GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **2626 - 2650** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
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
79867	tectonic family member 2	TCTN2
79865	triggering receptor expressed on myeloid cells like 2	TREML2
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
79834	pseudopodium enriched atypical kinase 1	PEAK1
79832	glutamine and serine rich 1	QSER1
79827	CXADR like membrane protein	CLMP
79823	calmodulin-lysine N-methyltransferase	CAMKMT
79820	cation channel sperm associated auxiliary subunit beta	CATSPERB
79819	dynein axonemal intermediate chain 4	DNAI4
79818	zinc finger protein 552	ZNF552
79815	NIPA like domain containing 2	NIPAL2
79813	euchromatic histone lysine methyltransferase 1	EHMT1
79812	multimerin 2	MMRN2
79811	SAFB like transcription modulator	SLTM
79805	vasohibin 2	VASH2
79802	HHIP like 2	HHIPL2
79799	UDP glucuronosyltransferase family 2 member A3	UGT2A3 FLJ21934
79796	ALG9 alpha-1,2-mannosyltransferase	ALG9 dol-P-Man dependent alpha-1,2-mannosyltransferase dolichyl-P-Man:Man(6)GlcNAc(2)-PP-dolichol alpha-1,2-mannosyltransferase dolichyl-P-Man:Man(8)GlcNAc(2)-PP-dolichol alpha-1,2-mannosyltransferase	Gilles de la Tourette syndrome Marfan syndrome Meckel syndrome 1 Meckel syndrome 2 Meckel syndrome 3 Meckel syndrome 4 Meckel syndrome 5 Meckel syndrome 6 Meckel syndrome 8 Meckel syndrome autosomal dominant polycystic kidney disease cardiovascular system disease congenital disorder of glycosylation Il congenital disorder of glycosylation type I congenital disorder of glycosylation congenital heart disease congestive heart failure craniosynostosis cystic kidney disease cystinuria enophthalmos epilepsy esotropia galactokinase deficiency galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease heart disease heart septal defect hemopericardium intellectual disability learning disability microcephaly monocular esotropia mucopolysaccharidosis IV multiple epiphyseal dysplasia neuroendocrine carcinoma neuroendocrine tumor obsolete exophthalmos orbital disease osteochondrodysplasia pericardial effusion polycystic kidney disease 1 polycystic liver disease psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder situs inversus tuberous sclerosis visual epilepsy
79794	SREBF pathway regulator in golgi 1	SPRING1
79792	gasdermin D	GSDMD
79791	F-box protein 31	FBXO31
79789	calmin	CLMN
79784	myosin heavy chain 14	MYH14
79781	IQ motif containing with AAA domain 1	IQCA1

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