keratosis follicularis spinulosa decalvans (KFSD)
Name: KFSD
Description: keratosis follicularis spinulosa decalvans
Orgname: Homo sapiens
Status: 1
CurrentID: 6303
Chromosome: X
GeneticSource: genomic
MapLocation: Xp22.2-p21.2
OtherAliases:
OtherDesignations:
NomenclatureSymbol: KFSD
NomenclatureName: keratosis follicularis spinulosa decalvans
NomenclatureStatus: Official
TaxID: 9606
Mim:
GenomicInfo:
GeneWeight: 0
Summary:
ChrSort: ~~last
ChrStart: 999999999
UniProtein db: KFSD UniProt protein knowledge database
Ensembl db: KFSD Ensembl genome database
Keratosis follicularis spinulosa decalvans (KFSD) or Siemens-1 syndrome is a rare ... So far, the gene has been mapped to Xp22.13p22.2 in two extended KFSD families. ...
Keratosis follicularis spinulosa decalvans (KFSD) is a rare X-chromosomal disorder. ... Dutch pedigree we performed DNA analysis in order to localize the KFSD gene. ...
Part 3. Disorders of the Skin Appendages > Section 15. Disorders of the Hair and ... follicularis; keratosis pilaris; keratosis pilaris atrophicans; kfsd gene. ...
KFSD is classified in the group of genetic skin disorders as keratosis pilaris ... linked keratosis follicularis spinulosa decalvans (KFSD) gene in Xp22.13-p22.2. J Med Genet. ...
kfsd gene. lichen planopilaris. perifolliculitis capitis abscedens ... Perform a full-text search for "Folliculitis decalvans" (supports Boolean) ...
Keratosis follicular spinulosa decalvans (KFSD) is a rare X-linked disorder, of ... This region contains gene implicated in KFSD, retinoschisis and spermidine ...
Use of type VII collagen gene (COL7A1) markers in prenatal diagnosis of ... (KFSD) gene in Xp22.13-p22.2. J Med Genet 1995;32:736-739 doi:10.1136 ...
The Schizophrenia Research Forum is an online scientific community dedicated to developing treatments and preventions for Schizophrenia.
Synonyms: KFSD, DC21, SSAT, SSAT-1, SAT. The data in COSMIC for SAT1 is from selected papers only and does not represent a wide survey of publications for this gene. ...
Chemical–Gene Interactions. Genes. Diseases. References. Tools. Overview ... acetyltransferase; diamine acetyltransferase 1; kfsd; sat; similar to spermidine ...
KFSD is a rare X-linked disorder affecting the skin and the eye. ... follicularis spinulosa decalvans: refinement of gene localization and evidence for genetic heterogeneity. ...
Complete information for SAT1 gene (protein-coding), spermidine/spermine N1-acetyltransferase 1
Just a single change in the gene's DNA code determines whether...
SAT1 (spermidine/spermine N1-acetyltransferase 1), Authors: Dessen P, Le Minor S. Published in: Atlas Genet Cytogenet Oncol Haematol.
SAT1 SAT2. Gene Name: spermidine/spermine N1-acetyltransferase 1. Gene Alias: SAT DC21 KFSD SSAT SSAT-1 ... the below pathway map to view gene annotation and product information. ...