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PMID: 7668254
Watkins PA, Gould SJ, Smith MA, Braiterman LT, Wei HM, Kok F, Moser AB, Moser HW, Smith KD
Altered expression of ALDP in X-linked adrenoleukodystrophy.
Am J Hum Genet. 1995 Aug;57(2):292-301.,
[PubMed]
Sentences
No.
Mutations
Sentence
Comment
176
ABCD1 p.Arg401Gln
X
ABCD1 p.Arg401Gln 7668254:176:602
status:
NEW
view ABCD1 p.Arg401Gln details
ABCD1 p.Arg660Trp
X
ABCD1 p.Arg660Trp 7668254:176:912
status:
NEW
view ABCD1 p.Arg660Trp details
ABCD1 p.Ala626Thr
X
ABCD1 p.Ala626Thr 7668254:176:788
status:
NEW
view ABCD1 p.Ala626Thr details
ABCD1 p.Arg617His
X
ABCD1 p.Arg617His 7668254:176:747
status:
NEW
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ABCD1 p.Ser606Leu
X
ABCD1 p.Ser606Leu 7668254:176:705
status:
NEW
view ABCD1 p.Ser606Leu details
ABCD1 p.Arg389His
X
ABCD1 p.Arg389His 7668254:176:558
status:
NEW
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ABCD1 p.Arg591Gln
X
ABCD1 p.Arg591Gln 7668254:176:669
status:
NEW
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ABCD1 p.Asp629His
X
ABCD1 p.Asp629His 7668254:176:829
status:
NEW
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ABCD1 p.Glu291Asp
X
ABCD1 p.Glu291Asp 7668254:176:476
status:
NEW
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ABCD1 p.Lys276Glu
X
ABCD1 p.Lys276Glu 7668254:176:394
status:
NEW
view ABCD1 p.Lys276Glu details
ABCD1 p.Gln645*
X
ABCD1 p.Gln645* 7668254:176:872
status:
NEW
view ABCD1 p.Gln645* details
In 11 patients, missense mutations that occurred throughout the protein were found: within the transmembrane domains (patients 1, 3, and 4), within the ATP-binding domain (patients 8-12), and on either side of the ATP-binding Table 3 Mutational Analysis of the ALD Gene in IS Unrelated Patients ALDP Patient Phenotype Mutation Consequence Immunoreactivity 1 .................. CALD 825 A-GG
K276E
+ 2.................. AMN 870-2AGAGE291,& 3 .................. CALD 872 G-C
E291D
4 .................. AMN 1023 T-IC S342P+ 5 .................. AMN 1166 G-C
R389H
+ 6 .................. CALD 1201 G-AA
R401Q
+ 7 ........ CALD 1415-6 AAG FS@472 8 ........ AMN 1771 G-AA
R591Q
+ 9 ........ Addison 1817 C-T
S606L
+ 10 ................ AMN 1850 G-AA
R617H
11 ................ CALD 1876 G-AA
A626T
12 ................ Fetus 1884 G-C
D629H
+ 13 ................ CALD 1932 C-UT
Q645X
14 ................ AMN 1978 C-OT
R660W
15 ........ AMN AExon7-10 Null Mutations in the ALD gene were determined, as described in Methods, in 15 of the ALD patients reported in table 2.
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178
ABCD1 p.Arg401Gln
X
ABCD1 p.Arg401Gln 7668254:178:606
status:
NEW
view ABCD1 p.Arg401Gln details
ABCD1 p.Arg660Trp
X
ABCD1 p.Arg660Trp 7668254:178:916
status:
NEW
view ABCD1 p.Arg660Trp details
ABCD1 p.Ala626Thr
X
ABCD1 p.Ala626Thr 7668254:178:792
status:
NEW
view ABCD1 p.Ala626Thr details
ABCD1 p.Arg617His
X
ABCD1 p.Arg617His 7668254:178:751
status:
NEW
view ABCD1 p.Arg617His details
ABCD1 p.Ser606Leu
X
ABCD1 p.Ser606Leu 7668254:178:709
status:
NEW
view ABCD1 p.Ser606Leu details
ABCD1 p.Arg389His
X
ABCD1 p.Arg389His 7668254:178:562
status:
NEW
view ABCD1 p.Arg389His details
ABCD1 p.Arg591Gln
X
ABCD1 p.Arg591Gln 7668254:178:673
status:
NEW
view ABCD1 p.Arg591Gln details
ABCD1 p.Ser342Pro
X
ABCD1 p.Ser342Pro 7668254:178:520
status:
NEW
view ABCD1 p.Ser342Pro details
ABCD1 p.Asp629His
X
ABCD1 p.Asp629His 7668254:178:833
status:
NEW
view ABCD1 p.Asp629His details
ABCD1 p.Glu291Asp
X
ABCD1 p.Glu291Asp 7668254:178:479
status:
NEW
view ABCD1 p.Glu291Asp details
ABCD1 p.Lys276Glu
X
ABCD1 p.Lys276Glu 7668254:178:394
status:
NEW
view ABCD1 p.Lys276Glu details
ABCD1 p.Gln645*
X
ABCD1 p.Gln645* 7668254:178:876
status:
NEW
view ABCD1 p.Gln645* details
In 11 patients, missense mutations that occurred throughout the protein were found: within the transmembrane domains (patients 1, 3, and 4), within the ATP-binding domain (patients 8-12), and on either side of the ATP-binding Table 3 Mutational Analysis of the ALD Gene in IS Unrelated Patients ALDP Patient Phenotype Mutation Consequence Immunoreactivity 1 .................. CALD 825 A-GG
K276E
+ 2 .................. AMN 870-2 AGAG E291,& 3 .................. CALD 872 G-C
E291D
4 .................. AMN 1023 T-IC
S342P
+ 5 .................. AMN 1166 G-C
R389H
+ 6 .................. CALD 1201 G-AA
R401Q
+ 7 ........ CALD 1415-6 AAG FS@472 8 ........ AMN 1771 G-AA
R591Q
+ 9 ........ Addison 1817 C-T
S606L
+ 10 ................ AMN 1850 G-AA
R617H
11 ................ CALD 1876 G-AA
A626T
12 ................ Fetus 1884 G-C
D629H
+ 13 ................ CALD 1932 C-UT
Q645X
14 ................ AMN 1978 C-OT
R660W
15 ........ AMN AExon7-10 Null Mutations in the ALD gene were determined, as described in Methods, in 15 of the ALD patients reported in table 2.
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