GlyCosmos Portal

Displaying entries **18301 - 18325** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	Disease Ontology
D6ML73	MHC class I antigen (Fragment)	HLA-C	1
Q8WVN6	Secreted and transmembrane protein 1	SECTM1 K12	1
A0A0A7C9Q4	MHC class I antigen (Fragment)	HLA-C	1
A0A0A7C4X8	MHC class I antigen (Fragment)	HLA-C	1
Q8NB37	Glutamine amidotransferase-like class 1 domain-containing protein 1	GATD1 FERRY5 PDDC1	1
P21452	Substance-K receptor	TACR2 NK2R NKNAR TAC2R	2
A7Y9J9	Mucin 5AC, oligomeric mucus/gel-forming	MUC5AC	1
A0A291ID98	MHC class I antigen	HLA-C	1
E2GJI1	MHC class I antigen (Fragment)	HLA-C	1
A0A1G4HPX8	MHC class I antigen	HLA-B	1
M1PPD1	MHC class I polypeptide-related sequence A (Fragment)	MICA	3
A0A0G2R1R3	MHC class I antigen (Fragment)	HLA-C	1
G3D6I0	MHC class I antigen (Fragment)	HLA-C	1
N0A8Y8	MHC class I antigen (Fragment)	HLA-C	1
D3XDG3	MHC class I antigen (Fragment)	HLA-B	1
A0A678ZHK9	MHC class I antigen	HLA-B	1
O75914	Serine/threonine-protein kinase PAK 3	PAK3 OPHN3	2
P19526	Galactoside alpha-(1,2)-fucosyltransferase 1	FUT1 H HSC	2	B-cell lymphoma Edwards syndrome Fanconi anemia complementation group A Fanconi anemia complementation group D2 Fanconi anemia Kawasaki disease MHC class II deficiency Scheie syndrome T-cell acute lymphoblastic leukemia Wiskott-Aldrich syndrome X-linked lymphoproliferative syndrome 1 X-linked lymphoproliferative syndrome 2 X-linked severe combined immunodeficiency acquired immunodeficiency syndrome acquired polycythemia acute myeloid leukemia acute promyelocytic leukemia adenosine deaminase deficiency adrenoleukodystrophy alcoholic hepatitis alcoholic liver cirrhosis anemia arthritis arthropathy autoimmune disease autoimmune lymphoproliferative syndrome azoospermia beta thalassemia bile duct adenocarcinoma bile duct carcinoma bone marrow cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma catecholaminergic polymorphic ventricular tachycardia 1 catecholaminergic polymorphic ventricular tachycardia 2 catecholaminergic polymorphic ventricular tachycardia 3 catecholaminergic polymorphic ventricular tachycardia 4 catecholaminergic polymorphic ventricular tachycardia 5 catecholaminergic polymorphic ventricular tachycardia cerebral infarction cerebrovascular disease childhood leukemia cholangiocarcinoma chronic myeloid leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma combined T cell and B cell immunodeficiency congenital hemolytic anemia cutaneous porphyria cystic fibrosis diarrhea distal arthrogryposis embryoma erythropoietic protoporphyria erythropoietin polycythemia essential thrombocythemia factor VIII deficiency familial erythrocytosis 2 gallbladder disease glycogen storage disease II head and neck squamous cell carcinoma hematologic cancer hematopoietic system disease hemochromatosis type 1 hemochromatosis hemoglobin C disease hemoglobin D disease hemoglobin E disease hemoglobinopathy hemophagocytic lymphohistiocytosis hepatitis C hepatocellular carcinoma human immunodeficiency virus infectious disease immune system disease inherited metabolic disorder intrahepatic cholangiocarcinoma juvenile myelomonocytic leukemia large intestine cancer leukemia liver cancer liver cirrhosis liver disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung squamous cell carcinoma lysosomal storage disease macrocytic anemia malignant teratoma mantle cell lymphoma mature teratoma melanoma metachromatic leukodystrophy mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis multiple myeloma myelodysplastic syndrome myeloproliferative neoplasm obsolete ymphosarcoma orofaciodigital syndrome VIII osteoarthritis ovarian cancer ovarian carcinoma pancytopenia paroxysmal nocturnal hemoglobinuria polycythemia vera polycythemia progressive muscular atrophy prostate cancer prostate carcinoma proteinuria psoriatic arthritis sarcomatoid carcinoma severe combined immunodeficiency sickle cell anemia skin benign neoplasm skin cancer skin melanoma skin squamous cell carcinoma spinal muscular atrophy squamous cell carcinoma stomach cancer stomach carcinoma stress polycythemia teratocarcinoma teratoma tongue squamous cell carcinoma
P38567	Hyaluronidase PH-20	SPAM1 HYAL3 PH20	6	bladder carcinoma breast cancer breast carcinoma cancer carcinoma chronic obstructive pulmonary disease embryoma endocrine exophthalmos endometrial cancer endometrial carcinoma melanoma mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis osteochondrodysplasia ovarian carcinoma prostate cancer prostate carcinoma skin melanoma squamous cell carcinoma thromboangiitis obliterans tongue squamous cell carcinoma urinary bladder cancer uterine corpus cancer
A0A288QRQ2	MHC class I antigen (Fragment)	HLA-C	1
O60931	Cystinosin	CTNS	7	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Fanconi anemia Fanconi syndrome Laron syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome achondroplasia androgen insensitivity syndrome anhidrosis autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy bacterial vaginosis bone disease cartilage disease cerebral degeneration cone-rod dystrophy connective tissue disease cystinosis diabetes mellitus diabetic ketoacidosis disease of metabolism distal myopathy eunuchism exocrine pancreatic insufficiency facioscapulohumeral muscular dystrophy fundus albipunctatus glomerulonephritis hypogonadism hypohidrosis hypokalemia hypophosphatemia kidney disease kidney failure limb-girdle muscular dystrophy lysosomal storage disease male infertility muscular dystrophy nephritis nephrolithiasis nephrosis obsolete asthenopia obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete constipation oculopharyngeal muscular dystrophy osteomalacia premature menopause proteinuria pyoureter recurrent corneal erosion retinal disease retinitis pigmentosa retinitis rickets spondyloepimetaphyseal dysplasia, Sponastrime type uric acid nephrolithiasis vaginitis vulvitis vulvovaginitis
Q2P9R7	MHC class I antigen (Fragment)	HLA-C	1
Q9TPU4	MHC class I antigen HLA-B (Fragment)	HLA-B	1
Q14943	Killer cell immunoglobulin-like receptor 3DS1	KIR3DS1 NKAT10	3
A0A1W2PPN1	MHC class I polypeptide-related sequence A	MICA	2

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