Incidental Mutation 'R7250:Myo5c'
ID |
563849 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Myo5c
|
Ensembl Gene |
ENSMUSG00000033590 |
Gene Name |
myosin VC |
Synonyms |
9130003O20Rik |
MMRRC Submission |
045350-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R7250 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
9 |
Chromosomal Location |
75139302-75212733 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 75169497 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Threonine to Alanine
at position 441
(T441A)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000042229
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000036555]
[ENSMUST00000216788]
|
AlphaFold |
E9Q1F5 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000036555
AA Change: T441A
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000042229 Gene: ENSMUSG00000033590 AA Change: T441A
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: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.0%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930480E11Rik |
G |
T |
X: 77,414,311 (GRCm39) |
M345I |
probably benign |
Het |
Actl7b |
T |
A |
4: 56,741,035 (GRCm39) |
M108L |
probably benign |
Het |
Adgrf3 |
T |
A |
5: 30,400,680 (GRCm39) |
I934L |
probably damaging |
Het |
Adprm |
A |
G |
11: 66,932,450 (GRCm39) |
V153A |
probably benign |
Het |
Aif1l |
G |
A |
2: 31,859,764 (GRCm39) |
V109M |
probably damaging |
Het |
Asphd1 |
T |
A |
7: 126,545,942 (GRCm39) |
E307V |
probably damaging |
Het |
Ate1 |
T |
A |
7: 130,121,701 (GRCm39) |
|
probably benign |
Het |
Borcs7 |
A |
G |
19: 46,688,047 (GRCm39) |
H64R |
probably damaging |
Het |
C1qtnf1 |
A |
G |
11: 118,339,176 (GRCm39) |
*282W |
probably null |
Het |
Cacna1c |
A |
G |
6: 118,574,966 (GRCm39) |
C1985R |
|
Het |
Cacna1c |
A |
T |
6: 118,673,412 (GRCm39) |
V647E |
|
Het |
Cacna1d |
A |
G |
14: 29,797,108 (GRCm39) |
S1497P |
probably damaging |
Het |
Cacna1e |
T |
A |
1: 154,576,235 (GRCm39) |
I133F |
possibly damaging |
Het |
Ccdc63 |
A |
T |
5: 122,260,906 (GRCm39) |
L206H |
probably damaging |
Het |
Cenatac |
A |
G |
9: 44,323,748 (GRCm39) |
|
probably null |
Het |
Cspg4b |
T |
G |
13: 113,455,349 (GRCm39) |
I465R |
|
Het |
D430041D05Rik |
T |
C |
2: 104,086,961 (GRCm39) |
T672A |
possibly damaging |
Het |
D630045J12Rik |
G |
T |
6: 38,119,546 (GRCm39) |
T1732K |
possibly damaging |
Het |
D930020B18Rik |
T |
C |
10: 121,507,736 (GRCm39) |
I158T |
probably damaging |
Het |
Ddx52 |
G |
A |
11: 83,835,392 (GRCm39) |
G106D |
probably benign |
Het |
Dock2 |
A |
G |
11: 34,586,032 (GRCm39) |
V550A |
probably benign |
Het |
Dock2 |
C |
T |
11: 34,586,120 (GRCm39) |
D521N |
probably damaging |
Het |
F13b |
T |
C |
1: 139,444,227 (GRCm39) |
|
probably null |
Het |
Fchsd2 |
A |
G |
7: 100,908,892 (GRCm39) |
K431R |
possibly damaging |
Het |
Fez1 |
C |
T |
9: 36,779,090 (GRCm39) |
R256C |
probably damaging |
Het |
Gjd4 |
T |
A |
18: 9,280,391 (GRCm39) |
Q229L |
probably benign |
Het |
Gpr45 |
T |
A |
1: 43,071,531 (GRCm39) |
I58N |
probably damaging |
Het |
Gstm1 |
T |
A |
3: 107,923,709 (GRCm39) |
I99F |
probably damaging |
Het |
Gtpbp8 |
T |
A |
16: 44,564,225 (GRCm39) |
T149S |
probably damaging |
Het |
H2-Ab1 |
A |
G |
17: 34,486,481 (GRCm39) |
D180G |
probably damaging |
Het |
Hdhd5 |
A |
G |
6: 120,494,016 (GRCm39) |
I188T |
possibly damaging |
Het |
Hfm1 |
T |
C |
5: 107,052,197 (GRCm39) |
I300V |
probably benign |
Het |
Hnrnpr |
T |
G |
4: 136,059,746 (GRCm39) |
D283E |
probably benign |
Het |
Hsp90b1 |
T |
C |
10: 86,527,572 (GRCm39) |
E768G |
unknown |
Het |
Kcna4 |
C |
A |
2: 107,126,663 (GRCm39) |
Q466K |
possibly damaging |
Het |
Kcnk6 |
A |
G |
7: 28,931,619 (GRCm39) |
L97P |
probably benign |
Het |
Kics2 |
T |
C |
10: 121,581,376 (GRCm39) |
S126P |
possibly damaging |
Het |
Klf5 |
A |
G |
14: 99,536,455 (GRCm39) |
S9G |
probably benign |
Het |
Kmt2c |
C |
A |
5: 25,504,489 (GRCm39) |
K3606N |
probably damaging |
Het |
Kmt2c |
T |
C |
5: 25,514,805 (GRCm39) |
T3013A |
probably benign |
Het |
Lancl1 |
A |
G |
1: 67,048,458 (GRCm39) |
Y207H |
possibly damaging |
Het |
Lipe |
G |
C |
7: 25,088,085 (GRCm39) |
|
probably benign |
Het |
Lrrc66 |
T |
A |
5: 73,768,224 (GRCm39) |
H239L |
probably benign |
Het |
Ltbp2 |
C |
T |
12: 84,834,166 (GRCm39) |
W1441* |
probably null |
Het |
Man2a1 |
T |
C |
17: 64,943,583 (GRCm39) |
S213P |
probably benign |
Het |
Mapre2 |
C |
T |
18: 23,991,119 (GRCm39) |
A171V |
possibly damaging |
Het |
Mdn1 |
T |
A |
4: 32,695,427 (GRCm39) |
D1155E |
probably damaging |
Het |
Mki67 |
T |
C |
7: 135,301,053 (GRCm39) |
D1327G |
possibly damaging |
Het |
Mx2 |
T |
C |
16: 97,348,664 (GRCm39) |
I279T |
probably damaging |
Het |
Nlrp9a |
T |
G |
7: 26,258,143 (GRCm39) |
V587G |
possibly damaging |
Het |
Npas2 |
A |
T |
1: 39,377,188 (GRCm39) |
T517S |
probably damaging |
Het |
Npy1r |
T |
C |
8: 67,157,712 (GRCm39) |
S341P |
probably benign |
Het |
Ntm |
A |
G |
9: 29,322,988 (GRCm39) |
W11R |
probably benign |
Het |
Nxpe2 |
A |
T |
9: 48,238,096 (GRCm39) |
I53N |
possibly damaging |
Het |
Onecut2 |
T |
C |
18: 64,519,511 (GRCm39) |
F443L |
probably benign |
Het |
Or10g6 |
T |
A |
9: 39,934,050 (GRCm39) |
Y120* |
probably null |
Het |
Or2r2 |
A |
G |
6: 42,463,689 (GRCm39) |
V146A |
probably benign |
Het |
Or52ac1 |
A |
T |
7: 104,245,738 (GRCm39) |
Y217N |
probably damaging |
Het |
Parp2 |
T |
A |
14: 51,054,801 (GRCm39) |
V248E |
probably benign |
Het |
Pcdh12 |
C |
A |
18: 38,415,029 (GRCm39) |
V699L |
probably benign |
Het |
Pja2 |
G |
A |
17: 64,616,451 (GRCm39) |
P148L |
probably benign |
Het |
Poglut3 |
C |
T |
9: 53,301,821 (GRCm39) |
Q158* |
probably null |
Het |
Ppip5k2 |
T |
G |
1: 97,673,187 (GRCm39) |
D415A |
probably benign |
Het |
Prss47 |
A |
G |
13: 65,200,355 (GRCm39) |
S74P |
probably benign |
Het |
Ptprg |
G |
T |
14: 12,166,767 (GRCm38) |
M723I |
probably benign |
Het |
Qsox2 |
A |
T |
2: 26,118,444 (GRCm39) |
I109N |
probably damaging |
Het |
Ranbp3l |
A |
G |
15: 9,041,853 (GRCm39) |
E217G |
probably benign |
Het |
Rgl2 |
C |
T |
17: 34,152,403 (GRCm39) |
R367W |
probably damaging |
Het |
Rgs12 |
T |
A |
5: 35,122,841 (GRCm39) |
F208Y |
probably damaging |
Het |
Rin3 |
C |
T |
12: 102,334,893 (GRCm39) |
T268I |
unknown |
Het |
Rttn |
T |
A |
18: 89,007,647 (GRCm39) |
D427E |
probably benign |
Het |
Samd13 |
G |
A |
3: 146,352,079 (GRCm39) |
P91S |
probably benign |
Het |
Samd9l |
T |
C |
6: 3,374,201 (GRCm39) |
D1020G |
possibly damaging |
Het |
Sec62 |
T |
G |
3: 30,866,496 (GRCm39) |
L201V |
possibly damaging |
Het |
Setdb1 |
C |
T |
3: 95,261,852 (GRCm39) |
|
probably null |
Het |
Sf3a3 |
A |
T |
4: 124,616,708 (GRCm39) |
T197S |
probably benign |
Het |
Slc20a1 |
A |
T |
2: 129,051,844 (GRCm39) |
I618F |
possibly damaging |
Het |
Slc38a3 |
A |
T |
9: 107,533,865 (GRCm39) |
M186K |
probably benign |
Het |
Slc39a13 |
T |
C |
2: 90,893,503 (GRCm39) |
T319A |
probably benign |
Het |
Slc44a4 |
T |
C |
17: 35,137,520 (GRCm39) |
|
probably null |
Het |
St3gal1 |
A |
C |
15: 66,978,578 (GRCm39) |
D314E |
possibly damaging |
Het |
Suclg1 |
A |
G |
6: 73,248,074 (GRCm39) |
N265S |
probably benign |
Het |
Sult2b1 |
A |
T |
7: 45,433,361 (GRCm39) |
V2D |
unknown |
Het |
Supv3l1 |
T |
A |
10: 62,280,846 (GRCm39) |
I182F |
probably damaging |
Het |
Tcp11l2 |
T |
C |
10: 84,423,105 (GRCm39) |
|
probably null |
Het |
Tenm2 |
C |
A |
11: 35,963,625 (GRCm39) |
L935F |
probably damaging |
Het |
Tnks |
T |
A |
8: 35,318,912 (GRCm39) |
I790F |
probably damaging |
Het |
Top2b |
C |
T |
14: 16,420,411 (GRCm38) |
T1274I |
probably benign |
Het |
Tpi1 |
A |
T |
6: 124,789,441 (GRCm39) |
I178N |
probably damaging |
Het |
Trav9d-1 |
A |
T |
14: 53,030,153 (GRCm39) |
S86C |
probably damaging |
Het |
Treml2 |
A |
G |
17: 48,616,155 (GRCm39) |
E265G |
probably benign |
Het |
Trpm7 |
A |
T |
2: 126,668,685 (GRCm39) |
S744T |
possibly damaging |
Het |
Usp33 |
T |
A |
3: 152,097,999 (GRCm39) |
L909* |
probably null |
Het |
Vcan |
A |
G |
13: 89,869,805 (GRCm39) |
I210T |
probably damaging |
Het |
Vcan |
A |
T |
13: 89,879,576 (GRCm39) |
|
probably null |
Het |
Vsig10l |
A |
T |
7: 43,113,099 (GRCm39) |
D17V |
probably benign |
Het |
Zbtb7b |
T |
A |
3: 89,286,976 (GRCm39) |
T498S |
probably benign |
Het |
Zfp366 |
T |
A |
13: 99,366,076 (GRCm39) |
H412Q |
probably damaging |
Het |
Zfp53 |
C |
A |
17: 21,729,840 (GRCm39) |
D624E |
probably damaging |
Het |
Zfp827 |
A |
T |
8: 79,916,721 (GRCm39) |
D432V |
|
Het |
Zic1 |
T |
C |
9: 91,247,028 (GRCm39) |
T15A |
probably damaging |
Het |
Zswim8 |
T |
C |
14: 20,770,036 (GRCm39) |
C1368R |
probably 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 |
R1635:Myo5c
|
UTSW |
9 |
75,184,357 (GRCm39) |
missense |
probably benign |
0.09 |
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 |
|
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'- TGACTGCCAGCTTAGAAGGAAC -3'
(R):5'- CAGGCATGCTTGGATTCCTG -3'
Sequencing Primer
(F):5'- GCTTTGAAGTAGTTTAAACTTGCCG -3'
(R):5'- CATGCTTGGATTCCTGAATGAG -3'
|
Posted On |
2019-06-26 |