GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **7051 - 7075** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▼	Disease Ontology
55033	FKBP prolyl isomerase 14	FKBP14
51303	FKBP prolyl isomerase 11	FKBP11
60681	FKBP prolyl isomerase 10	FKBP10
24147	four-jointed box kinase 1	FJX1
81608	factor interacting with PAPOLA and CPSF1	FIP1L1
11259	filamin A interacting protein 1 like	FILIP1L
27145	filamin A interacting protein 1	FILIP1
63979	fidgetin like 1	FIGNL1
55137	fidgetin, microtubule severing factor	FIGN
9896	FIG4 phosphoinositide 5-phosphatase	FIG4 ALS11 CMT4J SAC3 dJ249I4.1 hSac3	Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 3 Charcot-Marie-Tooth disease type 4 Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Joubert syndrome Laron syndrome Marfan syndrome Miller-Dieker lissencephaly syndrome Papillon-Lefevre disease Yunis-Varon syndrome achondroplasia agenesis of the corpus callosum with peripheral neuropathy amyotrophic lateral sclerosis type 11 amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis anterior horn cell disease anxiety disorder atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect autosomal recessive distal hereditary motor neuronopathy 1 bilateral parasagittal parieto-occipital polymicrogyria breast cancer breast carcinoma cardiomyopathy cataract communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 cortical dysplasia-focal epilepsy syndrome cryptorchidism demyelinating disease demyelinating polyneuropathy depressive disorder distal arthrogryposis dysthymic disorder endomyocardial fibrosis enophthalmos epilepsy essential hypertension generalized anxiety disorder gingival recession gliosarcoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 1 hereditary sensory and autonomic neuropathy type 2 hereditary spastic paraplegia 7 high grade glioma holoprosencephaly 1 holoprosencephaly hydranencephaly hydrocephalus hypertension hypertrophic cardiomyopathy hypospadias laryngostenosis lateral sclerosis lissencephaly lysosomal storage disease major depressive disorder melancholic depression microcephaly mixed glioma motor neuron disease motor peripheral neuropathy neuroblastoma neurodegenerative disease neuropathy neurotic disorder obsolete exophthalmos obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete melancholia obstructive hydrocephalus orbital disease patent foramen ovale peripheral nervous system disease placental insufficiency polyhydramnios polyneuropathy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 primary pulmonary hypertension progressive muscular atrophy pyloric stenosis renal artery obstruction renovascular hypertension sclerocornea senile degeneration of brain sensorineural hearing loss septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly situs inversus status epilepticus subacute delirium syndactyly syndromic X-linked intellectual disability Najm type tetralogy of Fallot tuberous sclerosis ventricular septal defect
11153	FIC domain protein adenylyltransferase	FICD HIP13 HYPE fic S-phase protein cell division homolog (E. coli) huntingtin interacting protein 13
387758	fin bud initiation factor homolog	FIBIN
84929	fibrinogen C domain containing 1	FIBCD1
80206	formin homology 2 domain containing 3	FHOD3
29109	formin homology 2 domain containing 1	FHOD1
2275	four and a half LIM domains 3	FHL3
2273	four and a half LIM domains 1	FHL1
57700	FHF complex subunit HOOK interacting protein 2A	FHIP2A
114827	forkhead associated phosphopeptide binding domain 1	FHAD1
2271	fumarate hydratase	FH fumarase	B-cell lymphoma Barrett's esophagus Burkitt lymphoma Crohn's colitis Crohn's disease Gilbert syndrome Hirschsprung's disease Langerhans-cell histiocytosis MELAS syndrome Parkinson's disease Richter's syndrome Tangier disease acquired polycythemia actinic keratosis acute lymphoblastic leukemia acute myeloid leukemia acute promyelocytic leukemia adenosarcoma adrenal carcinoma adrenal cortex cancer adrenal gland cancer adrenal gland hyperfunction adrenocortical carcinoma adult acute lymphocytic leukemia adult lymphoma aggressive systemic mastocytosis agranulocytosis aniridia aortic valve disease 2 aortic valve stenosis arthritis arthropathy autism spectrum disorder autistic disorder autoimmune disease autoimmune hepatitis autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome bilirubin metabolic disorder bizarre leiomyoma bladder carcinoma blindness brain disease breast cancer cancer carcinoma cataract central nervous system lymphoma cerebral degeneration cerebral malaria childhood acute lymphocytic leukemia childhood kidney cell carcinoma childhood lymphoma cholestasis chromophobe renal cell carcinoma chronic lymphocytic leukemia clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congenital adrenal hyperplasia congestive heart failure cutaneous leiomyosarcoma cutaneous leishmaniasis cystic kidney disease duodenum cancer embryoma endometrial cancer endometrial carcinoma epilepsy epithelioid leiomyosarcoma erythropoietin polycythemia familial adenomatous polyposis familial erythrocytosis 2 familial renal papillary carcinoma follicular lymphoma fumarase deficiency glomerulonephritis heart cancer hemangioblastoma hypercalcemia hypertensive retinopathy immune system disease indolent systemic mastocytosis inflammatory bowel disease 1 inflammatory bowel disease kidney cancer kidney disease kwashiorkor lactic acidosis large intestine cancer late onset Parkinson's disease leiomyoma cutis leiomyoma leiomyomatosis leiomyosarcoma leukopenia lung non-small cell carcinoma lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 mantle cell lymphoma marasmus mastocytosis microcephaly microphthalmia mucinous ovarian cystadenoma mucocutaneous leishmaniasis multiple endocrine neoplasia type 2A multiple myeloma multiple sclerosis muscle benign neoplasm muscle cancer myofibroma myxoid leiomyosarcoma nasopharynx carcinoma nephritis nephroblastoma nephrocalcinosis neuroblastoma neuroendocrine carcinoma neurofibromatosis 1 neurofibromatosis neutropenia non-Hodgkin lymphoma non-congenital cyst of kidney nonpapillary renal cell carcinoma nutrition disease obsolete Cushing's syndrome obsolete ymphosarcoma optic atrophy osteoarthritis oxyphilic adenoma pancreatic cancer pancreatic carcinoma panic disorder papillary adenocarcinoma papillary renal cell carcinoma paraganglioma pheochromocytoma phosphorus metabolism disease polycythemia vera polycythemia primary biliary cholangitis primary hyperaldosteronism prostate cancer prostate carcinoma protein-energy malnutrition proteinuria rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma renal osteodystrophy reticulosarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia seborrheic keratosis severe congenital neutropenia sickle cell anemia skin disease small intestine cancer smooth muscle tumor speech disorder status epilepticus stomach cancer stomach carcinoma stress polycythemia systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic lupus erythematosus systemic mastocytosis testicular cancer thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland papillary carcinoma trichohepatoenteric syndrome 1 trichohepatoenteric syndrome ulcerative colitis urinary bladder cancer uterine corpus cancer uterine fibroid uterus leiomyosarcoma vaginal cancer visceral leishmaniasis visual epilepsy
2268	FGR proto-oncogene, Src family tyrosine kinase	FGR
10875	fibrinogen like 2	FGL2
55277	FGGY carbohydrate kinase domain containing	FGGY
2266	fibrinogen gamma chain	FGG
53834	fibroblast growth factor receptor like 1	FGFRL1