GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **4176 - 4200** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
50839	taste 2 receptor member 10	TAS2R10
50838	taste 2 receptor member 13	TAS2R13
50837	taste 2 receptor member 7	TAS2R7
50836	taste 2 receptor member 8	TAS2R8
50835	taste 2 receptor member 9	TAS2R9
50834	taste 2 receptor member 1	TAS2R1
50833	taste 2 receptor member 16	TAS2R16
50832	taste 2 receptor member 4	TAS2R4
50831	taste 2 receptor member 3	TAS2R3
50814	NAD(P) dependent steroid dehydrogenase-like	NSDHL H105e3 SDR31E1 XAP104 short chain dehydrogenase/reductase family 31E, member 1	Bloch-Sulzberger syndrome CHILD syndrome CK syndrome Joubert syndrome Miller-Dieker lissencephaly syndrome Potter's syndrome Sjogren-Larsson syndrome X-linked chondrodysplasia punctata 1 X-linked chondrodysplasia punctata 2 acquired hyperkeratosis autosomal dominant chondrodysplasia punctata autosomal recessive congenital ichthyosis bilateral renal aplasia cancer chondrodysplasia punctata cleft lip complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 cortical dysplasia-focal epilepsy syndrome cutaneous fibrous histiocytoma epidermal nevus epilepsy granuloma annulare head and neck squamous cell carcinoma heart septal defect hidradenoma hydranencephaly hydronephrosis hypertropia hypomelanosis of Ito intellectual disability learning disability lissencephaly mechanical strabismus microcephaly obsolete congenital ichthyosiform erythroderma omphalocele ophthalmoplegia pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 scoliosis septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly skin papilloma skin tag strabismus syndromic X-linked intellectual disability Najm type syringoma umbilical hernia ventricular septal defect verruciform xanthoma of skin visual epilepsy
50810	HDGF like 3	HDGFL3
50809	heterochromatin protein 1 binding protein 3	HP1BP3
50808	adenylate kinase 3	AK3
50807	ArfGAP with SH3 domain, ankyrin repeat and PH domain 1	ASAP1
50801	potassium two pore domain channel subfamily K member 4	KCNK4
50649	Rho guanine nucleotide exchange factor 4	ARHGEF4
50640	patatin like phospholipase domain containing 8	PNPLA8 IPLA2-2 IPLA2G calcium-independent phospholipase A2-gamma iPLA2gamma
50636	anoctamin 7	ANO7
50632	calcyon neuron specific vesicular protein	CALY
50628	gem nuclear organelle associated protein 4	GEMIN4
50624	CUB and zona pellucida like domains 1	CUZD1
50618	intersectin 2	ITSN2
50617	ATPase H+ transporting V0 subunit a4	ATP6V0A4
50616	interleukin 22	IL22
50615	interleukin 21 receptor	IL21R

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