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YDR019C GCV1 / SGDID:S000002426

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 Escherichia coli
YDR019C	GCV1	SGDID:S000002426	gcvT yqhI BSU24570	Aminomethyltransferase (EC 2.1.2.10) (Glycine cleavage system T protein)	2.1.2.10	Bacillus subtilis		1yx2_b	P54378			100.00	6.00E-62	4.00E-66	448.10	0	0	0
YDR019C	GCV1	SGDID:S000002426	gcvT b2905 JW2873	Aminomethyltransferase (EC 2.1.2.10) (Glycine cleavage system T protein)	2.1.2.10	Escherichia coli		1vlo_a	P27248			100.00	1.60E-59	1.00E-63	433.50	0	0	1
YDR019C	GCV1	SGDID:S000002426	dmg	Dimethylglycine oxidase (DMGO) (EC 1.5.3.10)	1.5.3.10	Arthrobacter globiformis		1pj5_a	Q9AGP8			100.00	1.00E-58	6.60E-63	471.40	0	0	0
YDR019C	GCV1	SGDID:S000002426	gcvT PH1146	Probable aminomethyltransferase (EC 2.1.2.10) (Glycine cleavage system T protein)	2.1.2.10	Pyrococcus horikoshii		1v5v_a	O58888			100.00	1.80E-56	1.20E-60	415.70	0	0	0
YDR019C	GCV1	SGDID:S000002426	IBA57 C1orf69	Putative transferase CAF17, mitochondrial (EC 2.1.-.-) (Iron-sulfur cluster assembly factor homolog)	2.1.-.-	Homo sapiens	Multiple Mitochondrial Dysfunctions Syndrome,Paraplegia,Myopathy,Spastic Paraplegia 55, Autosomal Recessive,Hereditary Spastic Paraplegia,Leukodystrophy,Multiple Mitochondrial Dysfunctions Syndrome 3,Combined Oxidative Phosphorylation Deficiency 19,Lactic Acidosis,Anemia, Sideroblastic, 1,Multiple Mitochondrial Dysfunctions Syndrome 1,Glycine Encephalopathy,Multiple Mitochondrial Dysfunctions Syndrome 2 With Hyperglycinemia,Multiple Mitochondrial Dysfunctions Syndrome 4,Spastic Paraplegia 74, Autosomal Recessive,Pyruvate Dehydrogenase E1-Alpha Deficiency	6geu_a	Q5T440			100.00	3.90E-44	2.60E-48	321.10	1	1	0
YDR019C	GCV1	SGDID:S000002426	gcvT BH12840	gcvT BH12840		Bartonella henselae		3gir_a	A0A0H3M6H9			100.00	8.40E-62	5.60E-66	449.70	0	0	0
YDR019C	GCV1	SGDID:S000002426	soxA	soxA		Stenotrophomonas maltophilia		2gag_a	Q3ZDQ8			100.00	2.30E-56	1.50E-60	459.10	0	0	0
YDR019C	GCV1	SGDID:S000002426	AMT GCST	Aminomethyltransferase, mitochondrial (EC 2.1.2.10) (Glycine cleavage system T protein) (GCVT)	2.1.2.10	Homo sapiens	Histidine Metabolism Disease,Cohen Syndrome,T-Cell Lymphoblastic Leukemia/Lymphoma,Cystathioninuria,Kluver-Bucy Syndrome,Hypomagnesemia 1, Intestinal,Sucrase-Isomaltase Deficiency, Congenital,Atypical Glycine Encephalopathy,Early Myoclonic Encephalopathy,Cutis Laxa, Autosomal Dominant 1,Phosphoserine Aminotransferase Deficiency,Histidinemia,Carrion'S Disease,Neural Tube Defects,Glycine Encephalopathy,Mullegama-Klein-Martinez Syndrome,Autosomal Recessive Disease,Cutis Laxa, Autosomal Dominant 2,Dehydrated Hereditary Stomatocytosis 1 With Or Without Pseudohyperkalemia And/Or Perinatal Edema,Frank-Ter Haar Syndrome,Cutis Laxa, Autosomal Dominant 3,Pentosuria	1wsr_b	P48728	ENSG00000145020	AMT	100.00	1.60E-58	1.00E-62	426.10	1	1	0
YDR019C	GCV1	SGDID:S000002426	gcvT TM_0211	Aminomethyltransferase (EC 2.1.2.10) (Glycine cleavage system T protein)	2.1.2.10	Thermotoga maritima		1wor_a	Q9WY54			100.00	1.40E-59	9.00E-64	432.20	0	0	0
YDR019C	GCV1	SGDID:S000002426	ygfZ yzzW b2898 JW2866	tRNA-modifying protein YgfZ		Escherichia coli		1nrk_a	P0ADE8			100.00	1.10E-49	7.20E-54	360.00	0	0	1
YDR019C	GCV1	SGDID:S000002426	Dmgdh	Dimethylglycine dehydrogenase, mitochondrial (EC 1.5.8.4) (ME2GLYDH)	1.5.8.4	Rattus norvegicus		4paa_a	Q63342			100.00	3.60E-58	2.40E-62	468.00	0	0	0
YDR019C	GCV1	SGDID:S000002426	ligM SLG_12740	Vanillate/3-O-methylgallate O-demethylase (Vanillate/3MGA O-demethylase) (EC 2.1.1.341)	2.1.1.341	Sphingobium sp.		5tl4_c	G2IQS7			100.00	2.60E-50	1.70E-54	377.40	0	0	0
YDR019C	GCV1	SGDID:S000002426	dmdA SAR11_0246	Dimethylsulfonioproprionate demethylase DmdA (EC 2.1.1.269)	2.1.1.269	Pelagibacter ubique		3tfi_a	Q4FP21			100.00	1.30E-57	8.30E-62	419.40	0	0	0