GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **8751 - 8775** of **9988** in total

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Gene ID	Gene Name ▲	Gene Symbol	Disease Ontology
150159	solute carrier family 9 member B1	SLC9B1
284525	solute carrier family 9 member C2 (putative)	SLC9C2
6579	solute carrier organic anion transporter family member 1A2	SLCO1A2
10599	solute carrier organic anion transporter family member 1B1	SLCO1B1
28234	solute carrier organic anion transporter family member 1B3	SLCO1B3
53919	solute carrier organic anion transporter family member 1C1	SLCO1C1
6578	solute carrier organic anion transporter family member 2A1	SLCO2A1
11309	solute carrier organic anion transporter family member 2B1	SLCO2B1
28232	solute carrier organic anion transporter family member 3A1	SLCO3A1
28231	solute carrier organic anion transporter family member 4A1	SLCO4A1
353189	solute carrier organic anion transporter family member 4C1	SLCO4C1
81796	solute carrier organic anion transporter family member 5A1	SLCO5A1
133482	solute carrier organic anion transporter family member 6A1	SLCO6A1
157869	somatomedin B and thrombospondin type 1 domain containing	SBSPON
6751	somatostatin receptor 1	SSTR1
6752	somatostatin receptor 2	SSTR2
6753	somatostatin receptor 3	SSTR3
6754	somatostatin receptor 4	SSTR4
6755	somatostatin receptor 5	SSTR5
6469	sonic hedgehog signaling molecule	SHH
10580	sorbin and SH3 domain containing 1	SORBS1
8470	sorbin and SH3 domain containing 2	SORBS2
10174	sorbin and SH3 domain containing 3	SORBS3
6652	sorbitol dehydrogenase	SORD	Alzheimer's disease Bannayan-Riley-Ruvalcaba syndrome Clouston syndrome Coffin-Siris syndrome 1 Coffin-Siris syndrome Cowden syndrome Leber congenital amaurosis 1 MELAS syndrome Peutz-Jeghers syndrome adenocarcinoma adenoma adrenal gland cancer autosomal recessive distal hereditary motor neuronopathy 8 background diabetic retinopathy bladder carcinoma breast cancer cancer cardiomyopathy cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types cataract childhood kidney cell carcinoma chromophobe renal cell carcinoma chronic obstructive pulmonary disease clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer dementia diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic neuropathy diabetic retinopathy disease of metabolism duodenum cancer eclampsia embryoma endomyocardial fibrosis essential hypertension exudative vitreoretinopathy follicular adenoma gastrointestinal stromal tumor glomerulonephritis heart cancer hepatocellular carcinoma hyperglycemia hypertension hypertrophic cardiomyopathy kidney cancer kidney disease kwashiorkor large intestine cancer leiomyoma leukodystrophy liver cancer liver carcinoma marasmus mesenchymal cell neoplasm microcystic adenoma mitochondrial complex II deficiency mitochondrial metabolism disease mitochondrial myopathy multiple endocrine neoplasia type 1 myofibrillar myopathy 1 myofibroma nephritis nephrosis neuroblastoma neurofibromatosis 1 neurofibromatosis nonpapillary renal cell carcinoma nutrition disease obsolete eye and adnexa disease obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy papillary adenoma papillary renal cell carcinoma paraganglioma perinatal necrotizing enterocolitis pheochromocytoma proliferative diabetic retinopathy prostate cancer prostate carcinoma protein-energy malnutrition pyoureter renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma skin benign neoplasm skin cancer small intestine cancer steatotic liver disease thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland medullary carcinoma tuberous sclerosis 1 tuberous sclerosis type 2 diabetes mellitus urinary bladder cancer uterine fibroid von Hippel-Lindau disease
6272	sortilin 1	SORT1

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