Incidental Mutation 'R4852:Myo16'
| ID |
373633 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Myo16
|
| Ensembl Gene |
ENSMUSG00000039057 |
| Gene Name |
myosin XVI |
| Synonyms |
C230040D10Rik, BM140241, Nyap3 |
| MMRRC Submission |
042464-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.265)
|
| Stock # |
R4852 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
8 |
| Chromosomal Location |
10203911-10684742 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 10423474 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Leucine to Proline
at position 270
(L270P)
|
| 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: L270P
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000049345
Gene: ENSMUSG00000039057
AA Change: L270P
| 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: L270P
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000207477
AA Change: L270P
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000208309
AA Change: L270P
PolyPhen 2
Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000214643
|
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.3%
- 10x: 96.2%
- 20x: 92.0%
|
| Validation Efficiency |
|
| 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: 85 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2700049A03Rik |
G |
T |
12: 71,211,320 (GRCm39) |
E685* |
probably null |
Het |
| 2700049A03Rik |
A |
T |
12: 71,211,321 (GRCm39) |
E685V |
possibly damaging |
Het |
| 4921524L21Rik |
C |
G |
18: 6,623,487 (GRCm39) |
L66V |
possibly damaging |
Het |
| 4921524L21Rik |
T |
A |
18: 6,623,488 (GRCm39) |
L66Q |
probably damaging |
Het |
| Abca6 |
A |
G |
11: 110,135,029 (GRCm39) |
V252A |
probably benign |
Het |
| Ablim2 |
C |
T |
5: 35,959,766 (GRCm39) |
R73C |
possibly damaging |
Het |
| Acap1 |
C |
T |
11: 69,775,202 (GRCm39) |
V354M |
probably benign |
Het |
| Accs |
T |
C |
2: 93,674,605 (GRCm39) |
D99G |
probably damaging |
Het |
| Adam9 |
T |
C |
8: 25,493,317 (GRCm39) |
Y97C |
probably damaging |
Het |
| Akap6 |
T |
C |
12: 53,151,458 (GRCm39) |
V1174A |
probably damaging |
Het |
| Aknad1 |
C |
A |
3: 108,659,056 (GRCm39) |
D23E |
probably damaging |
Het |
| Ano2 |
T |
C |
6: 125,959,886 (GRCm39) |
C666R |
possibly damaging |
Het |
| Atp4a |
G |
A |
7: 30,423,693 (GRCm39) |
A933T |
probably benign |
Het |
| Atxn2 |
T |
C |
5: 121,952,474 (GRCm39) |
L224P |
probably damaging |
Het |
| Bin2 |
T |
C |
15: 100,543,169 (GRCm39) |
E338G |
probably damaging |
Het |
| Bloc1s5 |
T |
C |
13: 38,818,960 (GRCm39) |
K20E |
probably damaging |
Het |
| Bst1 |
A |
T |
5: 43,977,867 (GRCm39) |
D72V |
probably benign |
Het |
| Cacna1i |
T |
C |
15: 80,272,680 (GRCm39) |
F1631L |
probably damaging |
Het |
| Capn13 |
GCA |
G |
17: 73,658,501 (GRCm39) |
|
probably null |
Het |
| Cfap43 |
A |
G |
19: 47,885,550 (GRCm39) |
I355T |
possibly damaging |
Het |
| Chuk |
A |
T |
19: 44,077,197 (GRCm39) |
M383K |
possibly damaging |
Het |
| Cnga4 |
A |
G |
7: 105,054,937 (GRCm39) |
I174V |
probably benign |
Het |
| Cpd |
T |
C |
11: 76,675,976 (GRCm39) |
K1226E |
probably benign |
Het |
| Crip2 |
T |
C |
12: 113,104,204 (GRCm39) |
C5R |
probably damaging |
Het |
| Cyp3a11 |
T |
A |
5: 145,797,305 (GRCm39) |
D358V |
probably damaging |
Het |
| Ebag9 |
T |
C |
15: 44,487,915 (GRCm39) |
F21S |
probably damaging |
Het |
| Ercc1 |
A |
T |
7: 19,084,629 (GRCm39) |
H70L |
probably damaging |
Het |
| Exoc3 |
G |
A |
13: 74,347,764 (GRCm39) |
R69C |
probably damaging |
Het |
| Fgfr4 |
A |
T |
13: 55,308,969 (GRCm39) |
R363S |
possibly damaging |
Het |
| Gas2l3 |
CACTCGTCATACT |
CACT |
10: 89,266,820 (GRCm39) |
|
probably benign |
Het |
| Gm7489 |
T |
A |
15: 53,749,434 (GRCm39) |
|
probably benign |
Het |
| Gphn |
G |
A |
12: 78,673,984 (GRCm39) |
V526M |
probably damaging |
Het |
| Gpr152 |
G |
A |
19: 4,193,790 (GRCm39) |
V444I |
probably benign |
Het |
| Gss |
T |
C |
2: 155,406,785 (GRCm39) |
E330G |
probably benign |
Het |
| Hbs1l |
A |
G |
10: 21,234,287 (GRCm39) |
D556G |
possibly damaging |
Het |
| Helz2 |
T |
C |
2: 180,871,913 (GRCm39) |
T2619A |
probably damaging |
Het |
| Hk3 |
A |
G |
13: 55,160,409 (GRCm39) |
F304L |
probably damaging |
Het |
| Itgad |
A |
T |
7: 127,797,702 (GRCm39) |
N906Y |
probably damaging |
Het |
| Jakmip2 |
T |
C |
18: 43,710,465 (GRCm39) |
E246G |
probably damaging |
Het |
| L3mbtl4 |
A |
T |
17: 68,866,748 (GRCm39) |
H329L |
probably damaging |
Het |
| Mau2 |
A |
G |
8: 70,485,827 (GRCm39) |
|
probably null |
Het |
| Naa25 |
T |
C |
5: 121,568,755 (GRCm39) |
S606P |
probably damaging |
Het |
| Nags |
T |
A |
11: 102,037,447 (GRCm39) |
C179* |
probably null |
Het |
| Naip2 |
A |
G |
13: 100,298,044 (GRCm39) |
M664T |
probably benign |
Het |
| Ndufv3 |
T |
C |
17: 31,747,043 (GRCm39) |
I311T |
probably benign |
Het |
| Nipsnap1 |
G |
T |
11: 4,841,468 (GRCm39) |
E258* |
probably null |
Het |
| Nudc |
A |
G |
4: 133,261,660 (GRCm39) |
L208P |
probably damaging |
Het |
| Or1e32 |
T |
C |
11: 73,705,074 (GRCm39) |
Y278C |
probably benign |
Het |
| Or51a39 |
A |
T |
7: 102,362,750 (GRCm39) |
V290E |
probably damaging |
Het |
| Oscp1 |
A |
G |
4: 125,970,652 (GRCm39) |
D137G |
possibly damaging |
Het |
| Pcdhb5 |
C |
T |
18: 37,455,524 (GRCm39) |
P635S |
probably benign |
Het |
| Pcdhgb2 |
T |
A |
18: 37,825,103 (GRCm39) |
I698N |
probably damaging |
Het |
| Pde4b |
A |
G |
4: 102,454,967 (GRCm39) |
Y399C |
probably damaging |
Het |
| Pdf |
A |
T |
8: 107,774,812 (GRCm39) |
V140E |
probably damaging |
Het |
| Pglyrp2 |
T |
C |
17: 32,634,823 (GRCm39) |
N513S |
probably benign |
Het |
| Ranbp2 |
T |
A |
10: 58,312,878 (GRCm39) |
D1199E |
possibly damaging |
Het |
| Rell2 |
G |
T |
18: 38,089,621 (GRCm39) |
|
probably null |
Het |
| Rgl2 |
A |
G |
17: 34,156,147 (GRCm39) |
H745R |
probably benign |
Het |
| Rnf121 |
A |
G |
7: 101,672,592 (GRCm39) |
C264R |
probably damaging |
Het |
| Rnf181 |
A |
G |
6: 72,338,499 (GRCm39) |
F3S |
probably damaging |
Het |
| Rsrc1 |
T |
A |
3: 67,262,935 (GRCm39) |
D296E |
probably damaging |
Het |
| Rubcn |
A |
T |
16: 32,663,678 (GRCm39) |
D319E |
probably damaging |
Het |
| Scaf8 |
T |
C |
17: 3,228,494 (GRCm39) |
S431P |
unknown |
Het |
| Septin11 |
T |
A |
5: 93,310,112 (GRCm39) |
M305K |
possibly damaging |
Het |
| Serpinb12 |
A |
G |
1: 106,884,132 (GRCm39) |
K293E |
probably benign |
Het |
| Sh3bp1 |
T |
A |
15: 78,788,538 (GRCm39) |
H229Q |
probably benign |
Het |
| Slco4c1 |
G |
A |
1: 96,768,953 (GRCm39) |
P303L |
probably damaging |
Het |
| Specc1 |
T |
A |
11: 62,102,510 (GRCm39) |
V952E |
probably damaging |
Het |
| Spint2 |
G |
A |
7: 28,956,211 (GRCm39) |
T158I |
probably benign |
Het |
| St8sia4 |
A |
T |
1: 95,588,623 (GRCm39) |
W71R |
probably damaging |
Het |
| Tex48 |
C |
T |
4: 63,530,151 (GRCm39) |
V23I |
possibly damaging |
Het |
| Tmc5 |
G |
A |
7: 118,244,562 (GRCm39) |
G480D |
probably benign |
Het |
| Tmem8b |
T |
A |
4: 43,689,713 (GRCm39) |
M330K |
probably damaging |
Het |
| Tnrc18 |
C |
T |
5: 142,717,095 (GRCm39) |
R2453Q |
probably damaging |
Het |
| Trank1 |
A |
T |
9: 111,220,963 (GRCm39) |
N2567Y |
possibly damaging |
Het |
| Trps1 |
T |
C |
15: 50,709,705 (GRCm39) |
D211G |
probably damaging |
Het |
| Ttn |
T |
C |
2: 76,555,503 (GRCm39) |
R30501G |
probably damaging |
Het |
| Ttn |
T |
A |
2: 76,573,247 (GRCm39) |
Y25882F |
probably damaging |
Het |
| Unc79 |
T |
A |
12: 103,139,725 (GRCm39) |
V2495E |
probably damaging |
Het |
| Uqcr10 |
T |
A |
11: 4,652,198 (GRCm39) |
H58L |
possibly damaging |
Het |
| Usp7 |
A |
T |
16: 8,574,708 (GRCm39) |
C58* |
probably null |
Het |
| Vmn1r36 |
A |
T |
6: 66,693,872 (GRCm39) |
M1K |
probably null |
Het |
| Wdr7 |
T |
A |
18: 63,911,020 (GRCm39) |
M804K |
probably damaging |
Het |
| Zfp131 |
A |
C |
13: 120,250,394 (GRCm39) |
|
probably null |
Het |
| Zfp507 |
A |
G |
7: 35,493,480 (GRCm39) |
V521A |
probably benign |
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 |
|
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'- CTGATTCAGGTCCTCAGTGTTC -3'
(R):5'- CTGCGATCAGTAACCCACAG -3'
Sequencing Primer
(F):5'- TCTGGGTACTTATTGATTCTGATCC -3'
(R):5'- AGGAGAACACTGGCTCTCTCTC -3'
|
| Posted On |
2016-03-01 |
Incidental Mutation