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YKR017C HEL1 / SGDID:S000001725

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	Flag Drosophila melanogaster
YKR017C	HEL1	SGDID:S000001725	PML MYL PP8675 RNF71 TRIM19	Protein PML (Promyelocytic leukemia protein) (RING finger protein 71) (Tripartite motif-containing protein 19)		Homo sapiens	Leukemia, Chronic Myeloid,Primary Biliary Cholangitis,Leukemia,Leukemia, Acute Myeloid,Leukemia, Acute Lymphoblastic,Influenza,Herpes Simplex,Breast Cancer,Neuronal Intranuclear Inclusion Disease,Rabies,Dentatorubral-Pallidoluysian Atrophy,Acute Promyelocytic Leukemia,Nijmegen Breakage Syndrome,Mulibrey Nanism,Bloom Syndrome	1bor_a	P29590			97.30	3.00E-07	2.10E-11	63.60	1	1	0
YKR017C	HEL1	SGDID:S000001725	PRKN2 LOC105225264	PRKN2 LOC105225264		Bactrocera dorsalis		6djw_a	A0A034W4L8			98.30	1.90E-10	1.40E-14	113.80	0	0	0
YKR017C	HEL1	SGDID:S000001725	8230172 Phum_PHUM233570	8230172 Phum_PHUM233570	2.3.2.-	Pediculus humanus		5caw_a	E0VIU9			99.80	5.50E-25	4.00E-29	218.70	0	0	0
YKR017C	HEL1	SGDID:S000001725	PRKN PARK2	E3 ubiquitin-protein ligase parkin (Parkin) (EC 2.3.2.31) (Parkin RBR E3 ubiquitin-protein ligase) (Parkinson juvenile disease protein 2) (Parkinson disease protein 2)	2.3.2.31	Homo sapiens	Progressive Myoclonus Epilepsy,Supranuclear Palsy, Progressive, 1,Retinitis Pigmentosa,Rem Sleep Behavior Disorder,Lung Cancer Susceptibility 3,Tremor,Optic Nerve Disease,Prion Disease,Gaucher'S Disease,Sphingolipidosis,Alzheimer Disease,Ulnar Nerve Lesion,Radial Nerve Lesion,Amyotrophic Lateral Sclerosis 1,Angelman Syndrome,Motor Neuron Disease,Movement Disease,Neurodegeneration With Brain Iron Accumulation,Testicular Disease,Leber Plus Disease,Essential Tremor,Choreatic Disease,Machado-Joseph Disease,Dementia,Optic Atrophy 1,Cerebellar Disease,Leukoencephalopathy, Hereditary Diffuse, With Spheroids,Parkin Type Of Early-Onset Parkinson Disease,Dystonia,Nervous System Disease,Ovarian Cancer,Charcot-Marie-Tooth Disease,Paratyphoid Fever,Parkinson Disease, Late-Onset,Peripheral Nervous System Disease,Parkinson Disease 3, Autosomal Dominant,Parkinson Disease 1, Autosomal Dominant,Tooth Disease,Pick Disease Of Brain,Postencephalitic Parkinson Disease,Autosomal Dominant Cerebellar Ataxia,Fanconi Anemia, Complementation Group A,Disease Of Mental Health,Gaucher Disease, Type I,Toxic Encephalopathy,Body Mass Index Quantitative Trait Locus 11,Dentatorubral-Pallidoluysian Atrophy,Meier-Gorlin Syndrome 2,Dementia, Lewy Body,Dystonia 12,Schizophrenia,Ophthalmomyiasis,Restless Legs Syndrome,Parkinson Disease 21,Kufor-Rakeb Syndrome,Leprosy 3,Focal Dystonia,Parkinson Disease 10,Attention Deficit-Hyperactivity Disorder,Autism Spectrum Disorder,Multiple System Atrophy 1,Color Agnosia,Leber Hereditary Optic Neuropathy, Modifier Of,Leprosy 2,Mitochondrial Complex I Deficiency, Nuclear Type 1,Epilepsy, Idiopathic Generalized 9,Ptosis,Rett Syndrome,Myoclonic Epilepsy Of Lafora,Autism,Juvenile-Onset Parkinson'S Disease,Early-Onset Parkinson'S Disease,Parkinson Disease 2, Autosomal Recessive Juvenile,Lung Cancer,Parkinson Disease 15, Autosomal Recessive Early-Onset	4i1f_a	O60260	ENSG00000185345	PRKN	99.80	2.80E-25	2.00E-29	221.20	1	1	0
YKR017C	HEL1	SGDID:S000001725	MYCBP2 KIAA0916 PAM	E3 ubiquitin-protein ligase MYCBP2 (EC 2.3.2.33) (Myc-binding protein 2) (Protein associated with Myc)	2.3.2.33	Homo sapiens	Cerebral Degeneration,Reticulate Acropigmentation Of Kitamura,Pelizaeus-Merzbacher Disease,Hypomyelinating Leukodystrophy	5o6c_a	O75592	ENSG00000005810	MYCBP2	99.20	1.40E-15	1.00E-19	145.40	1	1	0
YKR017C	HEL1	SGDID:S000001725	park parkin CG10523	E3 ubiquitin-protein ligase parkin (EC 2.3.2.31)	2.3.2.31	Drosophila melanogaster		2lwr_a	Q7KTX7			97.80	1.50E-08	1.10E-12	74.00	0	0	1
YKR017C	HEL1	SGDID:S000001725	RNF31 ZIBRA	E3 ubiquitin-protein ligase RNF31 (EC 2.3.2.31) (HOIL-1-interacting protein) (HOIP) (RING finger protein 31) (RING-type E3 ubiquitin transferase RNF31) (Zinc in-between-RING-finger ubiquitin-associated domain protein)	2.3.2.31	Homo sapiens	Autoinflammation, Panniculitis, And Dermatosis Syndrome,Immunodeficiency 11,Glycogen Storage Disease Iv,Polyglucosan Body Myopathy 1 With Or Without Immunodeficiency,Tooth Agenesis,Incontinentia Pigmenti	4ljo_a	Q96EP0	ENSG00000092098	RNF31	97.50	1.10E-07	7.50E-12	85.80	1	1	0
YKR017C	HEL1	SGDID:S000001725	TRAF6 RNF85	TNF receptor-associated factor 6 (EC 2.3.2.27) (E3 ubiquitin-protein ligase TRAF6) (Interleukin-1 signal transducer) (RING finger protein 85) (RING-type E3 ubiquitin transferase TRAF6)	2.3.2.27	Homo sapiens	Diabetes Mellitus,Ectodermal Dysplasia,B-Cell Lymphoma,Toxoplasmosis,Noonan Syndrome 1,Paget'S Disease Of Bone,Osteoporosis,Osteopetrosis,Cone-Rod Dystrophy 2,Type 2 Diabetes Mellitus,Streptococcus Pneumonia,Ectodermal Dysplasia 10a, Hypohidrotic/Hair/Nail Type, Autosomal Dominant,Malaria,Inflammatory Bowel Disease,Tooth Agenesis,Lymphoma, Mucosa-Associated Lymphoid Type,Immunodeficiency With Hyper-Igm, Type 3,Lymphoma,Incontinentia Pigmenti,Systemic Lupus Erythematosus,Lung Cancer	3hcs_b	Q9Y4K3	ENSG00000175104	TRAF6	97.20	3.70E-07	2.80E-11	78.90	1	1	0
YKR017C	HEL1	SGDID:S000001725	ARIH1 ARI MOP6 UBCH7BP HUSSY-27	E3 ubiquitin-protein ligase ARIH1 (EC 2.3.2.31) (H7-AP2) (HHARI) (Monocyte protein 6) (MOP-6) (Protein ariadne-1 homolog) (ARI-1) (UbcH7-binding protein) (UbcM4-interacting protein) (Ubiquitin-conjugating enzyme E2-binding protein 1)	2.3.2.31	Homo sapiens	Parkinson Disease, Late-Onset,Glycogen Storage Disease Iv,Meester-Loeys Syndrome,Juvenile-Onset Parkinson'S Disease	5udh_a	Q9Y4X5	ENSG00000166233	ARIH1	100.00	1.60E-49	1.20E-53	419.20	1	1	0