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YLL001W DNM1 / SGDID:S000003924

SGD CSV

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
YLL001W	DNM1	SGDID:S000003924	Dnm1	Dnm1		Cyanidioschyzon merolae		6fgz_a	Q84Y91			100.00	1.90E-47	2.30E-51	409.90	0	0
YLL001W	DNM1	SGDID:S000003924	MX2	Interferon-induced GTP-binding protein Mx2 (Interferon-regulated resistance GTP-binding protein MxB) (Myxovirus resistance protein 2) (p78-related protein)		Homo sapiens	Influenza,Pediculus Humanus Corporis Infestation,Hantavirus Hemorrhagic Fever With Renal Syndrome,Danubian Endemic Familial Nephropathy,Aicardi-Goutieres Syndrome,Microphthalmia With Limb Anomalies	4whj_a	P20592	ENSG00000183486	MX2	100.00	8.40E-38	1.00E-41	325.10	1	1
YLL001W	DNM1	SGDID:S000003924	CTHT_0065850	CTHT_0065850		Chaetomium thermophilum		6ql4_a	G0SGC7			99.90	7.60E-31	7.20E-35	297.10	0	0
YLL001W	DNM1	SGDID:S000003924	DNM3 KIAA0820	Dynamin-3 (EC 3.6.5.5) (Dynamin, testicular) (T-dynamin)	3.6.5.5	Homo sapiens	Myopathy, Centronuclear, 1,Sezary'S Disease,Centronuclear Myopathy,Neuropathy, Hereditary Sensory, Type Id	5a3f_d	Q9UQ16	ENSG00000197959	DNM3	100.00	2.80E-51	3.40E-55	439.40	1	1
YLL001W	DNM1	SGDID:S000003924	DNM1 DNM	Dynamin-1 (EC 3.6.5.5)	3.6.5.5	Homo sapiens	Zellweger Syndrome,Seizure Disorder,Optic Nerve Disease,Cohen Syndrome,Myopathy, Centronuclear, 1,Undetermined Early-Onset Epileptic Encephalopathy,Peroxisome Biogenesis Disorder 1b,Optic Atrophy 1,Charcot-Marie-Tooth Disease,Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant 2,Neuronal Intranuclear Inclusion Disease,Centronuclear Myopathy,Disease Of Mental Health,Neuropathy, Hereditary Sensory, Type Id,Aceruloplasminemia,Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive,Lennox-Gastaut Syndrome,Early Infantile Epileptic Encephalopathy,Charcot-Marie-Tooth Disease, Dominant Intermediate B,Developmental And Epileptic Encephalopathy 31,Ceroid Lipofuscinosis, Neuronal, 4a, Autosomal Recessive,Rett Syndrome	6dlu_p	Q05193	ENSG00000106976	DNM1	100.00	1.00E-50	1.20E-54	433.90	1	1
YLL001W	DNM1	SGDID:S000003924	DNM1L DLP1 DRP1	Dynamin-1-like protein (EC 3.6.5.5) (Dnm1p/Vps1p-like protein) (DVLP) (Dynamin family member proline-rich carboxyl-terminal domain less) (Dymple) (Dynamin-like protein) (Dynamin-like protein 4) (Dynamin-like protein IV) (HdynIV) (Dynamin-related protein 1)	3.6.5.5	Homo sapiens	Myopathy, Lactic Acidosis, And Sideroblastic Anemia,Zellweger Syndrome,Myopathy,Optic Nerve Disease,Scotoma,Cockayne Syndrome A,Alzheimer Disease,Mitochondrial Myopathy,Paroxysmal Dystonia,Hereditary Spastic Paraplegia,Skin Amelanotic Melanoma,Autosomal Recessive Spastic Ataxia,Optic Atrophy 1,Brain Cancer,Obesity Due To Melanocortin 4 Receptor Deficiency,Spastic Paraplegia 8,Charcot-Marie-Tooth Disease,Cranial Nerve Disease,Parkinson Disease, Late-Onset,Peripheral Nervous System Disease,Microcephaly,Encephalopathy,Tooth Disease,Myopathy, Lactic Acidosis, And Sideroblastic Anemia 2,Disease Of Mental Health,Body Mass Index Quantitative Trait Locus 11,Contractures, Pterygia, And Spondylocarpotarsal Fusion Syndrome 1a,Lactic Acidosis,Optic Atrophy With Or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, And Neuropathy,Spinocerebellar Ataxia 12,Optic Atrophy 5,Encephalopathy Due To Defective Mitochondrial And Peroxisomal Fission 1,Spastic Ataxia,Leigh Syndrome,3-Methylglutaconic Aciduria, Type Iii	4bej_b	O00429	ENSG00000087470	DNM1L	100.00	1.40E-40	1.80E-44	339.90	1	1
YLL001W	DNM1	SGDID:S000003924	Dynamin_M	Dynamin central region		pfam Family		PF01031				99.90	5.50E-30	7.10E-34	236.90	0	0