FOXN1base: T-cell immunodeficiency, congenital alopecia, and nail dystrophy

Version 1.0 last updated 15 June, 2007 contains 2 public entries


Curated:	Mauno Vihinen and Claudio Pignata
Maintained by:	Jouni Väliaho
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Short description of the FOXN1base (previously known as WHNbase) :

Mutation in the FOXN1(WHN) gene cause an autosomal recessive syndrome characterised by decrease of mature T and a low number of helper T cells, whereas the number of suppressor/cytotoxic T cells was relatively normal. Two patients have been described until now.

Other IMT services:
Immunodeficiency Resource (IDR)
Immunodeficiency Mutation Databases (MUTbase)
IDdiagnostics
Immunome Knowledge Base (IKB) - An integrated service for immunome research
SH2base - Database for pathogenic SH2 domain mutations

IDbases are linked to University of California Santa Cruz (UCSC) genome browser: FOXN1base