Incidental Mutation 'R1635:Myo5c'
ID |
173084 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Myo5c
|
Ensembl Gene |
ENSMUSG00000033590 |
Gene Name |
myosin VC |
Synonyms |
9130003O20Rik |
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R1635 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
9 |
Chromosomal Location |
75139302-75212733 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 75184357 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Arginine to Serine
at position 949
(R949S)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000042229
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000036555]
[ENSMUST00000216788]
|
AlphaFold |
E9Q1F5 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000036555
AA Change: R949S
PolyPhen 2
Score 0.087 (Sensitivity: 0.93; Specificity: 0.85)
|
SMART Domains |
Protein: ENSMUSP00000042229 Gene: ENSMUSG00000033590 AA Change: R949S
Domain | Start | End | E-Value | Type |
MYSc
|
61 |
754 |
N/A |
SMART |
IQ
|
755 |
777 |
1.11e-3 |
SMART |
IQ
|
778 |
800 |
1.39e0 |
SMART |
IQ
|
806 |
828 |
8.98e-4 |
SMART |
IQ
|
829 |
851 |
4.19e-4 |
SMART |
IQ
|
854 |
876 |
2.54e-3 |
SMART |
coiled coil region
|
1160 |
1185 |
N/A |
INTRINSIC |
coiled coil region
|
1207 |
1245 |
N/A |
INTRINSIC |
DIL
|
1574 |
1679 |
5.54e-45 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000216788
|
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.3%
- 10x: 96.0%
- 20x: 91.9%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca2 |
A |
T |
2: 25,334,868 (GRCm39) |
I1947F |
probably benign |
Het |
Adgrd1 |
G |
T |
5: 129,205,971 (GRCm39) |
V182F |
probably damaging |
Het |
Agmat |
A |
G |
4: 141,474,380 (GRCm39) |
D87G |
probably damaging |
Het |
AI182371 |
T |
C |
2: 34,978,749 (GRCm39) |
|
probably null |
Het |
Anapc1 |
G |
T |
2: 128,470,452 (GRCm39) |
H1559Q |
probably damaging |
Het |
Ankar |
T |
C |
1: 72,689,297 (GRCm39) |
Y1278C |
probably damaging |
Het |
Arhgef2 |
A |
T |
3: 88,546,628 (GRCm39) |
|
probably null |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
Banp |
A |
T |
8: 122,727,750 (GRCm39) |
I130F |
probably damaging |
Het |
C130050O18Rik |
G |
T |
5: 139,400,248 (GRCm39) |
R100S |
probably benign |
Het |
Carmil3 |
A |
G |
14: 55,733,739 (GRCm39) |
T374A |
possibly damaging |
Het |
Cc2d2a |
T |
A |
5: 43,879,812 (GRCm39) |
W1076R |
probably damaging |
Het |
Cdc34 |
T |
G |
10: 79,523,888 (GRCm39) |
S235A |
probably benign |
Het |
Cdh8 |
G |
T |
8: 99,757,656 (GRCm39) |
H647Q |
probably damaging |
Het |
Cdk1 |
A |
T |
10: 69,174,377 (GRCm39) |
L282Q |
probably damaging |
Het |
Ceacam3 |
A |
G |
7: 16,893,902 (GRCm39) |
D471G |
probably damaging |
Het |
Ciao2b |
A |
T |
8: 105,367,620 (GRCm39) |
I108N |
possibly damaging |
Het |
Cltc |
A |
T |
11: 86,648,105 (GRCm39) |
I4N |
probably benign |
Het |
Cntfr |
T |
A |
4: 41,658,816 (GRCm39) |
E305V |
probably damaging |
Het |
Cwh43 |
T |
A |
5: 73,591,653 (GRCm39) |
I496N |
probably damaging |
Het |
Cyp2f2 |
A |
G |
7: 26,829,149 (GRCm39) |
N218S |
probably benign |
Het |
D16Ertd472e |
A |
G |
16: 78,343,392 (GRCm39) |
|
probably null |
Het |
Dab2 |
A |
G |
15: 6,459,351 (GRCm39) |
Q400R |
possibly damaging |
Het |
Dapl1 |
A |
T |
2: 59,326,906 (GRCm39) |
I51F |
probably benign |
Het |
Drc7 |
G |
A |
8: 95,800,960 (GRCm39) |
|
probably null |
Het |
Etl4 |
A |
G |
2: 20,811,219 (GRCm39) |
T1101A |
probably damaging |
Het |
Fam83c |
C |
A |
2: 155,671,971 (GRCm39) |
R488M |
possibly damaging |
Het |
Fbxo42 |
A |
G |
4: 140,927,840 (GRCm39) |
T707A |
probably damaging |
Het |
Fcmr |
A |
T |
1: 130,803,922 (GRCm39) |
|
probably null |
Het |
Fer1l6 |
G |
C |
15: 58,518,930 (GRCm39) |
K1687N |
probably damaging |
Het |
Fgd4 |
G |
A |
16: 16,292,893 (GRCm39) |
R275* |
probably null |
Het |
Fxr2 |
G |
A |
11: 69,532,139 (GRCm39) |
C87Y |
possibly damaging |
Het |
Gja4 |
A |
T |
4: 127,206,472 (GRCm39) |
I97N |
probably damaging |
Het |
Gm136 |
A |
G |
4: 34,750,919 (GRCm39) |
|
probably null |
Het |
Gm14496 |
A |
G |
2: 181,642,837 (GRCm39) |
D836G |
possibly damaging |
Het |
Grm3 |
T |
A |
5: 9,561,520 (GRCm39) |
T777S |
probably damaging |
Het |
Guca2b |
A |
G |
4: 119,514,912 (GRCm39) |
Y50H |
probably damaging |
Het |
Herc2 |
C |
T |
7: 55,786,415 (GRCm39) |
P1587S |
probably benign |
Het |
Hmcn1 |
C |
T |
1: 150,545,309 (GRCm39) |
S2766N |
probably benign |
Het |
Idi2 |
T |
A |
13: 9,009,455 (GRCm39) |
I224K |
probably damaging |
Het |
Kmt2a |
A |
T |
9: 44,735,666 (GRCm39) |
|
probably benign |
Het |
Lonp2 |
A |
T |
8: 87,440,078 (GRCm39) |
M693L |
possibly damaging |
Het |
Megf8 |
G |
T |
7: 25,046,172 (GRCm39) |
M1525I |
possibly damaging |
Het |
Mgme1 |
T |
C |
2: 144,121,018 (GRCm39) |
V276A |
possibly damaging |
Het |
Mief2 |
G |
T |
11: 60,622,234 (GRCm39) |
W268L |
probably damaging |
Het |
Mpped1 |
C |
T |
15: 83,676,191 (GRCm39) |
|
probably benign |
Het |
Mreg |
T |
C |
1: 72,231,356 (GRCm39) |
N34S |
probably benign |
Het |
Myf6 |
T |
C |
10: 107,330,534 (GRCm39) |
Y11C |
probably damaging |
Het |
Myh9 |
C |
A |
15: 77,655,367 (GRCm39) |
Q1196H |
probably benign |
Het |
Myh9 |
A |
T |
15: 77,660,099 (GRCm39) |
D56E |
probably benign |
Het |
Ncapg2 |
TAA |
TA |
12: 116,398,305 (GRCm39) |
|
probably null |
Het |
Nfx1 |
T |
A |
4: 40,977,004 (GRCm39) |
V226E |
probably benign |
Het |
Nlrp10 |
T |
A |
7: 108,523,737 (GRCm39) |
K581M |
possibly damaging |
Het |
Nmd3 |
T |
G |
3: 69,647,317 (GRCm39) |
I273S |
probably benign |
Het |
Or4c3 |
A |
T |
2: 89,852,314 (GRCm39) |
I32N |
possibly damaging |
Het |
P4hb |
T |
C |
11: 120,462,442 (GRCm39) |
E88G |
probably damaging |
Het |
Pcnx3 |
A |
T |
19: 5,715,773 (GRCm39) |
H1444Q |
probably benign |
Het |
Pdia4 |
A |
T |
6: 47,776,133 (GRCm39) |
F421L |
possibly damaging |
Het |
Picalm |
T |
A |
7: 89,840,459 (GRCm39) |
S538T |
probably damaging |
Het |
Ppp2r2b |
T |
A |
18: 43,192,275 (GRCm39) |
I11F |
probably benign |
Het |
Prb1c |
A |
G |
6: 132,339,969 (GRCm39) |
|
probably null |
Het |
Ptk7 |
C |
T |
17: 46,884,460 (GRCm39) |
E757K |
possibly damaging |
Het |
Rbm22 |
T |
G |
18: 60,694,340 (GRCm39) |
C24W |
probably damaging |
Het |
Rev3l |
A |
G |
10: 39,682,658 (GRCm39) |
D288G |
probably damaging |
Het |
Rgs18 |
T |
A |
1: 144,629,791 (GRCm39) |
H156L |
probably benign |
Het |
Rnf213 |
A |
G |
11: 119,333,405 (GRCm39) |
I2871M |
probably damaging |
Het |
Rrm2b |
A |
T |
15: 37,945,328 (GRCm39) |
M137K |
probably damaging |
Het |
Rrp12 |
A |
T |
19: 41,857,224 (GRCm39) |
D1183E |
probably benign |
Het |
Sacs |
G |
A |
14: 61,441,277 (GRCm39) |
V1108M |
probably damaging |
Het |
Scube2 |
A |
T |
7: 109,442,421 (GRCm39) |
D270E |
possibly damaging |
Het |
Serpina3a |
T |
A |
12: 104,082,737 (GRCm39) |
F170Y |
probably damaging |
Het |
Serpinb3b |
T |
C |
1: 107,082,403 (GRCm39) |
E287G |
probably benign |
Het |
Slamf8 |
C |
T |
1: 172,412,186 (GRCm39) |
V130M |
probably damaging |
Het |
Slc5a3 |
T |
C |
16: 91,874,284 (GRCm39) |
S114P |
possibly damaging |
Het |
Sos1 |
T |
A |
17: 80,730,108 (GRCm39) |
|
probably null |
Het |
Sox10 |
A |
T |
15: 79,040,660 (GRCm39) |
D293E |
probably damaging |
Het |
Sphk1 |
A |
G |
11: 116,426,596 (GRCm39) |
D177G |
probably damaging |
Het |
Sphkap |
T |
G |
1: 83,256,121 (GRCm39) |
M543L |
probably benign |
Het |
Syt13 |
A |
T |
2: 92,783,760 (GRCm39) |
K343N |
probably damaging |
Het |
Tatdn3 |
A |
G |
1: 190,792,373 (GRCm39) |
M34T |
probably benign |
Het |
Timd4 |
T |
G |
11: 46,732,989 (GRCm39) |
V305G |
possibly damaging |
Het |
Tnnc2 |
T |
C |
2: 164,619,512 (GRCm39) |
I111V |
probably benign |
Het |
Togaram2 |
C |
T |
17: 72,004,846 (GRCm39) |
P301L |
probably benign |
Het |
Trpc3 |
T |
C |
3: 36,694,776 (GRCm39) |
N726S |
probably damaging |
Het |
Tspear |
T |
A |
10: 77,706,253 (GRCm39) |
L341H |
possibly damaging |
Het |
Ugt1a5 |
T |
A |
1: 88,093,805 (GRCm39) |
|
probably benign |
Het |
Ulk3 |
A |
T |
9: 57,500,443 (GRCm39) |
|
probably null |
Het |
Unc5d |
T |
A |
8: 29,250,777 (GRCm39) |
I297L |
probably benign |
Het |
Usp20 |
A |
G |
2: 30,908,830 (GRCm39) |
I804V |
probably benign |
Het |
Usp22 |
G |
T |
11: 61,052,144 (GRCm39) |
C278* |
probably null |
Het |
Usp53 |
A |
T |
3: 122,727,872 (GRCm39) |
N903K |
probably benign |
Het |
V1rd19 |
T |
C |
7: 23,702,812 (GRCm39) |
F93L |
probably benign |
Het |
Zdbf2 |
T |
A |
1: 63,343,493 (GRCm39) |
V624E |
possibly damaging |
Het |
Zfyve16 |
A |
T |
13: 92,645,528 (GRCm39) |
S1073T |
probably damaging |
Het |
Zkscan8 |
T |
C |
13: 21,710,765 (GRCm39) |
H115R |
possibly damaging |
Het |
|
Other mutations in Myo5c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00093:Myo5c
|
APN |
9 |
75,150,162 (GRCm39) |
splice site |
probably benign |
|
IGL00848:Myo5c
|
APN |
9 |
75,196,463 (GRCm39) |
missense |
probably benign |
|
IGL01503:Myo5c
|
APN |
9 |
75,170,324 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01735:Myo5c
|
APN |
9 |
75,208,720 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01866:Myo5c
|
APN |
9 |
75,176,864 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01956:Myo5c
|
APN |
9 |
75,150,158 (GRCm39) |
splice site |
probably null |
|
IGL02127:Myo5c
|
APN |
9 |
75,208,184 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02268:Myo5c
|
APN |
9 |
75,153,519 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02272:Myo5c
|
APN |
9 |
75,173,442 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL03052:Myo5c
|
APN |
9 |
75,159,798 (GRCm39) |
splice site |
probably benign |
|
IGL03179:Myo5c
|
APN |
9 |
75,163,148 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL03224:Myo5c
|
APN |
9 |
75,185,525 (GRCm39) |
missense |
probably benign |
0.01 |
Marked
|
UTSW |
9 |
75,182,919 (GRCm39) |
critical splice donor site |
probably null |
|
pixie
|
UTSW |
9 |
75,193,860 (GRCm39) |
missense |
probably benign |
0.26 |
PIT4142001:Myo5c
|
UTSW |
9 |
75,191,230 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4431001:Myo5c
|
UTSW |
9 |
75,159,853 (GRCm39) |
missense |
possibly damaging |
0.75 |
R0126:Myo5c
|
UTSW |
9 |
75,176,807 (GRCm39) |
missense |
probably benign |
0.05 |
R0266:Myo5c
|
UTSW |
9 |
75,191,498 (GRCm39) |
splice site |
probably benign |
|
R0345:Myo5c
|
UTSW |
9 |
75,204,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R0387:Myo5c
|
UTSW |
9 |
75,192,303 (GRCm39) |
splice site |
probably benign |
|
R0602:Myo5c
|
UTSW |
9 |
75,173,478 (GRCm39) |
splice site |
probably null |
|
R0675:Myo5c
|
UTSW |
9 |
75,185,571 (GRCm39) |
missense |
probably benign |
|
R0798:Myo5c
|
UTSW |
9 |
75,165,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R0981:Myo5c
|
UTSW |
9 |
75,178,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R1051:Myo5c
|
UTSW |
9 |
75,198,165 (GRCm39) |
missense |
probably benign |
0.00 |
R1072:Myo5c
|
UTSW |
9 |
75,199,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R1144:Myo5c
|
UTSW |
9 |
75,193,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R1454:Myo5c
|
UTSW |
9 |
75,170,348 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1476:Myo5c
|
UTSW |
9 |
75,183,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R1484:Myo5c
|
UTSW |
9 |
75,208,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R1586:Myo5c
|
UTSW |
9 |
75,174,313 (GRCm39) |
missense |
probably damaging |
0.99 |
R1616:Myo5c
|
UTSW |
9 |
75,203,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R1800:Myo5c
|
UTSW |
9 |
75,153,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R1838:Myo5c
|
UTSW |
9 |
75,180,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R1840:Myo5c
|
UTSW |
9 |
75,157,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R1885:Myo5c
|
UTSW |
9 |
75,157,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R1897:Myo5c
|
UTSW |
9 |
75,199,523 (GRCm39) |
missense |
probably benign |
0.20 |
R1898:Myo5c
|
UTSW |
9 |
75,204,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R2029:Myo5c
|
UTSW |
9 |
75,196,337 (GRCm39) |
unclassified |
probably benign |
|
R2063:Myo5c
|
UTSW |
9 |
75,189,150 (GRCm39) |
missense |
probably benign |
0.19 |
R2230:Myo5c
|
UTSW |
9 |
75,180,888 (GRCm39) |
missense |
probably benign |
|
R2519:Myo5c
|
UTSW |
9 |
75,157,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R2520:Myo5c
|
UTSW |
9 |
75,204,931 (GRCm39) |
nonsense |
probably null |
|
R3034:Myo5c
|
UTSW |
9 |
75,193,859 (GRCm39) |
missense |
probably benign |
0.44 |
R3117:Myo5c
|
UTSW |
9 |
75,173,476 (GRCm39) |
critical splice donor site |
probably null |
|
R3432:Myo5c
|
UTSW |
9 |
75,170,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R3751:Myo5c
|
UTSW |
9 |
75,183,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R4132:Myo5c
|
UTSW |
9 |
75,159,850 (GRCm39) |
missense |
probably benign |
0.00 |
R4173:Myo5c
|
UTSW |
9 |
75,153,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R4239:Myo5c
|
UTSW |
9 |
75,191,224 (GRCm39) |
missense |
probably benign |
0.01 |
R4429:Myo5c
|
UTSW |
9 |
75,201,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R4574:Myo5c
|
UTSW |
9 |
75,176,893 (GRCm39) |
missense |
probably benign |
0.00 |
R4791:Myo5c
|
UTSW |
9 |
75,198,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R4804:Myo5c
|
UTSW |
9 |
75,152,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R4819:Myo5c
|
UTSW |
9 |
75,199,484 (GRCm39) |
missense |
probably damaging |
0.97 |
R4881:Myo5c
|
UTSW |
9 |
75,191,434 (GRCm39) |
missense |
probably benign |
0.00 |
R4900:Myo5c
|
UTSW |
9 |
75,180,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R4964:Myo5c
|
UTSW |
9 |
75,204,791 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4966:Myo5c
|
UTSW |
9 |
75,176,878 (GRCm39) |
missense |
probably benign |
0.03 |
R5057:Myo5c
|
UTSW |
9 |
75,208,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R5347:Myo5c
|
UTSW |
9 |
75,202,487 (GRCm39) |
missense |
probably null |
1.00 |
R5399:Myo5c
|
UTSW |
9 |
75,195,356 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5440:Myo5c
|
UTSW |
9 |
75,165,407 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5569:Myo5c
|
UTSW |
9 |
75,180,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R5600:Myo5c
|
UTSW |
9 |
75,196,436 (GRCm39) |
missense |
probably benign |
0.00 |
R5606:Myo5c
|
UTSW |
9 |
75,182,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R5704:Myo5c
|
UTSW |
9 |
75,180,185 (GRCm39) |
missense |
probably benign |
0.00 |
R5798:Myo5c
|
UTSW |
9 |
75,191,480 (GRCm39) |
missense |
probably benign |
0.04 |
R5865:Myo5c
|
UTSW |
9 |
75,204,770 (GRCm39) |
missense |
probably damaging |
0.97 |
R6034:Myo5c
|
UTSW |
9 |
75,163,187 (GRCm39) |
missense |
probably benign |
0.05 |
R6034:Myo5c
|
UTSW |
9 |
75,163,187 (GRCm39) |
missense |
probably benign |
0.05 |
R6143:Myo5c
|
UTSW |
9 |
75,157,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R6242:Myo5c
|
UTSW |
9 |
75,180,893 (GRCm39) |
missense |
probably benign |
|
R6253:Myo5c
|
UTSW |
9 |
75,152,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R6264:Myo5c
|
UTSW |
9 |
75,182,836 (GRCm39) |
missense |
probably benign |
|
R6307:Myo5c
|
UTSW |
9 |
75,180,198 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6358:Myo5c
|
UTSW |
9 |
75,203,294 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6450:Myo5c
|
UTSW |
9 |
75,193,860 (GRCm39) |
missense |
probably benign |
0.26 |
R6598:Myo5c
|
UTSW |
9 |
75,153,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R6618:Myo5c
|
UTSW |
9 |
75,182,919 (GRCm39) |
critical splice donor site |
probably null |
|
R6774:Myo5c
|
UTSW |
9 |
75,196,468 (GRCm39) |
missense |
probably benign |
0.05 |
R6865:Myo5c
|
UTSW |
9 |
75,176,878 (GRCm39) |
missense |
probably benign |
0.03 |
R6996:Myo5c
|
UTSW |
9 |
75,157,746 (GRCm39) |
missense |
probably benign |
0.01 |
R7023:Myo5c
|
UTSW |
9 |
75,208,738 (GRCm39) |
missense |
probably damaging |
0.98 |
R7123:Myo5c
|
UTSW |
9 |
75,196,505 (GRCm39) |
missense |
probably benign |
|
R7250:Myo5c
|
UTSW |
9 |
75,169,497 (GRCm39) |
missense |
probably damaging |
1.00 |
R7316:Myo5c
|
UTSW |
9 |
75,176,920 (GRCm39) |
missense |
probably benign |
0.00 |
R7340:Myo5c
|
UTSW |
9 |
75,196,423 (GRCm39) |
missense |
probably benign |
|
R7382:Myo5c
|
UTSW |
9 |
75,211,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R7426:Myo5c
|
UTSW |
9 |
75,158,809 (GRCm39) |
splice site |
probably null |
|
R7788:Myo5c
|
UTSW |
9 |
75,186,627 (GRCm39) |
missense |
probably damaging |
0.98 |
R7956:Myo5c
|
UTSW |
9 |
75,159,845 (GRCm39) |
missense |
probably benign |
|
R8082:Myo5c
|
UTSW |
9 |
75,182,793 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8290:Myo5c
|
UTSW |
9 |
75,196,178 (GRCm39) |
missense |
probably benign |
0.01 |
R8406:Myo5c
|
UTSW |
9 |
75,182,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R8481:Myo5c
|
UTSW |
9 |
75,208,726 (GRCm39) |
missense |
probably damaging |
1.00 |
R8489:Myo5c
|
UTSW |
9 |
75,180,128 (GRCm39) |
missense |
probably damaging |
0.98 |
R8505:Myo5c
|
UTSW |
9 |
75,153,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R8685:Myo5c
|
UTSW |
9 |
75,192,229 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8806:Myo5c
|
UTSW |
9 |
75,150,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R8871:Myo5c
|
UTSW |
9 |
75,185,585 (GRCm39) |
missense |
probably benign |
0.10 |
R9323:Myo5c
|
UTSW |
9 |
75,153,531 (GRCm39) |
missense |
probably damaging |
1.00 |
R9484:Myo5c
|
UTSW |
9 |
75,204,770 (GRCm39) |
missense |
probably damaging |
0.99 |
R9639:Myo5c
|
UTSW |
9 |
75,165,477 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Myo5c
|
UTSW |
9 |
75,152,341 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Myo5c
|
UTSW |
9 |
75,153,537 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- ACCTCCGCGTCTTTCTCTAGAACAG -3'
(R):5'- CTCATGCAGGTGGACAAGTGACAG -3'
Sequencing Primer
(F):5'- TTCTCTAGAACAGAGAGAACCACG -3'
(R):5'- TCAGCTTGTAAAGGCGGAC -3'
|
Posted On |
2014-04-24 |