GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (10109) Glycans (5831) Glycoproteins (15837) Lectins (297) Pathways (2074)

Displaying entries **9926 - 9950** of **10109** in total

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Gene ID	Gene Name ▼	Gene Symbol	Disease Ontology
84168	ANTXR cell adhesion molecule 1	ANTXR1	GAPO syndrome colorectal carcinoma
404734	ANKHD1-EIF4EBP3 readthrough	ANKHD1-EIF4EBP3
83607	AMMECR1 like	AMMECR1L
60529	ALX homeobox 4	ALX4	bronchiolo-alveolar adenocarcinoma colorectal cancer craniosynostosis frontonasal dysplasia 2 hepatocellular carcinoma lung adenocarcinoma lung cancer parietal foramina
7840	ALMS1 centrosome and basal body associated protein	ALMS1	Alstrom syndrome
238	ALK receptor tyrosine kinase	ALK
389658	ALK and LTK ligand 1	ALKAL1
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	congenital disorder of glycosylation Il
79053	ALG8 alpha-1,3-glucosyltransferase	ALG8 MGC2840 dolichyl-P-Glc:Glc(1)Man(9)GlcNAc(2)-PP-dolichol alpha- 1->3-glucosyltransferase	congenital disorder of glycosylation Ih polycystic liver disease 3
29929	ALG6 alpha-1,3-glucosyltransferase	ALG6 dolichyl-P-Glc:Man(9)GlcNAc(2)-PP-dolichol alpha- 1->3-glucosyltransferase	congenital disorder of glycosylation Ic
29880	ALG5 dolichyl-phosphate beta-glucosyltransferase	ALG5 bA421P11.2	polycystic kidney disease 7
10195	ALG3 alpha-1,3- mannosyltransferase	ALG3 CDGS4 D16Ertd36e NOT56L Not56 carbohydrate deficient glycoprotein syndrome type IV dol-P-Man dependent alpha-1,3- mannosyltransferase dol-P-Man:Man(5)GlcNAc(2)-PP-Dol alpha-1,3-mannosyltransferase	congenital disorder of glycosylation Id
85365	ALG2 alpha-1,3/1,6-mannosyltransferase	ALG2 CDG1I CDGIi FLJ14511 NET38 hALPG2	congenital disorder of glycosylation Ii congenital disorder of glycosylation type II congenital myasthenic syndrome 14
199857	ALG14 UDP-N-acetylglucosaminyltransferase subunit	ALG14 MGC19780	congenital myasthenic syndrome 15
79868	ALG13 UDP-N-acetylglucosaminyltransferase subunit	ALG13 CDG1S FLJ23018 MDS031 N-acetylglucosaminyldiphosphodolichol N-acetylglucosaminyltransferase TDRD13 YGL047W tudor domain containing 13	developmental and epileptic encephalopathy 36
79087	ALG12 alpha-1,6-mannosyltransferase	ALG12 CDG1G ECM39 dol-P-Man dependent alpha-1,6-mannosyltransferase dolichyl-P-Man:Man(7)GlcNAc(2)-PP-dolichol alpha-1,6-mannosyltransferase	congenital disorder of glycosylation Ig
440138	ALG11 alpha-1,2-mannosyltransferase	ALG11 CDG1P GDP-Man:Man(3)GlcNAc(2)-PP-dolichol alpha-1,2-mannosyltransferase KIAA0266	congenital disorder of glycosylation Ip
144245	ALG10 alpha-1,2-glucosyltransferase B	ALG10B KCR1 dolichyl-P-Glc:Glc(2)Man(9)GlcNAc(2)-PP-dolichol alpha-1,2- glucosyltransferase potassium channel regulator 1	long QT syndrome 2
84920	ALG10 alpha-1,2-glucosyltransferase	ALG10 ALG10A DIE2 FLJ14751 derepression of ITR1 expression 2 homolog (S. cerevisiae) dolichyl-P-Glc:Glc(2)Man(9)GlcNAc(2)-PP-dolichol alpha-1,2- glucosyltransferase
644974	ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase like 2	ALG1L2
56052	ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase	ALG1 CDG1K HMAT1 HMT-1 Mat-1	congenital disorder of glycosylation Ik
27125	ALF transcription elongation factor 4	AFF4
3899	ALF transcription elongation factor 3	AFF3	KINSSHIP syndrome
2334	ALF transcription elongation factor 2	AFF2	X-linked intellectual developmental disorder 109
84335	AKT1 substrate 1	AKT1S1

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