GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **7076 - 7100** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
64409	polypeptide N-acetylgalactosaminyltransferase 17	GALNT17 GALNTL3 GalNAc-T17 GalNAc-T19 GalNAc-T5L polypeptide GalNAc transferase 3 polypeptide N-acetylgalactosaminyltransferase-like 3 ppGalNAc-T17	allergic asthma asthma autism spectrum disorder autistic disorder intrinsic asthma
64411	ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3	ARAP3
64418	transmembrane protein 168	TMEM168
64419	myotubularin related protein 14	MTMR14 FLJ22405 FLJ90311 egg-derived tyrosine phosphatase homolog (Drosophila) hEDTP hJumpy	Bell's palsy agnosia asphyxia neonatorum autosomal dominant centronuclear myopathy autosomal recessive centronuclear myopathy cancer capillary hemangioma cardiomyopathy cavernous hemangioma centronuclear myopathy 1 centronuclear myopathy X-linked centronuclear myopathy congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital myopathy 1A congenital myopathy 4A congenital ptosis congenital structural myopathy cryptorchidism developmental coordination disorder endomyocardial fibrosis facial nerve disease facial paralysis familial periodic paralysis hemangioma hepatocellular carcinoma hypertrophic cardiomyopathy liver cancer liver carcinoma malignant hyperthermia megaconial type congenital muscular dystrophy muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 myopathy nemaline myopathy obesity ophthalmoplegia ovarian carcinoma polyhydramnios ptosis rigid spine muscular dystrophy 1 tubular aggregate myopathy 1
64420	sushi domain containing 1	SUSD1
64421	DNA cross-link repair 1C	DCLRE1C
64422	autophagy related 3	ATG3
64423	inverted formin 2	INF2
64426	SDS3 homolog, SIN3A corepressor complex component	SUDS3
64428	cytosolic iron-sulfur assembly component 3	CIAO3
64430	pecanex 4	PCNX4
64434	nucleolar protein with MIF4G domain 1	NOM1
64478	CUB and Sushi multiple domains 1	CSMD1
64499	tryptase beta 2	TPSB2
64506	cytoplasmic polyadenylation element binding protein 1	CPEB1
64518	tektin 3	TEKT3
64579	N-deacetylase and N-sulfotransferase 4	NDST4	arteriosclerotic cardiovascular disease atherosclerosis autism spectrum disorder azoospermia cancer colorectal cancer colorectal carcinoma coronary artery disease embryoma intellectual disability large intestine cancer nutmeg liver prostate cancer prostate carcinoma
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
64600	phospholipase A2 group IIF	PLA2G2F
64601	VPS16 core subunit of CORVET and HOPS complexes	VPS16
64645	major facilitator superfamily domain containing 14A	MFSD14A
64682	anaphase promoting complex subunit 1	ANAPC1
64699	transmembrane serine protease 3	TMPRSS3
64711	heparan sulfate-glucosamine 3-sulfotransferase 6	HS3ST6	anthracosilicosis asbestosis bagassosis hereditary angioedema herpes simplex pneumoconiosis siderosis
64714	protein disulfide isomerase family A member 2	PDIA2

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