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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YPL138C | SPP1 | SGDID:S000006059 | SIZ1 Os05g0125000 LOC_Os05g03430 OSJNBb0079L11.3 |
E3 SUMO-protein ligase SIZ1 (EC 2.3.2.-) (E3 SUMO-protein transferase SIZ1) |
2.3.2.- | Oryza sativa | 2rsd_a | Q6L4L4 | 95.70 | 0.00011 | 8.80E-09 | 48.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YPL138C | SPP1 | SGDID:S000006059 | KMT2D ALR MLL2 MLL4 |
Histone-lysine N-methyltransferase 2D (Lysine N-methyltransferase 2D) (EC 2.1.1.354) (ALL1-related protein) (Myeloid/lymphoid or mixed-lineage leukemia protein 2) |
2.1.1.354 | Homo sapiens | Charge Syndrome,Plasma Cell Neoplasm,Cold Agglutinin Disease,Kleefstra Syndrome,Cavernous Sinus Meningioma,Rasopathy,Holoprosencephaly,Hypoplastic Left Heart Syndrome,Leukemia, Acute Myeloid,Dandy-Walker Syndrome,Rubinstein Taybi Like Syndrome,Breast Malignant Phyllodes Tumor,Microphthalmia,Microcephaly,Weaver Syndrome,Sotos Syndrome 1,Alacrima, Achalasia, And Mental Retardation Syndrome,Fanconi Anemia, Complementation Group A,Disease Of Mental Health,Complement Component C1s Deficiency,Chromosome 16p13.3 Deletion Syndrome, Proximal,Mental Retardation, Autosomal Dominant 26,Childhood Medulloblastoma,Lung Squamous Cell Carcinoma,Smith-Magenis Syndrome,Spinocerebellar Ataxia 2,Tetralogy Of Fallot,Peripheral T-Cell Lymphoma,Congenital Disorder Of Glycosylation, Type Ig,Autism Spectrum Disorder,Lymphoma,Kabuki Syndrome 1,Kbg Syndrome,Methylmalonic Acidemia And Homocysteinemia, Cblx Type,Scoliosis,Autosomal Dominant Non-Syndromic Intellectual Disability,Myeloma, Multiple,Medulloblastoma,Isolated Growth Hormone Deficiency Type Iii,Postaxial Acrofacial Dysostosis |
6o7g_b | O14686 | ENSG00000167548 | KMT2D | 95.00 | 0.00046 | 3.60E-08 | 44.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YPL138C | SPP1 | SGDID:S000006059 | lid CG9088 |
Lysine-specific demethylase lid (EC 1.14.11.67) (Histone demethylase lid) (Jumonji/ARID domain-containing protein lid) (Protein little imaginal disks) (Retinoblastoma-binding protein 2 homolog) ([histone H3]-trimethyl-L-lysine(4) demethylase lid) |
1.14.11.67 | Drosophila melanogaster | 2miq_a | Q9VMJ7 | 95.20 | 0.00033 | 2.50E-08 | 49.60 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | |||
YPL138C | SPP1 | SGDID:S000006059 | SHPRH KIAA2023 |
E3 ubiquitin-protein ligase SHPRH (EC 2.3.2.27) (EC 3.6.4.-) (RING-type E3 ubiquitin transferase SHPRH) (SNF2, histone-linker, PHD and RING finger domain-containing helicase) |
2.3.2.27 | Homo sapiens | Xeroderma Pigmentosum, Variant Type |
2m85_a | Q149N8 | ENSG00000146414 | SHPRH | 95.50 | 0.00017 | 1.30E-08 | 48.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YPL138C | SPP1 | SGDID:S000006059 | BAZ1B WBSC10 WBSCR10 WBSCR9 WSTF |
Tyrosine-protein kinase BAZ1B (EC 2.7.10.2) (Bromodomain adjacent to zinc finger domain protein 1B) (Williams syndrome transcription factor) (Williams-Beuren syndrome chromosomal region 10 protein) (Williams-Beuren syndrome chromosomal region 9 protein) (hWALp2) |
2.7.10.2 | Homo sapiens | Myopathy, Centronuclear, 1,Klippel-Feil Syndrome,Helsmoortel-Van Der Aa Syndrome,Supravalvular Aortic Stenosis,Williams-Beuren Syndrome,Autosomal Dominant Non-Syndromic Intellectual Disability,Chromosomal Deletion Syndrome |
1f62_a | Q9UIG0 | 96.90 | 2.40E-06 | 1.70E-10 | 54.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
YPL138C | SPP1 | SGDID:S000006059 | ASH2L ASH2L1 |
Set1/Ash2 histone methyltransferase complex subunit ASH2 (ASH2-like protein) |
Homo sapiens | Kleefstra Syndrome,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Kabuki Syndrome 1 |
3rsn_a | Q9UBL3 | ENSG00000129691 | ASH2L | 98.70 | 4.60E-12 | 3.40E-16 | 105.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YPL138C | SPP1 | SGDID:S000006059 | KMT2A ALL1 CXXC7 HRX HTRX MLL MLL1 TRX1 |
Histone-lysine N-methyltransferase 2A (Lysine N-methyltransferase 2A) (EC 2.1.1.354) (ALL-1) (CXXC-type zinc finger protein 7) (Myeloid/lymphoid or mixed-lineage leukemia) (Myeloid/lymphoid or mixed-lineage leukemia protein 1) (Trithorax-like protein) (Zinc finger protein HRX) [Cleaved into: MLL cleavage product N320 (N-terminal cleavage product of 320 kDa) (p320); MLL cleavage product C180 (C-terminal cleavage product of 180 kDa) (p180)] |
2.1.1.354 | Homo sapiens | Childhood Acute Lymphocytic Leukemia,Lymphoblastic Lymphoma,Hypertrichosis,Chronic Neutrophilic Leukemia,Chronic Myelomonocytic Leukemia,Cornelia De Lange Syndrome,Leukemia, Chronic Myeloid,Acute Myeloid Leukemia With T(9;11)(P22;Q23),B-Lymphoblastic Leukemia/Lymphoma,B-Lymphoblastic Leukemia/Lymphoma With Bcr-Abl1,B-Lymphoblastic Leukemia/Lymphoma With Iamp21,Rare Genetic Intellectual Disability,Myeloproliferative Neoplasm,Leukemia,Pancytopenia,Mixed Phenotype Acute Leukemia,Childhood Leukemia,Acute Leukemia,Leukemia, Acute Myeloid,Acute Myeloid Leukemia With 11q23 Abnormalities,Intravascular Large B-Cell Lymphoma,Familial Isolated Trichomegaly,Myelodysplastic/Myeloproliferative Neoplasm,Hematologic Cancer,Leukemia, Acute Lymphoblastic,Ring Chromosome 21,Acute Megakaryoblastic Leukemia Without Down Syndrome,Rubinstein Taybi Like Syndrome,Central Nervous System Leukemia,Monocytic Leukemia,Ring Chromosome,Myeloid Sarcoma,Myeloid Leukemia,Acute Megakaryocytic Leukemia,Acute Monoblastic Leukemia,Colon Leiomyoma,Cytogenetically Normal Acute Myeloid Leukemia,Microcephaly,Hypoxia,Chronic Granulomatous Disease,Alacrima, Achalasia, And Mental Retardation Syndrome,Leukemia, Acute Lymphoblastic 3,Disease Of Mental Health,Cornelia De Lange Syndrome 1,Lymphoma, Non-Hodgkin, Familial,Wiedemann-Steiner Syndrome,Myelodysplastic Syndrome,Hairy Elbows,Acute Promyelocytic Leukemia,Wilms Tumor 1,Kabuki Syndrome 1,Kbg Syndrome,Leukemia, Acute Monocytic,Leukemia, Chronic Lymphocytic,Juvenile Myelomonocytic Leukemia,Autosomal Dominant Non-Syndromic Intellectual Disability,Autism |
2kyu_a | Q03164 | ENSG00000118058 | KMT2A | 95.20 | 0.00036 | 2.80E-08 | 45.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YPL138C | SPP1 | SGDID:S000006059 | KMT2E MLL5 |
Inactive histone-lysine N-methyltransferase 2E (Inactive lysine N-methyltransferase 2E) (Myeloid/lymphoid or mixed-lineage leukemia protein 5) |
Homo sapiens | Epilepsy,Non-Specific Syndromic Intellectual Disability,Kleefstra Syndrome 2,Disease Of Mental Health,O'Donnell-Luria-Rodan Syndrome,Cerebroretinal Microangiopathy With Calcifications And Cysts 1,Kabuki Syndrome 1,Agenesis Of Corpus Callosum, Cardiac, Ocular, And Genital Syndrome,Autism |
2lv9_a | Q8IZD2 | ENSG00000005483 | KMT2E | 95.40 | 0.00024 | 1.80E-08 | 51.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YPL138C | SPP1 | SGDID:S000006059 | SET3 YKR029C |
SET domain-containing protein 3 |
Saccharomyces cerevisiae | 5tdr_a | P36124 | 96.00 | 4.90E-05 | 3.80E-09 | 50.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YPL138C | SPP1 | SGDID:S000006059 | BCL9L DLNB11 |
B-cell CLL/lymphoma 9-like protein (B-cell lymphoma 9-like protein) (BCL9-like protein) (Protein BCL9-2) |
Homo sapiens | Acinar Cell Cystadenocarcinoma |
2xb1_c | Q86UU0 | ENSG00000186174 | BCL9L | 96.30 | 1.90E-05 | 1.40E-09 | 57.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YPL138C | SPP1 | SGDID:S000006059 | PHF2 CENP-35 KIAA0662 |
Lysine-specific demethylase PHF2 (EC 1.14.11.-) (GRC5) (PHD finger protein 2) |
1.14.11.- | Homo sapiens | Dissociative Disorder,Culler-Jones Syndrome |
3kqi_a | O75151 | ENSG00000197724 | PHF2 | 95.00 | 0.0005 | 4.00E-08 | 45.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YPL138C | SPP1 | SGDID:S000006059 | MTF2 PCL2 |
Metal-response element-binding transcription factor 2 (Metal regulatory transcription factor 2) (Metal-response element DNA-binding protein M96) (Polycomb-like protein 2) (hPCl2) |
Homo sapiens | Weaver Syndrome,Retinitis Pigmentosa 48,Hereditary Lymphedema,Hereditary Lymphedema I |
5xfr_a | Q9Y483 | ENSG00000143033 | MTF2 | 98.20 | 4.90E-10 | 3.80E-14 | 101.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YPL138C | SPP1 | SGDID:S000006059 | Pcl CG5109 |
Polycomb protein Pcl (Polycomblike protein) |
Drosophila melanogaster | 5oqd_c | Q24459 | 98.60 | 1.90E-11 | 1.40E-15 | 104.30 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | ||||
YPL138C | SPP1 | SGDID:S000006059 | EBS At4g22140 F1N20.240 |
Chromatin remodeling protein EBS (Protein EARLY BOLTING IN SHORT DAYS) |
Arabidopsis thaliana | 5z8l_a | F4JL28 | 95.10 | 0.00045 | 3.40E-08 | 58.00 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | ||||
YPL138C | SPP1 | SGDID:S000006059 | PHF8 KIAA1111 ZNF422 |
Histone lysine demethylase PHF8 (EC 1.14.11.27) (EC 1.14.11.65) (PHD finger protein 8) ([histone H3]-dimethyl-L-lysine(36) demethylase PHF8) ([histone H3]-dimethyl-L-lysine(9) demethylase PHF8) |
1.14.11.27,1.14.11.65, | Homo sapiens | Cleft Lip,Cleft Lip/Palate,X-Linked Intellectual Disability, Siderius Type,Sotos Syndrome 1,Alacrima, Achalasia, And Mental Retardation Syndrome,Van Der Woude Syndrome 1,Disease Of Mental Health,Orofacial Cleft,Non-Syndromic X-Linked Intellectual Disability,Borjeson-Forssman-Lehmann Syndrome,Acute Promyelocytic Leukemia,Kabuki Syndrome 1,Syndromic X-Linked Intellectual Disability,Autism,Syndromic X-Linked Intellectual Disability Siderius Type |
3kv4_a | Q9UPP1 | ENSG00000172943 | PHF8 | 95.60 | 0.00014 | 1.10E-08 | 67.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YPL138C | SPP1 | SGDID:S000006059 | BPTF FAC1 FALZ |
Nucleosome-remodeling factor subunit BPTF (Bromodomain and PHD finger-containing transcription factor) (Fetal Alz-50 clone 1 protein) (Fetal Alzheimer antigen) |
Homo sapiens | Seizure Disorder,Alzheimer Disease,Non-Specific Syndromic Intellectual Disability,17q24.2 Microdeletion Syndrome,Microcephaly,Alacrima, Achalasia, And Mental Retardation Syndrome,Neurodevelopmental Disorder With Dysmorphic Facies And Distal Limb Anomalies,Disease Of Mental Health,Legius Syndrome,Autism |
2ri7_a | Q12830 | ENSG00000171634 | BPTF | 95.10 | 0.0004 | 3.20E-08 | 54.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YPL138C | SPP1 | SGDID:S000006059 | PHF20 C20orf104 GLEA2 HCA58 NZF TZP |
PHD finger protein 20 (Glioma-expressed antigen 2) (Hepatocellular carcinoma-associated antigen 58) (Novel zinc finger protein) (Transcription factor TZP) |
Homo sapiens | Hepatocellular Carcinoma,Glycogen Storage Disease Iv |
5tab_a | Q9BVI0 | ENSG00000025293 | PHF20 | 95.10 | 0.0004 | 3.10E-08 | 42.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YPL138C | SPP1 | SGDID:S000006059 | SPP1 CPS40 SAF41 YPL138C |
COMPASS component SPP1 (Complex proteins associated with SET1 protein SPP1) (Set1C component SPP1) (Suppressor of PRP protein 1) |
Saccharomyces cerevisiae | 6bx3_f | Q03012 | 100.00 | 8.60E-49 | 6.20E-53 | 347.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YPL138C | SPP1 | SGDID:S000006059 | PHF13 |
PHD finger protein 13 (Survival time-associated PHD finger protein in ovarian cancer 1) (SPOC1) |
Homo sapiens | Ovarian Cancer,Pick Disease Of Brain,Chromosome 1p36 Deletion Syndrome,Ovarian Cancer 1 |
3o70_a | Q86YI8 | ENSG00000116273 | PHF13 | 95.50 | 0.00018 | 1.40E-08 | 47.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YPL138C | SPP1 | SGDID:S000006059 | BRD1 BRL BRPF2 |
Bromodomain-containing protein 1 (BR140-like protein) (Bromodomain and PHD finger-containing protein 2) |
Homo sapiens | Tuberculum Sellae Meningioma,Griscelli Syndrome, Type 3,Ohdo Syndrome, Sbbys Variant,Sella Turcica Neoplasm,Schizophrenia,Ohdo Syndrome |
2l43_a | O95696 | ENSG00000100425 | BRD1 | 95.00 | 0.00046 | 3.50E-08 | 48.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |