GlyCosmos Portal

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GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **108801 - 108825** of **126547** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs ▲	Disease Ontology
E9Q066	La ribonucleoprotein 4	Larp4	Mus musculus (house mouse)	0	1
Q5DU62	MFLJ00139 protein (Fragment)	Micall2 mFLJ00139	Mus musculus (house mouse)	0	1
Q9BZL1	Ubiquitin-like protein 5	UBL5	Homo sapiens (human)	0	1
Q3UA37	Transcriptional regulator QRICH1	Qrich1	Mus musculus (house mouse)	2	1
Q99469	SH3 and cysteine-rich domain-containing protein	STAC STAC1	Homo sapiens (human)	3	1
D3ZCV0	Actinin alpha 2	Actn2	Rattus norvegicus (Norway rat)	0	1
A0A0R4J038	Kininogen 1	Kng1	Mus musculus (house mouse)	3	1
Q6RUK3	Uncharacterized protein	109N23.4	Triticum monococcum	0	1
Q9H0K6	Pseudouridylate synthase PUS7L	PUS7L	Homo sapiens (human)	0	1
P15559	NAD(P)H dehydrogenase [quinone] 1	NQO1 DIA4 NMOR1	Homo sapiens (human)	0	1
Q8BW72	Lysine-specific demethylase 4A	Kdm4a Jhdm3a Jmjd2 Jmjd2a Kiaa0677	Mus musculus (house mouse)	0	1
Q8CIN4	Serine/threonine-protein kinase PAK 2	Pak2	Mus musculus (house mouse)	1	1
Q68FU3	Electron transfer flavoprotein subunit beta	Etfb	Rattus norvegicus (Norway rat)	1	1
A0A1B0GRV3	Regulatory factor X, 1 (influences HLA class II expression)	Rfx1	Mus musculus (house mouse)	0	1
V5BNT6	Uncharacterized protein	TCDM_01728	Trypanosoma cruzi Dm28c	0	1
Q6PAM1	Alpha-taxilin	Txlna Txln	Mus musculus (house mouse)	0	1
K2NHB5	Post-transcriptional regulator MKT1 N-terminal domain-containing protein	MOQ_001007	Trypanosoma cruzi marinkellei	0	1
V5BLF3	Uncharacterized protein	TCDM_04343	Trypanosoma cruzi Dm28c	0	1
Q70YC5	Protein ZNF365	ZNF365 DBZ KIAA0844	Homo sapiens (human)	0	1
P35573	Glycogen debranching enzyme	AGL GDE	Homo sapiens (human)	2	1	Duchenne muscular dystrophy Laron syndrome achondroplasia acute promyelocytic leukemia atrichia with papular lesions 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 bladder carcinoma cancer cardiomyopathy colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital muscular dystrophy cystinuria disease of metabolism distal myopathy endomyocardial fibrosis facioscapulohumeral muscular dystrophy familial hyperlipidemia familial partial lipodystrophy familial periodic paralysis galactosemia giardiasis glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease III glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease hepatitis C hypertrophic cardiomyopathy hypoglycemia isolated elevated serum creatine phosphokinase levels kidney failure large intestine cancer limb-girdle muscular dystrophy lipoatrophic diabetes mellitus lipodystrophy liver cirrhosis lung cancer lung non-small cell carcinoma muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy nodular nonsuppurative panniculitis 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 panniculitis primary immunodeficiency disease rippling muscle disease 2 uremia urinary bladder cancer
P08003	Protein disulfide-isomerase A4	Pdia4 Cai Erp72	Mus musculus (house mouse)	1	1
Q12451	Oxysterol-binding protein homolog 2	OSH2	Saccharomyces cerevisiae S288C	3	1
Q96F86	Enhancer of mRNA-decapping protein 3	EDC3 LSM16 YJDC YJEFN2	Homo sapiens (human)	2	1
Q05027	Transcription initiation factor TFIID subunit 9	TAF9 TAF17	Saccharomyces cerevisiae S288C	4	1
O60243	Heparan-sulfate 6-O-sulfotransferase 1	HS6ST1 HS6ST	Homo sapiens (human)	2	1	Kallmann syndrome Potter's syndrome Sheehan syndrome achromatopsia acquired color blindness anxiety disorder bilateral renal aplasia blindness blue color blindness cartilage-hair hypoplasia clubfoot color blindness congenital nystagmus congenital ptosis cryptorchidism depressive disorder diabetes mellitus diabetic ketoacidosis dissociated nystagmus dysthymic disorder epilepsy eunuchism generalized anxiety disorder gynecomastia 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 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 ichthyosis idiopathic interstitial pneumonia idiopathic pulmonary fibrosis impotence infant gynecomastia 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 major depressive disorder melancholic depression mucopolysaccharidosis IV multiple epiphyseal dysplasia neurotic disorder obesity obsolete melancholia osteochondrodysplasia osteoporosis panhypopituitarism paraplegia pathologic nystagmus premature ejaculation psychologic dyspareunia ptosis red color blindness red-green color blindness schizophrenia sensorineural hearing loss septooptic dysplasia spontaneous ocular nystagmus type 2 diabetes mellitus visual epilepsy

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