GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **8051 - 8075** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▼	Disease Ontology
131544	crystallin beta-gamma domain containing 3	CRYBG3 DKFZp667G2110	bronchus cancer bronchus carcinoma cancer embryoma lung cancer lung carcinoma
55057	crystallin beta-gamma domain containing 2	CRYBG2 FLJ38020 beta-gamma crystallin domain containing 2
202	crystallin beta-gamma domain containing 1	CRYBG1 suppression of tumorigenicity 4	allergic asthma asthma cancer intrinsic asthma melanoma multiple myeloma patent ductus arteriosus prostate cancer prostate carcinoma skin melanoma
1410	crystallin alpha B	CRYAB
1409	crystallin alpha A	CRYAA
1407	cryptochrome circadian regulator 1	CRY1	delayed sleep phase syndrome
64784	CREB regulated transcription coactivator 3	CRTC3
200186	CREB regulated transcription coactivator 2	CRTC2	type 2 diabetes mellitus
23373	CREB regulated transcription coactivator 1	CRTC1
10491	cartilage associated protein	CRTAP
56253	cytotoxic and regulatory T cell molecule	CRTAM
55118	cartilage acidic protein 1	CRTAC1
729920	CDP-L-ribitol pyrophosphorylase A	CRPPA 4-diphosphocytidyl-2C-methyl-D-erythritol synthase homolog (Arabidopsis) D-ribitol-5-phosphate cytidylyltransferase IspD Nip hCG_1745121 notch1-induced protein	Axenfeld-Rieger syndrome Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome agnosia anemia autosomal dominant Emery-Dreifuss muscular dystrophy 2 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 bilateral optic nerve hypoplasia cataract chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital muscular dystrophy due to integrin alpha-7 deficiency congenital muscular dystrophy-dystroglycanopathy A7 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy-dystroglycanopathy type A8 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism developmental coordination disorder distal myopathy epilepsy facioscapulohumeral muscular dystrophy familial periodic paralysis fibromyalgia fundus dystrophy glaucoma hydranencephaly hydrocephalus intellectual disability isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lissencephaly macrocytic anemia microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myositis nonpapillary renal cell carcinoma 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 obstructive hydrocephalus oculopharyngeal muscular dystrophy optic atrophy papillary renal cell carcinoma persistent hyperplastic primary vitreous pneumonia pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion renal carcinoma renal cell carcinoma retinal detachment rippling muscle disease 2 sarcomatoid renal cell carcinoma scoliosis senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly syndromic X-linked intellectual disability Najm type visual epilepsy
9696	ciliary rootlet coiled-coil, rootletin	CROCC
51340	crooked neck pre-mRNA splicing factor 1	CRNKL1
1400	collapsin response mediator protein 1	CRMP1
54675	cardiolipin synthase 1	CRLS1 CLS1 GCD10 GCD10 homolog (S. cerevisiae) dJ967N21.6	Coffin-Lowry syndrome adenosarcoma bilateral breast cancer breast cancer breast ductal carcinoma breast fibrocystic disease bronchus cancer bronchus carcinoma cancer colitis combined oxidative phosphorylation deficiency 57 depressive disorder dysthymic disorder gastroenteritis hepatitis C hepatocellular carcinoma ileitis ileocolitis liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma major depressive disorder mastitis melancholic depression microglandular adenosis nephroblastoma neurotic disorder obsolete melancholia paroxysmal nocturnal hemoglobinuria schizophrenia vascular dementia
51379	cytokine receptor like factor 3	CRLF3
64109	cytokine receptor like factor 2	CRLF2
9244	cytokine receptor like factor 1	CRLF1
1399	CRK like proto-oncogene, adaptor protein	CRKL
1398	CRK proto-oncogene, adaptor protein	CRK
83716	cysteine rich secretory protein LCCL domain containing 2	CRISPLD2
10321	cysteine rich secretory protein 3	CRISP3
167	cysteine rich secretory protein 1	CRISP1

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