ChromothripsisDB: a curated database of chromothripsis
 
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  Fusion Gene
  PubMed ID: 25799107 Case ID: Mother3 Disease: Congenital abnormality Genome Assembly: GRCh37/hg19
Gene Symbol 1 Chromosome1 Description 1 Gene Symbol 2 Chromosome2 Description 2
 
 
  Affected Gene
  PubMed ID: 25799107 Case ID: Mother3 Disease: Congenital abnormality Genome Assembly: GRCh37/hg19
Gene Symbol Entrez Gene Chromosome Start End Description
GFM1 85476 3 158362067 158410364 G elongation factor, mitochondrial 1
LXN 56925 3 158363611 158390482 latexin
TNK2 10188 3 195590235 195638816 tyrosine kinase, non-receptor, 2
SHE 126669 1 154442248 154474589 Src homology 2 domain containing E
IL6R 3570 1 154377669 154441926 interleukin 6 receptor
C1orf56 54964 1 151020216 151024462 chromosome 1 open reading frame 56
BNIPL 149428 1 151009046 151020076 BCL2/adenovirus E1B 19kD interacting protein like
CDC42SE1 56882 1 151023447 151042801 CDC42 small effector 1
MLLT11 10962 1 151030234 151040970 myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 11
LEKR1 389170 3 156543270 156763918 leucine, glutamate and lysine rich 1
SLC27A3 11000 1 153746830 153752633 solute carrier family 27 (fatty acid transporter), member 3
INTS3 65123 1 153700543 153746555 integrator complex subunit 3
 
Chromothripsis database. 2025 Cai Laboratory