Incidental Mutation 'IGL00823:Dmd'
ID |
10202 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Dmd
|
Ensembl Gene |
ENSMUSG00000045103 |
Gene Name |
dystrophin, muscular dystrophy |
Synonyms |
Duchenne muscular dystrophy, pke, dys, Dp71, Dp427, X-linked muscular dystrophy, mdx |
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.829)
|
Stock # |
IGL00823
|
Quality Score |
|
Status
|
|
Chromosome |
X |
Chromosomal Location |
81992476-84249747 bp(+) (GRCm39) |
Type of Mutation |
splice site (4 bp from exon) |
DNA Base Change (assembly) |
A to G
at 83469419 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000109633
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000114000]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably null
Transcript: ENSMUST00000114000
|
SMART Domains |
Protein: ENSMUSP00000109633 Gene: ENSMUSG00000045103
Domain | Start | End | E-Value | Type |
CH
|
17 |
117 |
5.94e-27 |
SMART |
CH
|
136 |
235 |
3.83e-21 |
SMART |
SPEC
|
344 |
448 |
7.39e-17 |
SMART |
SPEC
|
453 |
557 |
6.49e-13 |
SMART |
SPEC
|
564 |
668 |
9.73e-2 |
SMART |
low complexity region
|
672 |
695 |
N/A |
INTRINSIC |
SPEC
|
724 |
829 |
9.18e-13 |
SMART |
SPEC
|
835 |
935 |
2.28e-1 |
SMART |
SPEC
|
944 |
1046 |
9.34e-2 |
SMART |
SPEC
|
1053 |
1155 |
7.99e-13 |
SMART |
SPEC
|
1162 |
1264 |
7.52e-9 |
SMART |
SPEC
|
1271 |
1368 |
5.53e-7 |
SMART |
SPEC
|
1470 |
1569 |
7.29e-7 |
SMART |
SPEC
|
1576 |
1677 |
8.29e-1 |
SMART |
SPEC
|
1684 |
1781 |
1.82e-1 |
SMART |
SPEC
|
1786 |
1875 |
3.48e0 |
SMART |
SPEC
|
1882 |
1972 |
6.69e-2 |
SMART |
SPEC
|
2000 |
2102 |
1.45e0 |
SMART |
SPEC
|
2109 |
2209 |
6.15e-14 |
SMART |
SPEC
|
2216 |
2317 |
8.9e-11 |
SMART |
low complexity region
|
2325 |
2337 |
N/A |
INTRINSIC |
low complexity region
|
2432 |
2444 |
N/A |
INTRINSIC |
SPEC
|
2466 |
2569 |
1.65e-14 |
SMART |
SPEC
|
2576 |
2678 |
1.2e-7 |
SMART |
SPEC
|
2685 |
2794 |
9.84e-13 |
SMART |
SPEC
|
2801 |
2923 |
8.38e-7 |
SMART |
SPEC
|
2930 |
3032 |
1.21e-12 |
SMART |
WW
|
3049 |
3081 |
1.36e-10 |
SMART |
Pfam:EF-hand_2
|
3082 |
3200 |
1.7e-42 |
PFAM |
Pfam:EF-hand_3
|
3204 |
3295 |
6.6e-41 |
PFAM |
ZnF_ZZ
|
3300 |
3345 |
7.39e-18 |
SMART |
coiled coil region
|
3488 |
3598 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: This gene encodes a large, rod-like cytoskeletal protein which is found at the inner surface of muscle fibers in skeletal and cardiac muscles. The encoded protein, dystrophin, is part of the dystrophin-glycoprotein complex, which bridges the inner cytoskeleton (F-actin) and the extra-cellular matrix. This protein is required for proper development and organization of myofibers as contractile units in striated muscles. Mutations in the human gene cause Duchenne and Becker Muscular Dystrophies and a form of heart disease called DMD-associated dilated cardiomyopathy. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Sep 2015] PHENOTYPE: Mutations in this gene cause muscular dystrophy. Phenotypic variation has been observed in different backgrounds. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aasdh |
T |
C |
5: 77,026,381 (GRCm39) |
|
probably benign |
Het |
Adam5 |
T |
C |
8: 25,308,758 (GRCm39) |
E39G |
probably benign |
Het |
Anapc7 |
G |
A |
5: 122,571,540 (GRCm39) |
W205* |
probably null |
Het |
Arhgap5 |
C |
T |
12: 52,565,525 (GRCm39) |
T832I |
possibly damaging |
Het |
Arhgef10 |
T |
A |
8: 14,990,378 (GRCm39) |
|
probably benign |
Het |
Atg5 |
A |
G |
10: 44,239,040 (GRCm39) |
T274A |
probably benign |
Het |
Baiap2l2 |
G |
T |
15: 79,168,765 (GRCm39) |
|
probably benign |
Het |
Brap |
T |
A |
5: 121,803,290 (GRCm39) |
M146K |
probably damaging |
Het |
Brpf1 |
T |
C |
6: 113,298,847 (GRCm39) |
S1074P |
probably benign |
Het |
Camta1 |
A |
C |
4: 151,169,058 (GRCm39) |
I231R |
probably benign |
Het |
Ccdc15 |
C |
T |
9: 37,231,709 (GRCm39) |
G205D |
probably benign |
Het |
Cd6 |
G |
T |
19: 10,773,758 (GRCm39) |
|
probably benign |
Het |
Cdh17 |
T |
G |
4: 11,783,412 (GRCm39) |
S219R |
possibly damaging |
Het |
Cgn |
G |
A |
3: 94,674,519 (GRCm39) |
R873W |
probably damaging |
Het |
Ctnna3 |
C |
T |
10: 63,373,322 (GRCm39) |
P41L |
possibly damaging |
Het |
Dmbt1 |
T |
C |
7: 130,659,888 (GRCm39) |
W484R |
probably benign |
Het |
Dnah17 |
C |
T |
11: 117,937,987 (GRCm39) |
V3347I |
probably benign |
Het |
Fgd5 |
T |
A |
6: 91,965,440 (GRCm39) |
S400T |
possibly damaging |
Het |
Kitl |
C |
A |
10: 99,923,206 (GRCm39) |
|
probably benign |
Het |
Lamc3 |
A |
T |
2: 31,808,533 (GRCm39) |
D763V |
probably damaging |
Het |
Lgmn |
T |
C |
12: 102,364,435 (GRCm39) |
|
probably benign |
Het |
Lpcat2 |
T |
G |
8: 93,591,598 (GRCm39) |
W81G |
possibly damaging |
Het |
Myh13 |
A |
G |
11: 67,246,773 (GRCm39) |
I1165V |
probably benign |
Het |
Nf1 |
A |
G |
11: 79,456,343 (GRCm39) |
D599G |
probably damaging |
Het |
Nin |
T |
C |
12: 70,061,567 (GRCm39) |
N2099S |
probably benign |
Het |
Nlrc4 |
T |
C |
17: 74,754,985 (GRCm39) |
D77G |
probably benign |
Het |
Otub1 |
A |
G |
19: 7,181,416 (GRCm39) |
|
probably benign |
Het |
Pabir2 |
A |
T |
X: 52,334,208 (GRCm39) |
C222S |
probably damaging |
Het |
Pah |
A |
G |
10: 87,406,193 (GRCm39) |
Y174C |
probably null |
Het |
Rbbp5 |
G |
A |
1: 132,417,444 (GRCm39) |
V88I |
probably damaging |
Het |
Scn1a |
C |
T |
2: 66,155,279 (GRCm39) |
R560H |
probably benign |
Het |
Snx5 |
T |
C |
2: 144,097,485 (GRCm39) |
I217V |
probably benign |
Het |
Syne2 |
T |
C |
12: 76,036,016 (GRCm39) |
S3769P |
probably damaging |
Het |
Tent2 |
T |
C |
13: 93,322,905 (GRCm39) |
T15A |
probably benign |
Het |
Tmem255b |
T |
C |
8: 13,507,054 (GRCm39) |
M261T |
probably benign |
Het |
Top3b |
T |
C |
16: 16,705,486 (GRCm39) |
I417T |
probably damaging |
Het |
Tspan2 |
T |
C |
3: 102,665,549 (GRCm39) |
|
probably null |
Het |
Ttn |
T |
C |
2: 76,540,057 (GRCm39) |
T34310A |
possibly damaging |
Het |
Ush2a |
G |
A |
1: 188,643,640 (GRCm39) |
C4334Y |
possibly damaging |
Het |
Wdpcp |
A |
G |
11: 21,609,995 (GRCm39) |
D21G |
probably damaging |
Het |
Yy2 |
A |
C |
X: 156,351,207 (GRCm39) |
D186E |
probably benign |
Het |
|
Other mutations in Dmd |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00771:Dmd
|
APN |
X |
82,951,978 (GRCm39) |
splice site |
probably null |
|
IGL01160:Dmd
|
APN |
X |
82,968,567 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01285:Dmd
|
APN |
X |
84,153,590 (GRCm39) |
nonsense |
probably null |
|
IGL01294:Dmd
|
APN |
X |
83,475,604 (GRCm39) |
splice site |
probably null |
|
IGL02426:Dmd
|
APN |
X |
83,892,342 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02610:Dmd
|
APN |
X |
82,707,762 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02887:Dmd
|
APN |
X |
82,922,110 (GRCm39) |
missense |
probably benign |
0.44 |
IGL03268:Dmd
|
APN |
X |
82,849,814 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03301:Dmd
|
APN |
X |
82,952,120 (GRCm39) |
missense |
probably damaging |
1.00 |
R0480:Dmd
|
UTSW |
X |
83,469,344 (GRCm39) |
missense |
probably benign |
0.00 |
R0714:Dmd
|
UTSW |
X |
83,353,503 (GRCm39) |
missense |
probably benign |
0.00 |
R1296:Dmd
|
UTSW |
X |
82,922,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R1448:Dmd
|
UTSW |
X |
83,892,306 (GRCm39) |
missense |
probably damaging |
0.97 |
R1678:Dmd
|
UTSW |
X |
84,018,368 (GRCm39) |
missense |
probably benign |
0.43 |
R1714:Dmd
|
UTSW |
X |
83,008,356 (GRCm39) |
missense |
probably benign |
0.17 |
R1951:Dmd
|
UTSW |
X |
82,874,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R1952:Dmd
|
UTSW |
X |
82,874,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R1953:Dmd
|
UTSW |
X |
82,874,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R1955:Dmd
|
UTSW |
X |
82,922,163 (GRCm39) |
missense |
probably benign |
0.10 |
R2072:Dmd
|
UTSW |
X |
83,356,089 (GRCm39) |
missense |
probably benign |
0.33 |
R2073:Dmd
|
UTSW |
X |
83,356,089 (GRCm39) |
missense |
probably benign |
0.33 |
R2074:Dmd
|
UTSW |
X |
83,356,089 (GRCm39) |
missense |
probably benign |
0.33 |
R2075:Dmd
|
UTSW |
X |
83,356,089 (GRCm39) |
missense |
probably benign |
0.33 |
R2118:Dmd
|
UTSW |
X |
83,356,089 (GRCm39) |
missense |
probably benign |
0.33 |
R2119:Dmd
|
UTSW |
X |
83,356,089 (GRCm39) |
missense |
probably benign |
0.33 |
R2120:Dmd
|
UTSW |
X |
83,356,089 (GRCm39) |
missense |
probably benign |
0.33 |
R2122:Dmd
|
UTSW |
X |
83,356,089 (GRCm39) |
missense |
probably benign |
0.33 |
R4398:Dmd
|
UTSW |
X |
82,765,624 (GRCm39) |
missense |
probably benign |
0.01 |
X0025:Dmd
|
UTSW |
X |
83,690,800 (GRCm39) |
missense |
probably benign |
|
Z1088:Dmd
|
UTSW |
X |
83,619,366 (GRCm39) |
missense |
probably benign |
0.05 |
Z1088:Dmd
|
UTSW |
X |
82,922,101 (GRCm39) |
missense |
possibly damaging |
0.67 |
Z1176:Dmd
|
UTSW |
X |
82,922,090 (GRCm39) |
missense |
possibly damaging |
0.90 |
Z1176:Dmd
|
UTSW |
X |
82,670,892 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Dmd
|
UTSW |
X |
82,670,877 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Posted On |
2012-12-06 |