GlyCosmos Portal

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Displaying entries **2076 - 2100** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of GlyTouCan IDs	Disease Ontology
Q13127	RE1-silencing transcription factor	REST NRSF XBR	Homo sapiens (human)	1
O15056	Synaptojanin-2	SYNJ2 KIAA0348	Homo sapiens (human)	1	Duchenne muscular dystrophy Joubert syndrome 1 Joubert syndrome amyotrophic lateral sclerosis 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 breast cancer bronchus cancer bronchus carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congenital muscular dystrophy depressive disorder distal myopathy facioscapulohumeral muscular dystrophy giant cell glioblastoma glioblastoma large intestine cancer limb-girdle muscular dystrophy lung cancer lung carcinoma 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 oculopharyngeal muscular dystrophy progressive muscular atrophy rippling muscle disease 2
Q96A19	Coiled-coil domain-containing protein 102A	CCDC102A	Homo sapiens (human)	1
Q8TCX1	Cytoplasmic dynein 2 light intermediate chain 1	DYNC2LI1 D2LIC LIC3	Homo sapiens (human)	1
Q92519	Tribbles homolog 2	TRIB2 TRB2	Homo sapiens (human)	1
Q9BVL4	Protein adenylyltransferase SelO, mitochondrial	SELENOO SELO	Homo sapiens (human)	1
Q504T8	Midnolin	MIDN	Homo sapiens (human)	1
P51970	NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 8	NDUFA8	Homo sapiens (human)	1
Q96G46	tRNA-dihydrouridine(47) synthase [NAD(P)(+)]-like	DUS3L	Homo sapiens (human)	1
Q99661	Kinesin-like protein KIF2C	KIF2C KNSL6	Homo sapiens (human)	1
Q8TBE9	N-acylneuraminate-9-phosphatase	NANP C20orf147 HDHD4	Homo sapiens (human)	1	cancer cerebral degeneration colorectal cancer esophageal cancer esophageal carcinoma large intestine cancer malaria
Q9UNH7	Sorting nexin-6	SNX6	Homo sapiens (human)	1
Q7L5Y6	DET1 homolog	DET1	Homo sapiens (human)	1
Q9BW04	Specifically androgen-regulated gene protein	SARG C1orf116	Homo sapiens (human)	1
A6NHL2	Tubulin alpha chain-like 3	TUBAL3	Homo sapiens (human)	1
Q9BQ83	Structure-specific endonuclease subunit SLX1	SLX1A SLX1B GIYD1 GIYD2 SLX1	Homo sapiens (human)	1
Q92529	SHC-transforming protein 3	SHC3 NSHC SHCC	Homo sapiens (human)	1
Q8IX06	Putative exonuclease GOR	REXO1L1P GOR REXO1L1	Homo sapiens (human)	1
Q9C005	Protein dpy-30 homolog	DPY30	Homo sapiens (human)	1
P34913	Bifunctional epoxide hydrolase 2	EPHX2	Homo sapiens (human)	1	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 Crohn's colitis Crohn's disease IgA glomerulonephritis Langerhans-cell histiocytosis Lewy body dementia Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Sertoli cell-only syndrome Y-linked spermatogenic failure 1 abdominal obesity-metabolic syndrome 1 acute chest syndrome acute kidney failure acute myocardial infarction adenocarcinoma adenoma adult respiratory distress syndrome anorexia nervosa arcus senilis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation autism spectrum disorder autistic disorder blindness brain stem infarction bronchus cancer bronchus carcinoma cancer cardiovascular system disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cervical squamous cell carcinoma chronic kidney disease chronic obstructive pulmonary disease complement deficiency complex partial epilepsy congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma dementia depressive disorder diabetes mellitus embryoma essential hypertension exudative vitreoretinopathy 1 exudative vitreoretinopathy eyelid disease familial hypercholesterolemia gastrointestinal stromal tumor glomerulonephritis granular cell carcinoma heart disease hyperglycemia hypertension inflammatory bowel disease 1 inflammatory bowel disease kidney disease lobular neoplasia lung benign neoplasm lung cancer lung carcinoma lupus erythematosus lupus nephritis lymphoma major depressive disorder melancholic depression middle cerebral artery infarction myocardial infarction nephritis newborn respiratory distress syndrome non-Hodgkin lymphoma nutmeg liver obsolete melancholia obsolete ymphosarcoma oligospermia pancreatic cancer pancreatic carcinoma pneumonia primary pulmonary hypertension prostate cancer prostate carcinoma pulmonary emphysema pulmonary hypertension reticulosarcoma retinopathy of prematurity sarcoidosis schizophrenia sick sinus syndrome silent myocardial infarction sudden infant death syndrome systemic lupus erythematosus temporal lobe epilepsy tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis uveoparotid fever xanthomatosis
Q7Z6G3	N-terminal EF-hand calcium-binding protein 2	NECAB2 EFCBP2	Homo sapiens (human)	1
O76015	Keratin, type I cuticular Ha8	KRT38 HHA8 HKA8 KRTHA8	Homo sapiens (human)	1
P62424	Large ribosomal subunit protein eL8	RPL7A SURF-3 SURF3	Homo sapiens (human)	1
Q96EY4	Translation machinery-associated protein 16	TMA16 C4orf43	Homo sapiens (human)	1
O00408	cGMP-dependent 3',5'-cyclic phosphodiesterase	PDE2A	Homo sapiens (human)	1

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