GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **6226 - 6250** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
54913	ribonuclease P and MRP subunit p25	RPP25
54915	YTH N6-methyladenosine RNA binding protein F1	YTHDF1
54916	transmembrane protein 260	TMEM260	B-cell lymphoma Langerhans-cell histiocytosis T-cell non-Hodgkin lymphoma acute myeloid leukemia alcohol dependence alcohol use disorder cancer double outlet right ventricle embryoma kidney failure lymphoma non-Hodgkin lymphoma obsolete ymphosarcoma reticulosarcoma stomach cancer ventricular septal defect
54921	chromosome transmission fidelity factor 8	CHTF8
54922	Ras interacting protein 1	RASIP1
54926	ubiquitin conjugating enzyme E2 R2	UBE2R2
54927	coiled-coil-helix-coiled-coil-helix domain containing 3	CHCHD3
54928	3'(2'), 5'-bisphosphate nucleotidase 2	BPNT2 FLJ20421 Golgi-resident adenosine 3',5'-bisphosphate 3'-phosphatase IMPA3 gPAPP golgi-resident nucleotide phosphatase
54929	transmembrane protein 161A	TMEM161A
54931	tRNA methyltransferase 10C, mitochondrial RNase P subunit	TRMT10C
54936	ADP-ribosylserine hydrolase	ADPRS ADP-ribosylarginine hydrolase like 2 ARH3 FLJ20446	autosomal recessive hypercholesterolemia brain stem infarction breast cancer breast carcinoma cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease congenital nystagmus congenital ptosis dissociated nystagmus epilepsy hypertropia intellectual disability learning disability mechanical strabismus neurodegenerative disease ophthalmoplegia pathologic nystagmus ptosis spontaneous ocular nystagmus strabismus stress-induced childhood-onset neurodegeneration with variable ataxia and seizures visual epilepsy
54937	spermatogenesis and oogenesis specific basic helix-loop-helix 2	SOHLH2
54938	seryl-tRNA synthetase 2, mitochondrial	SARS2
54940	OCIA domain containing 1	OCIAD1
54947	lysophosphatidylcholine acyltransferase 2	LPCAT2 AGPAT11 FLJ20481 LPLAT9 LysoPAFAT lysophospholipid acyltransferase 9	colorectal cancer colorectal carcinoma large intestine cancer microphthalmia obsolete Matthew-Wood syndrome polycystic ovary syndrome prostate cancer prostate carcinoma
54948	mitochondrial ribosomal protein L16	MRPL16
54949	succinate dehydrogenase complex assembly factor 2	SDHAF2
54956	poly(ADP-ribose) polymerase family member 16	PARP16 ARTD15 FLJ20509 FLJ25281 pART15
54959	odontogenic, ameloblast associated	ODAM
54963	uridine-cytidine kinase 1 like 1	UCKL1
54964	chromosome 1 open reading frame 56	C1orf56
54965	phosphatidylinositol glycan anchor biosynthesis class X	PIGX FLJ20522 PIG-X	Bannayan-Riley-Ruvalcaba syndrome Bardet-Biedl syndrome 10 Bardet-Biedl syndrome 11 Bardet-Biedl syndrome 12 Bardet-Biedl syndrome 13 Bardet-Biedl syndrome 14 Bardet-Biedl syndrome 15 Bardet-Biedl syndrome 16 Bardet-Biedl syndrome 17 Bardet-Biedl syndrome 18 Bardet-Biedl syndrome 19 Bardet-Biedl syndrome 1 Bardet-Biedl syndrome 2 Bardet-Biedl syndrome 3 Bardet-Biedl syndrome 4 Bardet-Biedl syndrome 5 Bardet-Biedl syndrome 6 Bardet-Biedl syndrome 7 Bardet-Biedl syndrome 8 Bardet-Biedl syndrome 9 Bardet-Biedl syndrome Laurence-Moon syndrome allergic asthma allergic disease asthma breast cancer breast carcinoma cancer dermatitis embryoma intrinsic asthma polydactyly
54969	histone PARylation factor 1	HPF1
54972	transmembrane protein 132A	TMEM132A
54974	tRNA-histidine guanylyltransferase 1 like	THG1L

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