GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **7351 - 7375** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
79813	euchromatic histone lysine methyltransferase 1	EHMT1
79815	NIPA like domain containing 2	NIPAL2
79818	zinc finger protein 552	ZNF552
79819	dynein axonemal intermediate chain 4	DNAI4
79820	cation channel sperm associated auxiliary subunit beta	CATSPERB
79823	calmodulin-lysine N-methyltransferase	CAMKMT
79827	CXADR like membrane protein	CLMP
79832	glutamine and serine rich 1	QSER1
79834	pseudopodium enriched atypical kinase 1	PEAK1
79837	phosphatidylinositol-5-phosphate 4-kinase type 2 gamma	PIP4K2C FLJ22055	bipolar disorder breast cancer cancer diabetic ketoacidosis embryoma lingual-facial-buccal dyskinesia obsolete type 1 diabetes mellitus 9 schizophrenia type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus
79865	triggering receptor expressed on myeloid cells like 2	TREML2
79867	tectonic family member 2	TCTN2
79868	ALG13 UDP-N-acetylglucosaminyltransferase subunit	ALG13 CDG1S FLJ23018 MDS031 N-acetylglucosaminyldiphosphodolichol N-acetylglucosaminyltransferase TDRD13 YGL047W tudor domain containing 13	Bell's palsy Meckel's diverticulum West syndrome agnosia attention deficit hyperactivity disorder autistic disorder blindness cerebral degeneration choreatic disease clubfoot congenital disorder of glycosylation type I congenital disorder of glycosylation congenital nystagmus craniosynostosis developmental and epileptic encephalopathy 36 dissociated nystagmus epilepsy facial nerve disease facial paralysis focal segmental glomerulosclerosis hypophosphatemia intellectual disability learning disability lung cancer lung non-small cell carcinoma microcephaly non-syndromic X-linked intellectual disability obesity obsolete infantile epileptic encephalopathy optic atrophy pathologic nystagmus placental insufficiency pyloric stenosis spontaneous ocular nystagmus syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 visual epilepsy
79869	cleavage and polyadenylation specific factor 7	CPSF7
79871	RNA polymerase II associated protein 2	RPAP2
79872	Cbl proto-oncogene like 1	CBLL1
79875	thrombospondin type 1 domain containing 4	THSD4 ADAMTSL6 FLJ13710 FVSY9334 PRO34005
79879	coiled-coil domain containing 134	CCDC134
79882	zinc finger CCCH-type containing 14	ZC3H14
79883	podocan like 1	PODNL1
79887	phospholipase B domain containing 1	PLBD1 FLJ22662 PLB homolog 1 (Dictyostelium)
79888	lysophosphatidylcholine acyltransferase 1	LPCAT1 AGPAT10 AGPAT9 FLJ12443 LPLAT8 lysophospholipid acyltransferase 8	Leber congenital amaurosis adult respiratory distress syndrome allergic asthma asthma breast cancer breast carcinoma breast fibrocystic disease bronchus cancer bronchus carcinoma cancer carcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma cone-rod dystrophy cystic fibrosis embryoma fundus albipunctatus hepatitis C hepatocellular carcinoma hypereosinophilic syndrome intrinsic asthma liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma microglandular adenosis newborn respiratory distress syndrome nonpapillary renal cell carcinoma papillary renal cell carcinoma prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma retinitis pigmentosa sarcomatoid renal cell carcinoma sickle cell anemia
79891	zinc finger protein 671	ZNF671
79892	minichromosome maintenance complex binding protein	MCMBP
79895	ATPase phospholipid transporting 8B4 (putative)	ATP8B4

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