GlyCosmos Portal

Displaying entries **13176 - 13200** of **18496** in total

« First

‹ Prev

…

524

525

526

527

528

529

530

531

532

…

Next ›

Last »
UniProt ID	Protein Name	Gene Symbol ▼	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9H2X6	Homeodomain-interacting protein kinase 2	HIPK2	6	3
Q86Z02	Homeodomain-interacting protein kinase 1	HIPK1 KIAA0630 MYAK NBAK2	6	1
O75146	Huntingtin-interacting protein 1-related protein	HIP1R HIP12 KIAA0655	2	2
O00291	Huntingtin-interacting protein 1	HIP1	1	1
Q9NQE9	Adenosine 5'-monophosphoramidase HINT3	HINT3	0	1
P49773	Adenosine 5'-monophosphoramidase HINT1	HINT1 HINT PKCI1 PRKCNH1	0	1
Q9Y5L2	Hypoxia-inducible lipid droplet-associated protein	HILPDA C7orf68 HIG2	6	1
Q9Y241	HIG1 domain family member 1A, mitochondrial	HIGD1A HIG1	0	1
Q16665	Hypoxia-inducible factor 1-alpha	HIF1A BHLHE78 MOP1 PASD8	2	2
A8MVS5	Protein HIDE1	HIDE1 C19orf38	3	1
Q8IV36	Protein HID1	HID1 C17orf28 DMC1	3	1
Q14526	Hypermethylated in cancer 1 protein	HIC1 ZBTB29	0	1
Q6NVY1	3-hydroxyisobutyryl-CoA hydrolase, mitochondrial	HIBCH	0	1	Leigh disease Unverricht-Lundborg syndrome West syndrome agnosia arthritis arthropathy blepharospasm brain disease cancer colorectal cancer colorectal carcinoma congenital nystagmus cryptorchidism developmental coordination disorder dissociated nystagmus dystonia early myoclonic encephalopathy epilepsy focal hand dystonia generalized dystonia hydrocephalus hypertropia inherited metabolic disorder lactic acidosis large intestine cancer mechanical strabismus neurodegenerative disease obsolete infantile epileptic encephalopathy ophthalmoplegia osteoarthritis pathologic nystagmus spontaneous ocular nystagmus strabismus tetralogy of Fallot visual epilepsy
P31937	3-hydroxyisobutyrate dehydrogenase, mitochondrial	HIBADH	4	2
Q9UM44	HERV-H LTR-associating protein 2	HHLA2	3	1
C9JL84	HERV-H LTR-associating protein 1	HHLA1	3	0
Q6UWX4	HHIP-like protein 2	HHIPL2 HHIP3 KIAA1822L	1	0
Q96JK4	HHIP-like protein 1	HHIPL1 HHIP2 KIAA1822	1	0
Q96QV1	Hedgehog-interacting protein	HHIP HIP	4	2
Q68CP4	Heparan-alpha-glucosaminide N-acetyltransferase	HGSNAT TMEM76	5	19	Zollinger-Ellison syndrome agnosia amnestic disorder blindness bulimia nervosa cataract cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness corneal disease developmental coordination disorder diabetes mellitus diarrhea dissociated nystagmus echolalia enterocele epilepsy fundus albipunctatus fundus dystrophy glaucoma hyperinsulinism hypertrichosis hypertrophic cardiomyopathy 1 hypogonadism intellectual disability keratoconus learning disability mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIB mucopolysaccharidosis type IIIC mucopolysaccharidosis type IIID mucopolysaccharidosis night blindness obesity obsolete asthenopia ophthalmoplegia optic atrophy pathologic nystagmus peripheral retinal degeneration retinitis pigmentosa 73 retinitis pigmentosa retrograde amnesia scoliosis sensorineural hearing loss spontaneous ocular nystagmus stereotypic movement disorder type 2 diabetes mellitus visual epilepsy
O14964	Hepatocyte growth factor-regulated tyrosine kinase substrate	HGS HRS	8	1
Q9BTY7	Protein HGH1 homolog	HGH1 C8orf30A C8orf30B FAM203A FAM203B	0	1
Q04756	Hepatocyte growth factor activator	HGFAC	11	20
D6RAR4	HGF activator	HGFAC	1	0
P14210	Hepatocyte growth factor	HGF HPTA	5	31

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

Summary

International Collaboration

Acknowledgements