𝔖 Bobbio Scriptorium
✦   LIBER   ✦

TCOF1 mutation database: Novel mutation in the alternatively spliced exon 6A and update in mutation nomenclature

✍ Scribed by Alessandra Splendore; Roberto D. Fanganiello; Cibele Masotti; Lucas S.C. Morganti; M. Rita Passos-Bueno


Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
152 KB
Volume
25
Category
Article
ISSN
1059-7794

No coin nor oath required. For personal study only.

✦ Synopsis


Communicated by Marc Greenblatt

Recently, a novel exon was described in TCOF1 that, although alternatively spliced, is included in the major protein isoform. In addition, most published mutations in this gene do not conform to current mutation nomenclature guidelines. Given these observations, we developed an online database of TCOF1 mutations in which all the reported mutations are renamed according to standard recommendations and in reference to the genomic and novel cDNA reference sequences (www.genoma.ib.usp.br/TCOF1 _ database). We also report in this work: 1) results of the first screening for large deletions in TCOF1 by Southern blot in patients without mutation detected by direct sequencing; 2) the identification of the first pathogenic mutation in the newly described exon 6A; and 3) statistical analysis of pathogenic mutations and polymorphism distribution throughout the gene.


πŸ“œ SIMILAR VOLUMES


A family with attenuated familial adenom
✍ Joanne Young; Lisa A. Simms; Jabbar Tarish; Ron Buttenshaw; Ngaire Knight; Grego πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 196 KB πŸ‘ 2 views

A family is presented with attenuated familial adenomatous polyposis of variable phenotype. The clinical features range from sparse right-sided polyposis and cancer in the proximal colon at the age of 34 to pan-colonic polyposis and cancer at the age of 68. Rectal sparing is common to all affected m

A novel mutation in the CFTR gene: I506T
✍ Marie Desgeorges; Marie-Catherine Romey; Christine Coubes; Jacques Demaille; Mir πŸ“‚ Article πŸ“… 1995 πŸ› John Wiley and Sons 🌐 English βš– 70 KB πŸ‘ 1 views

A woman with a family history of cystic fibrosis (CF) requested DNA analysis at 4 months of pregnancy. Since her brother died at age of 10 in 1986, it was necessary to perform DGGE screening of CFTR exons on DNA from the 2 parents. An aberrant heteroduplex pattern was observed for exon 10 amplified

Maternal mosaicism for a second mutation
✍ Sima Davidson; Lucy Leshanski; Gad Rennert; Shmuel Eidelman; Dorit Amikam πŸ“‚ Article πŸ“… 2001 πŸ› John Wiley and Sons 🌐 English βš– 140 KB πŸ‘ 2 views

## Familial Adenomatous Polyposis (FAP) is an autosomal dominant heritable disorder caused by germ-line mutations in the APC gene. To date, more than 300 germ-line mutations within this gene have been described. Using PCR, SSCP and DNA sequencing, we have identified a new mutation in the alternativ