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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YBR233W | PBP2 | SGDID:S000000437 | KHDC4 BLOM7 KIAA0907 SNORA80EHG |
KH homology domain-containing protein 4 (Brings lots of money 7) (Pre-mRNA splicing factor protein KHDC4) |
Homo sapiens | 2yqr_a | Q7Z7F0 | 96.00 | 5.90E-05 | 4.10E-09 | 56.90 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR233W | PBP2 | SGDID:S000000437 | KRR1 SCRG_05350 |
KRR1 small subunit processome component (KRR-R motif-containing protein 1) (Ribosomal RNA assembly protein KRR1) |
Saccharomyces cerevisiae | 5wlc_nk | B3LU25 | 98.40 | 7.60E-11 | 5.10E-15 | 104.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR233W | PBP2 | SGDID:S000000437 | FUBP1 |
Far upstream element-binding protein 1 (FBP) (FUSE-binding protein 1) (DNA helicase V) (hDH V) |
Homo sapiens | Pediatric Meningioma,Temporal Lobe Neoplasm,Diffuse Astrocytoma,Mixed Glioma,Oligodendroglioma,Childhood Oligodendroglioma,Adult Oligodendroglioma,Hand, Foot And Mouth Disease,Mouth Disease,Brain Glioma |
1j4w_a | Q96AE4 | ENSG00000162613 | FUBP1 | 99.00 | 4.20E-14 | 3.00E-18 | 117.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR233W | PBP2 | SGDID:S000000437 | NOVA1 |
RNA-binding protein Nova-1 (Neuro-oncological ventral antigen 1) (Onconeural ventral antigen 1) (Paraneoplastic Ri antigen) (Ventral neuron-specific protein 1) |
Homo sapiens | Gait Apraxia,Low-Grade Astrocytoma,Paraneoplastic Polyneuropathy,Breast Cancer,Partial Fetal Alcohol Syndrome,Lung Cancer |
2anr_a | P51513 | ENSG00000139910 | NOVA1 | 99.00 | 1.30E-13 | 9.20E-18 | 114.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR233W | PBP2 | SGDID:S000000437 | gld-1 T23G11.3 |
Female germline-specific tumor suppressor gld-1 (Defective in germ line development protein 1) |
Caenorhabditis elegans | 2mjh_a | Q17339 | 96.70 | 5.60E-06 | 3.80E-10 | 64.80 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | ||||
YBR233W | PBP2 | SGDID:S000000437 | APE_0754.1 |
APE_0754.1 |
Aeropyrum pernix | 1tua_a | Q9YE16 | 98.70 | 5.20E-12 | 3.60E-16 | 106.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR233W | PBP2 | SGDID:S000000437 | NOVA2 ANOVA NOVA3 |
RNA-binding protein Nova-2 (Astrocytic NOVA1-like RNA-binding protein) (Neuro-oncological ventral antigen 2) |
Homo sapiens | Paraneoplastic Polyneuropathy,Fragile X Syndrome,Neurodevelopmental Disorder With Or Without Autistic Features And/Or Structural Brain Abnormalities |
1dtj_a | Q9UNW9 | 98.30 | 1.90E-10 | 1.30E-14 | 80.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YBR233W | PBP2 | SGDID:S000000437 | mina-1 C41G7.3 |
Messenger RNA-binding inhibitor of apoptosis 1 |
Caenorhabditis elegans | 6fbl_a | Q93367 | 97.10 | 8.10E-07 | 5.70E-11 | 63.20 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | ||||
YBR233W | PBP2 | SGDID:S000000437 | KRR1 YCL059C YCL59C |
KRR1 small subunit processome component (KRR-R motif-containing protein 1) (Ribosomal RNA assembly protein KRR1) |
Saccharomyces cerevisiae | 4qmf_b | P25586 | 98.60 | 1.70E-11 | 1.20E-15 | 102.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR233W | PBP2 | SGDID:S000000437 | NOVA2 ANOVA NOVA3 |
RNA-binding protein Nova-2 (Astrocytic NOVA1-like RNA-binding protein) (Neuro-oncological ventral antigen 2) |
Homo sapiens | Paraneoplastic Polyneuropathy,Fragile X Syndrome,Neurodevelopmental Disorder With Or Without Autistic Features And/Or Structural Brain Abnormalities |
1dtj_b | Q9UNW9 | ENSG00000104967 | NOVA2 | 96.90 | 2.70E-06 | 1.90E-10 | 58.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR233W | PBP2 | SGDID:S000000437 | PCBP1 |
Poly(rC)-binding protein 1 (Alpha-CP1) (Heterogeneous nuclear ribonucleoprotein E1) (hnRNP E1) (Nucleic acid-binding protein SUB2.3) |
Homo sapiens | Tremor, Hereditary Essential, 4,Burkitt Lymphoma,Deafness, Autosomal Recessive 17,Aceruloplasminemia |
1wvn_a | Q15365 | ENSG00000169564 | PCBP1 | 96.70 | 4.60E-06 | 3.20E-10 | 58.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR233W | PBP2 | SGDID:S000000437 | Fubp1 D3Ertd330e |
Far upstream element-binding protein 1 (FBP) (FUSE-binding protein 1) |
Mus musculus | 1x4n_a | Q91WJ8 | 96.80 | 3.40E-06 | 2.40E-10 | 60.30 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YBR233W | PBP2 | SGDID:S000000437 | PH1566 |
PH1566 |
Pyrococcus horikoshii | 2e3u_a | O59282 | 99.00 | 8.20E-14 | 5.70E-18 | 120.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR233W | PBP2 | SGDID:S000000437 | PNO1 |
RNA-binding protein PNO1 (Partner of NOB1) |
Homo sapiens | Diamond-Blackfan Anemia,Hermansky-Pudlak Syndrome 3 |
6g18_x | Q9NRX1 | ENSG00000186468 | RPS23 | 99.00 | 5.70E-14 | 3.90E-18 | 124.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR233W | PBP2 | SGDID:S000000437 | FMR1 |
Synaptic functional regulator FMR1 (Fragile X mental retardation protein 1) (FMRP) (Protein FMR-1) |
Homo sapiens | Learning Disability,Chromosomal Disease,Echolalia,Mutism,Retinitis Pigmentosa,Migraine With Or Without Aura 1,Fibromyalgia,Kagami-Ogata Syndrome,Tremor,Speech Disorder,Cataract 24,Phobia, Specific,Myotonic Disease,Gene Duplication Disease,Amyotrophic Lateral Sclerosis 1,Myotonic Dystrophy 1,Angelman Syndrome,Middle Cranial Fossa Meningioma,Intestinal Disaccharidase Deficiency,Muscular Dystrophy,Movement Disease,Spinocerebellar Ataxia 8,Myoclonic Cerebellar Dyssynergia,Essential Tremor,Influenza,Fmr1 Disorders,Spinocerebellar Ataxia 1,Dementia,Cerebellar Disease,Childhood Disintegrative Disease,Parkinson Disease, Late-Onset,Patella, Chondromalacia Of,Premature Menopause,Amenorrhea,Speech And Communication Disorders,Phobic Disorder,Myotonic Dystrophy 2,Chromosome 14q11-Q22 Deletion Syndrome,Schizoid Personality Disorder,Sotos Syndrome 1,Ovarian Disease,Alacrima, Achalasia, And Mental Retardation Syndrome,Autosomal Dominant Cerebellar Ataxia,Benign Epilepsy With Centrotemporal Spikes,Spinocerebellar Ataxia 10,Prader-Willi Syndrome,Social Phobia,Friedreich Ataxia,Turner Syndrome,Disease Of Mental Health,Lubs X-Linked Mental Retardation Syndrome,Dentatorubral-Pallidoluysian Atrophy,Meier-Gorlin Syndrome 2,Mental Retardation, X-Linked, With Cerebellar Hypoplasia And Distinctive Facial Appearance,Fragile X Tremor/Ataxia Syndrome,Fragile X Syndrome,Schizophrenia,Beckwith-Wiedemann Syndrome,Restless Legs Syndrome,Chromosome Xq27.3-Q28 Duplication Syndrome,Phelan-Mcdermid Syndrome,Digeorge Syndrome,X-Linked Monogenic Disease,Huntington Disease-Like 2,Kaufman Oculocerebrofacial Syndrome,Non-Syndromic X-Linked Intellectual Disability,Spinocerebellar Ataxia, X-Linked 3,Spinocerebellar Ataxia, X-Linked 4,Velocardiofacial Syndrome,Huntington Disease,Attention Deficit-Hyperactivity Disorder,Fragile X-Associated Tremor/Ataxia Syndrome,Williams-Beuren Syndrome,X-Linked Hereditary Ataxia,Specific Developmental Disorder,Pervasive Developmental Disorder,Autism Spectrum Disorder,Atypical Autism,Multiple System Atrophy 1,Epilepsy, Idiopathic Generalized 9,Mucopolysaccharidosis, Type Ii,Anxiety,Premature Ovarian Failure 1,Chromosomal Deletion Syndrome,Chromosomal Duplication Syndrome,Spinal And Bulbar Muscular Atrophy, X-Linked 1,Autism |
2qnd_b | Q06787 | ENSG00000102081 | FMR1 | 98.70 | 2.40E-12 | 1.70E-16 | 103.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR233W | PBP2 | SGDID:S000000437 | MEX3D KIAA2031 RKHD1 RNF193 |
RNA-binding protein MEX3D (RING finger and KH domain-containing protein 1) (RING finger protein 193) (TINO) |
Homo sapiens | Hemophagocytic Lymphohistiocytosis, Familial, 1,Hemophagocytic Lymphohistiocytosis, Familial, 2,Meckel Diverticulum |
2dgr_a | Q86XN8 | ENSG00000181588 | MEX3D | 96.10 | 4.40E-05 | 3.10E-09 | 52.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR233W | PBP2 | SGDID:S000000437 | PNO1 DIM2 CTHT_0030540 |
Pre-rRNA-processing protein PNO1 |
Chaetomium thermophilum | 5oql_h | G0S3T2 | 98.90 | 3.10E-13 | 2.10E-17 | 118.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR233W | PBP2 | SGDID:S000000437 | PNO1 DIM2 RRP20 YOR145C O3513 YOR3513C |
Pre-rRNA-processing protein PNO1 (Partner of NOB1) (Ribosomal RNA-processing protein 20) |
Saccharomyces cerevisiae | 6eml_p | Q99216 | 99.00 | 1.10E-13 | 7.60E-18 | 121.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR233W | PBP2 | SGDID:S000000437 | HNRNPK HNRPK |
Heterogeneous nuclear ribonucleoprotein K (hnRNP K) (Transformation up-regulated nuclear protein) (TUNP) |
Homo sapiens | Stomatitis,Melanomatosis,Neurodevelopmental Disorder-Craniofacial Dysmorphism-Cardiac Defect-Skeletal Anomalies Syndrome Due To 9q21.3 Microdeletion,Aplastic Anemia,Breast Cancer,Colorectal Cancer,Alacrima, Achalasia, And Mental Retardation Syndrome,Spinocerebellar Ataxia 10,Disease Of Mental Health,Fragile X Syndrome,Mouth Disease,Au-Kline Syndrome,Ptosis |
1zzi_a | P61978 | ENSG00000165119 | HNRNPK | 96.90 | 1.80E-06 | 1.30E-10 | 60.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR233W | PBP2 | SGDID:S000000437 | MEX3C RKHD2 RNF194 BM-013 |
RNA-binding E3 ubiquitin-protein ligase MEX3C (EC 2.3.2.27) (RING finger and KH domain-containing protein 2) (RING finger protein 194) (RING-type E3 ubiquitin transferase MEX3C) |
2.3.2.27 | Homo sapiens | Protoplasmic Astrocytoma,Smallpox |
5wwx_a | Q5U5Q3 | ENSG00000176624 | MEX3C | 96.00 | 5.50E-05 | 3.90E-09 | 52.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YBR233W | PBP2 | SGDID:S000000437 | IGF2BP3 |
IGF2BP3 |
Sus scrofa | 6gqe_a | A0A0B8RZH0 | 99.10 | 1.40E-14 | 9.60E-19 | 119.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR233W | PBP2 | SGDID:S000000437 | gld-3 T07F8.3 |
Defective in germ line development protein 3 (Germline development defective 3) |
Caenorhabditis elegans | 3n89_a | Q95ZK7 | 99.40 | 2.10E-17 | 1.50E-21 | 155.70 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | ||||
YBR233W | PBP2 | SGDID:S000000437 | FXR1 |
Fragile X mental retardation syndrome-related protein 1 (hFXR1p) |
Homo sapiens | Myopathy,Mixed Cell Uveal Melanoma,Cervical Non-Keratinizing Squamous Cell Carcinoma,Multiminicore Disease,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Fragile X Syndrome,X-Linked Monogenic Disease,Fragile X-Associated Tremor/Ataxia Syndrome,Specific Developmental Disorder,Myopathy, Congenital, With Respiratory Insufficiency And Bone Fractures,Myopathy, Congenital Proximal, With Minicore Lesions,Autism |
2cpq_a | P51114 | ENSG00000114416 | FXR1 | 95.80 | 0.0001 | 7.10E-09 | 52.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR233W | PBP2 | SGDID:S000000437 | PCBP2 |
Poly(rC)-binding protein 2 (Alpha-CP2) (Heterogeneous nuclear ribonucleoprotein E2) (hnRNP E2) |
Homo sapiens | Tremor, Hereditary Essential, 4,Leukemia, Chronic Myeloid,Hepatitis A,Semantic Dementia,Deficiency Anemia,Frontotemporal Dementia |
2jzx_a | Q15366 | ENSG00000197111 | PCBP2 | 99.10 | 2.80E-14 | 2.00E-18 | 116.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR233W | PBP2 | SGDID:S000000437 | nusA APE_1850 |
nusA APE_1850 |
Aeropyrum pernix | 2cxc_a | Q9YAU4 | 96.70 | 6.10E-06 | 4.30E-10 | 64.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR233W | PBP2 | SGDID:S000000437 | KHSRP FUBP2 |
Far upstream element-binding protein 2 (FUSE-binding protein 2) (KH type-splicing regulatory protein) (KSRP) (p75) |
Homo sapiens | Spinal Muscular Atrophy |
2jvz_a | Q92945 | ENSG00000088247 | KHSRP | 99.00 | 3.70E-14 | 2.70E-18 | 116.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR233W | PBP2 | SGDID:S000000437 | KHDRBS3 SALP SLM2 |
KH domain-containing, RNA-binding, signal transduction-associated protein 3 (RNA-binding protein T-Star) (Sam68-like mammalian protein 2) (SLM-2) (Sam68-like phosphotyrosine protein) |
Homo sapiens | Childhood Absence Epilepsy,Osteopetrosis,Hypophosphatasia,Localized Osteosarcoma,Corneal Dystrophy, Fleck,Hypophosphatasia, Infantile,Hypophosphatasia, Adult,Atrial Septal Defect 2 |
5el3_d | O75525 | ENSG00000131773 | KHDRBS3 | 95.50 | 0.0002 | 1.30E-08 | 53.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR233W | PBP2 | SGDID:S000000437 | IGF2BP1 CRDBP VICKZ1 ZBP1 |
Insulin-like growth factor 2 mRNA-binding protein 1 (IGF2 mRNA-binding protein 1) (IMP-1) (IMP1) (Coding region determinant-binding protein) (CRD-BP) (IGF-II mRNA-binding protein 1) (VICKZ family member 1) (Zipcode-binding protein 1) (ZBP-1) |
Homo sapiens | Skin Squamous Cell Carcinoma,Cone-Rod Dystrophy 2,Meningioma, Familial |
3krm_b | Q9NZI8 | ENSG00000159217 | IGF2BP1 | 99.00 | 3.70E-14 | 2.60E-18 | 116.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR233W | PBP2 | SGDID:S000000437 | MSL5 BBP SF1 YLR116W L2949 |
Branchpoint-bridging protein (Mud synthetic-lethal 5 protein) (Splicing factor 1) (Zinc finger protein BBP) |
Saccharomyces cerevisiae | 4wal_a | Q12186 | 96.70 | 4.80E-06 | 3.30E-10 | 64.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR233W | PBP2 | SGDID:S000000437 | PNPT1 PNPASE |
Polyribonucleotide nucleotidyltransferase 1, mitochondrial (EC 2.7.7.8) (3'-5' RNA exonuclease OLD35) (PNPase old-35) (Polynucleotide phosphorylase 1) (PNPase 1) (Polynucleotide phosphorylase-like protein) |
2.7.7.8 | Homo sapiens | Melanoma,Myopathy, Centronuclear, 1,Combined Oxidative Phosphorylation Deficiency 13,Deafness, Autosomal Recessive 70,Nonsyndromic Deafness,Optic Atrophy 3, Autosomal Dominant,Prostate Carcinoma In Situ,Autosomal Recessive Non-Syndromic Sensorineural Deafness Type Dfnb,Autosomal Recessive Nonsyndromic Deafness,Aicardi-Goutieres Syndrome,Spastic Ataxia 5,Agenesis Of Corpus Callosum, Cardiac, Ocular, And Genital Syndrome,2-Aminoadipic 2-Oxoadipic Aciduria,Combined Oxidative Phosphorylation Deficiency,Leigh Syndrome |
3u1k_c | Q8TCS8 | ENSG00000138035 | PNPT1 | 95.40 | 0.00026 | 1.80E-08 | 69.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YBR233W | PBP2 | SGDID:S000000437 | IGF2BP1 VICKZ1 ZBP1 |
Insulin-like growth factor 2 mRNA-binding protein 1 (IGF2 mRNA-binding protein 1) (IMP-1) (IGF-II mRNA-binding protein 1) (VICKZ family member 1) (Zip-code binding polypeptide) (Zipcode-binding protein 1) (ZBP-1) |
Gallus gallus | 2n8l_a | O42254 | 99.00 | 9.80E-14 | 6.90E-18 | 117.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR233W | PBP2 | SGDID:S000000437 | Khdc3 |
KH domain-containing protein 3 (Protein Filia) |
Mus musculus | 3v69_a | Q9CWU5 | 97.70 | 3.60E-08 | 2.40E-12 | 77.10 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YBR233W | PBP2 | SGDID:S000000437 | HDLBP HBP VGL |
Vigilin (High density lipoprotein-binding protein) (HDL-binding protein) |
Homo sapiens | Epilepsy, Idiopathic Generalized 5,Chromosome 2q37 Deletion Syndrome |
2ctf_a | Q00341 | ENSG00000115677 | HDLBP | 97.00 | 1.20E-06 | 8.50E-11 | 64.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |