GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (10109) Glycans (5831) Glycoproteins (15834) Lectins (297) Pathways (2074)

Displaying entries **10076 - 10100** of **10109** in total

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Gene ID	Gene Name	Gene Symbol ▼	Disease Ontology
22	ATP binding cassette subfamily B member 7	ABCB7	X-linked sideroblastic anemia with ataxia
10058	ATP binding cassette subfamily B member 6 (LAN blood group)	ABCB6	dyschromatosis universalis hereditaria
340273	ATP binding cassette subfamily B member 5	ABCB5
5244	ATP binding cassette subfamily B member 4	ABCB4	cholestasis intrahepatic cholestasis of pregnancy 3 intrahepatic cholestasis liver cirrhosis primary biliary cholangitis progressive familial intrahepatic cholestasis 3
8647	ATP binding cassette subfamily B member 11	ABCB11	benign recurrent intrahepatic cholestasis 2 intrahepatic cholestasis liver cirrhosis progressive familial intrahepatic cholestasis 2
23456	ATP binding cassette subfamily B member 10	ABCB10
5243	ATP binding cassette subfamily B member 1	ABCB1	Behcet's disease Crohn's disease acquired immunodeficiency syndrome acute lymphoblastic leukemia allergic rhinitis antisocial personality disorder cannabis dependence chronic myeloid leukemia colorectal adenocarcinoma cryoglobulinemia drug dependence epilepsy familial Mediterranean fever familial hyperlipidemia hepatocellular carcinoma heroin dependence human immunodeficiency virus infectious disease inflammatory bowel disease 13 invasive ductal carcinoma lung non-small cell carcinoma malaria opiate dependence osteonecrosis pulmonary tuberculosis renal cell carcinoma toxic encephalopathy type 2 diabetes mellitus ulcerative colitis
10350	ATP binding cassette subfamily A member 9	ABCA9
10351	ATP binding cassette subfamily A member 8	ABCA8
10347	ATP binding cassette subfamily A member 7	ABCA7	Alzheimer's disease 9
23460	ATP binding cassette subfamily A member 6	ABCA6
23461	ATP binding cassette subfamily A member 5	ABCA5
24	ATP binding cassette subfamily A member 4	ABCA4	age related macular degeneration 2 cone-rod dystrophy 3 fundus dystrophy macular degeneration retinal degeneration retinitis pigmentosa 19 retinitis pigmentosa
21	ATP binding cassette subfamily A member 3	ABCA3	pulmonary alveolar proteinosis
20	ATP binding cassette subfamily A member 2	ABCA2
154664	ATP binding cassette subfamily A member 13	ABCA13	gastric adenocarcinoma
26154	ATP binding cassette subfamily A member 12	ABCA12	autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis 4A autosomal recessive congenital ichthyosis 4B
19	ATP binding cassette subfamily A member 1	ABCA1	Alzheimer's disease Tangier disease coronary artery disease hypolipoproteinemia obesity primary hypoalphalipoproteinemia 1 type 2 diabetes mellitus
18	4-aminobutyrate aminotransferase	ABAT 4-aminobutyrate transaminase GABA transaminase GABA-T GABAT gamma-aminobutyrate aminotransferase	Alzheimer's disease GABA aminotransferase deficiency Huntington's disease
26574	apoptosis antagonizing transcription factor	AATF
57505	alanyl-tRNA synthetase 2, mitochondrial	AARS2	combined oxidative phosphorylation deficiency 8 progressive leukoencephalopathy with ovarian failure
16	alanyl-tRNA synthetase 1	AARS1	Charcot-Marie-Tooth disease axonal type 2N developmental and epileptic encephalopathy 29 leukodystrophy trichothiodystrophy
25980	AAR2 splicing factor	AAR2
22848	AP2 associated kinase 1	AAK1
343066	arylacetamide deacetylase like 4	AADACL4 OTTHUMG00000001889

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