GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **8276 - 8300** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▼	Disease Ontology
22883	calsyntenin 1	CLSTN1
63967	claspin	CLSPN
119467	clarin 3	CLRN3
645104	clarin 2	CLRN2
7401	clarin 1	CLRN1
10845	caseinolytic mitochondrial matrix peptidase chaperone subunit X	CLPX
81037	CLPTM1 like	CLPTM1L
1209	CLPTM1 regulator of GABA type A receptor forward trafficking	CLPTM1
9575	clock circadian regulator	CLOCK
1207	chloride nucleotide-sensitive channel 1A	CLNS1A
116449	cytokine dependent hematopoietic cell linker	CLNK
1203	CLN5 intracellular trafficking protein	CLN5	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 Lafora disease MERRF syndrome Pick's disease Reye syndrome Unverricht-Lundborg syndrome agnosia blepharospasm blindness brain disease cerebellar ataxia cerebellar disease cerebral degeneration early myoclonic encephalopathy epilepsy eye disease focal hand dystonia intellectual disability learning disability neurodegenerative disease neuronal ceroid lipofuscinosis 10 neuronal ceroid lipofuscinosis 11 neuronal ceroid lipofuscinosis 13 neuronal ceroid lipofuscinosis 1 neuronal ceroid lipofuscinosis 2 neuronal ceroid lipofuscinosis 3 neuronal ceroid lipofuscinosis 4 neuronal ceroid lipofuscinosis 5 neuronal ceroid lipofuscinosis 6A neuronal ceroid lipofuscinosis 6B neuronal ceroid lipofuscinosis 7 neuronal ceroid lipofuscinosis 8 northern epilepsy variant neuronal ceroid lipofuscinosis 8 neuronal ceroid lipofuscinosis 9 neuronal ceroid lipofuscinosis retinal degeneration visual epilepsy
1201	CLN3 lysosomal/endosomal transmembrane protein, battenin	CLN3
79827	CXADR like membrane protein	CLMP
79789	calmin	CLMN
1195	CDC like kinase 1	CLK1
79745	CAP-Gly domain containing linker protein family member 4	CLIP4
7461	CAP-Gly domain containing linker protein 2	CLIP2
6249	CAP-Gly domain containing linker protein 1	CLIP1
9685	clathrin interactor 1	CLINT1
1192	chloride intracellular channel 1	CLIC1
1047	calmegin	CLGN	breast cancer breast carcinoma prostate cancer prostate carcinoma seminoma testicular cancer testicular germ cell cancer testis seminoma
283420	C-type lectin domain containing 9A	CLEC9A CD370 DNGR-1 HEEE9341 UNQ9341	acquired immunodeficiency syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis cancer coronary artery disease herpes simplex human immunodeficiency virus infectious disease influenza leprosy pneumonia primary immunodeficiency disease tuberculosis viral infectious disease
64581	C-type lectin domain containing 7A	CLEC7A CD369 DECTIN-1 SCARE2 hDectin-1	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 Behcet's disease Bloch-Sulzberger syndrome Kawasaki disease Meier-Gorlin syndrome 1 Meier-Gorlin syndrome Pick's disease Reye syndrome acquired hyperkeratosis acute myeloid leukemia adult-onset Still's disease allergic asthma amyloidosis angular cheilitis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy aspergillosis asthma atherosclerosis atopic dermatitis autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autoimmune polyendocrine syndrome type 1 autoimmune polyendocrine syndrome bacterial infectious disease bacterial sepsis black piedra blastomycosis cancer candidiasis cerebral degeneration cheilitis cholesteatoma chromoblastomycosis chronic mucocutaneous candidiasis chronic obstructive pulmonary disease chronic ulcer of skin coccidioidomycosis colitis congenital intrinsic factor deficiency coronary artery disease cryptococcosis cutaneous leishmaniasis cystic fibrosis dermatitis dermatomycosis dermatophytosis diverticulitis embryoma epilepsy exanthem fungal infectious disease gastroenteritis granuloma annulare hepatitis B hepatitis hepatocellular carcinoma histoplasmosis hypomelanosis of Ito ileitis ileocolitis immune system disease inflammatory bowel disease 1 inflammatory bowel disease influenza intrinsic asthma keratitis keratoconjunctivitis lip disease liver cancer liver carcinoma liver cirrhosis lupus nephritis male infertility mycotic corneal ulcer nutmeg liver obesity oral candidiasis osteoarthritis pancreatic cancer pancreatic carcinoma paracoccidioidomycosis parapsoriasis parasitic helminthiasis infectious disease patent ductus arteriosus pneumocystosis pneumonia polyp of middle ear psoriasis pustulosis of palm and sole rheumatoid arthritis shigellosis sporotrichosis superficial mycosis systemic lupus erythematosus tinea favosa tuberculosis ulcerative colitis urinary tract obstruction vasculitis visual epilepsy vulvovaginal candidiasis white piedra
93978	C-type lectin domain containing 6A	CLEC6A dectin-2 hDECTIN-2	Kawasaki disease acute myocardial infarction arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis cancer candidiasis cholesteatoma coronary artery disease coronary thrombosis cryptococcosis cystic fibrosis dermatomycosis dermatophytosis embryoma fungal infectious disease myocardial infarction pneumocystosis pneumonia polyp of middle ear rheumatoid arthritis silent myocardial infarction superficial mycosis tinea favosa tuberculosis vasculitis

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