ZM fibroblastHomo sapiens (Human)Transformed cell line

AI Summary

No AI-generated summary available for this cell line.

Basic Information

Database IDCVCL_B7LG
SpeciesHomo sapiens (Human)
Tissue SourceSkin[UBERON:UBERON_0002097]

Disease Information

DiseaseImmunodeficiency by defective expression of MHC class II

DepMap Information

Known Sequence Variations

TypeGene/ProteinDescriptionZygosityNoteSource
MutationSimpleRFXAPp.Ser123Thrfs*14 (c.368delG) (484delG)Homozygous-PubMed=9287230

Publications

Genetic and molecular definition of complementation group D in MHC class II deficiency.

Fischer A., Lisowska-Grospierre B.

Hum. Mol. Genet. 7:879-885(1998).

Mutation of RFXAP, a regulator of MHC class II genes, in primary MHC class II deficiency.

Reith W., Mach B.

N. Engl. J. Med. 337:748-753(1997).