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GlyCosmos Genes

Integrated list of glycan-related genes extracted KEGG GENES Database, UniProt, GlycoGene Database (GGDB), Plant GARDEN and FlyGlycoDB. Glycan-related genes including glycosyltransferase, hydrolase activity (acting on glycosyl bonds), carbohydrate metabolic process, etc .

Source	Last Updated
FlyGlycoDB	March 25, 2024
GlycoGene Database (GGDB)	January 26, 2018
KEGG GENES Database	September 20, 2023
Plant GARDEN	May 28, 2020
UniProt	October 29, 2024

Selecting the function you want to look up from the categories displays a list narrowed down to glycan-related genes with that function (Gene Ontology).

Catalytic activity

glycosyltransferase activity

hydrolase activity, acting on glycosyl bonds

Binding

carbohydrate binding

Response to carbohydrate

Primary metabolic process

Displaying entries **226 - 250** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
412	steroid sulfatase	STS Aliases: ARSC arylsulfatase C steryl-sulfatase	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease B-cell lymphoma Barrett's esophagus Chagas disease Cockayne syndrome Cornelia de Lange syndrome Creutzfeldt-Jakob disease Down syndrome Dubowitz syndrome Evans' syndrome Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Joubert syndrome Kallmann syndrome Kawasaki disease Klinefelter syndrome Laron syndrome Miller-Dieker lissencephaly syndrome Mycobacterium avium complex disease Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Patau syndrome Pick's disease Prader-Willi syndrome Renpenning syndrome Reye syndrome Robinow syndrome Seckel syndrome Sertoli cell-only syndrome Sheehan syndrome Silver-Russell syndrome Sjogren's syndrome Sjogren-Larsson syndrome Smith-Lemli-Opitz syndrome Smith-Magenis syndrome Streptococcus pneumonia T-cell acute lymphoblastic leukemia Usher syndrome type 1 X-linked Aarskog syndrome X-linked chondrodysplasia punctata 1 X-linked chondrodysplasia punctata 2 X-linked ichthyosis Y-linked spermatogenic failure 1 abdominal obesity-metabolic syndrome 1 achondroplasia achromatopsia acoustic neuroma acquired color blindness acquired hyperkeratosis acquired immunodeficiency syndrome actinic keratosis acute biphenotypic leukemia acute leukemia acute myeloid leukemia adenocarcinoma in situ adenocarcinoma adenoma adult fibrosarcoma adult liposarcoma adult lymphoma alcoholic hepatitis allergic asthma alopecia amnestic disorder amyloidosis anaplastic astrocytoma androgen insensitivity syndrome androgenic alopecia angioimmunoblastic T-cell lymphoma angiomatous meningioma anhidrosis anogenital venereal wart antithrombin III deficiency aortic valve disease 1 aortic valve disease 2 aortic valve disease aortic valve insufficiency aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy ascending cholangitis asthma ataxia with oculomotor apraxia type 1 atherosclerosis atrial fibrillation attention deficit hyperactivity disorder autism spectrum disorder autistic disorder autoimmune thrombocytopenic purpura autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal dominant chondrodysplasia punctata autosomal recessive Robinow syndrome autosomal recessive congenital ichthyosis 10 autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis 2 autosomal recessive congenital ichthyosis 3 autosomal recessive congenital ichthyosis 4A autosomal recessive congenital ichthyosis 5 autosomal recessive congenital ichthyosis 6 autosomal recessive congenital ichthyosis 7 autosomal recessive congenital ichthyosis 8 autosomal recessive congenital ichthyosis 9 autosomal recessive congenital ichthyosis azoospermia bacterial infectious disease bacterial sepsis benign meningioma bicuspid aortic valve disease bile duct adenocarcinoma bile duct carcinoma bladder carcinoma blastomycosis blue color blindness bone osteosarcoma brain cancer brain infarction breast cancer breast carcinoma breast fibroadenoma bronchus cancer bronchus carcinoma calcinosis calcium metabolism disease cancer carcinoma cataract 9 multiple types cellular schwannoma central nervous system lymphoma cerebral cavernous malformation 1 cerebral convexity meningioma cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ childhood cerebral astrocytoma childhood liposarcoma childhood lymphoma childhood osteosarcoma cholangiocarcinoma cholangitis cholera cholesteatoma chondrodysplasia punctata chondrodysplasia-pseudohermaphroditism syndrome chorioamnionitis chromophobe renal cell carcinoma chronic fatigue syndrome chronic kidney disease chronic obstructive pulmonary disease clear cell meningioma clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colonic benign neoplasm color blindness colorectal cancer colorectal carcinoma common wart communication disorder complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital nystagmus congestive heart failure corneal dystrophy coronary artery disease cribriform carcinoma cryptorchidism cutaneous fibrous histiocytoma cystic fibrosis dedifferentiated liposarcoma dermatitis diabetes mellitus diabetic ketoacidosis diffuse large B-cell lymphoma disease of metabolism dissociated nystagmus distal arthrogryposis embryoma encephalitis encephalomyelitis endometrial cancer endometrial carcinoma endometrial hyperplasia endometriosis of uterus endometriosis epidermodysplasia verruciformis epidermolysis bullosa dystrophica epidermolytic hyperkeratosis epilepsy epithelioid sarcoma esophagus adenocarcinoma essential hypertension essential thrombocythemia essential tremor eunuchism familial mediterranean fever familial nephrotic syndrome fibrillary astrocytoma fibrosarcoma fibrous meningioma gallbladder disease gastroenteritis gastrointestinal system disease gastroparesis gastroschisis gemistocytic astrocytoma generalized anxiety disorder giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis granular cell carcinoma hemochromatosis type 1 hemochromatosis hepatic coma hepatic encephalopathy hepatitis C hepatocellular carcinoma hidradenoma high grade glioma human immunodeficiency virus infectious disease hydranencephaly hyperandrogenism hypercalcemia hypertension hypogonadism hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypohidrosis hypoparathyroidism-deafness-renal disease syndrome hypoparathyroidism hypopituitarism ichthyosis vulgaris ichthyosis ileitis ileocolitis in situ carcinoma inflammatory bowel disease inherited metabolic disorder intellectual disability intestinal disease intrahepatic cholangiocarcinoma intraorbital meningioma intraventricular meningioma intrinsic asthma isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency juvenile pilocytic astrocytoma keratoconjunctivitis sicca keratosis follicularis kidney disease kidney failure language disorder large intestine cancer laryngeal squamous cell carcinoma learning disability leprosy lipoid nephrosis liposarcoma lissencephaly liver cancer liver carcinoma liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung oat cell carcinoma lung small cell carcinoma lymphoma malignant astrocytoma malignant peripheral nerve sheath tumor melanoma melanotic neurilemmoma melioidosis meningioma meningothelial meningioma metachromatic leukodystrophy mevalonic aciduria microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcystic meningioma middle cerebral artery infarction migraine mixed glioma mixed oligodendroglioma-astrocytoma mongolian spot mood disorder mucosulfatidosis myelitis myelodysplastic syndrome myelofibrosis nephritis nephrocalcinosis nephronophthisis 1 nephrosis nephrotic syndrome neurilemmoma neurodegenerative disease nodular prostate non-suppurative otitis media non-syndromic X-linked intellectual disability nonpapillary renal cell carcinoma obesity obsolete congenital ichthyosiform erythroderma obsolete ymphosarcoma ocular albinism 1 olfactory groove meningioma oligospermia osteoarthritis osteosarcoma otitis media ovarian cancer ovarian carcinoma palindromic rheumatism pancreatic adenocarcinoma panhypopituitarism papillary renal cell carcinoma papilloma paracoccidioidomycosis parapsoriasis parasagittal meningioma patent ductus arteriosus pathologic nystagmus periodontitis peripheral vascular disease phosphorus metabolism disease pilocytic astrocytoma pituitary adenoma pituitary cancer pituitary carcinoma placental choriocarcinoma pleomorphic adenoma pleomorphic liposarcoma plexiform schwannoma pneumocystosis pneumonia polycystic ovary syndrome polyp of middle ear pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 postpartum depression primary sclerosing cholangitis prostate cancer prostate carcinoma prostatic adenoma protein C deficiency protein S deficiency protoplasmic astrocytoma psammomatous meningioma pseudohypoparathyroidism pseudoxanthoma elasticum psoriasis pustulosis of palm and sole pyoureter recessive dystrophic epidermolysis bullosa recurrent corneal erosion red color blindness red-green color blindness renal carcinoma renal cell carcinoma respiratory syncytial virus infectious disease retinal disease retinitis retrograde amnesia rheumatoid arthritis rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia sclerosing cholangitis seborrheic keratosis secretory meningioma seminoma septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly skin disease skin melanoma skin papilloma skin tag speech disorder spinal meningioma spindle cell sarcoma spontaneous ocular nystagmus squamous cell carcinoma squamous cell papilloma steatotic liver disease stomach cancer stomach carcinoma subependymal giant cell astrocytoma suppurative cholangitis syndromic X-linked intellectual disability Najm type syringoma testicular cancer testicular germ cell cancer testis seminoma thrombophilia tick-borne encephalitis tongue squamous cell carcinoma transitional meningioma trichohepatoenteric syndrome 1 trichohepatoenteric syndrome trypanosomiasis tuberculosis tubular adenocarcinoma type 2 diabetes mellitus urinary bladder cancer uterine corpus cancer varicose veins vasculitis visual epilepsy
414	arylsulfatase D	ARSD Aliases: ASD	Homo sapiens (human)	Asperger syndrome Bannayan-Riley-Ruvalcaba syndrome Beckwith-Wiedemann syndrome CLOVES syndrome Cockayne syndrome Cornelia de Lange syndrome 1 Cornelia de Lange syndrome Cowden syndrome Down syndrome Dubowitz syndrome Lown-Ganong-Levine syndrome Marfan syndrome Mowat-Wilson syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Perlman syndrome Prader-Willi syndrome Rett syndrome Richter's syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome Sotos syndrome Williams-Beuren syndrome Wolff-Parkinson-White syndrome X-linked Aarskog syndrome acute kidney tubular necrosis acute myeloid leukemia acute promyelocytic leukemia adult respiratory distress syndrome alexia amnestic disorder aniridia anxiety disorder aortic valve disease 1 aortic valve disease 2 aortic valve stenosis argininosuccinic aciduria arteriosclerotic cardiovascular disease atherosclerosis 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 atrioventricular block atrioventricular septal defect attention deficit hyperactivity disorder autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome bicuspid aortic valve disease breast cancer breast carcinoma buphthalmos cardiomyopathy cardiovascular system disease cerebral palsy chondrodysplasia-pseudohermaphroditism syndrome chronic lymphocytic leukemia citrullinemia communication disorder conduct disorder congenital heart disease congestive heart failure coronary artery disease depressive disorder developmental coordination disorder disease of mental health dyslexia dysthymic disorder eating disorder endocarditis endometriosis of uterus endometriosis endomyocardial fibrosis epilepsy essential hypertension excessive tearing familial hypertrophic cardiomyopathy fragile X syndrome generalized anxiety disorder glaucoma heart disease hemiplegia hydrophthalmos hyperargininemia hypertension hypertrophic cardiomyopathy hypospadias immune system disease infective endocarditis intellectual disability juvenile glaucoma lacrimal apparatus disease language disorder learning disability major depressive disorder melancholic depression microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microphthalmia neurotic disorder newborn respiratory distress syndrome nicotine dependence obesity obsolete melancholia patent ductus arteriosus patent foramen ovale phobic disorder polycystic ovary syndrome post-traumatic stress disorder primary open angle glaucoma psychotic disorder pulmonary valve stenosis retrograde amnesia schizophrenia sclerocornea situs inversus spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy subacute bacterial endocarditis substance abuse substance-related disorder supravalvular aortic stenosis syndromic X-linked intellectual disability 94 tuberous sclerosis ventricular septal defect visual epilepsy
415	arylsulfatase L	ARSL Aliases: chondrodysplasia punctata 1	Homo sapiens (human)
416	arylsulfatase F	ARSF Aliases: ASF	Homo sapiens (human)	Kuhnt-Junius degeneration breast cancer cancer embryoma epithelioid sarcoma hepatocellular carcinoma inflammatory bowel disease influenza liver cancer lung benign neoplasm lung cancer lung non-small cell carcinoma multiple sclerosis myositis neuroblastoma papilloma progressive multifocal leukoencephalopathy progressive muscular atrophy prostate cancer prostate carcinoma sarcoma spinal muscular atrophy spindle cell sarcoma squamous cell carcinoma squamous cell papilloma stomach cancer stomach carcinoma substance abuse substance-related disorder systemic lupus erythematosus tongue squamous cell carcinoma
417	ADP-ribosyltransferase 1	ART1 Aliases: ART2 ARTC1 CD296	Homo sapiens (human)	arthritis arthropathy astigmatism cancer central nervous system cancer colon carcinoma colorectal cancer colorectal carcinoma embryoma giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis hepatocellular carcinoma high grade glioma kidney disease large intestine cancer liver cancer mixed glioma nasopharynx carcinoma nephritis pancreatic cancer pancreatic carcinoma squamous cell carcinoma tongue squamous cell carcinoma tuberculosis
419	ADP-ribosyltransferase 3 (inactive)	ART3 Aliases: ARTC3	Homo sapiens (human)	azoospermia cancer melanoma patent ductus arteriosus skin melanoma steatotic liver disease
420	ADP-ribosyltransferase 4 (inactive) (Dombrock blood group)	ART4 Aliases: ARTC4 CD297 DOK1 NAD(+)--protein-arginine ADP-ribosyltransferase 4	Homo sapiens (human)	carotid artery thrombosis carotid stenosis conjunctivitis
427	N-acylsphingosine amidohydrolase 1	ASAH1 Aliases: AC ACDase FLJ21558 PHP32 acid ceramidase acylsphingosine deacylase	Homo sapiens (human)	Albright's hereditary osteodystrophy Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Beckwith-Wiedemann syndrome Bell's palsy CLOVES syndrome Erdheim-Chester disease Ewing sarcoma Fabry disease Farber lipogranulomatosis IGSF1 deficiency syndrome Krabbe disease Laron syndrome Lewy body dementia Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Perlman syndrome Pick's disease Reye syndrome Sotos syndrome Turner syndrome Unverricht-Lundborg syndrome Usher syndrome type 2 Usher syndrome type 3 Usher syndrome Wolman disease achondroplasia acute monocytic leukemia acute myeloid leukemia adult medulloblastoma agnosia amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 anterior horn cell disease arthritis arthropathy atrial fibrillation autosomal recessive distal hereditary motor neuronopathy 1 benign ependymoma benign epilepsy with centrotemporal spikes blepharospasm brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cellular ependymoma cerebral degeneration childhood ependymoma childhood medulloblastoma chylomicron retention disease colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma combined saposin deficiency congenital hypothyroidism congenital nongoitrous hypothyroidism 1 congenital nongoitrous hypothyroidism 2 congenital nongoitrous hypothyroidism 3 congenital nongoitrous hypothyroidism 4 congenital nongoitrous hypothyroidism 5 congenital nongoitrous hypothyroidism 6 congenital nystagmus cystic fibrosis dementia dentatorubral-pallidoluysian atrophy developmental coordination disorder dissociated nystagmus early myoclonic encephalopathy embryoma epilepsy facial nerve disease facial paralysis focal hand dystonia gastroenteritis gastrointestinal system cancer giant cell glioblastoma glaucoma glioblastoma gonadal dysgenesis head and neck cancer head and neck squamous cell carcinoma herpes simplex high grade glioma hyperglycemia hypoparathyroidism hypothyroidism idiopathic generalized epilepsy idiopathic interstitial pneumonia ileitis ileocolitis intellectual disability invasive ductal carcinoma large intestine cancer lateral sclerosis learning disability lipid storage disease lung benign neoplasm lung cancer lung carcinoma lysosomal storage disease measles medulloblastoma medullomyoblastoma melanoma melanotic medulloblastoma motor neuron disease myxedema myxopapillary ependymoma neonatal diabetes neurodegenerative disease neuroectodermal tumor obesity ocular melanoma osteoporosis pancreatic cancer pancreatic carcinoma papillary carcinoma papillary ependymoma pathologic nystagmus pneumonia postinflammatory pulmonary fibrosis progressive muscular atrophy progressive myoclonus epilepsy 1A progressive myoclonus epilepsy prostate cancer prostate carcinoma pseudohypoparathyroidism type IB pseudohypoparathyroidism pseudopseudohypoparathyroidism pulmonary fibrosis rectal benign neoplasm rectum adenocarcinoma rectum cancer recurrent corneal erosion retinitis pigmentosa-deafness syndrome retinoblastoma rheumatoid arthritis sarcomatoid carcinoma schizophrenia scoliosis sensorineural hearing loss skin melanoma speech disorder sphingolipidosis spinal muscular atrophy with progressive myoclonic epilepsy spinal muscular atrophy spontaneous ocular nystagmus tanycytic ependymoma thyroid adenoma thyroid cancer thyroid gland carcinoma transient neonatal diabetes mellitus viral infectious disease
432	asialoglycoprotein receptor 1	ASGR1 Aliases: CLEC4H1	Homo sapiens (human)	acrodermatitis arteriosclerotic cardiovascular disease atherosclerosis cancer coronary artery disease dermatitis hepatocellular carcinoma liver cancer nutmeg liver thrombocytopenia
433	asialoglycoprotein receptor 2	ASGR2 Aliases: CLEC4H2	Homo sapiens (human)
434	agouti signaling protein	ASIP	Homo sapiens (human)
444	aspartate beta-hydroxylase	ASPH	Homo sapiens (human)
445	argininosuccinate synthase 1	ASS1	Homo sapiens (human)
460	astrotactin 1	ASTN1	Homo sapiens (human)
462	serpin family C member 1	SERPINC1	Homo sapiens (human)
463	zinc finger homeobox 3	ZFHX3	Homo sapiens (human)
466	activating transcription factor 1	ATF1	Homo sapiens (human)
467	activating transcription factor 3	ATF3	Homo sapiens (human)	prostate cancer pulmonary tuberculosis
468	activating transcription factor 4	ATF4	Homo sapiens (human)	borna disease prostate carcinoma pulmonary venoocclusive disease
471	5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase	ATIC Aliases: AICARFT IMPCHASE PURH phosphoribosylaminoimidazolecarboxamide formyltransferase/IMP cyclohydrolase	Homo sapiens (human)
472	ATM serine/threonine kinase	ATM	Homo sapiens (human)
473	arginine-glutamic acid dipeptide repeats	RERE	Homo sapiens (human)
476	ATPase Na+/K+ transporting subunit alpha 1	ATP1A1	Homo sapiens (human)
477	ATPase Na+/K+ transporting subunit alpha 2	ATP1A2	Homo sapiens (human)	alcohol use disorder alternating hemiplegia of childhood benign neonatal seizures developmental and epileptic encephalopathy 98 epilepsy familial hemiplegic migraine 2 familial hemiplegic migraine hyperhomocysteinemia hypertension migraine with aura nervous system disease
481	ATPase Na+/K+ transporting subunit beta 1	ATP1B1	Homo sapiens (human)

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