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YDL120W YFH1 / SGDID:S000002278

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
YDL120W	YFH1	SGDID:S000002278	FXN FRDA X25	Frataxin, mitochondrial (EC 1.16.3.1) (Friedreich ataxia protein) (Fxn) [Cleaved into: Frataxin intermediate form (i-FXN); Frataxin(56-210) (m56-FXN); Frataxin(78-210) (d-FXN) (m78-FXN); Frataxin mature form (Frataxin(81-210)) (m81-FXN)]	1.16.3.1	Homo sapiens	Bone Structure Disease,Heart Disease,Sideroblastic Anemia,Retinitis Pigmentosa,Optic Nerve Disease,Diabetes Mellitus,Neuromuscular Disease,Hypertrophic Cardiomyopathy,Myotonic Disease,Myotonic Dystrophy 1,Neurodegeneration With Brain Iron Accumulation,Spastic Ataxia, Charlevoix-Saguenay Type,Tertiary Neurosyphilis,Mitochondrial Dna Depletion Syndrome 7,Sensory Peripheral Neuropathy,Choreatic Disease,Spinocerebellar Ataxia 1,Tabes Dorsalis,Mitochondrial Complex Iii Deficiency, Nuclear Type 2,Cerebellar Disease,Mitochondrial Disorders,Friedreich Ataxia 2,Peripheral Nervous System Disease,Ataxia With Vitamin 3 Deficiency,Myotonic Dystrophy 2,Deficiency Anemia,Autosomal Dominant Cerebellar Ataxia,Spinocerebellar Ataxia 10,Friedreich Ataxia,Disease Of Mental Health,Dentatorubral-Pallidoluysian Atrophy,Aceruloplasminemia,Mental Retardation, X-Linked, With Cerebellar Hypoplasia And Distinctive Facial Appearance,Hemochromatosis, Type 1,Fragile X Syndrome,Anemia, Sideroblastic, 1,Spinocerebellar Ataxia 6,Spinocerebellar Ataxia, Autosomal Recessive, With Axonal Neuropathy 2,Neurodegeneration With Brain Iron Accumulation 3,Autosomal Recessive Disease,Autosomal Genetic Disease,Anemia, Sideroblastic, And Spinocerebellar Ataxia,Perrault Syndrome,Fragile X-Associated Tremor/Ataxia Syndrome,Marinesco-Sjogren Syndrome,Autosomal Recessive Cerebellar Ataxia,Hereditary Ataxia,Spastic Ataxia,X-Linked Hereditary Ataxia,Leber Hereditary Optic Neuropathy, Modifier Of,Mitochondrial Complex I Deficiency, Nuclear Type 1,Scoliosis,Spinal And Bulbar Muscular Atrophy, X-Linked 1,Ataxia, Early-Onset, With Oculomotor Apraxia And Hypoalbuminemia,Kearns-Sayre Syndrome,Leigh Syndrome,3-Methylglutaconic Aciduria, Type Iii	1ekg_a	Q16595			100.00	1.30E-35	1.10E-39	224.10	1	1
YDL120W	YFH1	SGDID:S000002278	cyaY Ping_0042	Iron-sulfur cluster assembly protein CyaY		Psychromonas ingrahamii		4hs5_b	A1SR01			99.90	2.00E-32	1.70E-36	201.20	0	0
YDL120W	YFH1	SGDID:S000002278	cyaY BceJ2315_02750 BCAL0273	Iron-sulfur cluster assembly protein CyaY		Burkholderia cenocepacia		4jpd_a	B4E5Z6			99.90	1.30E-33	1.10E-37	209.90	0	0
YDL120W	YFH1	SGDID:S000002278	CTHT_0015430	CTHT_0015430	1.16.3.1	Chaetomium thermophilum		6fco_b	G0S1Z8			99.90	1.40E-32	1.10E-36	209.10	0	0
YDL120W	YFH1	SGDID:S000002278	ISU1 NUA1 YPL135W	Iron sulfur cluster assembly protein 1, mitochondrial (Iron sulfur cluster scaffold protein 1)		Saccharomyces cerevisiae		5tre_l	Q03020			100.00	1.40E-35	1.10E-39	223.80	0	0
YDL120W	YFH1	SGDID:S000002278	YFH1 YDL120W	Frataxin homolog, mitochondrial (EC 1.16.3.1) [Cleaved into: Frataxin homolog intermediate form]	1.16.3.1	Saccharomyces cerevisiae		3oeq_a	Q07540			100.00	3.70E-36	3.10E-40	227.60	0	0
YDL120W	YFH1	SGDID:S000002278	FXN FRDA X25	Frataxin, mitochondrial (EC 1.16.3.1) (Friedreich ataxia protein) (Fxn) [Cleaved into: Frataxin intermediate form (i-FXN); Frataxin(56-210) (m56-FXN); Frataxin(78-210) (d-FXN) (m78-FXN); Frataxin mature form (Frataxin(81-210)) (m81-FXN)]	1.16.3.1	Homo sapiens	Bone Structure Disease,Heart Disease,Sideroblastic Anemia,Retinitis Pigmentosa,Optic Nerve Disease,Diabetes Mellitus,Neuromuscular Disease,Hypertrophic Cardiomyopathy,Myotonic Disease,Myotonic Dystrophy 1,Neurodegeneration With Brain Iron Accumulation,Spastic Ataxia, Charlevoix-Saguenay Type,Tertiary Neurosyphilis,Mitochondrial Dna Depletion Syndrome 7,Sensory Peripheral Neuropathy,Choreatic Disease,Spinocerebellar Ataxia 1,Tabes Dorsalis,Mitochondrial Complex Iii Deficiency, Nuclear Type 2,Cerebellar Disease,Mitochondrial Disorders,Friedreich Ataxia 2,Peripheral Nervous System Disease,Ataxia With Vitamin 3 Deficiency,Myotonic Dystrophy 2,Deficiency Anemia,Autosomal Dominant Cerebellar Ataxia,Spinocerebellar Ataxia 10,Friedreich Ataxia,Disease Of Mental Health,Dentatorubral-Pallidoluysian Atrophy,Aceruloplasminemia,Mental Retardation, X-Linked, With Cerebellar Hypoplasia And Distinctive Facial Appearance,Hemochromatosis, Type 1,Fragile X Syndrome,Anemia, Sideroblastic, 1,Spinocerebellar Ataxia 6,Spinocerebellar Ataxia, Autosomal Recessive, With Axonal Neuropathy 2,Neurodegeneration With Brain Iron Accumulation 3,Autosomal Recessive Disease,Autosomal Genetic Disease,Anemia, Sideroblastic, And Spinocerebellar Ataxia,Perrault Syndrome,Fragile X-Associated Tremor/Ataxia Syndrome,Marinesco-Sjogren Syndrome,Autosomal Recessive Cerebellar Ataxia,Hereditary Ataxia,Spastic Ataxia,X-Linked Hereditary Ataxia,Leber Hereditary Optic Neuropathy, Modifier Of,Mitochondrial Complex I Deficiency, Nuclear Type 1,Scoliosis,Spinal And Bulbar Muscular Atrophy, X-Linked 1,Ataxia, Early-Onset, With Oculomotor Apraxia And Hypoalbuminemia,Kearns-Sayre Syndrome,Leigh Syndrome,3-Methylglutaconic Aciduria, Type Iii	3t3l_a	Q16595	ENSG00000165060	FXN	99.90	2.90E-33	2.40E-37	213.20	1	1
YDL120W	YFH1	SGDID:S000002278	ISCU NIFUN	Iron-sulfur cluster assembly enzyme ISCU, mitochondrial (NifU-like N-terminal domain-containing protein) (NifU-like protein)		Homo sapiens	Multiple Mitochondrial Dysfunctions Syndrome,Myopathy,Mitochondrial Myopathy,Cerebellar Disease,Myopathy With Deficiency Of Iscu,Siderosis,Combined Oxidative Phosphorylation Deficiency 19,Lactic Acidosis,Anemia, Sideroblastic, 1,Multiple Mitochondrial Dysfunctions Syndrome 1,Mend Syndrome,Anemia, Sideroblastic, And Spinocerebellar Ataxia,Autosomal Recessive Cerebellar Ataxia,Myopathy With Lactic Acidosis, Hereditary	5kz5_b	Q9H1K1	ENSG00000136003	ISCU	100.00	1.90E-37	1.50E-41	246.60	1	1