA helicase HFM1	HFM1 SEC3D1	1	1
Q30201	Hereditary hemochromatosis protein	HFE HLAH	3	4
Q14006	HF protein (Fragment)	HF	6	0
Q9Y5J3	Hairy/enhancer-of-split related with YRPW motif protein 1	HEY1 BHLHB31 CHF2 HERP2 HESR1 HRT1	0	1
O94992	Protein HEXIM1	HEXIM1 CLP1 EDG1 HIS1 MAQ1	3	3
P07686	Beta-hexosaminidase subunit beta	HEXB	6	47	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 spontaneous ocular nystagmus visual epilepsy
P06865	Beta-hexosaminidase subunit alpha	HEXA	7	27	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
Q9HCC6	Transcription factor HES-4	HES4 BHLHB42	0	1
Q14469	Transcription factor HES-1	HES1 BHLHB39 HL HRY	2	1
Q902F9	Endogenous retrovirus group K member 113 Env polyprotein	HERVK_113	12	0
Q8IVU3	Probable E3 ubiquitin-protein ligase HERC6	HERC6	1	2
Q9UII4	E3 ISG15--protein ligase HERC5	HERC5 CEB1 CEBP1	1	1
Q5GLZ8	Probable E3 ubiquitin-protein ligase HERC4	HERC4 KIAA1593	0	1
O95714	E3 ubiquitin-protein ligase HERC2	HERC2	8	7
Q15751	Probable E3 ubiquitin-protein ligase HERC1	HERC1	6	2
Q6MZM0	Ferroxidase HEPHL1	HEPHL1	6	0
Q9BQS7	Hephaestin	HEPH KIAA0698	13	3
C9JN07	HEPACAM family member 2	HEPACAM2	1	0
A8MVW5	HEPACAM family member 2	HEPACAM2 MIKI	5	0
Q14CZ8	Hepatic and glial cell adhesion molecule	HEPACAM	5	1
Q5T8I9	Small RNA 2'-O-methyltransferase	HENMT1 C1orf59	0	1
Q9BXL5	Hemogen	HEMGN EDAG NDR	0	1
P42694	Probable helicase with zinc finger domain	HELZ DRHC KIAA0054	6	3
Q8TDG4	Helicase POLQ-like	HELQ HEL308	2	7

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