Incidental Mutation 'IGL03268:Dmd'
| ID |
415144 |
| 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 # |
IGL03268
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
X |
| Chromosomal Location |
81992476-84249747 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 82849814 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glutamic Acid to Glycine
at position 1084
(E1084G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000109633
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000114000]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000114000
AA Change: E1084G
PolyPhen 2
Score 0.980 (Sensitivity: 0.75; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000109633
Gene: ENSMUSG00000045103
AA Change: E1084G
| 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: 49 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1500002C15Rik |
G |
T |
4: 155,818,648 (GRCm39) |
|
probably benign |
Het |
| Acvrl1 |
A |
T |
15: 101,033,803 (GRCm39) |
I162F |
possibly damaging |
Het |
| Adprhl1 |
A |
G |
8: 13,296,170 (GRCm39) |
|
probably benign |
Het |
| Anapc7 |
G |
A |
5: 122,567,669 (GRCm39) |
|
probably null |
Het |
| Ankrd13a |
T |
C |
5: 114,930,296 (GRCm39) |
L227P |
probably damaging |
Het |
| Anxa5 |
T |
C |
3: 36,504,828 (GRCm39) |
I245V |
probably benign |
Het |
| Arf1 |
A |
T |
11: 59,103,663 (GRCm39) |
V123E |
possibly damaging |
Het |
| Catsperg1 |
G |
A |
7: 28,899,668 (GRCm39) |
R338C |
probably damaging |
Het |
| Cc2d1a |
A |
C |
8: 84,860,154 (GRCm39) |
L855R |
probably damaging |
Het |
| Cdh18 |
G |
A |
15: 23,366,953 (GRCm39) |
A220T |
probably damaging |
Het |
| Cep350 |
T |
C |
1: 155,829,295 (GRCm39) |
H203R |
probably benign |
Het |
| Cep78 |
G |
T |
19: 15,951,806 (GRCm39) |
S333* |
probably null |
Het |
| Chrna2 |
T |
A |
14: 66,388,395 (GRCm39) |
|
probably benign |
Het |
| Dact1 |
T |
C |
12: 71,364,257 (GRCm39) |
V346A |
probably damaging |
Het |
| Dcn |
A |
G |
10: 97,319,240 (GRCm39) |
I6V |
probably benign |
Het |
| Dlg3 |
A |
G |
X: 99,853,493 (GRCm39) |
Y600C |
probably damaging |
Het |
| Epb41 |
A |
C |
4: 131,655,806 (GRCm39) |
D825E |
probably damaging |
Het |
| Galc |
T |
A |
12: 98,188,852 (GRCm39) |
|
probably benign |
Het |
| Hmcn1 |
T |
A |
1: 150,648,261 (GRCm39) |
D675V |
probably damaging |
Het |
| Igkv2-137 |
A |
G |
6: 67,533,092 (GRCm39) |
D85G |
probably benign |
Het |
| Kxd1 |
A |
G |
8: 70,961,136 (GRCm39) |
I78T |
probably damaging |
Het |
| Lama1 |
G |
A |
17: 68,111,531 (GRCm39) |
G2261R |
probably damaging |
Het |
| Lama2 |
A |
T |
10: 27,298,649 (GRCm39) |
I149N |
probably damaging |
Het |
| Mbnl2 |
G |
T |
14: 120,616,569 (GRCm39) |
C61F |
probably damaging |
Het |
| Mcts1 |
T |
C |
X: 37,690,859 (GRCm39) |
I22T |
possibly damaging |
Het |
| Or4k15b |
T |
C |
14: 50,272,024 (GRCm39) |
T279A |
probably damaging |
Het |
| Or52e3 |
T |
G |
7: 102,869,848 (GRCm39) |
F308V |
probably benign |
Het |
| Pde12 |
T |
A |
14: 26,389,614 (GRCm39) |
E365V |
probably benign |
Het |
| Prl8a2 |
A |
G |
13: 27,537,938 (GRCm39) |
K204R |
probably benign |
Het |
| Rnf25 |
A |
T |
1: 74,638,217 (GRCm39) |
|
probably benign |
Het |
| Rragb |
A |
G |
X: 151,923,493 (GRCm39) |
D5G |
unknown |
Het |
| Rsrc2 |
T |
A |
5: 123,878,790 (GRCm39) |
K56* |
probably null |
Het |
| Scn5a |
T |
C |
9: 119,350,297 (GRCm39) |
Q859R |
probably damaging |
Het |
| Septin4 |
G |
A |
11: 87,480,529 (GRCm39) |
V388M |
probably damaging |
Het |
| Slc29a2 |
C |
T |
19: 5,074,531 (GRCm39) |
|
probably benign |
Het |
| Slc30a5 |
G |
A |
13: 100,943,211 (GRCm39) |
T549I |
probably damaging |
Het |
| Slc7a2 |
A |
G |
8: 41,365,554 (GRCm39) |
T462A |
probably benign |
Het |
| Spsb2 |
A |
G |
6: 124,786,450 (GRCm39) |
E61G |
probably damaging |
Het |
| Srr |
A |
G |
11: 74,803,943 (GRCm39) |
Y5H |
probably benign |
Het |
| Suclg2 |
T |
C |
6: 95,546,573 (GRCm39) |
D301G |
probably damaging |
Het |
| Syt14 |
A |
G |
1: 192,669,142 (GRCm39) |
V37A |
probably benign |
Het |
| Syt9 |
A |
G |
7: 107,035,612 (GRCm39) |
N210D |
probably benign |
Het |
| Tenm3 |
T |
C |
8: 48,688,558 (GRCm39) |
D2343G |
probably damaging |
Het |
| Tma7 |
A |
G |
9: 108,907,450 (GRCm39) |
|
probably benign |
Het |
| Tor3a |
T |
C |
1: 156,497,020 (GRCm39) |
D175G |
probably damaging |
Het |
| Tpo |
G |
T |
12: 30,144,964 (GRCm39) |
A595D |
possibly damaging |
Het |
| Tpst2 |
T |
C |
5: 112,456,091 (GRCm39) |
V210A |
probably damaging |
Het |
| Uchl1 |
A |
T |
5: 66,839,824 (GRCm39) |
E122V |
probably benign |
Het |
| Vmn1r210 |
A |
T |
13: 23,011,405 (GRCm39) |
F294I |
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 |
|
|
IGL00823:Dmd
|
APN |
X |
83,469,419 (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 |
|
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 |
2016-08-02 |
Incidental Mutation