Incidental Mutation 'R1733:Myo16'
| ID |
199488 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Myo16
|
| Ensembl Gene |
ENSMUSG00000039057 |
| Gene Name |
myosin XVI |
| Synonyms |
C230040D10Rik, BM140241, Nyap3 |
| MMRRC Submission |
039765-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.325)
|
| Stock # |
R1733 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
8 |
| Chromosomal Location |
10203911-10684742 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 10492283 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Proline
at position 742
(S742P)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000049345
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000042103]
[ENSMUST00000207204]
[ENSMUST00000207477]
|
| AlphaFold |
Q5DU14 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000042103
AA Change: S742P
PolyPhen 2
Score 0.983 (Sensitivity: 0.75; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000049345
Gene: ENSMUSG00000039057
AA Change: S742P
| 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: S686P
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000207477
AA Change: S742P
|
| Meta Mutation Damage Score |
0.5305 |
| Coding Region Coverage |
- 1x: 97.5%
- 3x: 96.9%
- 10x: 95.2%
- 20x: 91.9%
|
| Validation Efficiency |
95% (95/100) |
| 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: 93 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adamts19 |
T |
G |
18: 59,165,001 (GRCm39) |
C1034W |
probably damaging |
Het |
| Agbl2 |
G |
T |
2: 90,641,089 (GRCm39) |
K737N |
probably damaging |
Het |
| Aqp9 |
T |
A |
9: 71,019,624 (GRCm39) |
I279F |
possibly damaging |
Het |
| Aspm |
T |
A |
1: 139,384,855 (GRCm39) |
N166K |
probably benign |
Het |
| Atp13a3 |
A |
T |
16: 30,176,084 (GRCm39) |
I186N |
probably benign |
Het |
| Btaf1 |
A |
T |
19: 36,972,362 (GRCm39) |
I1366L |
probably benign |
Het |
| Camk4 |
A |
C |
18: 33,211,074 (GRCm39) |
K60Q |
possibly damaging |
Het |
| Card11 |
G |
T |
5: 140,892,388 (GRCm39) |
Q226K |
possibly damaging |
Het |
| Ccdc187 |
T |
C |
2: 26,183,670 (GRCm39) |
D110G |
possibly damaging |
Het |
| Col5a2 |
C |
T |
1: 45,446,192 (GRCm39) |
R462Q |
possibly damaging |
Het |
| Cp |
A |
T |
3: 20,022,383 (GRCm39) |
|
probably benign |
Het |
| Cpz |
A |
T |
5: 35,675,102 (GRCm39) |
V38E |
probably damaging |
Het |
| Cxcr6 |
G |
A |
9: 123,639,181 (GRCm39) |
V68I |
probably damaging |
Het |
| Cyp2a22 |
C |
A |
7: 26,634,187 (GRCm39) |
E322D |
possibly damaging |
Het |
| D130052B06Rik |
C |
T |
11: 33,573,784 (GRCm39) |
T127I |
probably benign |
Het |
| Daam2 |
T |
A |
17: 49,797,231 (GRCm39) |
M185L |
possibly damaging |
Het |
| Dnaja3 |
G |
A |
16: 4,502,029 (GRCm39) |
R11K |
probably null |
Het |
| Dnttip2 |
T |
A |
3: 122,070,397 (GRCm39) |
S537R |
probably benign |
Het |
| Dock9 |
G |
T |
14: 121,864,292 (GRCm39) |
H572Q |
probably benign |
Het |
| Dpp4 |
T |
A |
2: 62,203,213 (GRCm39) |
|
probably null |
Het |
| Enc1 |
T |
G |
13: 97,381,550 (GRCm39) |
I20S |
possibly damaging |
Het |
| Ephb6 |
T |
A |
6: 41,596,654 (GRCm39) |
H900Q |
probably benign |
Het |
| Ercc3 |
T |
C |
18: 32,400,218 (GRCm39) |
V690A |
possibly damaging |
Het |
| Fam90a1a |
C |
T |
8: 22,453,385 (GRCm39) |
Q247* |
probably null |
Het |
| Fkbp10 |
G |
A |
11: 100,314,757 (GRCm39) |
R423H |
probably benign |
Het |
| Fus |
A |
G |
7: 127,580,717 (GRCm39) |
M265V |
probably benign |
Het |
| Gas2l3 |
T |
A |
10: 89,250,127 (GRCm39) |
K330N |
probably damaging |
Het |
| Gpam |
T |
G |
19: 55,069,901 (GRCm39) |
L410F |
probably damaging |
Het |
| Gpr37l1 |
A |
T |
1: 135,089,273 (GRCm39) |
V264E |
possibly damaging |
Het |
| Grk6 |
A |
T |
13: 55,600,979 (GRCm39) |
|
probably benign |
Het |
| Gsto1 |
G |
T |
19: 47,843,674 (GRCm39) |
V19F |
probably damaging |
Het |
| H1f7 |
G |
T |
15: 98,154,016 (GRCm39) |
Q378K |
unknown |
Het |
| Hgfac |
G |
A |
5: 35,201,018 (GRCm39) |
C194Y |
probably damaging |
Het |
| Hivep1 |
A |
G |
13: 42,311,407 (GRCm39) |
N1216D |
probably damaging |
Het |
| Hrg |
C |
T |
16: 22,769,997 (GRCm39) |
A42V |
probably damaging |
Het |
| Irx4 |
A |
G |
13: 73,414,824 (GRCm39) |
D136G |
probably benign |
Het |
| Kcnn3 |
G |
T |
3: 89,559,397 (GRCm39) |
V556L |
probably benign |
Het |
| Klk1b8 |
T |
C |
7: 43,451,545 (GRCm39) |
Y179H |
possibly damaging |
Het |
| Klrb1f |
T |
A |
6: 129,031,322 (GRCm39) |
L173* |
probably null |
Het |
| Kremen2 |
A |
T |
17: 23,962,373 (GRCm39) |
|
probably null |
Het |
| Krt25 |
A |
T |
11: 99,207,378 (GRCm39) |
Y400* |
probably null |
Het |
| Lingo4 |
A |
T |
3: 94,310,485 (GRCm39) |
R474S |
probably benign |
Het |
| Lnpep |
T |
C |
17: 17,773,575 (GRCm39) |
K599E |
probably benign |
Het |
| Mapk8ip3 |
A |
T |
17: 25,155,824 (GRCm39) |
M2K |
possibly damaging |
Het |
| Mat2b |
A |
T |
11: 40,570,904 (GRCm39) |
S307T |
probably benign |
Het |
| Mcph1 |
C |
A |
8: 18,681,979 (GRCm39) |
A372D |
probably benign |
Het |
| Mfsd6 |
T |
A |
1: 52,748,524 (GRCm39) |
I114F |
probably damaging |
Het |
| Mlkl |
A |
G |
8: 112,049,380 (GRCm39) |
S248P |
probably damaging |
Het |
| Mmrn1 |
A |
T |
6: 60,954,085 (GRCm39) |
T789S |
probably benign |
Het |
| Mphosph8 |
A |
G |
14: 56,930,916 (GRCm39) |
Y735C |
probably damaging |
Het |
| Mrc1 |
T |
A |
2: 14,261,910 (GRCm39) |
Y300N |
probably damaging |
Het |
| Mrps11 |
A |
G |
7: 78,442,460 (GRCm39) |
H180R |
probably damaging |
Het |
| Msh4 |
T |
C |
3: 153,573,404 (GRCm39) |
D556G |
probably damaging |
Het |
| Myh10 |
C |
A |
11: 68,693,122 (GRCm39) |
D1472E |
probably benign |
Het |
| Nlrp5-ps |
C |
T |
7: 14,316,978 (GRCm39) |
|
noncoding transcript |
Het |
| Nrp1 |
C |
T |
8: 129,194,974 (GRCm39) |
P477S |
probably benign |
Het |
| Oplah |
G |
T |
15: 76,186,683 (GRCm39) |
C665* |
probably null |
Het |
| Or4f14b |
T |
A |
2: 111,775,625 (GRCm39) |
M59L |
probably benign |
Het |
| Or4f54 |
T |
C |
2: 111,123,210 (GRCm39) |
V199A |
probably damaging |
Het |
| Or51b17 |
T |
C |
7: 103,542,118 (GRCm39) |
S275G |
probably benign |
Het |
| Or8g22 |
G |
T |
9: 38,958,678 (GRCm39) |
H57N |
unknown |
Het |
| Otogl |
T |
C |
10: 107,619,573 (GRCm39) |
T1696A |
possibly damaging |
Het |
| Pdzrn4 |
A |
G |
15: 92,299,855 (GRCm39) |
I242V |
probably benign |
Het |
| Phgdh |
G |
A |
3: 98,235,451 (GRCm39) |
T141I |
probably benign |
Het |
| Pigv |
T |
C |
4: 133,392,237 (GRCm39) |
Y311C |
probably damaging |
Het |
| Pik3c2a |
T |
G |
7: 116,017,755 (GRCm39) |
M1L |
possibly damaging |
Het |
| Pitpnm1 |
A |
T |
19: 4,159,960 (GRCm39) |
K760* |
probably null |
Het |
| Pnrc1 |
G |
A |
4: 33,246,438 (GRCm39) |
H174Y |
probably damaging |
Het |
| Ptgis |
A |
G |
2: 167,033,888 (GRCm39) |
|
probably benign |
Het |
| Ptpn4 |
T |
C |
1: 119,643,773 (GRCm39) |
|
probably null |
Het |
| Rin3 |
T |
A |
12: 102,335,589 (GRCm39) |
L420* |
probably null |
Het |
| Sacs |
T |
G |
14: 61,442,903 (GRCm39) |
F1650V |
probably damaging |
Het |
| Sbno2 |
T |
A |
10: 79,894,342 (GRCm39) |
N1081Y |
possibly damaging |
Het |
| Sema5b |
C |
T |
16: 35,466,737 (GRCm39) |
P213L |
probably damaging |
Het |
| Sharpin |
T |
C |
15: 76,232,136 (GRCm39) |
K240R |
probably benign |
Het |
| Skint6 |
T |
A |
4: 113,034,234 (GRCm39) |
|
probably benign |
Het |
| Slc4a2 |
A |
G |
5: 24,634,565 (GRCm39) |
E68G |
probably damaging |
Het |
| Srcin1 |
C |
T |
11: 97,424,327 (GRCm39) |
V634I |
probably benign |
Het |
| Srsf10 |
T |
A |
4: 135,590,476 (GRCm39) |
F134I |
possibly damaging |
Het |
| Stab1 |
C |
A |
14: 30,867,260 (GRCm39) |
G1700V |
probably damaging |
Het |
| Sun1 |
T |
G |
5: 139,216,544 (GRCm39) |
C290W |
possibly damaging |
Het |
| Svs6 |
T |
A |
2: 164,159,577 (GRCm39) |
|
probably benign |
Het |
| Tmem8b |
G |
A |
4: 43,690,228 (GRCm39) |
|
probably null |
Het |
| Usp49 |
A |
G |
17: 47,983,238 (GRCm39) |
D81G |
probably damaging |
Het |
| Vmn1r215 |
T |
A |
13: 23,260,848 (GRCm39) |
V296D |
probably benign |
Het |
| Vmn1r6 |
T |
A |
6: 56,979,607 (GRCm39) |
S90T |
probably damaging |
Het |
| Wbp2 |
A |
G |
11: 115,974,709 (GRCm39) |
F42L |
probably benign |
Het |
| Wdr20rt |
C |
T |
12: 65,274,055 (GRCm39) |
T333I |
possibly damaging |
Het |
| Zfp341 |
C |
T |
2: 154,483,298 (GRCm39) |
A552V |
probably benign |
Het |
| Zfp607b |
A |
T |
7: 27,391,949 (GRCm39) |
H8L |
possibly damaging |
Het |
| Zfp758 |
G |
T |
17: 22,594,830 (GRCm39) |
D439Y |
probably damaging |
Het |
| Zfp946 |
T |
C |
17: 22,672,538 (GRCm39) |
Y46H |
probably damaging |
Het |
| Zic2 |
G |
A |
14: 122,716,359 (GRCm39) |
E432K |
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 |
|
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 |
|
|
R9287:Myo16
|
UTSW |
8 |
10,526,114 (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'- CATGGCGGACATCATAGAGTGTGAG -3'
(R):5'- CAGAGTAACACTTGGGCCACCATC -3'
Sequencing Primer
(F):5'- CATCATAGAGTGTGAGTGGGAC -3'
(R):5'- AGCACCTGTAATCCTGAGTTG -3'
|
| Posted On |
2014-05-23 |
Incidental Mutation