Gene: [11p155/BWSCR1B] Beckwith-Wiedemann syndrome chromosome region 1, candidate b; [BWR1B ]


REF

 COD,SEQ,FAG "Schwienbacher C &: PNAS, 95, 3873-3878, 1998

CLA

 coding, basic

LOC

 11 p15.5

MIM

 ?

SYN

 BWR1B

Смотрите также:

  • Gene: [11p155/CDKN1C] cyclin-dependent kinase inhibitor 1C (p57, Kip2); Beckwith-Wiedemann syndrome (exomphalos-macroglossia-gigantism; MIM:130650); [Kip2 ]
  • Gene: [11p155/BWSCR1A] Beckwith-Wiedemann syndrome chromosome region 1, candidate a; imprinted polyspecific membrane transporter 1; organic cation transporter-like 2; solute carrier family 22, member 1-like; [BWR1A IMPT1 ]