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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	July 8, 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 **1451 - 1475** of **1582** in total

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Gene ID	Gene Name	Gene Symbol	Organism	Disease Ontology ▼
8803	succinate-CoA ligase ADP-forming subunit beta	SUCLA2 Aliases: succinate--CoA ligase (ADP-forming)	Homo sapiens (human)	3-methylglutaconic aciduria type 4 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 3 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Creutzfeldt-Jakob disease Crohn's colitis Crohn's disease Down syndrome Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Laron syndrome Leigh disease Lewy body dementia Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome achondroplasia age related macular degeneration alternating hemiplegia of childhood amnestic disorder amyloidosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autonomic neuropathy blindness central nervous system disease cerebral degeneration congenital ptosis congestive heart failure coronary artery disease cutaneous porphyria degeneration of macula and posterior pole dementia depressive disorder diabetes mellitus diabetic ketoacidosis dissociative amnesia dysthymic disorder dystonia enterocele epilepsy erythropoietic protoporphyria familial retinoblastoma focal hand dystonia frontotemporal dementia generalized dystonia herpes simplex hydrocephalus hypertropia inflammatory bowel disease 1 inflammatory bowel disease isolated elevated serum creatine phosphokinase levels lactic acidosis leukopenia lingual-facial-buccal dyskinesia macular degeneration major depressive disorder mechanical strabismus melancholic depression methylmalonic acidemia microcephaly mitochondrial DNA depletion syndrome 5 mitochondrial DNA depletion syndrome 9 mitochondrial DNA depletion syndrome mitochondrial encephalomyopathy movement disease nervous system disease neuroblastoma neurodegenerative disease neuropathy neurotic disorder obesity obsolete melancholia ophthalmoplegia parasitic helminthiasis infectious disease peripheral nervous system disease ptosis retinoblastoma retrocochlear disease retrograde amnesia sensorineural hearing loss sideroblastic anemia 1 strabismus trichohepatoenteric syndrome 1 trichohepatoenteric syndrome trilateral retinoblastoma tuberculosis type 2 diabetes mellitus ulcerative colitis vascular dementia visual epilepsy
8455	attractin	ATRN Aliases: DPPT-L MGCA mahogany protein	Homo sapiens (human)	3-methylglutaconic aciduria type 3 Barth syndrome allergic asthma anaplastic astrocytoma asthma cancer cardiomyopathy central nervous system cancer childhood cerebral astrocytoma endomyocardial fibrosis fibrillary astrocytoma gemistocytic astrocytoma gliosarcoma high grade glioma hypertrophic cardiomyopathy intrinsic asthma juvenile pilocytic astrocytoma leukodystrophy malignant astrocytoma mixed glioma obesity pilocytic astrocytoma protoplasmic astrocytoma restless legs syndrome skin benign neoplasm skin cancer squamous cell carcinoma subependymal giant cell astrocytoma tongue squamous cell carcinoma
6576	solute carrier family 25 member 1	SLC25A1	Homo sapiens (human)	2-hydroxyglutaric aciduria DiGeorge syndrome chromosome 22q11.2 deletion syndrome, distal combined D-2- and L-2-hydroxyglutaric aciduria congenital myasthenic syndrome mitochondrial metabolism disease
79944	L-2-hydroxyglutarate dehydrogenase	L2HGDH Aliases: 2-hydroxyglutarate dehydrogenase FLJ12618	Homo sapiens (human)	2-hydroxyglutaric aciduria D-2-hydroxyglutaric aciduria 1 D-2-hydroxyglutaric aciduria L-2-hydroxyglutaric aciduria brain cancer cerebellar ataxia chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma congenital nystagmus disease of metabolism dissociated nystagmus dystonia encephalitis encephalomyelitis epilepsy giant cell glioblastoma glioblastoma hereditary spastic paraplegia high grade glioma hypertropia intellectual disability learning disability mechanical strabismus myelitis nervous system cancer neurodegenerative disease nonpapillary renal cell carcinoma ophthalmoplegia optic atrophy papillary renal cell carcinoma pathologic nystagmus renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma sensorineural hearing loss spontaneous ocular nystagmus strabismus syndromic X-linked intellectual disability 94 vascular dementia visual epilepsy
3417	isocitrate dehydrogenase (NADP(+)) 1	IDH1	Homo sapiens (human)	2-hydroxyglutaric aciduria 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 Cenani-Lenz syndactyly syndrome Chediak-Higashi syndrome Crohn's colitis Crohn's disease D-2-hydroxyglutaric aciduria Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Langerhans-cell histiocytosis Laron syndrome Li-Fraumeni syndrome 1 Li-Fraumeni syndrome Maffucci syndrome Marfan syndrome Nijmegen breakage syndrome Ollier disease Pelger-Huet anomaly Pick's disease Reye syndrome Richter's syndrome T-cell acute lymphoblastic leukemia achondroplasia acoustic neuroma acquired immunodeficiency syndrome acute biphenotypic leukemia acute leukemia acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia acute promyelocytic leukemia adamantinous craniopharyngioma adenocarcinoma adenoid cystic carcinoma adenoma adrenal cortex cancer adrenal gland cancer adult acute lymphocytic leukemia adult astrocytic tumor adult fibrosarcoma adult lymphoma adult medulloblastoma adult oligodendroglioma alpha thalassemia-X-linked intellectual disability syndrome anaplastic astrocytoma anemia angioimmunoblastic T-cell lymphoma angiokeratoma aortic valve insufficiency aromatase excess syndrome astroblastoma ataxia with oculomotor apraxia type 1 atypical chronic myeloid leukemia, BCR-ABL1 negative autoimmune disease benign ependymoma benign giant cell tumor bile duct adenocarcinoma bile duct carcinoma biliary tract cancer bipolar disorder bladder urothelial carcinoma bone cancer bone marrow cancer bone osteosarcoma brain cancer brain stem glioma breast adenocarcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cataract 4 multiple types cavernous hemangioma cellular ependymoma central nervous system cancer central nervous system lymphoma central neurocytoma cerebellar liponeurocytoma cerebral degeneration cerebral palsy cherubism childhood acute lymphocytic leukemia childhood acute myeloid leukemia childhood astrocytic tumor childhood cerebral astrocytoma childhood ependymoma childhood leukemia childhood lymphoma childhood medulloblastoma childhood oligodendroglioma childhood osteosarcoma childhood pilocytic astrocytoma cholangiocarcinoma cholangiolocellular carcinoma chondroblastic osteosarcoma chondroma chondrosarcoma chordoma chorioangioma chromophobe renal cell carcinoma chronic lymphocytic leukemia chronic monocytic leukemia chronic myeloid leukemia chronic ulcer of skin clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma connective tissue benign neoplasm cranial nerve disease cranial nerve palsy craniopharyngioma cribriform carcinoma degenerative disc disease dementia demyelinating polyneuropathy diffuse infiltrative lymphocytosis syndrome diffuse large B-cell lymphoma dilated cardiomyopathy 1A dilated cardiomyopathy disease of mental health disease of metabolism distal arthrogryposis duodenum cancer dysembryoplastic neuroepithelial tumor dysplastic nevus syndrome embryoma embryonal cancer endometrial cancer endometrial carcinoma epilepsy epithelioid sarcoma esophagus squamous cell carcinoma essential thrombocythemia exanthem exostosis familial retinoblastoma fibrillary astrocytoma fibrosarcoma follicular adenoma gallbladder cancer gallbladder carcinoma ganglioglioma gastrointestinal system cancer gemistocytic astrocytoma germ cell and embryonal cancer germ cell cancer giant cell glioblastoma glioblastoma gliomatosis cerebri gliosarcoma glomus tumor goiter granular cell carcinoma heart cancer hemangioma hematologic cancer hemiplegia hepatocellular carcinoma hepatocellular clear cell carcinoma hereditary multiple exostoses hidradenitis suppurativa hidradenitis high grade glioma histiocytoid hemangioma human immunodeficiency virus infectious disease inflammatory bowel disease 1 inflammatory bowel disease inflammatory liposarcoma intellectual disability intrahepatic cholangiocarcinoma intramuscular hemangioma invasive ductal carcinoma invasive lobular carcinoma juvenile pilocytic astrocytoma kidney cancer large intestine cancer learning disability leukemia liver cancer liver carcinoma liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma lung squamous cell carcinoma lymphangioma lymphoblastic lymphoma lymphoid leukemia lymphoma macrocytic anemia malignant astrocytoma malignant fibrous histiocytoma medulloblastoma medullomyoblastoma melanoma melanotic medulloblastoma meningioma microcystic adenoma microphthalmia mixed glioma mixed oligodendroglioma-astrocytoma monocytic leukemia mononeuritis multiplex mononeuropathy multiple myeloma myelodysplastic syndrome myelofibrosis myeloid leukemia myeloproliferative neoplasm myxopapillary ependymoma nervous system cancer neurofibromatosis 1 neurofibromatosis neuropathy non-Hodgkin lymphoma nonpapillary renal cell carcinoma nontoxic goiter obsolete Matthew-Wood syndrome obsolete ymphosarcoma oligodendroglioma osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary adenocarcinoma papillary adenoma papillary craniopharyngioma papillary ependymoma papillary renal cell carcinoma paraganglioma parathyroid adenoma parathyroid carcinoma paroxysmal nocturnal hemoglobinuria patent ductus arteriosus periarthritis peripheral T-cell lymphoma peripheral nervous system disease pheochromocytoma pilocytic astrocytoma of cerebellum pilocytic astrocytoma pituitary adenoma pituitary cancer pituitary carcinoma plasmacytoma pleomorphic xanthoastrocytoma polycythemia vera polycythemia polyneuropathy pompholyx primary immunodeficiency disease prostate adenocarcinoma prostate cancer prostate carcinoma protoplasmic astrocytoma psychotic disorder renal carcinoma renal cell carcinoma respiratory failure reticulosarcoma retinoblastoma rheumatic fever salivary gland adenoid cystic carcinoma sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma sclerosing liposarcoma scoliosis situs inversus skin melanoma small intestine cancer spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spindle cell hemangioma spindle cell sarcoma squamous cell carcinoma status epilepticus stomach cancer stomach carcinoma subependymal giant cell astrocytoma supratentorial cancer tanycytic ependymoma tendinitis thalamic neoplasm thrombophilia thyroid adenoma thyroid cancer thyroid gland anaplastic carcinoma thyroid gland carcinoma thyroid gland disease thyroid gland follicular carcinoma thyroid gland papillary carcinoma tongue squamous cell carcinoma trilateral retinoblastoma tuberous sclerosis tubular adenocarcinoma ulcerative colitis uterine corpus cancer uveal melanoma vascular cancer visual epilepsy vulvar dystrophy well-differentiated liposarcoma
3418	isocitrate dehydrogenase (NADP(+)) 2	IDH2 Aliases: IDH-2	Homo sapiens (human)	2-hydroxyglutaric aciduria 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 Balo concentric sclerosis Burkitt lymphoma Cenani-Lenz syndactyly syndrome Chediak-Higashi syndrome D-2-hydroxyglutaric aciduria 1 D-2-hydroxyglutaric aciduria 2 D-2-hydroxyglutaric aciduria Duchenne muscular dystrophy Keshan disease Langerhans-cell histiocytosis Laron syndrome Maffucci syndrome Marinesco-Sjogren syndrome Ollier disease Pelger-Huet anomaly Peutz-Jeghers syndrome Pick's disease Reye syndrome Richter's syndrome T-cell acute lymphoblastic leukemia T-cell adult acute lymphocytic leukemia achondroplasia acoustic neuroma acute biphenotypic leukemia acute leukemia acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia acute promyelocytic leukemia adenocarcinoma adenoma adrenal cortex cancer adrenal gland cancer adrenoleukodystrophy adult acute lymphocytic leukemia adult astrocytic tumor adult lymphoma adult medulloblastoma adult oligodendroglioma alpha thalassemia-X-linked intellectual disability syndrome anaplastic astrocytoma anemia angioimmunoblastic T-cell lymphoma angiokeratoma aortic valve insufficiency aromatase excess syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atypical chronic myeloid leukemia, BCR-ABL1 negative 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 benign ependymoma benign mastocytoma bile duct adenocarcinoma bile duct cancer bile duct carcinoma biliary tract cancer bipolar disorder bone cancer bone giant cell tumor bone marrow cancer bone osteosarcoma bone remodeling disease brain cancer brain stem glioma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy cardiovascular system disease cavernous hemangioma cellular ependymoma central nervous system cancer central nervous system disease central nervous system lymphoma cerebral degeneration cerebral palsy cherubism childhood acute lymphocytic leukemia childhood acute myeloid leukemia childhood astrocytic tumor childhood cerebral astrocytoma childhood leukemia childhood lymphoma childhood medulloblastoma childhood oligodendroglioma childhood osteosarcoma childhood pilocytic astrocytoma cholangiocarcinoma chondroblastoma chondroma chondrosarcoma chorioangioma chronic lymphocytic leukemia chronic monocytic leukemia chronic myeloid leukemia chronic ulcer of skin colitis colorectal cancer colorectal carcinoma cone-rod dystrophy congenital muscular dystrophy coronary artery disease cranial nerve disease cranial nerve palsy cribriform carcinoma degenerative disc disease demyelinating polyneuropathy diffuse infiltrative lymphocytosis syndrome diffuse large B-cell lymphoma disease of metabolism distal arthrogryposis distal myopathy duodenum cancer embryoma embryonal cancer endomyocardial fibrosis epilepsy epithelioid sarcoma esophagus squamous cell carcinoma essential hypertension essential thrombocythemia exanthem exostosis extracutaneous mastocytoma facioscapulohumeral muscular dystrophy familial hypertrophic cardiomyopathy familial retinoblastoma fibrillary astrocytoma focal epilepsy fundus albipunctatus ganglioglioma gastroenteritis gemistocytic astrocytoma germ cell and embryonal cancer germ cell cancer germinoma giant cell glioblastoma glioblastoma gliosarcoma glomus tumor goiter granular cell carcinoma head and neck squamous cell carcinoma heart cancer heart disease hemangioma hematologic cancer hematopoietic system disease hemiplegia hepatocellular carcinoma hepatocellular clear cell carcinoma hereditary multiple exostoses hidradenitis suppurativa hidradenitis high grade glioma histiocytoid hemangioma hydronephrosis hypertension hypertrophic cardiomyopathy ileitis ileocolitis indolent systemic mastocytosis inflammatory bowel disease inflammatory breast carcinoma inflammatory liposarcoma intellectual disability intrahepatic cholangiocarcinoma intramuscular hemangioma juvenile pilocytic astrocytoma kidney failure large intestine cancer learning disability leukemia limb-girdle muscular dystrophy liver cancer liver carcinoma luminal breast carcinoma A lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung squamous cell carcinoma lymphangioma lymphoblastic lymphoma lymphoid leukemia lymphoma macrocytic anemia malignant astrocytoma malignant fibrous histiocytoma mast cell neoplasm mastocytosis medulloblastoma medullomyoblastoma melanoma melanotic medulloblastoma meningioma mixed glioma mixed oligodendroglioma-astrocytoma mononeuritis multiplex mononeuropathy multiple myeloma muscular dystrophy myelodysplastic syndrome myelofibrosis myeloid leukemia myeloproliferative neoplasm myofibrillar myopathy 1 myofibrillar myopathy 3 myxopapillary ependymoma narcolepsy nervous system disease neurodegenerative disease neuroendocrine carcinoma neurofibromatosis 1 neurofibromatosis neuropathy non-Hodgkin lymphoma nontoxic goiter 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 obsolete ymphosarcoma oculopharyngeal muscular dystrophy olfactory neuroblastoma oligodendroglioma osteoarthritis osteoporosis osteosarcoma ovarian cancer ovarian carcinoma papillary carcinoma papillary ependymoma paraganglioma parathyroid adenoma parathyroid carcinoma partial motor epilepsy periarthritis peripheral T-cell lymphoma peripheral nervous system disease pheochromocytoma pilocytic astrocytoma pituitary adenoma pituitary cancer pituitary carcinoma plasmacytoma pleomorphic xanthoastrocytoma polycythemia vera polycythemia polyneuropathy pompholyx primary cerebellar degeneration prostate cancer prostate carcinoma protoplasmic astrocytoma pulmonary large cell neuroendocrine carcinoma reflex sympathetic dystrophy reticulosarcoma retinitis pigmentosa retinoblastoma rippling muscle disease 2 sarcoma sarcomatoid carcinoma sclerosing liposarcoma scoliosis sensorineural hearing loss skin melanoma small intestine cancer spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spindle cell hemangioma spindle cell sarcoma status epilepticus steatotic liver disease stomach cancer stomach carcinoma subependymal giant cell astrocytoma tanycytic ependymoma telangiectatic osteogenic sarcoma tendinitis thrombophilia thyroid adenoma thyroid cancer thyroid gland anaplastic carcinoma thyroid gland carcinoma thyroid gland disease thyroid gland follicular carcinoma transitional cell carcinoma trilateral retinoblastoma tubular adenocarcinoma uremia urticaria pigmentosa visual epilepsy von Hippel-Lindau disease vulvar dystrophy well-differentiated liposarcoma
55526	dehydrogenase E1 and transketolase domain containing 1	DHTKD1	Homo sapiens (human)	2-aminoadipic 2-oxoadipic aciduria Charcot-Marie-Tooth disease axonal type 2Q
3293	hydroxysteroid 17-beta dehydrogenase 3	HSD17B3 Aliases: SDR12C2 short chain dehydrogenase/reductase family 12C, member 2	Homo sapiens (human)	17-beta hydroxysteroid dehydrogenase 3 deficiency Alzheimer's disease Kallmann syndrome Sheehan syndrome acne androgen insensitivity syndrome autoimmune hepatitis cancer congenital adrenal hyperplasia congenital hypothyroidism cryptorchidism diabetes mellitus disorder of sexual development endometriosis of uterus endometriosis gynecomastia hepatitis hermaphroditism hypertrophy of breast 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 23 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 hypopituitarism hypospadias hypothyroidism infant gynecomastia infertility 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 myxedema nicotine dependence nodular prostate obesity panhypopituitarism premature menopause prostate cancer prostate carcinoma prostatic adenoma pseudohermaphroditism type 2 diabetes mellitus
283209	phosphoglucomutase 2 like 1	PGM2L1 Aliases: BM32A FLJ32029 glucose-1,6-bisphosphate synthase	Homo sapiens (human)
154790	C-type lectin domain family 2 member L	CLEC2L Aliases: FLJ32986	Homo sapiens (human)
388581	C1q and TNF related 12	C1QTNF12	Homo sapiens (human)
79799	UDP glucuronosyltransferase family 2 member A3	UGT2A3 Aliases: FLJ21934	Homo sapiens (human)
55811	adenylate cyclase 10	ADCY10	Homo sapiens (human)
339665	solute carrier family 35 member E4	SLC35E4	Homo sapiens (human)
391013	phospholipase A2 group IIC	PLA2G2C	Homo sapiens (human)
55326	1-acylglycerol-3-phosphate O-acyltransferase 5	AGPAT5 Aliases: 1-acyl-sn-glycerol-3-phosphate acyltransferase epsilon FLJ11210 LPAAT-e LPAAT-epsilon LPLAT5 lysophosphatidic acid acyltransferase, epsilon lysophospholipid acyltransferase 5	Homo sapiens (human)
133121	ectonucleotide pyrophosphatase/phosphodiesterase 6	ENPP6 Aliases: MGC33971	Homo sapiens (human)
79691	queuine tRNA-ribosyltransferase accessory subunit 2	QTRT2 Aliases: FLJ12960	Homo sapiens (human)
142683	intelectin 2	ITLN2 Aliases: HL-2	Homo sapiens (human)
729201	sperm acrosome associated 5B	SPACA5B Aliases: LYZL5B	Homo sapiens (human)
84569	lysozyme like 1	LYZL1 Aliases: LYC2 MGC33408	Homo sapiens (human)
9962	solute carrier family 23 member 2	SLC23A2	Homo sapiens (human)
51006	solute carrier family 35 member C2	SLC35C2 Aliases: CGI-15 bA394O2.1	Homo sapiens (human)
5504	protein phosphatase 1 regulatory inhibitor subunit 2	PPP1R2	Homo sapiens (human)
7165	TPD52 like 2	TPD52L2	Homo sapiens (human)

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