BTKbase, mutation database for X-linked agammaglobulinemia (XLA)
Vihinen, Mauno LU
; Belohradsky, BH
; Haire, RN
; HolinskiFeder, E
; Kwan, SP
; Lappalainen, I
; Lehvaslaiho, H
; Lester, T
; Meindl, A
and Ochs, HD
, et al.
(1997)
In Nucleic Acids Research
25(1).
p.166-171
- Abstract
- X-linked agammaglobulinemia (XLA) is an immunodeficiency caused by mutations in the gene coding for Bruton's agammaglobulinemia tyrosine kinase (BTK). A database (BTKbase) of BTK mutations has been compiled and the recent update lists 368 entries from 318 unrelated families showing 228 unique molecular events. In addition to mutations the database lists also some polymorphisms and site-directed mutations. Each patient is given a unique patient identity number (PIN). Information is provided regarding the phenotype including symptoms. Mutations in all the five domains of BTK have been noticed to cause the disease, the most common event being missense mutations, The mutations appear almost uniformly throughout the molecule and frequently... (More)
- X-linked agammaglobulinemia (XLA) is an immunodeficiency caused by mutations in the gene coding for Bruton's agammaglobulinemia tyrosine kinase (BTK). A database (BTKbase) of BTK mutations has been compiled and the recent update lists 368 entries from 318 unrelated families showing 228 unique molecular events. In addition to mutations the database lists also some polymorphisms and site-directed mutations. Each patient is given a unique patient identity number (PIN). Information is provided regarding the phenotype including symptoms. Mutations in all the five domains of BTK have been noticed to cause the disease, the most common event being missense mutations, The mutations appear almost uniformly throughout the molecule and frequently affect CpG sites forming arginine residues. These hot spots have generally pyrimidines 5' and purines 3' to the mutated cytosine. A decreased frequency of missense mutations was found in the TH, SH3 and the upper lobe of the kinase domain, The putative structural implications of all the missense mutations are given in the database showing 228 unique molecular events, including a novel missense mutation causing an R28C substitution as previously seen in the Xid mouse. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/3852889
- author
- Vihinen, Mauno
LU
; Belohradsky, BH
; Haire, RN
; HolinskiFeder, E
; Kwan, SP
; Lappalainen, I
; Lehvaslaiho, H
; Lester, T
; Meindl, A
and Ochs, HD
, et al. (More)
- Vihinen, Mauno
LU
; Belohradsky, BH
; Haire, RN
; HolinskiFeder, E
; Kwan, SP
; Lappalainen, I
; Lehvaslaiho, H
; Lester, T
; Meindl, A
; Ochs, HD
; Ollila, J
; Vorechovsky, I
; Weiss, M
and Smith, CIE
(Less)
- publishing date
- 1997
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Nucleic Acids Research
- volume
- 25
- issue
- 1
- pages
- 166 - 171
- publisher
- Oxford University Press
- external identifiers
-
- wos:A1997WD44300040
- scopus:0030862611
- ISSN
- 1362-4962
- DOI
- 10.1093/nar/25.1.166
- language
- English
- LU publication?
- no
- id
- 6e71014b-1756-4428-8e4d-627380e39504 (old id 3852889)
- date added to LUP
- 2016-04-01 11:45:20
- date last changed
- 2022-01-26 17:45:33
@article{6e71014b-1756-4428-8e4d-627380e39504,
abstract = {{X-linked agammaglobulinemia (XLA) is an immunodeficiency caused by mutations in the gene coding for Bruton's agammaglobulinemia tyrosine kinase (BTK). A database (BTKbase) of BTK mutations has been compiled and the recent update lists 368 entries from 318 unrelated families showing 228 unique molecular events. In addition to mutations the database lists also some polymorphisms and site-directed mutations. Each patient is given a unique patient identity number (PIN). Information is provided regarding the phenotype including symptoms. Mutations in all the five domains of BTK have been noticed to cause the disease, the most common event being missense mutations, The mutations appear almost uniformly throughout the molecule and frequently affect CpG sites forming arginine residues. These hot spots have generally pyrimidines 5' and purines 3' to the mutated cytosine. A decreased frequency of missense mutations was found in the TH, SH3 and the upper lobe of the kinase domain, The putative structural implications of all the missense mutations are given in the database showing 228 unique molecular events, including a novel missense mutation causing an R28C substitution as previously seen in the Xid mouse.}},
author = {{Vihinen, Mauno and Belohradsky, BH and Haire, RN and HolinskiFeder, E and Kwan, SP and Lappalainen, I and Lehvaslaiho, H and Lester, T and Meindl, A and Ochs, HD and Ollila, J and Vorechovsky, I and Weiss, M and Smith, CIE}},
issn = {{1362-4962}},
language = {{eng}},
number = {{1}},
pages = {{166--171}},
publisher = {{Oxford University Press}},
series = {{Nucleic Acids Research}},
title = {{BTKbase, mutation database for X-linked agammaglobulinemia (XLA)}},
url = {{http://dx.doi.org/10.1093/nar/25.1.166}},
doi = {{10.1093/nar/25.1.166}},
volume = {{25}},
year = {{1997}},
}