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 **126351 - 126375** of **126547** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of GlyTouCan IDs	Disease Ontology
P13533	Myosin-6	MYH6 MYHCA	Homo sapiens (human)	1
Q9D8S4	Oligoribonuclease, mitochondrial	Rexo2 Smfn	Mus musculus (house mouse)	1
Q96A26	Protein FAM162A	FAM162A C3orf28 E2IG5	Homo sapiens (human)	1
O95198	Kelch-like protein 2	KLHL2	Homo sapiens (human)	1
Q8BFY6	Peflin	Pef1	Mus musculus (house mouse)	1
P50479	PDZ and LIM domain protein 4	PDLIM4 RIL	Homo sapiens (human)	1
Q9CWX4	Pseudouridylate synthase RPUSD4, mitochondrial	Rpusd4	Mus musculus (house mouse)	1
Q9VXH7	FI17510p1	Dmel\CG9917 CG9917-RA anon-WO0140519.229	Drosophila melanogaster (fruit fly)	1
P53657	Pyruvate kinase PKLR	Pklr	Mus musculus (house mouse)	1
Q02551	Flagellin	flaA	Listeria monocytogenes EGD-e	1
Q86UQ8	Transcription factor NF-E4	NFE4	Homo sapiens (human)	1
P50607	Tubby protein homolog	TUB	Homo sapiens (human)	1
V5B262	DUF1935 domain-containing protein	TCDM_04034	Trypanosoma cruzi Dm28c	1
Q4DCI5	Prohibitin	Tc00.1047053511469.70	Trypanosoma cruzi strain CL Brener	1
Q9NRR6	Phosphatidylinositol polyphosphate 5-phosphatase type IV	INPP5E	Homo sapiens (human)	1	Bannayan-Riley-Ruvalcaba syndrome Bardet-Biedl syndrome 10 Bardet-Biedl syndrome 11 Bardet-Biedl syndrome 12 Bardet-Biedl syndrome 13 Bardet-Biedl syndrome 14 Bardet-Biedl syndrome 15 Bardet-Biedl syndrome 16 Bardet-Biedl syndrome 17 Bardet-Biedl syndrome 18 Bardet-Biedl syndrome 19 Bardet-Biedl syndrome 1 Bardet-Biedl syndrome 2 Bardet-Biedl syndrome 3 Bardet-Biedl syndrome 4 Bardet-Biedl syndrome 5 Bardet-Biedl syndrome 6 Bardet-Biedl syndrome 7 Bardet-Biedl syndrome 8 Bardet-Biedl syndrome 9 Bardet-Biedl syndrome Cogan syndrome Hirschsprung's disease Joubert syndrome 1 Joubert syndrome Kartagener syndrome Klippel-Feil syndrome Laurence-Moon syndrome Meckel syndrome 1 Meckel syndrome adult medulloblastoma autosomal dominant polycystic kidney disease autosomal recessive polycystic kidney disease blindness cancer cataract central sleep apnea childhood medulloblastoma cleft palate clubfoot coloboma of optic nerve coloboma communicating hydrocephalus congenital nystagmus congenital ptosis cystic kidney disease dextrocardia diffuse interstitial keratitis dissociated nystagmus embryoma epilepsy episodic kinesigenic dyskinesia 1 fundus dystrophy glomerulonephritis hepatocellular carcinoma hydrocephalus hypertropia inguinal hernia intellectual disability interstitial lung disease isolated cleft palate kidney disease kidney failure learning disability leukoplakia of penis liver cancer liver cirrhosis mechanical strabismus medulloblastoma medullomyoblastoma melanoma melanotic medulloblastoma nephritis nephrosis non-congenital cyst of kidney obesity obstructive hydrocephalus oculocerebrorenal syndrome ophthalmoplegia patent ductus arteriosus pathologic nystagmus polycystic kidney disease 4 polydactyly portal hypertension primary ciliary dyskinesia 1 primary ciliary dyskinesia ptosis pyoureter scoliosis senile degeneration of brain skin melanoma spondylolisthesis spontaneous ocular nystagmus strabismus viral infectious disease visual epilepsy visual pathway disease
Q4W5G0	Tigger transposable element-derived protein 2	TIGD2	Homo sapiens (human)	1
B6KL08	Microneme protein MIC1	BN1205_084920	Toxoplasma gondii VEG	1
Q4DAV0	SET domain-containing protein	Tc00.1047053507739.30	Trypanosoma cruzi strain CL Brener	1
V5AR01	T-complex protein 1 subunit delta	TCDM_09015	Trypanosoma cruzi Dm28c	1
Q9QXY2	SRC kinase signaling inhibitor 1	Srcin1 P140 Snip	Rattus norvegicus (Norway rat)	1
Q9FM71	RNA-binding (RRM/RBD/RNP motifs) family protein	MDF20.11 MDF20_11	Arabidopsis thaliana (thale cress)	1
P21281	V-type proton ATPase subunit B, brain isoform	ATP6V1B2 ATP6B2 VPP3	Homo sapiens (human)	1
P14060	3 beta-hydroxysteroid dehydrogenase/Delta 5-->4-isomerase type 1	HSD3B1 3BH HSDB3A	Homo sapiens (human)	1	Bartter disease Conn's syndrome Waterhouse-Friderichsen syndrome acne adenocarcinoma adenoma adrenal gland hyperfunction alopecia aortic valve insufficiency bladder carcinoma breast cancer breast carcinoma cancer carcinoma choriocarcinoma congenital adrenal hyperplasia congenital hypothyroidism diabetes mellitus diabetic ketoacidosis disorder of sexual development endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis essential hypertension follicular adenoma hermaphroditism hyperprolactinemia hypertension hypogonadism hypothyroidism kwashiorkor lesion of sciatic nerve marasmus microcystic adenoma myxedema nutrition disease obsolete Cushing's syndrome papillary adenoma placenta cancer polycystic ovary syndrome pre-eclampsia primary cutaneous amyloidosis primary hyperaldosteronism prostate cancer prostate carcinoma protein-energy malnutrition pseudohermaphroditism sarcomatoid carcinoma sciatic neuropathy stomach cancer stomach carcinoma trophoblastic neoplasm type 2 diabetes mellitus urinary bladder cancer uterine corpus cancer
P11182	Lipoamide acyltransferase component of branched-chain alpha-keto acid dehydrogenase complex, mitochondrial	DBT BCATE2 BCKDHE2	Homo sapiens (human)	1	acute pancreatitis autoimmune hepatitis borderline personality disorder brain edema breast cancer breast carcinoma cancer carcinoma cardiovascular system disease central nervous system cancer dilated cardiomyopathy 1A dilated cardiomyopathy dystonia eating disorder embryoma epilepsy focal hand dystonia generalized dystonia giant cell glioblastoma glioblastoma gliosarcoma heart disease high grade glioma hypoglycemia intellectual disability intermittent explosive disorder lactic acidosis learning disability maple syrup urine disease melanoma mixed glioma pancreatitis post-traumatic stress disorder primary biliary cholangitis skin melanoma substance abuse substance-related disorder syndromic X-linked intellectual disability 94 visual epilepsy
A0A0G2JDI9	ATP-binding cassette, sub-family D (ALD), member 3	Abcd3	Mus musculus (house mouse)	1

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