Gene: [0Xp11/IP1] incontinentia pigmenti, type I (sporadic; X-arrangement-associated);


HET

Basing on the data (Sefiani-1988,1989) about teh linkage of IP locus with DNA markers on the distal end of the chr X long arm, the HGM and GEM catalogues register the second IP gene (GEM:0Xq2/IP2), which determines the familial form of the incontinentia pigmenti syndrome (male-lethal)."

REF

LOC "de Grouchy J &: Ann Genet, 28, 86-89, 1985
LOC "Gilgenkrantz S &: Ann Genet, 28, 90-92, 1985
LOC "Hodgson SV &: Hum Genet, 71, 231-234, 1985
COM,FAG "Sefiani A &: Hum Genet, 80, 282-286, 1988
COM,FAG "see GEM:0Xq2/IP2

KEY

derm

CLA

unknown, basic

LOC

0X p11.21-.1

MIM

MIM: 308300

Смотрите также:

  • Gene: [09q34/ITO] hypomelanosis of Ito (incontinentia pigmenti achromians, IPA); [HMI IPA ]