GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **7901 - 7925** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
85455	dispatched RND transporter family member 2	DISP2
85456	tankyrase 1 binding protein 1	TNKS1BP1
85459	centrosomal protein 295	CEP295
85461	tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 1	TANC1
85463	zinc finger CCCH-type containing 12C	ZC3H12C
85464	slingshot protein phosphatase 2	SSH2
85465	selenoprotein I	SELENOI KIAA1724 SELI SEPI	Charcot-Marie-Tooth disease type 5 MASA syndrome Mast syndrome SPOAN syndrome Troyer syndrome cancer cleft palate coronary artery disease hepatoblastoma hepatocellular carcinoma hereditary spastic paraplegia 10 hereditary spastic paraplegia 11 hereditary spastic paraplegia 12 hereditary spastic paraplegia 13 hereditary spastic paraplegia 14 hereditary spastic paraplegia 15 hereditary spastic paraplegia 16 hereditary spastic paraplegia 17 hereditary spastic paraplegia 18 hereditary spastic paraplegia 19 hereditary spastic paraplegia 23 hereditary spastic paraplegia 24 hereditary spastic paraplegia 25 hereditary spastic paraplegia 26 hereditary spastic paraplegia 27 hereditary spastic paraplegia 28 hereditary spastic paraplegia 29 hereditary spastic paraplegia 2 hereditary spastic paraplegia 30 hereditary spastic paraplegia 31 hereditary spastic paraplegia 32 hereditary spastic paraplegia 34 hereditary spastic paraplegia 35 hereditary spastic paraplegia 36 hereditary spastic paraplegia 37 hereditary spastic paraplegia 38 hereditary spastic paraplegia 39 hereditary spastic paraplegia 3A hereditary spastic paraplegia 41 hereditary spastic paraplegia 42 hereditary spastic paraplegia 43 hereditary spastic paraplegia 44 hereditary spastic paraplegia 45 hereditary spastic paraplegia 46 hereditary spastic paraplegia 48 hereditary spastic paraplegia 49 hereditary spastic paraplegia 4 hereditary spastic paraplegia 53 hereditary spastic paraplegia 54 hereditary spastic paraplegia 55 hereditary spastic paraplegia 56 hereditary spastic paraplegia 57 hereditary spastic paraplegia 5A hereditary spastic paraplegia 61 hereditary spastic paraplegia 62 hereditary spastic paraplegia 63 hereditary spastic paraplegia 64 hereditary spastic paraplegia 6 hereditary spastic paraplegia 72A hereditary spastic paraplegia 73 hereditary spastic paraplegia 75 hereditary spastic paraplegia 77 hereditary spastic paraplegia 7 hereditary spastic paraplegia 81 hereditary spastic paraplegia 8 hereditary spastic paraplegia 9A hereditary spastic paraplegia 9B hereditary spastic paraplegia isolated cleft palate liver cancer microcephaly
85476	G elongation factor mitochondrial 1	GFM1
85480	thymic stromal lymphopoietin	TSLP
85508	scratch family transcriptional repressor 2	SCRT2
87178	polyribonucleotide nucleotidyltransferase 1	PNPT1
89766	uromodulin like 1	UMODL1
89780	Wnt family member 3A	WNT3A
89790	sialic acid binding Ig like lectin 10	SIGLEC10 MGC126774 PRO940 SIGLEC-10 SLG2 sialic acid binding Ig-like lectin 10 Ig-like lectin 7 siglec-like gene 2	B-cell lymphoma cancer childhood leukemia leukemia obsolete ymphosarcoma
89792	galactose-3-O-sulfotransferase 3	GAL3ST3 GAL3ST2
89795	neuron navigator 3	NAV3
89796	neuron navigator 1	NAV1
89797	neuron navigator 2	NAV2
89801	protein phosphatase 1 regulatory subunit 3F	PPP1R3F
89822	potassium two pore domain channel subfamily K member 17	KCNK17
89832	CHRNA7 (exons 5-10) and FAM7A (exons A-E) fusion	CHRFAM7A
89845	ATP binding cassette subfamily C member 10	ABCC10
89846	FYVE, RhoGEF and PH domain containing 3	FGD3
89853	multivesicular body subunit 12B	MVB12B
89858	sialic acid binding Ig like lectin 12	SIGLEC12 S2V SLG Siglec-12 Siglec-L1 Siglec-XII	carcinoma chronic fatigue syndrome disease of metabolism encephalomyelitis obesity prostate cancer prostate carcinoma sarcomatoid carcinoma systemic lupus erythematosus

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