ChromothripsisDB: a curated database of chromothripsis
 
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  Fusion Gene
  PubMed ID: 23334667 Case ID: MEN0017 Disease: Meningioma Genome Assembly: GRCh37/hg19
Gene Symbol 1 Chromosome1 Description 1 Gene Symbol 2 Chromosome2 Description 2
AGBL4 1 ATP/GTP binding protein-like 4 INADL 1 InaD-like (Drosophila)
DAB1 1 Dab, reelin signal transducer, homolog 1 (Drosophila) FAM46C 1 family with sequence similarity 46, member C
DAB1 1 Dab, reelin signal transducer, homolog 1 (Drosophila) VAV3 1 vav 3 guanine nucleotide exchange factor
DNM3 1 dynamin 3 TDRD5 1 tudor domain containing 5
FRRS1 1 ferric-chelate reductase 1 DNM3 1 dynamin 3
FRRS1 1 ferric-chelate reductase 1 NPHS2 1 nephrosis 2, idiopathic, steroid-resistant (podocin)
GNL2 1 guanine nucleotide binding protein-like 2 (nucleolar) MACF1 1 microtubule-actin crosslinking factor 1
MACF1 1 microtubule-actin crosslinking factor 1 SLC30A7 1 solute carrier family 30 (zinc transporter), member 7
METTL13 1 methyltransferase like 13 DNM3 1 dynamin 3
PIGK 1 phosphatidylinositol glycan anchor biosynthesis, class K DNM3 1 dynamin 3
SPATA6 1 spermatogenesis associated 6 PIGK 1 phosphatidylinositol glycan anchor biosynthesis, class K
TTC39A 1 tetratricopeptide repeat domain 39A PIGK 1 phosphatidylinositol glycan anchor biosynthesis, class K
 
 
  Affected Gene
  PubMed ID: 23334667 Case ID: MEN0017 Disease: Meningioma Genome Assembly: GRCh37/hg19
Gene Symbol Entrez Gene Chromosome Start End Description
NEGR1 257194 1 71861623 72748417 neuronal growth regulator 1
 
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