Incidental Mutation 'R7316:Myo5c'
ID |
567978 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Myo5c
|
Ensembl Gene |
ENSMUSG00000033590 |
Gene Name |
myosin VC |
Synonyms |
9130003O20Rik |
MMRRC Submission |
045413-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R7316 (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 T
at 75176920 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Threonine to Serine
at position 622
(T622S)
|
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: T622S
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
SMART Domains |
Protein: ENSMUSP00000042229 Gene: ENSMUSG00000033590 AA Change: T622S
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: 99.6%
- 20x: 98.9%
|
Validation Efficiency |
99% (93/94) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933434E20Rik |
G |
A |
3: 89,969,020 (GRCm39) |
M214I |
probably benign |
Het |
Aadat |
G |
T |
8: 60,979,668 (GRCm39) |
G177C |
probably damaging |
Het |
Adam4 |
T |
C |
12: 81,466,498 (GRCm39) |
I708V |
probably benign |
Het |
Aip |
T |
C |
19: 4,164,793 (GRCm39) |
N264S |
probably benign |
Het |
Alox8 |
A |
T |
11: 69,077,064 (GRCm39) |
D505E |
probably benign |
Het |
Ap3d1 |
A |
T |
10: 80,553,693 (GRCm39) |
I518N |
probably damaging |
Het |
Arf3 |
G |
A |
15: 98,638,874 (GRCm39) |
Q128* |
probably null |
Het |
Asph |
A |
G |
4: 9,537,746 (GRCm39) |
V344A |
probably benign |
Het |
Birc6 |
A |
T |
17: 74,911,489 (GRCm39) |
R1500S |
probably damaging |
Het |
Bptf |
G |
A |
11: 106,963,935 (GRCm39) |
T1753I |
probably damaging |
Het |
Bptf |
A |
T |
11: 107,001,740 (GRCm39) |
C457* |
probably null |
Het |
Brpf3 |
T |
A |
17: 29,033,660 (GRCm39) |
I568N |
probably damaging |
Het |
Btnl4 |
G |
C |
17: 34,688,031 (GRCm39) |
N582K |
probably benign |
Het |
Camsap3 |
C |
A |
8: 3,654,648 (GRCm39) |
P773T |
possibly damaging |
Het |
Capsl |
A |
T |
15: 9,461,888 (GRCm39) |
I95L |
probably benign |
Het |
Cd96 |
T |
A |
16: 45,890,016 (GRCm39) |
M336L |
probably benign |
Het |
Cdan1 |
A |
T |
2: 120,558,813 (GRCm39) |
|
probably null |
Het |
Chd3 |
A |
T |
11: 69,236,394 (GRCm39) |
L1939Q |
probably damaging |
Het |
Cngb3 |
A |
T |
4: 19,425,599 (GRCm39) |
Y469F |
probably benign |
Het |
Cp |
T |
C |
3: 20,026,916 (GRCm39) |
L448P |
probably damaging |
Het |
Csnk1g2 |
T |
C |
10: 80,475,687 (GRCm39) |
V418A |
possibly damaging |
Het |
Dag1 |
A |
T |
9: 108,086,701 (GRCm39) |
S147T |
probably benign |
Het |
Dnajc25 |
T |
A |
4: 59,017,693 (GRCm39) |
Y117* |
probably null |
Het |
Dpysl2 |
A |
T |
14: 67,100,044 (GRCm39) |
M64K |
possibly damaging |
Het |
Dus3l |
A |
G |
17: 57,072,551 (GRCm39) |
H38R |
possibly damaging |
Het |
Eme2 |
G |
A |
17: 25,113,840 (GRCm39) |
R62W |
probably damaging |
Het |
Enox1 |
A |
T |
14: 77,958,298 (GRCm39) |
M616L |
probably benign |
Het |
Epb41l4b |
T |
A |
4: 57,019,867 (GRCm39) |
T708S |
probably benign |
Het |
Fat2 |
A |
T |
11: 55,176,893 (GRCm39) |
I1534N |
probably damaging |
Het |
Fer1l5 |
A |
G |
1: 36,457,197 (GRCm39) |
T1649A |
probably benign |
Het |
Fmo9 |
A |
G |
1: 166,491,215 (GRCm39) |
V421A |
probably benign |
Het |
Fsip2 |
A |
C |
2: 82,820,035 (GRCm39) |
Y5256S |
possibly damaging |
Het |
Gapvd1 |
G |
A |
2: 34,594,681 (GRCm39) |
L804F |
probably damaging |
Het |
Garin1a |
A |
G |
6: 29,286,101 (GRCm39) |
M187V |
probably benign |
Het |
Gen1 |
A |
G |
12: 11,291,470 (GRCm39) |
V838A |
probably benign |
Het |
Gnptab |
A |
T |
10: 88,236,572 (GRCm39) |
N59I |
probably damaging |
Het |
Grm5 |
A |
G |
7: 87,624,473 (GRCm39) |
T347A |
probably benign |
Het |
Gsdmc3 |
T |
C |
15: 63,730,251 (GRCm39) |
N438D |
possibly damaging |
Het |
Hmcn1 |
A |
G |
1: 150,608,697 (GRCm39) |
L1495S |
probably damaging |
Het |
Ift70a1 |
A |
T |
2: 75,811,201 (GRCm39) |
L294Q |
probably damaging |
Het |
Islr2 |
T |
C |
9: 58,105,250 (GRCm39) |
E714G |
probably damaging |
Het |
Larp4 |
A |
T |
15: 99,898,898 (GRCm39) |
M430L |
probably benign |
Het |
Lpcat2b |
A |
G |
5: 107,580,979 (GRCm39) |
I103V |
not run |
Het |
Lrguk |
C |
T |
6: 34,080,191 (GRCm39) |
S1142F |
unknown |
Het |
Lrit2 |
G |
T |
14: 36,790,815 (GRCm39) |
V165F |
probably damaging |
Het |
Mast3 |
T |
A |
8: 71,232,432 (GRCm39) |
I1182F |
probably damaging |
Het |
Mcm6 |
C |
T |
1: 128,287,245 (GRCm39) |
D20N |
probably damaging |
Het |
Mief1 |
A |
G |
15: 80,133,598 (GRCm39) |
I218M |
probably damaging |
Het |
Mmp2 |
A |
G |
8: 93,567,038 (GRCm39) |
T453A |
probably benign |
Het |
Ms4a18 |
T |
A |
19: 10,979,360 (GRCm39) |
S219C |
probably damaging |
Het |
Neb |
A |
T |
2: 52,161,450 (GRCm39) |
M2114K |
possibly damaging |
Het |
Nemp1 |
T |
A |
10: 127,525,212 (GRCm39) |
L122* |
probably null |
Het |
Nkx2-1 |
T |
C |
12: 56,581,583 (GRCm39) |
N88S |
probably benign |
Het |
Nr2c2 |
T |
A |
6: 92,131,444 (GRCm39) |
C202S |
probably damaging |
Het |
Ntsr1 |
A |
C |
2: 180,142,545 (GRCm39) |
D112A |
probably damaging |
Het |
Or14j3 |
A |
G |
17: 37,901,026 (GRCm39) |
S73P |
probably damaging |
Het |
Or56a41 |
A |
T |
7: 104,740,107 (GRCm39) |
H246Q |
probably damaging |
Het |
Or6n2 |
A |
T |
1: 173,897,727 (GRCm39) |
I288F |
probably benign |
Het |
Osbp2 |
C |
A |
11: 3,676,431 (GRCm39) |
R73L |
probably damaging |
Het |
Pbp2 |
T |
A |
6: 135,286,830 (GRCm39) |
E172D |
probably damaging |
Het |
Pcdhgc3 |
T |
C |
18: 37,941,501 (GRCm39) |
I634T |
probably benign |
Het |
Pcnx1 |
T |
C |
12: 82,042,323 (GRCm39) |
S38P |
probably benign |
Het |
Phyh |
A |
T |
2: 4,940,855 (GRCm39) |
K252* |
probably null |
Het |
Plcb3 |
C |
T |
19: 6,943,753 (GRCm39) |
|
probably null |
Het |
Ppargc1b |
T |
C |
18: 61,440,909 (GRCm39) |
S670G |
probably damaging |
Het |
Prorp |
A |
G |
12: 55,351,429 (GRCm39) |
D246G |
probably damaging |
Het |
Ptprc |
T |
C |
1: 137,992,509 (GRCm39) |
Y1067C |
probably damaging |
Het |
Pwwp2b |
A |
C |
7: 138,836,140 (GRCm39) |
E527A |
probably benign |
Het |
Pzp |
T |
C |
6: 128,490,736 (GRCm39) |
D409G |
probably damaging |
Het |
Rbfox2 |
A |
T |
15: 77,016,929 (GRCm39) |
N148K |
possibly damaging |
Het |
Resf1 |
T |
C |
6: 149,228,136 (GRCm39) |
L394P |
probably damaging |
Het |
Rps24 |
T |
C |
14: 24,540,757 (GRCm39) |
|
probably benign |
Het |
Slc35e4 |
T |
C |
11: 3,862,584 (GRCm39) |
K202E |
probably damaging |
Het |
Spata7 |
C |
T |
12: 98,624,871 (GRCm39) |
R258W |
probably damaging |
Het |
Spen |
A |
T |
4: 141,204,365 (GRCm39) |
S1421T |
unknown |
Het |
Svep1 |
T |
A |
4: 58,068,763 (GRCm39) |
I3008F |
possibly damaging |
Het |
Tbc1d1 |
G |
T |
5: 64,492,620 (GRCm39) |
|
probably null |
Het |
Thsd4 |
T |
A |
9: 59,894,642 (GRCm39) |
H772L |
probably benign |
Het |
Tle1 |
T |
C |
4: 72,036,529 (GRCm39) |
I769V |
probably benign |
Het |
Tm4sf19 |
T |
A |
16: 32,226,466 (GRCm39) |
S127T |
possibly damaging |
Het |
Tmprss9 |
C |
A |
10: 80,730,813 (GRCm39) |
R780S |
probably benign |
Het |
Tpp2 |
T |
C |
1: 44,009,591 (GRCm39) |
V475A |
probably benign |
Het |
Ttn |
A |
G |
2: 76,692,509 (GRCm39) |
V471A |
|
Het |
Ttn |
A |
T |
2: 76,597,257 (GRCm39) |
N19885K |
probably damaging |
Het |
Tub |
A |
T |
7: 108,629,378 (GRCm39) |
T478S |
possibly damaging |
Het |
Ube2q2l |
T |
C |
6: 136,378,276 (GRCm39) |
K185E |
possibly damaging |
Het |
Vmn2r88 |
A |
T |
14: 51,651,712 (GRCm39) |
Y342F |
|
Het |
Wdr18 |
C |
A |
10: 79,801,059 (GRCm39) |
D157E |
probably benign |
Het |
Xrra1 |
A |
T |
7: 99,525,423 (GRCm39) |
|
probably null |
Het |
Zc3h4 |
G |
C |
7: 16,169,260 (GRCm39) |
G1198A |
unknown |
Het |
Zfp568 |
A |
T |
7: 29,721,681 (GRCm39) |
I209F |
possibly damaging |
Het |
Zfp787 |
C |
A |
7: 6,158,523 (GRCm39) |
|
probably benign |
Het |
Zfp974 |
A |
T |
7: 27,609,863 (GRCm39) |
Y621N |
possibly damaging |
Het |
Zyg11b |
A |
G |
4: 108,107,699 (GRCm39) |
I493T |
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 |
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 |
|
R7250:Myo5c
|
UTSW |
9 |
75,169,497 (GRCm39) |
missense |
probably damaging |
1.00 |
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'- GAGATAGCCGTCATGACTGTG -3'
(R):5'- TGTGGGTTACAGATGCACCC -3'
Sequencing Primer
(F):5'- AGATAGCCGTCATGACTGTGTATTTG -3'
(R):5'- GGTTACAGATGCACCCTACCTG -3'
|
Posted On |
2019-06-26 |