Incidental Mutation 'R4739:Myo16'
ID |
359526 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Myo16
|
Ensembl Gene |
ENSMUSG00000039057 |
Gene Name |
myosin XVI |
Synonyms |
C230040D10Rik, BM140241, Nyap3 |
MMRRC Submission |
042025-MU
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.265)
|
Stock # |
R4739 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
8 |
Chromosomal Location |
10203911-10684742 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to T
at 10423527 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glycine to Tryptophan
at position 288
(G288W)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000049345
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000042103]
[ENSMUST00000207204]
[ENSMUST00000207477]
[ENSMUST00000208309]
[ENSMUST00000214643]
|
AlphaFold |
Q5DU14 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000042103
AA Change: G288W
PolyPhen 2
Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000049345 Gene: ENSMUSG00000039057 AA Change: G288W
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: G288W
|
Predicted Effect |
unknown
Transcript: ENSMUST00000207477
AA Change: G288W
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000208309
AA Change: G288W
PolyPhen 2
Score 0.960 (Sensitivity: 0.78; Specificity: 0.95)
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000214643
|
Meta Mutation Damage Score |
0.6467 |
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.5%
- 10x: 96.9%
- 20x: 94.5%
|
Validation Efficiency |
96% (102/106) |
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: 98 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1600012P17Rik |
C |
T |
1: 158,796,904 (GRCm39) |
|
noncoding transcript |
Het |
2300002M23Rik |
A |
G |
17: 35,878,403 (GRCm39) |
|
probably benign |
Het |
Aadat |
T |
C |
8: 60,993,140 (GRCm39) |
V360A |
probably benign |
Het |
Abcc5 |
T |
A |
16: 20,218,376 (GRCm39) |
D283V |
probably damaging |
Het |
Abraxas1 |
T |
A |
5: 100,959,886 (GRCm39) |
K155N |
probably damaging |
Het |
Acot3 |
T |
C |
12: 84,105,364 (GRCm39) |
I277T |
probably benign |
Het |
Ankrd45 |
G |
A |
1: 160,982,960 (GRCm39) |
C157Y |
probably damaging |
Het |
Apol10a |
C |
T |
15: 77,372,841 (GRCm39) |
T159I |
possibly damaging |
Het |
Arhgef11 |
G |
A |
3: 87,605,306 (GRCm39) |
V214M |
possibly damaging |
Het |
Ash1l |
A |
C |
3: 88,890,152 (GRCm39) |
N677T |
probably benign |
Het |
Atg13 |
A |
G |
2: 91,515,040 (GRCm39) |
S254P |
probably damaging |
Het |
Atg16l2 |
A |
G |
7: 100,946,385 (GRCm39) |
L129P |
probably damaging |
Het |
Avl9 |
T |
A |
6: 56,703,294 (GRCm39) |
V120D |
probably damaging |
Het |
Castor1 |
A |
G |
11: 4,169,004 (GRCm39) |
E57G |
possibly damaging |
Het |
Cc2d1b |
T |
C |
4: 108,485,239 (GRCm39) |
V527A |
probably benign |
Het |
Ccnl1 |
A |
G |
3: 65,854,092 (GRCm39) |
|
probably benign |
Het |
Cenpl |
T |
A |
1: 160,910,837 (GRCm39) |
D261E |
probably damaging |
Het |
Cep192 |
T |
G |
18: 67,984,803 (GRCm39) |
I1604M |
probably benign |
Het |
Cep95 |
A |
G |
11: 106,706,560 (GRCm39) |
I573V |
probably benign |
Het |
Cfap100 |
A |
G |
6: 90,389,825 (GRCm39) |
|
probably null |
Het |
Ciao3 |
A |
T |
17: 26,000,283 (GRCm39) |
H322L |
probably damaging |
Het |
Cmc1 |
T |
A |
9: 117,904,245 (GRCm39) |
M49L |
probably benign |
Het |
Cyfip2 |
G |
T |
11: 46,170,820 (GRCm39) |
N176K |
probably damaging |
Het |
Cyp2w1 |
T |
C |
5: 139,342,430 (GRCm39) |
F408L |
probably damaging |
Het |
D630045J12Rik |
G |
A |
6: 38,172,971 (GRCm39) |
S399F |
possibly damaging |
Het |
Dcbld2 |
T |
A |
16: 58,281,339 (GRCm39) |
L528Q |
probably damaging |
Het |
Dip2b |
T |
C |
15: 100,105,658 (GRCm39) |
V1138A |
probably damaging |
Het |
Dip2c |
T |
A |
13: 9,583,375 (GRCm39) |
L119Q |
probably damaging |
Het |
Dnah3 |
T |
C |
7: 119,677,169 (GRCm39) |
D444G |
possibly damaging |
Het |
Dsg1c |
A |
T |
18: 20,408,246 (GRCm39) |
N432Y |
possibly damaging |
Het |
Dst |
T |
A |
1: 34,230,228 (GRCm39) |
I2785N |
probably benign |
Het |
Dynap |
A |
T |
18: 70,374,296 (GRCm39) |
Y77N |
possibly damaging |
Het |
Eif4g3 |
T |
C |
4: 137,910,510 (GRCm39) |
L1330P |
possibly damaging |
Het |
Eif4g3 |
T |
A |
4: 137,925,408 (GRCm39) |
S1584T |
probably benign |
Het |
Enpp1 |
A |
T |
10: 24,555,146 (GRCm39) |
C67S |
probably null |
Het |
Enpp5 |
C |
T |
17: 44,392,027 (GRCm39) |
T152I |
probably damaging |
Het |
Erbb4 |
T |
C |
1: 68,383,059 (GRCm39) |
M313V |
probably damaging |
Het |
Erc2 |
T |
G |
14: 27,498,838 (GRCm39) |
L238R |
probably damaging |
Het |
Eya3 |
T |
A |
4: 132,448,698 (GRCm39) |
|
probably benign |
Het |
Farp1 |
T |
C |
14: 121,476,199 (GRCm39) |
F339L |
probably damaging |
Het |
Fsip2 |
A |
C |
2: 82,805,697 (GRCm39) |
D672A |
possibly damaging |
Het |
Gap43 |
G |
T |
16: 42,112,581 (GRCm39) |
P60Q |
probably benign |
Het |
Gpr37l1 |
T |
A |
1: 135,094,783 (GRCm39) |
I154F |
probably damaging |
Het |
Greb1 |
A |
G |
12: 16,746,329 (GRCm39) |
S1314P |
probably damaging |
Het |
Hectd4 |
A |
T |
5: 121,486,505 (GRCm39) |
M3167L |
probably benign |
Het |
Hps3 |
C |
T |
3: 20,084,574 (GRCm39) |
|
probably null |
Het |
Hps5 |
A |
G |
7: 46,436,013 (GRCm39) |
C178R |
probably benign |
Het |
Hspg2 |
T |
A |
4: 137,297,384 (GRCm39) |
|
probably benign |
Het |
Impdh2-ps |
A |
G |
8: 100,757,839 (GRCm39) |
|
noncoding transcript |
Het |
Josd2 |
T |
A |
7: 44,120,678 (GRCm39) |
N138K |
probably damaging |
Het |
Mtmr6 |
T |
G |
14: 60,529,546 (GRCm39) |
M315R |
probably damaging |
Het |
Mtrf1 |
G |
A |
14: 79,650,520 (GRCm39) |
V323M |
probably damaging |
Het |
Myo18a |
T |
C |
11: 77,714,149 (GRCm39) |
Y748H |
probably damaging |
Het |
Nek1 |
A |
T |
8: 61,551,545 (GRCm39) |
N853I |
probably benign |
Het |
Npnt |
T |
G |
3: 132,610,452 (GRCm39) |
T272P |
possibly damaging |
Het |
Obi1 |
C |
T |
14: 104,747,819 (GRCm39) |
D43N |
probably damaging |
Het |
Or2ag1b |
C |
A |
7: 106,288,351 (GRCm39) |
E196* |
probably null |
Het |
Or2b6 |
T |
A |
13: 21,823,340 (GRCm39) |
M118L |
possibly damaging |
Het |
Or2y17 |
G |
A |
11: 49,232,148 (GRCm39) |
G263D |
probably benign |
Het |
Or51e1 |
T |
A |
7: 102,359,378 (GRCm39) |
I304N |
probably damaging |
Het |
Or52n2c |
G |
A |
7: 104,574,017 (GRCm39) |
T318I |
possibly damaging |
Het |
Or5a1 |
A |
G |
19: 12,097,234 (GRCm39) |
Y269H |
possibly damaging |
Het |
Pappa2 |
T |
C |
1: 158,784,582 (GRCm39) |
R143G |
probably benign |
Het |
Pappa2 |
T |
G |
1: 158,784,572 (GRCm39) |
D146A |
probably damaging |
Het |
Pcsk9 |
C |
T |
4: 106,304,353 (GRCm39) |
G496R |
probably damaging |
Het |
Pes1 |
A |
G |
11: 3,914,058 (GRCm39) |
K8E |
probably damaging |
Het |
Phlpp2 |
G |
A |
8: 110,667,052 (GRCm39) |
G1194S |
probably damaging |
Het |
Pkn1 |
A |
C |
8: 84,398,378 (GRCm39) |
V763G |
probably damaging |
Het |
Pkp2 |
C |
A |
16: 16,048,588 (GRCm39) |
A331E |
probably damaging |
Het |
Plb1 |
T |
A |
5: 32,507,023 (GRCm39) |
|
probably null |
Het |
Plxna1 |
A |
T |
6: 89,309,657 (GRCm39) |
|
probably null |
Het |
Polq |
C |
T |
16: 36,862,109 (GRCm39) |
T264M |
probably damaging |
Het |
Prkag3 |
T |
C |
1: 74,779,864 (GRCm39) |
*490W |
probably null |
Het |
Prl2c1 |
T |
C |
13: 28,041,661 (GRCm39) |
C228R |
probably damaging |
Het |
Pus7l |
T |
C |
15: 94,438,591 (GRCm39) |
S85G |
probably benign |
Het |
Rfc3 |
A |
C |
5: 151,568,241 (GRCm39) |
|
probably benign |
Het |
Riox2 |
A |
G |
16: 59,309,732 (GRCm39) |
N362S |
probably benign |
Het |
Scaper |
A |
T |
9: 55,650,932 (GRCm39) |
D904E |
probably damaging |
Het |
Scn11a |
T |
C |
9: 119,583,627 (GRCm39) |
M1663V |
probably benign |
Het |
Slc13a3 |
A |
T |
2: 165,272,209 (GRCm39) |
I278N |
possibly damaging |
Het |
Slc22a7 |
T |
C |
17: 46,745,923 (GRCm39) |
E278G |
probably damaging |
Het |
Snrnp48 |
T |
A |
13: 38,393,893 (GRCm39) |
M66K |
probably damaging |
Het |
Styk1 |
T |
G |
6: 131,277,429 (GRCm39) |
E404A |
probably damaging |
Het |
Synj1 |
T |
A |
16: 90,752,307 (GRCm39) |
H1016L |
probably benign |
Het |
Tbc1d8 |
G |
A |
1: 39,441,959 (GRCm39) |
T211I |
possibly damaging |
Het |
Tjp2 |
T |
C |
19: 24,097,475 (GRCm39) |
|
probably null |
Het |
Tmem87a |
A |
G |
2: 120,190,518 (GRCm39) |
|
probably null |
Het |
Trappc9 |
T |
G |
15: 72,808,909 (GRCm39) |
Y718S |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,641,587 (GRCm39) |
L5176Q |
possibly damaging |
Het |
Ubqlnl |
C |
T |
7: 103,798,925 (GRCm39) |
V191M |
probably benign |
Het |
Ugt2a3 |
C |
T |
5: 87,475,054 (GRCm39) |
G397R |
probably damaging |
Het |
Wdr33 |
T |
A |
18: 32,019,139 (GRCm39) |
M454K |
probably benign |
Het |
Wdtc1 |
G |
T |
4: 133,029,110 (GRCm39) |
N325K |
possibly damaging |
Het |
Whrn |
T |
C |
4: 63,336,402 (GRCm39) |
H720R |
probably damaging |
Het |
Xirp2 |
A |
T |
2: 67,349,609 (GRCm39) |
D3268V |
probably damaging |
Het |
Zc3h7a |
A |
T |
16: 10,959,573 (GRCm39) |
H793Q |
probably damaging |
Het |
Zfp518b |
C |
T |
5: 38,831,841 (GRCm39) |
A55T |
possibly damaging |
Het |
Zmynd8 |
G |
A |
2: 165,647,249 (GRCm39) |
T901M |
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 |
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'- GATTCTGATCCTTAGTACCCTGG -3'
(R):5'- TGGCTTTACCCACTGCGATC -3'
Sequencing Primer
(F):5'- TGATCCTTAGTACCCTGGATATTTG -3'
(R):5'- AGGAGAACACTGGCTCTCTCTC -3'
|
Posted On |
2015-11-11 |