GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **8676 - 8700** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
148789	beta-1,3-N-acetylgalactosaminyltransferase 2	B3GALNT2 MGC39558	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome agnosia 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 blindness breast cancer breast carcinoma cancer cataract cerebral degeneration choreatic disease coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital muscular dystrophy-dystroglycanopathy type A11 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism depressive disorder developmental coordination disorder distal myopathy dysthymic disorder dystonia embryoma epilepsy facioscapulohumeral muscular dystrophy familial periodic paralysis focal epilepsy fundus dystrophy glaucoma hepatocellular carcinoma holoprosencephaly 1 holoprosencephaly hydranencephaly hydrocephalus hypertropia intellectual disability isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia lissencephaly liver cancer major depressive disorder mechanical strabismus melancholic depression meningocele microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myopia neurotic disorder 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 infantile epileptic encephalopathy obsolete melancholia obstructive hydrocephalus oculopharyngeal muscular dystrophy ophthalmoplegia optic atrophy partial motor epilepsy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion retinal detachment rippling muscle disease 2 senile degeneration of brain sensorineural hearing loss septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly speech disorder stereotypic movement disorder strabismus syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability Najm type syndromic X-linked intellectual disability type 10 visual epilepsy
148808	major facilitator superfamily domain containing 4A	MFSD4A
148811	peptidase M20 domain containing 1	PM20D1
149041	ring finger and CCCH-type domains 1	RC3H1
149076	zinc finger protein 362	ZNF362
149095	DC-STAMP domain containing 1	DCST1
149175	mannosidase endo-alpha like	MANEAL FLJ31434	alternating hemiplegia of childhood autonomic neuropathy central nervous system disease nervous system disease neurodegenerative disease
149233	interleukin 23 receptor	IL23R
149466	chromosome 1 open reading frame 210	C1orf210
149499	leucine rich repeat containing 71	LRRC71
149628	pyrin and HIN domain family member 1	PYHIN1
149647	golgi associated RAB2 interactor family member 4	GARIN4
149954	BPI fold containing family B member 4	BPIFB4
149998	lipase I	LIPI CT17 LPDL PLA1C PRED5 cancer/testis antigen 17 mPA-PLA1beta membrane-associated phospholipase A1 beta
150082	lebercilin LCA5 like	LCA5L
150084	immunoglobulin superfamily member 5	IGSF5
150094	salt inducible kinase 1	SIK1
150159	solute carrier family 9 member B1	SLC9B1
150223	YdjC chitooligosaccharide deacetylase homolog	YDJC	bronchus cancer bronchus carcinoma celiac disease hepatitis B inflammatory bowel disease 1 inflammatory bowel disease lung cancer lung carcinoma parapsoriasis psoriasis pustulosis of palm and sole ulcerative colitis
150297	chromosome 22 open reading frame 42	C22orf42
150356	chondroadherin like	CHADL
150365	meiotic double-stranded break formation protein 1	MEI1
150372	NFAT activating protein with ITAM motif 1	NFAM1
150468	cytoskeleton associated protein 2 like	CKAP2L
150483	tektin 4	TEKT4

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