Incidental Mutation 'IGL01285:Des'
| ID |
72697 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Des
|
| Ensembl Gene |
ENSMUSG00000026208 |
| Gene Name |
desmin |
| Synonyms |
|
| Accession Numbers |
|
| Essential gene? |
Possibly essential
(E-score: 0.642)
|
| Stock # |
IGL01285
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
1 |
| Chromosomal Location |
75336973-75345223 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 75339227 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Alanine to Threonine
at position 251
(A251T)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000027409
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000027409]
|
| AlphaFold |
P31001 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000027409
AA Change: A251T
PolyPhen 2
Score 0.019 (Sensitivity: 0.95; Specificity: 0.80)
|
| SMART Domains |
Protein: ENSMUSP00000027409
Gene: ENSMUSG00000026208
AA Change: A251T
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Filament_head
|
9 |
105 |
1.3e-25 |
PFAM |
|
Filament
|
106 |
414 |
7.41e-148 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000125948
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000144894
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: This gene encodes a muscle-specific class III intermediate filament. Homopolymers of this protein form a stable intracytoplasmic filamentous network connecting myofibrils to each other and to the plasma membrane and are essential for maintaining the strength and integrity of skeletal, cardiac and smooth muscle fibers. Mutations in this gene affect assembly of intermediate filaments. Mice lacking this gene are able to develop and reproduce but exhibit abnormal muscle fibers. Mutations in the human gene are associated with myofibrillar myopathy, dilated cardiomyopathy, neurogenic scapuloperoneal syndrome and autosomal recessive limb-girdle muscular dystrophy, type 2R. [provided by RefSeq, Jan 2014]
PHENOTYPE: Homozygotes for targeted null mutations exhibit histologically detectable defects of cardiac, skeletal, and smooth muscle. Defects in the heart are most severe, and lead to calcification, progressive degeneration, and necrosis of the myocardium. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 47 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adam5 |
T |
C |
8: 25,271,610 (GRCm39) |
N599S |
probably benign |
Het |
| Adam6a |
A |
T |
12: 113,509,893 (GRCm39) |
*755Y |
probably null |
Het |
| Adgrb3 |
G |
T |
1: 25,132,868 (GRCm39) |
T1166K |
probably benign |
Het |
| Ano1 |
T |
C |
7: 144,198,479 (GRCm39) |
Y345C |
probably benign |
Het |
| Ano1 |
A |
G |
7: 144,149,275 (GRCm39) |
V862A |
probably damaging |
Het |
| Asap2 |
C |
T |
12: 21,279,264 (GRCm39) |
A382V |
probably damaging |
Het |
| Asb18 |
A |
G |
1: 89,923,963 (GRCm39) |
V100A |
probably benign |
Het |
| Bdnf |
G |
A |
2: 109,553,931 (GRCm39) |
A102T |
probably benign |
Het |
| Ccser2 |
G |
A |
14: 36,660,626 (GRCm39) |
T509M |
probably damaging |
Het |
| Cfap47 |
A |
G |
X: 78,532,764 (GRCm39) |
I767T |
possibly damaging |
Het |
| Dmd |
C |
T |
X: 84,153,590 (GRCm39) |
Q3224* |
probably null |
Het |
| Endog |
G |
T |
2: 30,061,975 (GRCm39) |
|
probably null |
Het |
| Ggt7 |
A |
G |
2: 155,342,691 (GRCm39) |
V269A |
probably damaging |
Het |
| Gucy2c |
A |
G |
6: 136,686,739 (GRCm39) |
F808S |
probably damaging |
Het |
| Hira |
A |
G |
16: 18,730,930 (GRCm39) |
T210A |
probably benign |
Het |
| Ifitm5 |
C |
A |
7: 140,530,076 (GRCm39) |
R16L |
probably benign |
Het |
| Igdcc4 |
T |
C |
9: 65,031,273 (GRCm39) |
C404R |
probably damaging |
Het |
| Ints7 |
G |
A |
1: 191,347,890 (GRCm39) |
R754H |
probably benign |
Het |
| Irf9 |
A |
G |
14: 55,845,058 (GRCm39) |
E258G |
probably damaging |
Het |
| Megf11 |
T |
C |
9: 64,567,728 (GRCm39) |
C406R |
probably damaging |
Het |
| Olfml1 |
A |
G |
7: 107,189,364 (GRCm39) |
N143S |
possibly damaging |
Het |
| Or4m1 |
A |
G |
14: 50,557,713 (GRCm39) |
F193S |
possibly damaging |
Het |
| Or6c66b |
T |
A |
10: 129,376,711 (GRCm39) |
F102I |
probably benign |
Het |
| Or7g30 |
A |
G |
9: 19,352,266 (GRCm39) |
D19G |
probably benign |
Het |
| Otof |
G |
T |
5: 30,562,527 (GRCm39) |
Q254K |
probably damaging |
Het |
| Pate7 |
A |
T |
9: 35,688,044 (GRCm39) |
N65K |
possibly damaging |
Het |
| Plcd3 |
A |
G |
11: 102,968,696 (GRCm39) |
F332L |
probably benign |
Het |
| Plxnc1 |
T |
C |
10: 94,635,230 (GRCm39) |
D1332G |
probably damaging |
Het |
| Rnasel |
A |
T |
1: 153,634,130 (GRCm39) |
D521V |
probably benign |
Het |
| Sema5a |
T |
A |
15: 32,575,143 (GRCm39) |
V417D |
possibly damaging |
Het |
| Senp6 |
G |
A |
9: 80,044,000 (GRCm39) |
R877Q |
probably benign |
Het |
| Shroom2 |
A |
T |
X: 151,442,353 (GRCm39) |
D937E |
probably damaging |
Het |
| Slc35a3 |
A |
G |
3: 116,488,262 (GRCm39) |
S142P |
probably damaging |
Het |
| Srpx |
A |
T |
X: 9,905,298 (GRCm39) |
V398E |
probably damaging |
Het |
| Stk10 |
A |
T |
11: 32,560,653 (GRCm39) |
K669N |
possibly damaging |
Het |
| Sumf2 |
A |
G |
5: 129,878,811 (GRCm39) |
D49G |
probably damaging |
Het |
| Syde1 |
T |
A |
10: 78,424,721 (GRCm39) |
E370D |
probably damaging |
Het |
| Tas2r115 |
G |
T |
6: 132,714,641 (GRCm39) |
S103R |
probably damaging |
Het |
| Top2a |
G |
A |
11: 98,896,985 (GRCm39) |
|
probably benign |
Het |
| Ttn |
T |
A |
2: 76,550,842 (GRCm39) |
T23190S |
probably damaging |
Het |
| Ttyh3 |
C |
A |
5: 140,615,167 (GRCm39) |
C407F |
probably damaging |
Het |
| Vmn2r27 |
G |
T |
6: 124,169,370 (GRCm39) |
H587N |
possibly damaging |
Het |
| Vmn2r74 |
A |
G |
7: 85,606,692 (GRCm39) |
I218T |
possibly damaging |
Het |
| Vsig10 |
A |
G |
5: 117,462,954 (GRCm39) |
N60S |
probably benign |
Het |
| Zc3h7a |
A |
G |
16: 10,956,979 (GRCm39) |
S877P |
probably damaging |
Het |
| Zfp979 |
G |
T |
4: 147,699,853 (GRCm39) |
T29N |
probably damaging |
Het |
| Znfx1 |
G |
A |
2: 166,880,615 (GRCm39) |
R390C |
possibly damaging |
Het |
|
| Other mutations in Des |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02416:Des
|
APN |
1 |
75,339,372 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL02953:Des
|
APN |
1 |
75,340,288 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
IGL03156:Des
|
APN |
1 |
75,339,640 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03288:Des
|
APN |
1 |
75,338,985 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R0032:Des
|
UTSW |
1 |
75,338,810 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R0849:Des
|
UTSW |
1 |
75,337,272 (GRCm39) |
missense |
probably benign |
|
|
R0885:Des
|
UTSW |
1 |
75,337,374 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1271:Des
|
UTSW |
1 |
75,337,290 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1452:Des
|
UTSW |
1 |
75,340,121 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1559:Des
|
UTSW |
1 |
75,337,230 (GRCm39) |
missense |
probably benign |
0.11 |
|
R1929:Des
|
UTSW |
1 |
75,340,137 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2144:Des
|
UTSW |
1 |
75,343,448 (GRCm39) |
missense |
probably benign |
0.45 |
|
R2145:Des
|
UTSW |
1 |
75,340,108 (GRCm39) |
splice site |
probably benign |
|
|
R2271:Des
|
UTSW |
1 |
75,340,137 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4182:Des
|
UTSW |
1 |
75,339,228 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4184:Des
|
UTSW |
1 |
75,339,228 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4383:Des
|
UTSW |
1 |
75,337,413 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R5268:Des
|
UTSW |
1 |
75,339,572 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R5787:Des
|
UTSW |
1 |
75,340,290 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5974:Des
|
UTSW |
1 |
75,339,628 (GRCm39) |
missense |
probably benign |
0.10 |
|
R6044:Des
|
UTSW |
1 |
75,340,113 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R6985:Des
|
UTSW |
1 |
75,343,431 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R7359:Des
|
UTSW |
1 |
75,337,596 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7467:Des
|
UTSW |
1 |
75,339,605 (GRCm39) |
missense |
possibly damaging |
0.48 |
|
R7798:Des
|
UTSW |
1 |
75,339,003 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R8878:Des
|
UTSW |
1 |
75,337,137 (GRCm39) |
missense |
unknown |
|
|
R8957:Des
|
UTSW |
1 |
75,340,295 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9245:Des
|
UTSW |
1 |
75,343,406 (GRCm39) |
missense |
probably benign |
0.17 |
|
R9258:Des
|
UTSW |
1 |
75,340,289 (GRCm39) |
missense |
probably benign |
0.21 |
|
R9507:Des
|
UTSW |
1 |
75,343,434 (GRCm39) |
missense |
probably benign |
0.02 |
|
R9707:Des
|
UTSW |
1 |
75,337,533 (GRCm39) |
missense |
possibly damaging |
0.51 |
|
| Posted On |
2013-10-07 |
Incidental Mutation