GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **5301 - 5325** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
10946	splicing factor 3a subunit 3	SF3A3
10942	serine protease 21	PRSS21 ESP-1 TEST1 testisin	Behcet's disease Down syndrome acquired immunodeficiency syndrome alcohol dependence alcohol use disorder atrial fibrillation cancer cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood germ cell cancer diabetes mellitus diabetic ketoacidosis disorder of sexual development embryonal cancer germ cell and embryonal cancer germ cell cancer germinoma hepatitis B hermaphroditism human immunodeficiency virus infectious disease monoclonal gammopathy of uncertain significance monoclonal paraproteinemia ovarian cancer ovarian carcinoma plasma cell neoplasm pseudohermaphroditism type 2 diabetes mellitus
10941	UDP glucuronosyltransferase family 2 member A1 complex locus	UGT2A1	cancer embryoma laryngeal disease ovarian cancer ovarian carcinoma tracheal disease
10940	POP1 homolog, ribonuclease P/MRP subunit	POP1
10936	G protein-coupled receptor 75	GPR75
10926	DBF4-CDC7 kinase regulatory subunit	DBF4
10924	sphingomyelin phosphodiesterase acid like 3A	SMPDL3A ASM3A ASML3a FLJ20177 acid sphingomyelinase-like phosphodiesterase 3a yR36GH4.1	Niemann-Pick disease endometriosis of ovary endometriosis of uterus endometriosis sphingolipidosis urinary bladder cancer
10923	SUB1 regulator of transcription	SUB1
10922	Fas activated serine/threonine kinase	FASTK
10921	RNA binding protein with serine rich domain 1	RNPS1
10920	COP9 signalosome subunit 8	COPS8
10919	euchromatic histone lysine methyltransferase 2	EHMT2
10916	MAGE family member D2	MAGED2
10915	transcription elongation regulator 1	TCERG1
10914	poly(A) polymerase alpha	PAPOLA
10913	ectodysplasin A receptor	EDAR
10910	SGT1 homolog, MIS12 kinetochore complex assembly cochaperone	SUGT1
10908	patatin like phospholipase domain containing 6	PNPLA6 NTE SPG39 iPLA2delta neuropathy target esterase sws	Bardet-Biedl syndrome Boucher-Neuhauser syndrome Brooke-Spiegler syndrome Charcot-Marie-Tooth disease type 5 Henoch-Schoenlein purpura Kallmann syndrome Klinefelter syndrome Laron syndrome Laurence-Moon syndrome Leber congenital amaurosis MASA syndrome MYH-9 related disease Mast syndrome Oliver-McFarlane syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Patau syndrome Peutz-Jeghers syndrome SPOAN syndrome Sheehan syndrome Stargardt disease Troyer syndrome achondroplasia adiposis dolorosa alopecia alternating hemiplegia of childhood amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis anterior horn cell disease autonomic neuropathy autosomal dominant cerebellar ataxia autosomal recessive congenital ichthyosis 1 autosomal recessive distal hereditary motor neuronopathy 1 autosomal recessive polycystic kidney disease biliary tract disease blindness blue cone monochromacy cancer cataract cavernous hemangioma central nervous system disease cerebellar ataxia cerebellar disease chorioangioma coloboma cone-rod dystrophy congenital nystagmus craniosynostosis critical illness polyneuropathy cryptorchidism dementia depressive disorder diabetes mellitus diabetic autonomic neuropathy diabetic neuropathy diabetic polyneuropathy dissociated nystagmus dysthymic disorder embryoma epilepsy focal epilepsy fundus albipunctatus fundus dystrophy glomus tumor gynecomastia hemangioma 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 8 hereditary spastic paraplegia 9A hereditary spastic paraplegia 9B hereditary spastic paraplegia histiocytoid hemangioma hypersensitivity vasculitis hypertrophy of breast hypertropia hypogonadism hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism ichthyosis infant gynecomastia inflammatory and toxic neuropathy intellectual disability intramuscular hemangioma isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency keratosis follicularis kidney failure lateral sclerosis learning disability lipomatosis liver cirrhosis lymphangioma major depressive disorder mechanical strabismus melancholic depression meningoencephalitis migraine without aura mongolian spot motor neuron disease multiple symmetric lipomatosis muscular atrophy nervous system disease neuroblastoma neurodegenerative disease neuropathy neurotic disorder obesity obsolete asthenopia obsolete congenital ichthyosiform erythroderma obsolete melancholia obsolete multiple symmetrical lipomatosis obstructive jaundice ophthalmoplegia optic atrophy panhypopituitarism paraplegia partial motor epilepsy pathologic nystagmus peripheral nervous system disease placental insufficiency polycystic kidney disease 4 polydactyly polyneuropathy progressive muscular atrophy pseudoxanthoma elasticum recurrent hypersomnia retinal degeneration retinitis pigmentosa sensorineural hearing loss sick building syndrome speech disorder spontaneous ocular nystagmus steatotic liver disease strabismus type 2 diabetes mellitus viral infectious disease visual epilepsy von Hippel-Lindau disease
10907	thioredoxin like 4A	TXNL4A
10906	TRAF-type zinc finger domain containing 1	TRAFD1
10905	mannosidase alpha class 1A member 2	MAN1A2 MAN1B	hepatocellular carcinoma liver cancer
10903	myotubularin related protein 11	MTMR11
10902	bromodomain containing 8	BRD8
10899	jumping translocation breakpoint	JTB
10898	cleavage and polyadenylation specific factor 4	CPSF4

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