GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **4026 - 4050** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
9543	immunoglobulin superfamily DCC subclass member 3	IGDCC3
9552	sperm associated antigen 7	SPAG7
9553	mitochondrial ribosomal protein L33	MRPL33
9554	SEC22 homolog B, vesicle trafficking protein	SEC22B
9555	macroH2A.1 histone	MACROH2A1
9557	chromodomain helicase DNA binding protein 1 like	CHD1L ALC1 amplified in liver cancer 1
9559	VPS26 retromer complex component A	VPS26A
9562	multiple inositol-polyphosphate phosphatase 1	MINPP1 MIPP	actinic keratosis cancer carcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colonic benign neoplasm colorectal cancer head and neck cancer large intestine cancer multiple myeloma nodular goiter papillary adenocarcinoma papillary renal cell carcinoma pontocerebellar hypoplasia type 16 renal cell carcinoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma seborrheic keratosis skin disease spinal cord disease thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland follicular carcinoma thyroid gland papillary carcinoma
9563	hexose-6-phosphate dehydrogenase/glucose 1-dehydrogenase	H6PD 6-phosphogluconolactonase GDH/6PGL endoplasmic bifunctional protein H6PDH	Alzheimer's disease B-cell lymphoma Laron syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 achondroplasia acne aromatase excess syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis beta thalassemia breast cancer breast carcinoma cancer cardiovascular system disease cholangiocarcinoma colorectal cancer cone-rod dystrophy 2 cone-rod dystrophy coronary artery disease cortisone reductase deficiency 1 cortisone reductase deficiency dementia diabetes insipidus diabetes mellitus diabetic ketoacidosis diarrhea gallbladder disease giardiasis heart disease hemolytic anemia hyperandrogenism hyperinsulinism hypertrichosis hypoglycemia infertility intrahepatic cholangiocarcinoma large intestine cancer leishmaniasis liver disease luminal breast carcinoma A malaria multiple sclerosis neurohypophyseal diabetes insipidus obesity obsolete ymphosarcoma placental insufficiency polycystic ovary syndrome primary hyperoxaluria steatotic liver disease thalassemia type 2 diabetes mellitus visceral leishmaniasis
9564	BCAR1 scaffold protein, Cas family member	BCAR1
9567	GTP binding protein 1	GTPBP1
9568	gamma-aminobutyric acid type B receptor subunit 2	GABBR2
9572	nuclear receptor subfamily 1 group D member 1	NR1D1	alcoholic liver cirrhosis brain small vessel disease hyperthyroidism hypothyroidism portal hypertension type 2 diabetes mellitus
9573	growth differentiation factor 3	GDF3
9575	clock circadian regulator	CLOCK
9578	CDC42 binding protein kinase beta	CDC42BPB
9580	SRY-box transcription factor 13	SOX13
9583	ectonucleoside triphosphate diphosphohydrolase 4	ENTPD4 KIAA0392 LALP70 LAP70 NTPDase-4 UDPase
9585	kinesin family member 20B	KIF20B
9586	cAMP responsive element binding protein 5	CREB5
9590	A-kinase anchoring protein 12	AKAP12
9600	phosphatidylinositol transfer protein membrane associated 1	PITPNM1
9601	protein disulfide isomerase family A member 4	PDIA4
9604	ring finger protein 14	RNF14
9611	nuclear receptor corepressor 1	NCOR1

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