Incidental Mutation 'R9287:Myo16'
ID |
704017 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Myo16
|
Ensembl Gene |
ENSMUSG00000039057 |
Gene Name |
myosin XVI |
Synonyms |
C230040D10Rik, BM140241, Nyap3 |
MMRRC Submission |
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.325)
|
Stock # |
R9287 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
8 |
Chromosomal Location |
10203911-10684742 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 10526114 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Methionine
at position 885
(V885M)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000146677
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000042103]
[ENSMUST00000207204]
[ENSMUST00000207477]
|
AlphaFold |
Q5DU14 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000042103
AA Change: V885M
PolyPhen 2
Score 0.007 (Sensitivity: 0.96; Specificity: 0.75)
|
SMART Domains |
Protein: ENSMUSP00000049345 Gene: ENSMUSG00000039057 AA Change: V885M
Domain | Start | End | E-Value | Type |
ANK
|
92 |
121 |
1.65e-1 |
SMART |
ANK
|
125 |
154 |
3.46e-4 |
SMART |
ANK
|
158 |
189 |
2.11e2 |
SMART |
ANK
|
221 |
250 |
2.85e-5 |
SMART |
ANK
|
254 |
283 |
3.51e-5 |
SMART |
low complexity region
|
333 |
349 |
N/A |
INTRINSIC |
MYSc
|
394 |
1144 |
2.27e-144 |
SMART |
IQ
|
1144 |
1166 |
4.06e-2 |
SMART |
Pfam:NYAP_N
|
1207 |
1591 |
4.1e-135 |
PFAM |
low complexity region
|
1670 |
1690 |
N/A |
INTRINSIC |
low complexity region
|
1841 |
1860 |
N/A |
INTRINSIC |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000207204
AA Change: V829M
|
Predicted Effect |
unknown
Transcript: ENSMUST00000207477
AA Change: V885M
|
Meta Mutation Damage Score |
0.0852 |
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.1%
|
Validation Efficiency |
100% (109/109) |
MGI Phenotype |
PHENOTYPE: Triple KO of Nyap1, Nyap2 and Myo16 results in decreased brain weight and cortex and striatum size and reduced neurite length in cortical neurons. [provided by MGI curators]
|
Allele List at MGI |
All alleles(3) : Targeted(2) Gene trapped(1)
|
Other mutations in this stock |
Total: 108 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9430097D07Rik |
T |
A |
2: 32,465,178 (GRCm39) |
|
probably benign |
Het |
Aadacl2 |
C |
A |
3: 59,932,573 (GRCm39) |
H363N |
probably damaging |
Het |
Ace3 |
T |
G |
11: 105,888,246 (GRCm39) |
S319A |
probably damaging |
Het |
Amer3 |
C |
T |
1: 34,627,900 (GRCm39) |
P713L |
possibly damaging |
Het |
Aoah |
T |
C |
13: 21,186,879 (GRCm39) |
L453P |
probably damaging |
Het |
Asz1 |
A |
T |
6: 18,051,290 (GRCm39) |
L463Q |
possibly damaging |
Het |
Bpifb6 |
T |
A |
2: 153,746,535 (GRCm39) |
V143D |
probably damaging |
Het |
Cad |
T |
A |
5: 31,230,000 (GRCm39) |
M1499K |
possibly damaging |
Het |
Casp9 |
T |
A |
4: 141,534,471 (GRCm39) |
C294S |
probably benign |
Het |
Ccdc7b |
T |
A |
8: 129,890,321 (GRCm39) |
S65T |
probably benign |
Het |
Cdh23 |
G |
A |
10: 60,143,306 (GRCm39) |
A3005V |
possibly damaging |
Het |
Cfap54 |
T |
C |
10: 92,805,565 (GRCm39) |
Y1515C |
possibly damaging |
Het |
Chrm5 |
A |
C |
2: 112,309,610 (GRCm39) |
F502C |
probably damaging |
Het |
Cnst |
A |
T |
1: 179,407,108 (GRCm39) |
T52S |
possibly damaging |
Het |
Cntn6 |
T |
C |
6: 104,809,471 (GRCm39) |
I502T |
possibly damaging |
Het |
Col7a1 |
G |
A |
9: 108,787,457 (GRCm39) |
V617M |
unknown |
Het |
Ctsb |
A |
G |
14: 63,370,875 (GRCm39) |
D29G |
probably benign |
Het |
Cyp3a44 |
T |
A |
5: 145,725,202 (GRCm39) |
Q333L |
possibly damaging |
Het |
Dnajc27 |
T |
C |
12: 4,146,256 (GRCm39) |
V95A |
possibly damaging |
Het |
Eea1 |
T |
A |
10: 95,831,445 (GRCm39) |
Y179N |
probably damaging |
Het |
Erbb2 |
T |
C |
11: 98,326,107 (GRCm39) |
M961T |
probably damaging |
Het |
Fat4 |
G |
A |
3: 38,945,781 (GRCm39) |
G1558D |
probably damaging |
Het |
Foxh1 |
T |
C |
15: 76,553,126 (GRCm39) |
E196G |
probably damaging |
Het |
Gcc2 |
T |
A |
10: 58,105,217 (GRCm39) |
L151* |
probably null |
Het |
Gcdh |
C |
T |
8: 85,616,313 (GRCm39) |
G294D |
probably damaging |
Het |
Gcnt3 |
A |
T |
9: 69,941,693 (GRCm39) |
F292I |
probably damaging |
Het |
Glod4 |
T |
C |
11: 76,128,510 (GRCm39) |
S131G |
probably benign |
Het |
Gpc2 |
G |
A |
5: 138,272,586 (GRCm39) |
L576F |
unknown |
Het |
Gphn |
G |
A |
12: 78,609,646 (GRCm39) |
S330N |
possibly damaging |
Het |
Heatr5a |
C |
T |
12: 51,967,260 (GRCm39) |
C872Y |
probably damaging |
Het |
Hephl1 |
G |
A |
9: 14,995,775 (GRCm39) |
S449L |
probably benign |
Het |
Hrh2 |
G |
T |
13: 54,368,358 (GRCm39) |
M111I |
probably benign |
Het |
Igfn1 |
A |
G |
1: 135,925,544 (GRCm39) |
V70A |
probably benign |
Het |
Il2 |
G |
A |
3: 37,179,988 (GRCm39) |
T23I |
probably damaging |
Het |
Irak4 |
A |
G |
15: 94,460,917 (GRCm39) |
T382A |
possibly damaging |
Het |
Itih2 |
A |
G |
2: 10,128,297 (GRCm39) |
S135P |
possibly damaging |
Het |
Kansl3 |
C |
T |
1: 36,388,497 (GRCm39) |
D457N |
probably damaging |
Het |
Kcns3 |
A |
G |
12: 11,141,601 (GRCm39) |
I366T |
probably damaging |
Het |
Kif26a |
C |
A |
12: 112,145,719 (GRCm39) |
Y1743* |
probably null |
Het |
Lama4 |
A |
T |
10: 38,981,960 (GRCm39) |
I1730F |
probably damaging |
Het |
Lax1 |
T |
C |
1: 133,607,931 (GRCm39) |
N270S |
probably benign |
Het |
Lrp1 |
G |
T |
10: 127,403,233 (GRCm39) |
D2113E |
probably damaging |
Het |
Lrp6 |
A |
G |
6: 134,483,259 (GRCm39) |
V482A |
probably benign |
Het |
Luzp2 |
A |
G |
7: 54,914,108 (GRCm39) |
|
probably benign |
Het |
Mc5r |
C |
A |
18: 68,472,200 (GRCm39) |
D186E |
probably damaging |
Het |
Mcph1 |
A |
T |
8: 18,657,293 (GRCm39) |
|
probably null |
Het |
Mgam |
A |
G |
6: 40,705,905 (GRCm39) |
|
probably benign |
Het |
Mmrn1 |
A |
C |
6: 60,952,939 (GRCm39) |
T407P |
probably damaging |
Het |
Mrpl1 |
T |
C |
5: 96,386,806 (GRCm39) |
V265A |
probably benign |
Het |
Mrpl15 |
C |
T |
1: 4,846,856 (GRCm39) |
G240D |
probably damaging |
Het |
Msx1 |
A |
T |
5: 37,978,795 (GRCm39) |
M240K |
probably damaging |
Het |
Mtf1 |
T |
C |
4: 124,724,934 (GRCm39) |
L337P |
probably damaging |
Het |
Muc5ac |
T |
A |
7: 141,361,626 (GRCm39) |
C1646S |
probably damaging |
Het |
Mvb12a |
C |
A |
8: 71,999,638 (GRCm39) |
T219N |
probably damaging |
Het |
N4bp2 |
T |
A |
5: 65,960,855 (GRCm39) |
S509T |
probably benign |
Het |
Nckap1 |
A |
G |
2: 80,383,750 (GRCm39) |
V144A |
possibly damaging |
Het |
Nkx2-6 |
G |
T |
14: 69,412,404 (GRCm39) |
G191C |
possibly damaging |
Het |
Nmnat2 |
T |
C |
1: 152,962,138 (GRCm39) |
I126T |
probably damaging |
Het |
Nrp2 |
C |
T |
1: 62,835,014 (GRCm39) |
R863W |
probably damaging |
Het |
Nup188 |
C |
T |
2: 30,226,726 (GRCm39) |
R1168C |
probably damaging |
Het |
Oas3 |
T |
A |
5: 120,892,754 (GRCm39) |
D1091V |
probably damaging |
Het |
Optn |
T |
A |
2: 5,036,126 (GRCm39) |
Q452L |
probably damaging |
Het |
Or8b47 |
C |
T |
9: 38,435,082 (GRCm39) |
T18I |
probably damaging |
Het |
Pcca |
G |
A |
14: 122,854,178 (GRCm39) |
V157I |
probably benign |
Het |
Pcdha9 |
A |
G |
18: 37,132,281 (GRCm39) |
D450G |
probably benign |
Het |
Pcnx1 |
T |
A |
12: 82,042,323 (GRCm39) |
S38T |
probably benign |
Het |
Phrf1 |
C |
G |
7: 140,840,055 (GRCm39) |
D1083E |
probably benign |
Het |
Plaat5 |
T |
A |
19: 7,596,691 (GRCm39) |
Y159* |
probably null |
Het |
Plcb4 |
G |
A |
2: 135,829,817 (GRCm39) |
A947T |
probably benign |
Het |
Ppp1r3g |
G |
A |
13: 36,152,834 (GRCm39) |
D85N |
possibly damaging |
Het |
Pramel34 |
G |
A |
5: 93,785,969 (GRCm39) |
H104Y |
possibly damaging |
Het |
Prom2 |
A |
C |
2: 127,380,185 (GRCm39) |
V349G |
probably damaging |
Het |
Prrc2c |
C |
T |
1: 162,541,843 (GRCm39) |
S382N |
probably benign |
Het |
Rai14 |
A |
T |
15: 10,592,204 (GRCm39) |
N230K |
probably benign |
Het |
Rexo5 |
A |
T |
7: 119,402,025 (GRCm39) |
K142I |
probably damaging |
Het |
Rgs22 |
T |
C |
15: 36,098,409 (GRCm39) |
H484R |
probably damaging |
Het |
Rims2 |
C |
T |
15: 39,543,086 (GRCm39) |
A1440V |
probably damaging |
Het |
Serpinb1a |
T |
C |
13: 33,026,946 (GRCm39) |
E332G |
probably damaging |
Het |
Sh2b1 |
TGGGGACCAGCTCAGCCACGGGGACCAGCTC |
TGGGGACCAGCTCAGCCACGGGGACCAGCTCAGCCACGGGGACCAGCTC |
7: 126,066,742 (GRCm39) |
|
probably benign |
Het |
Slc26a7 |
C |
T |
4: 14,516,165 (GRCm39) |
G555S |
possibly damaging |
Het |
Slc4a2 |
A |
T |
5: 24,639,123 (GRCm39) |
D386V |
probably damaging |
Het |
Slc6a17 |
C |
T |
3: 107,384,551 (GRCm39) |
V350M |
probably damaging |
Het |
Smc2 |
A |
G |
4: 52,449,361 (GRCm39) |
Y174C |
probably damaging |
Het |
Smoc2 |
A |
G |
17: 14,619,686 (GRCm39) |
Y355C |
probably damaging |
Het |
Smpd1 |
T |
A |
7: 105,204,442 (GRCm39) |
V107E |
probably benign |
Het |
Snapc1 |
T |
C |
12: 74,018,773 (GRCm39) |
|
probably benign |
Het |
Spata31e2 |
T |
C |
1: 26,722,426 (GRCm39) |
D918G |
possibly damaging |
Het |
Steap4 |
T |
G |
5: 8,026,683 (GRCm39) |
F215L |
probably benign |
Het |
Tbc1d1 |
T |
A |
5: 64,435,364 (GRCm39) |
S501T |
probably damaging |
Het |
Tec |
A |
G |
5: 72,926,117 (GRCm39) |
Y312H |
probably damaging |
Het |
Ticrr |
C |
A |
7: 79,343,516 (GRCm39) |
T1127K |
possibly damaging |
Het |
Tlk2 |
A |
G |
11: 105,147,722 (GRCm39) |
D438G |
probably benign |
Het |
Tln2 |
C |
A |
9: 67,277,980 (GRCm39) |
V343L |
probably benign |
Het |
Tmem156 |
T |
A |
5: 65,231,148 (GRCm39) |
I241F |
probably damaging |
Het |
Tmtc1 |
G |
T |
6: 148,186,390 (GRCm39) |
N559K |
probably benign |
Het |
Trbv4 |
A |
T |
6: 41,036,696 (GRCm39) |
I74F |
probably benign |
Het |
Trmt1l |
C |
T |
1: 151,328,899 (GRCm39) |
P524S |
probably damaging |
Het |
Trpa1 |
A |
T |
1: 14,956,040 (GRCm39) |
C776* |
probably null |
Het |
Ttc41 |
T |
A |
10: 86,599,830 (GRCm39) |
S1043R |
probably benign |
Het |
Ttn |
A |
G |
2: 76,576,646 (GRCm39) |
L24749S |
probably damaging |
Het |
Ube2o |
C |
T |
11: 116,471,942 (GRCm39) |
G100R |
probably damaging |
Het |
Unc5b |
T |
C |
10: 60,609,532 (GRCm39) |
E588G |
possibly damaging |
Het |
Usp43 |
G |
T |
11: 67,770,922 (GRCm39) |
Q571K |
probably damaging |
Het |
Vmn1r127 |
G |
A |
7: 21,052,927 (GRCm39) |
P287L |
possibly damaging |
Het |
Wasf3 |
T |
A |
5: 146,397,857 (GRCm39) |
M208K |
possibly damaging |
Het |
Xab2 |
A |
G |
8: 3,663,000 (GRCm39) |
F527S |
possibly damaging |
Het |
Zfp644 |
T |
G |
5: 106,785,774 (GRCm39) |
N258H |
possibly damaging |
Het |
Zfp947 |
A |
C |
17: 22,364,594 (GRCm39) |
F360C |
probably damaging |
Het |
|
Other mutations in Myo16 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00421:Myo16
|
APN |
8 |
10,488,889 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00567:Myo16
|
APN |
8 |
10,512,154 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00671:Myo16
|
APN |
8 |
10,411,067 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00897:Myo16
|
APN |
8 |
10,365,518 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01458:Myo16
|
APN |
8 |
10,485,853 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01523:Myo16
|
APN |
8 |
10,420,908 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01532:Myo16
|
APN |
8 |
10,450,551 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01680:Myo16
|
APN |
8 |
10,322,630 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01747:Myo16
|
APN |
8 |
10,654,877 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02084:Myo16
|
APN |
8 |
10,411,088 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02203:Myo16
|
APN |
8 |
10,620,132 (GRCm39) |
missense |
possibly damaging |
0.52 |
IGL02506:Myo16
|
APN |
8 |
10,440,217 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02819:Myo16
|
APN |
8 |
10,372,600 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02935:Myo16
|
APN |
8 |
10,582,990 (GRCm39) |
missense |
probably benign |
0.41 |
IGL02943:Myo16
|
APN |
8 |
10,450,595 (GRCm39) |
splice site |
probably benign |
|
IGL03347:Myo16
|
APN |
8 |
10,426,120 (GRCm39) |
critical splice acceptor site |
probably null |
|
3-1:Myo16
|
UTSW |
8 |
10,488,869 (GRCm39) |
missense |
probably damaging |
0.99 |
P0016:Myo16
|
UTSW |
8 |
10,450,596 (GRCm39) |
splice site |
probably benign |
|
R0006:Myo16
|
UTSW |
8 |
10,525,988 (GRCm39) |
missense |
probably damaging |
0.98 |
R0006:Myo16
|
UTSW |
8 |
10,525,988 (GRCm39) |
missense |
probably damaging |
0.98 |
R0033:Myo16
|
UTSW |
8 |
10,420,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R0033:Myo16
|
UTSW |
8 |
10,420,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R0142:Myo16
|
UTSW |
8 |
10,619,790 (GRCm39) |
missense |
probably benign |
0.01 |
R0195:Myo16
|
UTSW |
8 |
10,365,538 (GRCm39) |
splice site |
probably benign |
|
R0418:Myo16
|
UTSW |
8 |
10,619,918 (GRCm39) |
missense |
probably benign |
0.01 |
R0576:Myo16
|
UTSW |
8 |
10,612,318 (GRCm39) |
critical splice donor site |
probably null |
|
R0627:Myo16
|
UTSW |
8 |
10,489,689 (GRCm39) |
missense |
probably benign |
0.15 |
R0826:Myo16
|
UTSW |
8 |
10,426,285 (GRCm39) |
splice site |
probably benign |
|
R0835:Myo16
|
UTSW |
8 |
10,322,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R1015:Myo16
|
UTSW |
8 |
10,440,183 (GRCm39) |
missense |
probably benign |
0.17 |
R1052:Myo16
|
UTSW |
8 |
10,620,181 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1180:Myo16
|
UTSW |
8 |
10,446,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R1185:Myo16
|
UTSW |
8 |
10,683,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R1185:Myo16
|
UTSW |
8 |
10,683,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R1474:Myo16
|
UTSW |
8 |
10,552,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R1484:Myo16
|
UTSW |
8 |
10,610,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R1503:Myo16
|
UTSW |
8 |
10,552,817 (GRCm39) |
missense |
probably benign |
0.44 |
R1733:Myo16
|
UTSW |
8 |
10,492,283 (GRCm39) |
missense |
probably damaging |
0.98 |
R1873:Myo16
|
UTSW |
8 |
10,322,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R1885:Myo16
|
UTSW |
8 |
10,372,656 (GRCm39) |
missense |
probably damaging |
1.00 |
R1943:Myo16
|
UTSW |
8 |
10,644,905 (GRCm39) |
missense |
possibly damaging |
0.63 |
R2013:Myo16
|
UTSW |
8 |
10,552,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R2019:Myo16
|
UTSW |
8 |
10,426,260 (GRCm39) |
missense |
probably benign |
0.05 |
R2022:Myo16
|
UTSW |
8 |
10,322,633 (GRCm39) |
missense |
probably benign |
0.08 |
R2214:Myo16
|
UTSW |
8 |
10,488,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R2228:Myo16
|
UTSW |
8 |
10,644,905 (GRCm39) |
missense |
possibly damaging |
0.63 |
R2351:Myo16
|
UTSW |
8 |
10,644,905 (GRCm39) |
missense |
possibly damaging |
0.63 |
R2352:Myo16
|
UTSW |
8 |
10,644,905 (GRCm39) |
missense |
possibly damaging |
0.63 |
R2357:Myo16
|
UTSW |
8 |
10,644,905 (GRCm39) |
missense |
possibly damaging |
0.63 |
R2566:Myo16
|
UTSW |
8 |
10,644,820 (GRCm39) |
missense |
probably benign |
0.43 |
R3402:Myo16
|
UTSW |
8 |
10,434,719 (GRCm39) |
missense |
probably benign |
|
R3870:Myo16
|
UTSW |
8 |
10,492,239 (GRCm39) |
missense |
probably benign |
0.25 |
R4080:Myo16
|
UTSW |
8 |
10,612,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R4498:Myo16
|
UTSW |
8 |
10,485,869 (GRCm39) |
missense |
probably benign |
0.01 |
R4631:Myo16
|
UTSW |
8 |
10,556,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R4689:Myo16
|
UTSW |
8 |
10,488,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R4736:Myo16
|
UTSW |
8 |
10,423,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R4738:Myo16
|
UTSW |
8 |
10,423,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R4739:Myo16
|
UTSW |
8 |
10,423,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R4764:Myo16
|
UTSW |
8 |
10,485,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R4778:Myo16
|
UTSW |
8 |
10,619,694 (GRCm39) |
missense |
probably damaging |
0.97 |
R4852:Myo16
|
UTSW |
8 |
10,423,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R4885:Myo16
|
UTSW |
8 |
10,488,892 (GRCm39) |
missense |
probably damaging |
0.98 |
R4993:Myo16
|
UTSW |
8 |
10,526,094 (GRCm39) |
missense |
probably damaging |
0.99 |
R5077:Myo16
|
UTSW |
8 |
10,372,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R5135:Myo16
|
UTSW |
8 |
10,526,114 (GRCm39) |
missense |
probably benign |
|
R5170:Myo16
|
UTSW |
8 |
10,619,745 (GRCm39) |
missense |
probably benign |
0.30 |
R5203:Myo16
|
UTSW |
8 |
10,410,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R5246:Myo16
|
UTSW |
8 |
10,612,212 (GRCm39) |
nonsense |
probably null |
|
R5517:Myo16
|
UTSW |
8 |
10,610,226 (GRCm39) |
missense |
probably benign |
0.22 |
R5567:Myo16
|
UTSW |
8 |
10,372,676 (GRCm39) |
missense |
probably damaging |
1.00 |
R5694:Myo16
|
UTSW |
8 |
10,619,606 (GRCm39) |
missense |
probably benign |
0.01 |
R5749:Myo16
|
UTSW |
8 |
10,463,245 (GRCm39) |
missense |
probably benign |
0.01 |
R6131:Myo16
|
UTSW |
8 |
10,619,877 (GRCm39) |
missense |
probably benign |
|
R6213:Myo16
|
UTSW |
8 |
10,420,963 (GRCm39) |
critical splice donor site |
probably null |
|
R6216:Myo16
|
UTSW |
8 |
10,365,494 (GRCm39) |
missense |
probably benign |
0.01 |
R6240:Myo16
|
UTSW |
8 |
10,420,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R6628:Myo16
|
UTSW |
8 |
10,620,638 (GRCm39) |
missense |
probably damaging |
0.99 |
R6935:Myo16
|
UTSW |
8 |
10,619,820 (GRCm39) |
missense |
probably benign |
0.37 |
R6996:Myo16
|
UTSW |
8 |
10,619,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R7103:Myo16
|
UTSW |
8 |
10,619,673 (GRCm39) |
missense |
unknown |
|
R7164:Myo16
|
UTSW |
8 |
10,619,585 (GRCm39) |
missense |
unknown |
|
R7255:Myo16
|
UTSW |
8 |
10,549,169 (GRCm39) |
missense |
unknown |
|
R7266:Myo16
|
UTSW |
8 |
10,322,687 (GRCm39) |
missense |
unknown |
|
R7319:Myo16
|
UTSW |
8 |
10,526,185 (GRCm39) |
splice site |
probably null |
|
R7398:Myo16
|
UTSW |
8 |
10,612,183 (GRCm39) |
missense |
unknown |
|
R7442:Myo16
|
UTSW |
8 |
10,322,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R7498:Myo16
|
UTSW |
8 |
10,450,589 (GRCm39) |
missense |
unknown |
|
R7539:Myo16
|
UTSW |
8 |
10,411,095 (GRCm39) |
critical splice donor site |
probably null |
|
R7622:Myo16
|
UTSW |
8 |
10,426,238 (GRCm39) |
missense |
unknown |
|
R7794:Myo16
|
UTSW |
8 |
10,619,913 (GRCm39) |
missense |
unknown |
|
R7903:Myo16
|
UTSW |
8 |
10,426,265 (GRCm39) |
missense |
probably null |
|
R8055:Myo16
|
UTSW |
8 |
10,612,186 (GRCm39) |
missense |
unknown |
|
R8078:Myo16
|
UTSW |
8 |
10,612,078 (GRCm39) |
missense |
unknown |
|
R8081:Myo16
|
UTSW |
8 |
10,372,743 (GRCm39) |
missense |
unknown |
|
R8679:Myo16
|
UTSW |
8 |
10,411,042 (GRCm39) |
missense |
unknown |
|
R8700:Myo16
|
UTSW |
8 |
10,463,172 (GRCm39) |
missense |
unknown |
|
R8939:Myo16
|
UTSW |
8 |
10,524,679 (GRCm39) |
missense |
probably damaging |
0.99 |
R8955:Myo16
|
UTSW |
8 |
10,426,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R8968:Myo16
|
UTSW |
8 |
10,619,700 (GRCm39) |
missense |
unknown |
|
R9187:Myo16
|
UTSW |
8 |
10,492,233 (GRCm39) |
missense |
unknown |
|
R9219:Myo16
|
UTSW |
8 |
10,492,236 (GRCm39) |
missense |
unknown |
|
R9327:Myo16
|
UTSW |
8 |
10,489,705 (GRCm39) |
critical splice donor site |
probably null |
|
R9763:Myo16
|
UTSW |
8 |
10,450,528 (GRCm39) |
missense |
unknown |
|
R9765:Myo16
|
UTSW |
8 |
10,620,401 (GRCm39) |
missense |
probably damaging |
0.97 |
R9790:Myo16
|
UTSW |
8 |
10,619,925 (GRCm39) |
missense |
unknown |
|
R9791:Myo16
|
UTSW |
8 |
10,619,925 (GRCm39) |
missense |
unknown |
|
X0066:Myo16
|
UTSW |
8 |
10,426,185 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Myo16
|
UTSW |
8 |
10,524,691 (GRCm39) |
missense |
unknown |
|
|
Predicted Primers |
PCR Primer
(F):5'- AGAGCGTATGTCAAGGATGCC -3'
(R):5'- TGACTGCAGGCTGTTCATG -3'
Sequencing Primer
(F):5'- CGTATGTCAAGGATGCCAAGTG -3'
(R):5'- GGCCTTTGAATGTGGAATAGTAACAC -3'
|
Posted On |
2022-03-25 |