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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | |
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 | 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 | 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 | 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 |