GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **8051 - 8075** of **9988** in total

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Gene ID	Gene Name ▲	Gene Symbol	Disease Ontology
5948	retinol binding protein 2	RBP2
5949	retinol binding protein 3	RBP3
5950	retinol binding protein 4	RBP4	acute pyelonephritis atherosclerosis cerebral infarction chronic kidney disease colon adenoma congestive heart failure coronary artery disease diabetic angiopathy diabetic retinopathy dilated cardiomyopathy essential hypertension familial hypercholesterolemia gallbladder cancer gestational diabetes hyperinsulinism hypertension liver cirrhosis myocardial infarction obesity pre-eclampsia proliferative diabetic retinopathy psoriasis severe pre-eclampsia systemic scleroderma type 2 diabetes mellitus
51109	retinol dehydrogenase 11	RDH11
57665	retinol dehydrogenase 14	RDH14
5959	retinol dehydrogenase 5	RDH5
79680	retrotransposon Gag like 10	RTL10
84247	retrotransposon Gag like 6	RTL6
8434	reversion inducing cysteine rich protein with kazal motifs	RECK hRECK	abdominal aortic aneurysm acute interstitial pneumonia adenocarcinoma adenoid cystic carcinoma adenoma adenosarcoma adult respiratory distress syndrome ameloblastoma anaplastic astrocytoma arthritis arthropathy atrial fibrillation bile duct adenocarcinoma bile duct carcinoma bladder carcinoma bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system cancer cervical adenocarcinoma cervical cancer cervix carcinoma cervix disease childhood cerebral astrocytoma childhood osteosarcoma cholangiocarcinoma chorioamnionitis chronic obstructive pulmonary disease cocaine abuse cocaine dependence colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma complement deficiency cribriform carcinoma cutaneous fibrous histiocytoma cystic fibrosis distal arthrogryposis dysplastic nevus syndrome embryoma epilepsy epithelioid malignant peripheral nerve sheath tumor esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma fibrillary astrocytoma fibrosarcoma gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hematologic cancer hepatitis C hepatocellular carcinoma hidradenoma high grade glioma idiopathic interstitial pneumonia intrahepatic cholangiocarcinoma juvenile pilocytic astrocytoma large intestine cancer leiomyoma liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma malignant astrocytoma malignant peripheral nerve sheath tumor melanoma mixed glioma multiple myeloma myofibroma nasopharyngitis nasopharynx carcinoma necrotizing fasciitis nephroblastoma neurilemmoma neuroblastoma neurofibrosarcoma nodular prostate osteoarthritis osteosarcoma pancreatic cancer pancreatic ductal adenocarcinoma papillary adenocarcinoma papillary renal cell carcinoma patent ductus arteriosus periodontal disease periodontitis pilocytic astrocytoma prostate cancer prostate carcinoma prostatic adenoma protoplasmic astrocytoma rheumatoid arthritis salivary gland adenoid cystic carcinoma sarcoidosis sarcomatoid carcinoma skin melanoma skin papilloma skin tag squamous cell carcinoma stomach cancer stomach carcinoma subependymal giant cell astrocytoma syringoma systemic lupus erythematosus thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland papillary carcinoma tongue squamous cell carcinoma transitional cell carcinoma tubular adenocarcinoma urinary bladder cancer uterine fibroid uveoparotid fever viral infectious disease
6010	rhodopsin	RHO
64285	rhomboid 5 homolog 1	RHBDF1
79651	rhomboid 5 homolog 2	RHBDF2
57414	rhomboid domain containing 2	RHBDD2
83853	rhophilin associated tail protein 1 like	ROPN1L
219790	rhotekin 2	RTKN2
10329	ribitol xylosyltransferase 1	RXYLT1 HP10481	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Turner syndrome Walker-Warburg syndrome autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy cataract coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital disorder of glycosylation congenital muscular dystrophy-dystroglycanopathy type A10 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism distal myopathy epilepsy facioscapulohumeral muscular dystrophy fundus dystrophy glaucoma gonadal dysgenesis hydranencephaly hydrocephalus intellectual disability learning disability limb-girdle muscular dystrophy lissencephaly microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obstructive hydrocephalus oculopharyngeal muscular dystrophy optic atrophy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion retinal detachment rippling muscle disease 2 senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly syndromic X-linked intellectual disability Najm type visual epilepsy
64080	ribokinase	RBKS DKFZp686G13268 RBSK	bipolar disorder schizophrenia tuberculosis
6035	ribonuclease A family member 1, pancreatic	RNASE1
122651	ribonuclease A family member 11 (inactive)	RNASE11
440163	ribonuclease A family member 13 (inactive)	RNASE13
6036	ribonuclease A family member 2	RNASE2
6037	ribonuclease A family member 3	RNASE3
6039	ribonuclease A family member 6	RNASE6
84659	ribonuclease A family member 7	RNASE7
390443	ribonuclease A family member 9 (inactive)	RNASE9

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