chromosomal translocation t(X;7)(p11.3;q11.21)

- chromosomal translocation t(X;7)(p11.3;q11.21) involving ZNF41 has been found in a patient with severe mental retardation

Properties

GENERAL: chromosomal translocation FORM: t(X;7)(p11.3;q11.21) LOCUS: human X-chromosome P11.3 human chromosome-7 Q11.21 SPLICED-GENES: zinc finger protein 41

References

UniProt :accession P51814