CLDN1
Gene name: claudin 1OMIM ID: 603718
Chromosome location: 3q28
Mutations
Disease/Phenotype | Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis |
---|---|
Reference transcript | NM_021101.4 |
DNA Change | c.200_201delTT |
A.A. Change | p.Phe67X |
Exon/Intron | exon 1 |
Mutation Type | deletion |
Reference | Nagtzaam IF, van Geel M, Driessen A, Steijlen PM, van Steensel MA.Bile duct paucity is part of the neonatal ichthyosis-sclerosing cholangitis phenotype. Br J Dermatol. 2010 Jul;163(1):205-7. |