Incidental Mutation 'R4620:Myo18a'
ID |
345252 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Myo18a
|
Ensembl Gene |
ENSMUSG00000000631 |
Gene Name |
myosin XVIIIA |
Synonyms |
MyoPDZ |
MMRRC Submission |
042008-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R4620 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
11 |
Chromosomal Location |
77654072-77756806 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 77708773 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Arginine to Histidine
at position 48
(R48H)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000131771
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000000645]
[ENSMUST00000092884]
[ENSMUST00000092887]
[ENSMUST00000100794]
[ENSMUST00000102488]
[ENSMUST00000108375]
[ENSMUST00000108376]
[ENSMUST00000164334]
[ENSMUST00000168348]
[ENSMUST00000169105]
[ENSMUST00000130305]
[ENSMUST00000172303]
[ENSMUST00000130627]
[ENSMUST00000151373]
[ENSMUST00000167856]
|
AlphaFold |
Q9JMH9 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000000645
AA Change: R379H
PolyPhen 2
Score 0.787 (Sensitivity: 0.85; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000000645 Gene: ENSMUSG00000000631 AA Change: R379H
Domain | Start | End | E-Value | Type |
low complexity region
|
6 |
27 |
N/A |
INTRINSIC |
low complexity region
|
202 |
227 |
N/A |
INTRINSIC |
PDZ
|
229 |
311 |
5.72e-10 |
SMART |
MYSc
|
399 |
1183 |
1.53e-45 |
SMART |
IQ
|
1184 |
1206 |
1.11e-3 |
SMART |
Pfam:Myosin_tail_1
|
1219 |
1867 |
1.7e-34 |
PFAM |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000092884
AA Change: R48H
PolyPhen 2
Score 0.867 (Sensitivity: 0.83; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000090560 Gene: ENSMUSG00000000631 AA Change: R48H
Domain | Start | End | E-Value | Type |
MYSc
|
68 |
851 |
4.16e-47 |
SMART |
IQ
|
852 |
874 |
1.11e-3 |
SMART |
Pfam:Myosin_tail_1
|
888 |
1534 |
2e-34 |
PFAM |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000092887
AA Change: R379H
PolyPhen 2
Score 0.783 (Sensitivity: 0.85; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000090563 Gene: ENSMUSG00000000631 AA Change: R379H
Domain | Start | End | E-Value | Type |
low complexity region
|
6 |
27 |
N/A |
INTRINSIC |
low complexity region
|
202 |
227 |
N/A |
INTRINSIC |
PDZ
|
229 |
311 |
5.72e-10 |
SMART |
MYSc
|
399 |
1182 |
4.16e-47 |
SMART |
IQ
|
1183 |
1205 |
1.11e-3 |
SMART |
Pfam:Myosin_tail_1
|
1218 |
1866 |
3e-34 |
PFAM |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000100794
AA Change: R48H
PolyPhen 2
Score 0.893 (Sensitivity: 0.82; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000098358 Gene: ENSMUSG00000000631 AA Change: R48H
Domain | Start | End | E-Value | Type |
MYSc
|
68 |
847 |
1.45e-46 |
SMART |
IQ
|
848 |
870 |
1.11e-3 |
SMART |
Pfam:Myosin_tail_1
|
884 |
1530 |
4.9e-35 |
PFAM |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000102488
AA Change: R379H
PolyPhen 2
Score 0.783 (Sensitivity: 0.85; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000099546 Gene: ENSMUSG00000000631 AA Change: R379H
Domain | Start | End | E-Value | Type |
low complexity region
|
6 |
27 |
N/A |
INTRINSIC |
low complexity region
|
202 |
227 |
N/A |
INTRINSIC |
PDZ
|
229 |
311 |
5.72e-10 |
SMART |
MYSc
|
399 |
1182 |
4.16e-47 |
SMART |
IQ
|
1183 |
1205 |
1.11e-3 |
SMART |
Pfam:Myosin_tail_1
|
1218 |
1866 |
3e-34 |
PFAM |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000108375
AA Change: R379H
PolyPhen 2
Score 0.783 (Sensitivity: 0.85; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000104012 Gene: ENSMUSG00000000631 AA Change: R379H
Domain | Start | End | E-Value | Type |
low complexity region
|
6 |
27 |
N/A |
INTRINSIC |
low complexity region
|
202 |
227 |
N/A |
INTRINSIC |
PDZ
|
229 |
311 |
5.72e-10 |
SMART |
MYSc
|
399 |
1182 |
4.16e-47 |
SMART |
IQ
|
1183 |
1205 |
1.11e-3 |
SMART |
Pfam:Myosin_tail_1
|
1218 |
1838 |
6.8e-36 |
PFAM |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000108376
AA Change: R379H
PolyPhen 2
Score 0.783 (Sensitivity: 0.85; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000104013 Gene: ENSMUSG00000000631 AA Change: R379H
Domain | Start | End | E-Value | Type |
low complexity region
|
6 |
27 |
N/A |
INTRINSIC |
low complexity region
|
202 |
227 |
N/A |
INTRINSIC |
PDZ
|
229 |
311 |
5.72e-10 |
SMART |
MYSc
|
399 |
1182 |
4.16e-47 |
SMART |
IQ
|
1183 |
1205 |
1.11e-3 |
SMART |
Blast:MYSc
|
1258 |
1387 |
1e-14 |
BLAST |
low complexity region
|
1396 |
1407 |
N/A |
INTRINSIC |
low complexity region
|
1743 |
1762 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000164334
AA Change: R48H
PolyPhen 2
Score 0.933 (Sensitivity: 0.80; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000131771 Gene: ENSMUSG00000000631 AA Change: R48H
Domain | Start | End | E-Value | Type |
MYSc
|
68 |
851 |
4.16e-47 |
SMART |
IQ
|
852 |
874 |
1.11e-3 |
SMART |
Pfam:Myosin_tail_1
|
888 |
1505 |
4e-36 |
PFAM |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000168348
AA Change: R427H
PolyPhen 2
Score 0.871 (Sensitivity: 0.83; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000130696 Gene: ENSMUSG00000000631 AA Change: R427H
Domain | Start | End | E-Value | Type |
low complexity region
|
6 |
27 |
N/A |
INTRINSIC |
low complexity region
|
202 |
227 |
N/A |
INTRINSIC |
PDZ
|
229 |
311 |
5.72e-10 |
SMART |
MYSc
|
447 |
1230 |
4.16e-47 |
SMART |
IQ
|
1231 |
1253 |
1.11e-3 |
SMART |
Blast:MYSc
|
1306 |
1435 |
1e-14 |
BLAST |
low complexity region
|
1444 |
1455 |
N/A |
INTRINSIC |
low complexity region
|
1828 |
1847 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000169105
AA Change: R391H
PolyPhen 2
Score 0.669 (Sensitivity: 0.86; Specificity: 0.91)
|
SMART Domains |
Protein: ENSMUSP00000132149 Gene: ENSMUSG00000000631 AA Change: R391H
Domain | Start | End | E-Value | Type |
low complexity region
|
6 |
27 |
N/A |
INTRINSIC |
low complexity region
|
202 |
227 |
N/A |
INTRINSIC |
PDZ
|
229 |
311 |
5.72e-10 |
SMART |
MYSc
|
411 |
1194 |
4.16e-47 |
SMART |
IQ
|
1195 |
1217 |
1.11e-3 |
SMART |
Pfam:Myosin_tail_1
|
1230 |
1878 |
7.3e-35 |
PFAM |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000130305
AA Change: R60H
PolyPhen 2
Score 0.861 (Sensitivity: 0.83; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000119574 Gene: ENSMUSG00000000631 AA Change: R60H
Domain | Start | End | E-Value | Type |
MYSc
|
80 |
863 |
4.16e-47 |
SMART |
IQ
|
864 |
886 |
1.11e-3 |
SMART |
Pfam:Myosin_tail_1
|
902 |
1547 |
2.6e-34 |
PFAM |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000172303
AA Change: R60H
PolyPhen 2
Score 0.783 (Sensitivity: 0.85; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000129098 Gene: ENSMUSG00000000631 AA Change: R60H
Domain | Start | End | E-Value | Type |
MYSc
|
80 |
863 |
4.16e-47 |
SMART |
IQ
|
864 |
886 |
1.11e-3 |
SMART |
Pfam:Myosin_tail_1
|
902 |
1547 |
2.6e-34 |
PFAM |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000130627
AA Change: R391H
PolyPhen 2
Score 0.933 (Sensitivity: 0.80; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000119839 Gene: ENSMUSG00000000631 AA Change: R391H
Domain | Start | End | E-Value | Type |
low complexity region
|
6 |
27 |
N/A |
INTRINSIC |
low complexity region
|
202 |
227 |
N/A |
INTRINSIC |
PDZ
|
229 |
311 |
5.72e-10 |
SMART |
MYSc
|
411 |
1194 |
4.16e-47 |
SMART |
IQ
|
1195 |
1217 |
1.11e-3 |
SMART |
Pfam:Myosin_tail_1
|
1230 |
1850 |
6.9e-36 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000151373
|
SMART Domains |
Protein: ENSMUSP00000123256 Gene: ENSMUSG00000000631
Domain | Start | End | E-Value | Type |
low complexity region
|
13 |
34 |
N/A |
INTRINSIC |
Blast:MYSc
|
45 |
89 |
3e-19 |
BLAST |
low complexity region
|
90 |
105 |
N/A |
INTRINSIC |
internal_repeat_1
|
115 |
134 |
4.34e-5 |
PROSPERO |
low complexity region
|
135 |
164 |
N/A |
INTRINSIC |
internal_repeat_1
|
188 |
209 |
4.34e-5 |
PROSPERO |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000167856
|
SMART Domains |
Protein: ENSMUSP00000128487 Gene: ENSMUSG00000000631
Domain | Start | End | E-Value | Type |
MYSc
|
16 |
789 |
1.3e-32 |
SMART |
IQ
|
790 |
812 |
1.11e-3 |
SMART |
Blast:MYSc
|
865 |
994 |
1e-14 |
BLAST |
low complexity region
|
1003 |
1014 |
N/A |
INTRINSIC |
low complexity region
|
1387 |
1406 |
N/A |
INTRINSIC |
internal_repeat_1
|
1569 |
1627 |
2.13e-5 |
PROSPERO |
|
Meta Mutation Damage Score |
0.1394 |
Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.6%
- 10x: 97.2%
- 20x: 95.1%
|
Validation Efficiency |
99% (80/81) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene can bind GOLPH3, linking the Golgi to the cytoskeleton and influencing Golgi membrane trafficking. The encoded protein is also part of a complex that assembles lamellar actomyosin bundles and may be required for cell migration. [provided by RefSeq, Oct 2016]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310057M21Rik |
A |
T |
7: 130,945,335 (GRCm39) |
Y433* |
probably null |
Het |
Apba2 |
C |
T |
7: 64,364,215 (GRCm39) |
R331C |
probably damaging |
Het |
Apod |
T |
C |
16: 31,116,211 (GRCm39) |
D173G |
probably benign |
Het |
B3gnt5 |
A |
T |
16: 19,588,632 (GRCm39) |
M284L |
probably benign |
Het |
Birc6 |
A |
C |
17: 74,947,145 (GRCm39) |
T2955P |
probably benign |
Het |
Blvra |
T |
C |
2: 126,938,885 (GRCm39) |
I287T |
probably damaging |
Het |
Capn5 |
T |
C |
7: 97,778,578 (GRCm39) |
Y347C |
probably damaging |
Het |
Cdcp2 |
A |
G |
4: 106,963,927 (GRCm39) |
E259G |
probably damaging |
Het |
Cdh2 |
A |
G |
18: 16,781,665 (GRCm39) |
V85A |
probably benign |
Het |
Cdk5rap2 |
A |
G |
4: 70,184,943 (GRCm39) |
I1169T |
probably benign |
Het |
Cenpj |
A |
G |
14: 56,772,911 (GRCm39) |
V1043A |
probably damaging |
Het |
Cfap54 |
T |
A |
10: 92,805,619 (GRCm39) |
H1497L |
probably benign |
Het |
Chat |
A |
G |
14: 32,175,775 (GRCm39) |
M95T |
probably damaging |
Het |
Csmd1 |
T |
C |
8: 16,052,694 (GRCm39) |
|
probably null |
Het |
Csmd3 |
T |
C |
15: 47,449,149 (GRCm39) |
E3615G |
probably benign |
Het |
Cyp2c68 |
A |
T |
19: 39,701,006 (GRCm39) |
|
probably null |
Het |
Dll1 |
C |
T |
17: 15,590,828 (GRCm39) |
A332T |
probably benign |
Het |
Dmrta1 |
A |
T |
4: 89,577,021 (GRCm39) |
Q159L |
probably benign |
Het |
Dnai3 |
A |
T |
3: 145,748,564 (GRCm39) |
L850Q |
probably damaging |
Het |
Eci3 |
A |
T |
13: 35,132,741 (GRCm39) |
M212K |
probably damaging |
Het |
Eml4 |
T |
C |
17: 83,768,962 (GRCm39) |
F557L |
probably benign |
Het |
Fat3 |
A |
T |
9: 15,908,190 (GRCm39) |
V2604D |
probably damaging |
Het |
Frem3 |
T |
C |
8: 81,395,586 (GRCm39) |
V1871A |
possibly damaging |
Het |
Gart |
T |
C |
16: 91,422,321 (GRCm39) |
N732S |
probably damaging |
Het |
Gas2l2 |
T |
C |
11: 83,313,924 (GRCm39) |
I463V |
probably benign |
Het |
H2-M3 |
C |
A |
17: 37,583,310 (GRCm39) |
T257K |
probably damaging |
Het |
Hdgf |
A |
G |
3: 87,821,883 (GRCm39) |
N166S |
possibly damaging |
Het |
Hoxb3 |
A |
T |
11: 96,236,599 (GRCm39) |
N226Y |
probably damaging |
Het |
Itgav |
T |
C |
2: 83,586,246 (GRCm39) |
Y169H |
probably benign |
Het |
Kalrn |
T |
G |
16: 33,849,075 (GRCm39) |
I426L |
probably damaging |
Het |
Kcnh3 |
G |
A |
15: 99,131,982 (GRCm39) |
V646M |
probably damaging |
Het |
Kif6 |
T |
C |
17: 50,208,324 (GRCm39) |
V735A |
probably benign |
Het |
Krt1c |
T |
A |
15: 101,726,026 (GRCm39) |
I171F |
probably damaging |
Het |
Megf8 |
G |
A |
7: 25,054,523 (GRCm39) |
A1880T |
possibly damaging |
Het |
Miox |
A |
T |
15: 89,220,324 (GRCm39) |
Y172F |
probably benign |
Het |
Ndufb7 |
T |
C |
8: 84,293,487 (GRCm39) |
S14P |
probably damaging |
Het |
Npepps |
A |
T |
11: 97,129,070 (GRCm39) |
H371Q |
probably damaging |
Het |
Or10d5j |
C |
T |
9: 39,868,205 (GRCm39) |
V9M |
probably damaging |
Het |
Or52e15 |
T |
A |
7: 104,645,830 (GRCm39) |
I94F |
probably damaging |
Het |
Or52e19 |
C |
T |
7: 102,959,165 (GRCm39) |
T79I |
probably benign |
Het |
Or8b12c |
A |
G |
9: 37,716,115 (GRCm39) |
T303A |
probably benign |
Het |
Orc5 |
A |
T |
5: 22,734,174 (GRCm39) |
D203E |
probably damaging |
Het |
Pappa |
A |
G |
4: 65,245,265 (GRCm39) |
T1518A |
probably benign |
Het |
Pde6a |
A |
G |
18: 61,395,563 (GRCm39) |
D602G |
probably damaging |
Het |
Pnliprp2 |
G |
A |
19: 58,750,718 (GRCm39) |
V136I |
possibly damaging |
Het |
Postn |
A |
C |
3: 54,284,414 (GRCm39) |
D627A |
probably damaging |
Het |
Prpf39 |
T |
C |
12: 65,089,337 (GRCm39) |
V25A |
probably benign |
Het |
Pxdc1 |
A |
G |
13: 34,836,297 (GRCm39) |
I41T |
probably damaging |
Het |
Rab11fip1 |
T |
A |
8: 27,644,243 (GRCm39) |
E514V |
probably damaging |
Het |
Rag1 |
A |
T |
2: 101,474,025 (GRCm39) |
H372Q |
probably damaging |
Het |
Ranbp1 |
A |
G |
16: 18,057,968 (GRCm39) |
|
probably benign |
Het |
Rexo5 |
A |
G |
7: 119,426,526 (GRCm39) |
I317V |
probably benign |
Het |
Rragc |
A |
G |
4: 123,818,622 (GRCm39) |
Q279R |
probably damaging |
Het |
Sbf1 |
A |
G |
15: 89,191,129 (GRCm39) |
S187P |
probably damaging |
Het |
Senp3 |
T |
A |
11: 69,567,944 (GRCm39) |
Y432F |
probably benign |
Het |
Slfn5 |
G |
A |
11: 82,852,478 (GRCm39) |
C868Y |
probably damaging |
Het |
Sorcs2 |
C |
T |
5: 36,194,838 (GRCm39) |
A722T |
probably benign |
Het |
Sptb |
A |
T |
12: 76,630,581 (GRCm39) |
C2244* |
probably null |
Het |
Srbd1 |
A |
T |
17: 86,416,693 (GRCm39) |
F488L |
probably benign |
Het |
Sucnr1 |
A |
G |
3: 59,994,190 (GRCm39) |
I239M |
possibly damaging |
Het |
Themis2 |
A |
G |
4: 132,513,333 (GRCm39) |
W298R |
probably damaging |
Het |
Tmem168 |
T |
G |
6: 13,594,952 (GRCm39) |
N37T |
probably benign |
Het |
Tmem62 |
A |
G |
2: 120,826,845 (GRCm39) |
|
probably benign |
Het |
Tmprss15 |
T |
C |
16: 78,818,358 (GRCm39) |
D524G |
probably damaging |
Het |
Trav5-4 |
G |
T |
14: 53,941,853 (GRCm39) |
M75I |
probably benign |
Het |
Trio |
T |
A |
15: 27,871,257 (GRCm39) |
H620L |
probably damaging |
Het |
Ubap2 |
C |
T |
4: 41,233,698 (GRCm39) |
G64E |
probably damaging |
Het |
Usp32 |
C |
A |
11: 84,949,953 (GRCm39) |
|
probably null |
Het |
Wdfy3 |
A |
T |
5: 102,054,011 (GRCm39) |
F1603Y |
probably damaging |
Het |
Xpo4 |
A |
T |
14: 57,867,782 (GRCm39) |
L155Q |
probably damaging |
Het |
Zbtb21 |
T |
C |
16: 97,751,092 (GRCm39) |
T1092A |
possibly damaging |
Het |
Zfp780b |
A |
T |
7: 27,662,178 (GRCm39) |
Y792* |
probably null |
Het |
|
Other mutations in Myo18a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00089:Myo18a
|
APN |
11 |
77,738,764 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00753:Myo18a
|
APN |
11 |
77,715,977 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01137:Myo18a
|
APN |
11 |
77,718,655 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01536:Myo18a
|
APN |
11 |
77,711,677 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01642:Myo18a
|
APN |
11 |
77,755,558 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01728:Myo18a
|
APN |
11 |
77,668,682 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01780:Myo18a
|
APN |
11 |
77,741,073 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02286:Myo18a
|
APN |
11 |
77,668,811 (GRCm39) |
nonsense |
probably null |
|
IGL02350:Myo18a
|
APN |
11 |
77,741,073 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02357:Myo18a
|
APN |
11 |
77,741,073 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02420:Myo18a
|
APN |
11 |
77,709,519 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02643:Myo18a
|
APN |
11 |
77,668,998 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02667:Myo18a
|
APN |
11 |
77,748,678 (GRCm39) |
splice site |
probably benign |
|
IGL02869:Myo18a
|
APN |
11 |
77,720,699 (GRCm39) |
splice site |
probably benign |
|
IGL02869:Myo18a
|
APN |
11 |
77,755,612 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02962:Myo18a
|
APN |
11 |
77,669,061 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02963:Myo18a
|
APN |
11 |
77,732,844 (GRCm39) |
splice site |
probably benign |
|
IGL03410:Myo18a
|
APN |
11 |
77,738,830 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03050:Myo18a
|
UTSW |
11 |
77,709,596 (GRCm39) |
missense |
probably benign |
0.00 |
R0022:Myo18a
|
UTSW |
11 |
77,734,059 (GRCm39) |
critical splice donor site |
probably null |
|
R0064:Myo18a
|
UTSW |
11 |
77,738,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R0064:Myo18a
|
UTSW |
11 |
77,738,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R0098:Myo18a
|
UTSW |
11 |
77,736,591 (GRCm39) |
missense |
probably damaging |
1.00 |
R0322:Myo18a
|
UTSW |
11 |
77,720,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R0373:Myo18a
|
UTSW |
11 |
77,711,868 (GRCm39) |
missense |
probably benign |
0.01 |
R0379:Myo18a
|
UTSW |
11 |
77,741,632 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0513:Myo18a
|
UTSW |
11 |
77,702,420 (GRCm39) |
intron |
probably benign |
|
R0688:Myo18a
|
UTSW |
11 |
77,714,966 (GRCm39) |
missense |
probably damaging |
1.00 |
R0734:Myo18a
|
UTSW |
11 |
77,738,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R0790:Myo18a
|
UTSW |
11 |
77,731,535 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1099:Myo18a
|
UTSW |
11 |
77,709,727 (GRCm39) |
splice site |
probably null |
|
R1103:Myo18a
|
UTSW |
11 |
77,714,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R1183:Myo18a
|
UTSW |
11 |
77,748,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R1216:Myo18a
|
UTSW |
11 |
77,709,473 (GRCm39) |
missense |
probably benign |
0.35 |
R1331:Myo18a
|
UTSW |
11 |
77,732,405 (GRCm39) |
missense |
probably benign |
0.28 |
R1479:Myo18a
|
UTSW |
11 |
77,733,020 (GRCm39) |
missense |
probably benign |
0.04 |
R1723:Myo18a
|
UTSW |
11 |
77,744,140 (GRCm39) |
missense |
probably damaging |
0.97 |
R1742:Myo18a
|
UTSW |
11 |
77,732,293 (GRCm39) |
missense |
probably damaging |
0.99 |
R1796:Myo18a
|
UTSW |
11 |
77,720,170 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1823:Myo18a
|
UTSW |
11 |
77,715,923 (GRCm39) |
splice site |
probably benign |
|
R1827:Myo18a
|
UTSW |
11 |
77,709,597 (GRCm39) |
missense |
probably benign |
0.00 |
R2033:Myo18a
|
UTSW |
11 |
77,733,925 (GRCm39) |
splice site |
probably null |
|
R2043:Myo18a
|
UTSW |
11 |
77,714,189 (GRCm39) |
missense |
probably damaging |
0.99 |
R2105:Myo18a
|
UTSW |
11 |
77,741,060 (GRCm39) |
missense |
probably benign |
|
R2191:Myo18a
|
UTSW |
11 |
77,709,441 (GRCm39) |
missense |
probably damaging |
0.99 |
R2264:Myo18a
|
UTSW |
11 |
77,710,798 (GRCm39) |
splice site |
probably benign |
|
R2370:Myo18a
|
UTSW |
11 |
77,668,596 (GRCm39) |
missense |
probably benign |
0.03 |
R3015:Myo18a
|
UTSW |
11 |
77,749,846 (GRCm39) |
intron |
probably benign |
|
R3433:Myo18a
|
UTSW |
11 |
77,708,870 (GRCm39) |
splice site |
probably null |
|
R3739:Myo18a
|
UTSW |
11 |
77,736,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R3825:Myo18a
|
UTSW |
11 |
77,668,292 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4056:Myo18a
|
UTSW |
11 |
77,702,839 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4163:Myo18a
|
UTSW |
11 |
77,720,534 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4184:Myo18a
|
UTSW |
11 |
77,748,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R4628:Myo18a
|
UTSW |
11 |
77,714,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R4647:Myo18a
|
UTSW |
11 |
77,708,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R4701:Myo18a
|
UTSW |
11 |
77,708,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R4729:Myo18a
|
UTSW |
11 |
77,668,511 (GRCm39) |
splice site |
probably null |
|
R4731:Myo18a
|
UTSW |
11 |
77,720,585 (GRCm39) |
missense |
probably benign |
0.00 |
R4739:Myo18a
|
UTSW |
11 |
77,714,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R4814:Myo18a
|
UTSW |
11 |
77,750,062 (GRCm39) |
intron |
probably benign |
|
R4889:Myo18a
|
UTSW |
11 |
77,723,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R4988:Myo18a
|
UTSW |
11 |
77,736,347 (GRCm39) |
critical splice donor site |
probably null |
|
R5172:Myo18a
|
UTSW |
11 |
77,714,924 (GRCm39) |
missense |
probably damaging |
1.00 |
R5177:Myo18a
|
UTSW |
11 |
77,755,668 (GRCm39) |
utr 3 prime |
probably benign |
|
R5394:Myo18a
|
UTSW |
11 |
77,744,176 (GRCm39) |
missense |
probably benign |
0.14 |
R5643:Myo18a
|
UTSW |
11 |
77,745,513 (GRCm39) |
missense |
probably benign |
0.12 |
R5808:Myo18a
|
UTSW |
11 |
77,720,127 (GRCm39) |
missense |
probably benign |
0.34 |
R5871:Myo18a
|
UTSW |
11 |
77,723,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R5936:Myo18a
|
UTSW |
11 |
77,709,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R6017:Myo18a
|
UTSW |
11 |
77,732,349 (GRCm39) |
missense |
probably damaging |
0.96 |
R6053:Myo18a
|
UTSW |
11 |
77,709,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R6271:Myo18a
|
UTSW |
11 |
77,711,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R6486:Myo18a
|
UTSW |
11 |
77,755,648 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6558:Myo18a
|
UTSW |
11 |
77,741,678 (GRCm39) |
missense |
probably damaging |
0.99 |
R6884:Myo18a
|
UTSW |
11 |
77,709,875 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6983:Myo18a
|
UTSW |
11 |
77,736,341 (GRCm39) |
missense |
probably benign |
0.06 |
R6993:Myo18a
|
UTSW |
11 |
77,749,900 (GRCm39) |
intron |
probably benign |
|
R7071:Myo18a
|
UTSW |
11 |
77,714,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R7074:Myo18a
|
UTSW |
11 |
77,733,387 (GRCm39) |
missense |
probably benign |
0.03 |
R7238:Myo18a
|
UTSW |
11 |
77,733,059 (GRCm39) |
missense |
probably damaging |
0.96 |
R7328:Myo18a
|
UTSW |
11 |
77,698,737 (GRCm39) |
missense |
|
|
R7527:Myo18a
|
UTSW |
11 |
77,734,406 (GRCm39) |
missense |
probably benign |
0.00 |
R7598:Myo18a
|
UTSW |
11 |
77,738,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R7671:Myo18a
|
UTSW |
11 |
77,750,246 (GRCm39) |
missense |
|
|
R7958:Myo18a
|
UTSW |
11 |
77,732,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R8098:Myo18a
|
UTSW |
11 |
77,736,227 (GRCm39) |
missense |
probably damaging |
0.97 |
R8168:Myo18a
|
UTSW |
11 |
77,711,968 (GRCm39) |
missense |
probably damaging |
0.99 |
R8318:Myo18a
|
UTSW |
11 |
77,714,215 (GRCm39) |
missense |
probably benign |
0.02 |
R8685:Myo18a
|
UTSW |
11 |
77,745,520 (GRCm39) |
missense |
probably benign |
0.00 |
R8778:Myo18a
|
UTSW |
11 |
77,714,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R9023:Myo18a
|
UTSW |
11 |
77,718,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R9059:Myo18a
|
UTSW |
11 |
77,668,899 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9186:Myo18a
|
UTSW |
11 |
77,749,847 (GRCm39) |
missense |
|
|
R9321:Myo18a
|
UTSW |
11 |
77,733,370 (GRCm39) |
missense |
probably damaging |
0.97 |
R9357:Myo18a
|
UTSW |
11 |
77,733,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R9407:Myo18a
|
UTSW |
11 |
77,709,596 (GRCm39) |
missense |
probably benign |
0.00 |
R9430:Myo18a
|
UTSW |
11 |
77,709,410 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9576:Myo18a
|
UTSW |
11 |
77,709,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R9585:Myo18a
|
UTSW |
11 |
77,709,495 (GRCm39) |
missense |
probably benign |
0.06 |
R9698:Myo18a
|
UTSW |
11 |
77,720,681 (GRCm39) |
missense |
probably damaging |
0.99 |
R9743:Myo18a
|
UTSW |
11 |
77,723,304 (GRCm39) |
missense |
probably benign |
0.10 |
R9777:Myo18a
|
UTSW |
11 |
77,733,080 (GRCm39) |
missense |
possibly damaging |
0.94 |
Y5407:Myo18a
|
UTSW |
11 |
77,668,641 (GRCm39) |
missense |
probably benign |
0.44 |
Z1177:Myo18a
|
UTSW |
11 |
77,732,821 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1187:Myo18a
|
UTSW |
11 |
77,744,643 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
Predicted Primers |
PCR Primer
(F):5'- TTGAGTCAGAACTGGCATGAG -3'
(R):5'- GCCAGATCTTCTAGACGGTC -3'
Sequencing Primer
(F):5'- AAATGCCTCTGCCCCTGGTAAG -3'
(R):5'- GCCAGATCTTCTAGACGGTCACATG -3'
|
Posted On |
2015-09-25 |