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AnalogYeast
One stop shop for finding analogs for your favorite yeast protein

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YPR192W AQY1 / SGDID:S000006396
SGD CSV
Disease Associated
Homo Sapiens
Mus Musculus
Danio Rerio
Drosophila Melanogaster
Caenorhabditis Elegans
Arabidopsis Thaliana
Escherichia Coli
Yeast Systematic Name Yeast Symbol SGDID Analog Name Analog Description EC Organism Disease Structure Uniprot Human ID Human Symbol HHsearch Probability HHsearch E_value HHsearch P_value HHsearch Score Flag Disease related Flag Homo sapiens Flag Mus musculus Flag Danio rerio Flag Drosophila melanogaster Flag Caenorhabditis elegans Flag Arabidopsis thaliana Flag Escherichia coli
YPR192W AQY1 SGDID:S000006396
glpF b3927 JW3898
Glycerol uptake facilitator protein (Aquaglyceroporin)
Escherichia coli
1fx8_a P0AER0 100.00 2.90E-36 2.20E-40 266.70 0 0 0 0 0 0 0 1
YPR192W AQY1 SGDID:S000006396
AQY1 PP7435_Chr3-0430
AQY1 PP7435_Chr3-0430
Komagataella phaffii
2w1p_a F2QVG4 99.90 1.20E-31 9.20E-36 240.10 0 0 0 0 0 0 0 0
YPR192W AQY1 SGDID:S000006396
glpF b3927 JW3898
Glycerol uptake facilitator protein (Aquaglyceroporin)
Escherichia coli
1ldf_a P0AER0 99.90 1.00E-31 8.20E-36 240.40 0 0 0 0 0 0 0 1
YPR192W AQY1 SGDID:S000006396
AQP2
Aquaporin-2 (AQP-2) (ADH water channel) (Aquaporin-CD) (AQP-CD) (Collecting duct water channel protein) (WCH-CD) (Water channel protein for renal collecting duct)
Homo sapiens
Meniere Disease,Autosomal Dominant Polycystic Kidney Disease,Central Pontine Myelinolysis,Polycystic Kidney Disease,Hepatorenal Syndrome,Nephrotic Syndrome,Diabetes Insipidus,Bartter Disease,Renal Tubular Transport Disease,Hypokalemia,Peripheral Vertigo,Chronic Kidney Disease,Bartter Syndrome, Type 1, Antenatal,Liver Cirrhosis,Ureteral Obstruction,Urinary Tract Obstruction,Hereditary Nephrogenic Diabetes Insipidus,Cystic Kidney Disease,Kidney Disease,Pendred Syndrome,Kidney Papillary Necrosis,Congestive Heart Failure,Ureteral Disease,Polycystic Kidney Disease 1 With Or Without Polycystic Liver Disease,Hydronephrosis,Inappropriate Adh Syndrome,Vestibular Disease,Liddle Syndrome 1,Diabetes Insipidus, Neurohypophyseal,Renal Glucosuria,Diabetes Insipidus, Nephrogenic, Autosomal,Nephrogenic Syndrome Of Inappropriate Antidiuresis,Metabolic Acidosis,Congenital Anomalies Of Kidney And Urinary Tract 2,Hypertension, Essential,Joubert Syndrome 1,Polycystic Kidney Disease 4 With Or Without Polycystic Liver Disease
4nef_a P41181 ENSG00000167580 AQP2 99.90 9.10E-31 7.10E-35 229.40 1 1 0 0 0 0 0 0
YPR192W AQY1 SGDID:S000006396
AQP5
Homo sapiens
Aquaporin 5
Pulmonary Edema,Acrokeratoderma, Hereditary Papulotranslucent,Accommodative Spasm,Presbyopia,Potocki-Shaffer Syndrome,Dacryoadenitis,Sjogren Syndrome,Brain Edema,Cataract,Keratoconjunctivitis Sicca,Sensorineural Hearing Loss,Eye Accommodation Disease,Xerophthalmia,Dry Eye Syndrome,Sialadenitis,Diffuse Pulmonary Fibrosis,Neuromyelitis Optica,Lacrimal Apparatus Disease,Diabetes Insipidus, Nephrogenic, Autosomal,Aplasia Of Lacrimal And Salivary Glands,Autoimmune Disease Of Exocrine System,Palmoplantar Keratoderma, Bothnian Type
3d9s_b P55064 ENSG00000161798 AQP5 99.90 9.80E-31 7.60E-35 232.40 1 0 0 0 0 0 0 0
YPR192W AQY1 SGDID:S000006396
AQP4
Homo sapiens
Homo sapiens
Brown-Sequard Syndrome,Narcolepsy,Myopathy,Central Pontine Myelinolysis,Neuritis,Acute Disseminated Encephalomyelitis,Spinal Cord Injury,Traumatic Brain Injury,Optic Nerve Disease,Scotoma,Autoimmune Disease Of The Nervous System,Intracranial Hypertension,Neuroma,Bacterial Meningitis,Meningitis,Alzheimer Disease,Neonatal Stroke,Constipation,Nutritional Optic Neuropathy,Optic Neuritis,Transverse Myelitis,Encephalitis,Arachnoiditis,Stroke, Ischemic,Brain Edema,Acute Transverse Myelitis,Idiopathic Acute Transverse Myelitis,Relapsing-Remitting Multiple Sclerosis,Wernicke Encephalopathy,Acoustic Neuroma,Autoimmune Disease,Miller Fisher Syndrome,Dysferlinopathy,Sudden Infant Death Syndrome,Skin Amelanotic Melanoma,Branch Retinal Artery Occlusion,Cerebral Artery Occlusion,Brain Cancer,Optic Papillitis,Internuclear Ophthalmoplegia,Subependymoma,Toxic Optic Neuropathy,Nervous System Disease,Inner Ear Disease,Neurosarcoidosis,Cranial Nerve Disease,Neuromyelitis Optica,Peripheral Nervous System Disease,Acquired Color Blindness,Abducens Nerve Disease,Hand, Foot And Mouth Disease,Spinal Cord Disease,Vascular Myelopathy,Demyelinating Disease,Brain Injury,Myelitis,Acute Retrobulbar Neuritis,Obstructive Hydrocephalus,Hydrocephalus,Syringomyelia,Bullous Keratopathy,Alacrima, Achalasia, And Mental Retardation Syndrome,Combined Oxidative Phosphorylation Deficiency 7,Cerebral Degeneration,Temporal Lobe Epilepsy,Papilledema,Inappropriate Adh Syndrome,Cerebritis,Disease Of Mental Health,Creutzfeldt-Jakob Disease,Megalencephalic Leukoencephalopathy With Subcortical Cysts 1,Normal Pressure Hydrocephalus,Communicating Hydrocephalus,Diabetes Insipidus, Nephrogenic, Autosomal,Multiple Sclerosis,Cranial Nerve Palsy,Autoimmune Optic Neuritis,Schizophrenia,Mouth Disease,Intraocular Pressure Quantitative Trait Locus,Immune Deficiency Disease,Intracranial Hypertension, Idiopathic,Acute Hemorrhagic Leukoencephalitis,Autoimmune Disease Of Central Nervous System,Autoimmune Disease Of Exocrine System,Autoimmune Disease Of Peripheral Nervous System,Color Agnosia,Leber Hereditary Optic Neuropathy, Modifier Of,Balo Concentric Sclerosis,Muscular Dystrophy, Duchenne Type
3gd8_a P55087 ENSG00000171885 AQP4 99.90 5.90E-30 4.70E-34 221.00 1 1 0 0 0 0 0 0
YPR192W AQY1 SGDID:S000006396
SOVF_195660
SOVF_195660
Spinacia oleracea
3cn5_a Q41372 99.90 1.80E-31 1.40E-35 241.60 0 0 0 0 0 0 0 0
YPR192W AQY1 SGDID:S000006396
MIP AQP0
Lens fiber major intrinsic protein (Aquaporin-0)
Ovis aries
2b6o_a Q6J8I9 99.90 2.60E-31 2.00E-35 235.90 0 0 0 0 0 0 0 0
YPR192W AQY1 SGDID:S000006396
aqpZ2 Atu5361 AGR_pAT_521
Agrobacterium fabrum
Aquaporin Z
3llq_a Q8UJW4 99.90 2.80E-32 2.20E-36 241.10 0 0 0 0 0 0 0 0
YPR192W AQY1 SGDID:S000006396
AQP
AQP
Plasmodium falciparum
3c02_a Q8WPZ6 99.90 7.90E-30 6.20E-34 225.20 0 0 0 0 0 0 0 0
YPR192W AQY1 SGDID:S000006396
AQP10
Homo sapiens
Homo sapiens
Pompholyx,Fox-Fordyce Disease,Diabetes Insipidus, Nephrogenic, Autosomal
6f7h_d Q96PS8 ENSG00000143595 AQP10 99.90 3.70E-32 2.80E-36 246.00 1 1 0 0 0 0 0 0

Weizmann Institute of Science | Maya Schuldiner Lab