Incidental Mutation 'R1474:Myo16'
ID |
163915 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Myo16
|
Ensembl Gene |
ENSMUSG00000039057 |
Gene Name |
myosin XVI |
Synonyms |
C230040D10Rik, BM140241, Nyap3 |
MMRRC Submission |
039527-MU
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.265)
|
Stock # |
R1474 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
8 |
Chromosomal Location |
10203911-10684742 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 10552796 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Phenylalanine to Isoleucine
at position 945
(F945I)
|
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: F945I
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000049345 Gene: ENSMUSG00000039057 AA Change: F945I
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: F889I
|
Predicted Effect |
unknown
Transcript: ENSMUST00000207477
AA Change: F945I
|
Meta Mutation Damage Score |
0.3993 |
Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.4%
- 10x: 96.6%
- 20x: 93.6%
|
Validation Efficiency |
95% (104/110) |
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: 106 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8a |
C |
A |
11: 109,960,635 (GRCm39) |
A628S |
probably damaging |
Het |
Abca9 |
T |
C |
11: 110,036,405 (GRCm39) |
N568S |
probably damaging |
Het |
Ada |
C |
T |
2: 163,574,814 (GRCm39) |
A108T |
possibly damaging |
Het |
Adam6a |
T |
A |
12: 113,508,069 (GRCm39) |
D147E |
possibly damaging |
Het |
Ampd1 |
A |
T |
3: 103,006,154 (GRCm39) |
T655S |
probably damaging |
Het |
Ankk1 |
A |
G |
9: 49,327,139 (GRCm39) |
F680S |
probably damaging |
Het |
Asap1 |
G |
A |
15: 63,991,869 (GRCm39) |
T783I |
probably benign |
Het |
Astn1 |
T |
A |
1: 158,329,923 (GRCm39) |
N259K |
probably damaging |
Het |
Birc6 |
T |
C |
17: 74,886,673 (GRCm39) |
V667A |
probably damaging |
Het |
Brat1 |
G |
A |
5: 140,698,382 (GRCm39) |
V185I |
probably benign |
Het |
Btnl6 |
T |
C |
17: 34,732,620 (GRCm39) |
Y318C |
probably damaging |
Het |
Caskin2 |
G |
A |
11: 115,694,522 (GRCm39) |
P360S |
probably benign |
Het |
Ccdc121rt3 |
T |
C |
5: 112,503,642 (GRCm39) |
T21A |
probably benign |
Het |
Cd68 |
T |
A |
11: 69,555,754 (GRCm39) |
|
probably benign |
Het |
Cdca2 |
T |
C |
14: 67,952,355 (GRCm39) |
|
probably benign |
Het |
Cdk6 |
G |
A |
5: 3,523,217 (GRCm39) |
M212I |
probably benign |
Het |
Ceacam5 |
T |
A |
7: 17,481,159 (GRCm39) |
F302Y |
probably damaging |
Het |
Celsr2 |
T |
C |
3: 108,301,055 (GRCm39) |
E2746G |
possibly damaging |
Het |
Clec4a4 |
G |
A |
6: 122,989,703 (GRCm39) |
V115I |
probably benign |
Het |
Clip3 |
C |
A |
7: 29,998,307 (GRCm39) |
A251E |
possibly damaging |
Het |
Cmah |
T |
C |
13: 24,623,180 (GRCm39) |
L350P |
probably damaging |
Het |
Cntnap5a |
C |
T |
1: 116,370,103 (GRCm39) |
R907* |
probably null |
Het |
Cntnap5b |
T |
C |
1: 99,999,814 (GRCm39) |
Y191H |
probably benign |
Het |
Col4a4 |
A |
T |
1: 82,458,207 (GRCm39) |
C1122* |
probably null |
Het |
Coq5 |
A |
G |
5: 115,433,842 (GRCm39) |
|
probably benign |
Het |
Cpxcr1 |
A |
G |
X: 115,387,136 (GRCm39) |
K16E |
possibly damaging |
Het |
Dclk3 |
T |
C |
9: 111,298,304 (GRCm39) |
I616T |
probably benign |
Het |
Dhrs3 |
A |
T |
4: 144,646,057 (GRCm39) |
T122S |
probably damaging |
Het |
Dnm1 |
T |
C |
2: 32,210,596 (GRCm39) |
I502V |
probably benign |
Het |
Dscaml1 |
G |
T |
9: 45,596,519 (GRCm39) |
G788W |
probably damaging |
Het |
Dusp10 |
C |
T |
1: 183,769,645 (GRCm39) |
|
probably null |
Het |
Ehbp1l1 |
C |
A |
19: 5,769,112 (GRCm39) |
L730F |
possibly damaging |
Het |
Eif2ak1 |
C |
T |
5: 143,808,785 (GRCm39) |
H75Y |
probably damaging |
Het |
Evi2a |
T |
C |
11: 79,418,398 (GRCm39) |
T71A |
probably benign |
Het |
Fam184a |
A |
T |
10: 53,511,461 (GRCm39) |
S1073T |
probably damaging |
Het |
Fam227a |
T |
C |
15: 79,499,582 (GRCm39) |
Y591C |
probably damaging |
Het |
Fam83a |
C |
T |
15: 57,873,272 (GRCm39) |
T367M |
probably benign |
Het |
Fam83g |
A |
G |
11: 61,593,819 (GRCm39) |
D451G |
probably damaging |
Het |
Fbn1 |
A |
G |
2: 125,203,185 (GRCm39) |
F1213L |
possibly damaging |
Het |
Fcgbp |
G |
A |
7: 27,791,273 (GRCm39) |
V845I |
probably benign |
Het |
Fermt1 |
C |
T |
2: 132,766,942 (GRCm39) |
E342K |
probably benign |
Het |
Foxn1 |
T |
A |
11: 78,251,933 (GRCm39) |
M433L |
probably benign |
Het |
Gm6632 |
T |
G |
5: 59,211,679 (GRCm39) |
|
noncoding transcript |
Het |
Gnl3 |
A |
T |
14: 30,738,418 (GRCm39) |
|
probably benign |
Het |
Hhipl1 |
C |
T |
12: 108,277,996 (GRCm39) |
T108I |
probably damaging |
Het |
Hs2st1 |
A |
T |
3: 144,141,256 (GRCm39) |
F271I |
possibly damaging |
Het |
Ido1 |
T |
C |
8: 25,074,462 (GRCm39) |
S303G |
probably damaging |
Het |
Ints2 |
C |
T |
11: 86,117,607 (GRCm39) |
R705H |
probably damaging |
Het |
Kcnc2 |
A |
G |
10: 112,292,305 (GRCm39) |
K49E |
probably damaging |
Het |
Kif3b |
T |
A |
2: 153,162,235 (GRCm39) |
V482E |
probably damaging |
Het |
Ldlrad2 |
G |
A |
4: 137,299,525 (GRCm39) |
P100S |
probably benign |
Het |
Lrba |
G |
T |
3: 86,687,573 (GRCm39) |
|
probably benign |
Het |
Lsm11 |
A |
T |
11: 45,824,730 (GRCm39) |
W266R |
probably benign |
Het |
Mob3a |
A |
T |
10: 80,522,988 (GRCm39) |
M215K |
probably benign |
Het |
Mterf1b |
T |
G |
5: 4,247,163 (GRCm39) |
L268R |
probably damaging |
Het |
Mvk |
T |
C |
5: 114,598,157 (GRCm39) |
F365L |
probably damaging |
Het |
Myo1f |
G |
T |
17: 33,813,001 (GRCm39) |
K602N |
possibly damaging |
Het |
Nr2c2ap |
A |
T |
8: 70,585,765 (GRCm39) |
M108L |
probably benign |
Het |
Ofcc1 |
C |
T |
13: 40,362,305 (GRCm39) |
G206R |
probably benign |
Het |
Ogfrl1 |
A |
G |
1: 23,414,890 (GRCm39) |
F206L |
probably damaging |
Het |
Ola1 |
A |
T |
2: 72,987,188 (GRCm39) |
I148N |
probably damaging |
Het |
Or14c46 |
G |
T |
7: 85,918,270 (GRCm39) |
H242Q |
probably damaging |
Het |
Or4d10b |
T |
A |
19: 12,036,844 (GRCm39) |
T91S |
probably benign |
Het |
Or51f1d |
A |
G |
7: 102,701,288 (GRCm39) |
Y261C |
probably damaging |
Het |
Or6c2 |
A |
T |
10: 129,362,824 (GRCm39) |
M243L |
probably benign |
Het |
Or9m2 |
A |
G |
2: 87,821,334 (GRCm39) |
N293S |
probably damaging |
Het |
Otof |
A |
G |
5: 30,536,876 (GRCm39) |
|
probably null |
Het |
Pah |
G |
T |
10: 87,414,175 (GRCm39) |
K341N |
probably damaging |
Het |
Pfdn5 |
T |
A |
15: 102,236,946 (GRCm39) |
|
probably null |
Het |
Piezo2 |
A |
G |
18: 63,216,202 (GRCm39) |
C960R |
probably damaging |
Het |
Pitx2 |
T |
C |
3: 129,012,488 (GRCm39) |
V306A |
probably damaging |
Het |
Pkd1l2 |
C |
A |
8: 117,792,236 (GRCm39) |
|
probably benign |
Het |
Plekho1 |
T |
C |
3: 95,896,878 (GRCm39) |
E197G |
probably damaging |
Het |
Polr2i |
A |
G |
7: 29,932,227 (GRCm39) |
N34S |
probably damaging |
Het |
Psph |
A |
T |
5: 129,848,614 (GRCm39) |
D22E |
probably damaging |
Het |
Ptprs |
C |
A |
17: 56,731,128 (GRCm39) |
A687S |
probably damaging |
Het |
Ralgapa1 |
T |
C |
12: 55,788,265 (GRCm39) |
K606R |
probably benign |
Het |
Rigi |
A |
G |
4: 40,208,868 (GRCm39) |
V703A |
possibly damaging |
Het |
Rims1 |
A |
G |
1: 22,577,362 (GRCm39) |
|
probably benign |
Het |
Rnf213 |
C |
T |
11: 119,328,576 (GRCm39) |
P2002L |
probably damaging |
Het |
Ryr3 |
A |
T |
2: 112,740,307 (GRCm39) |
C555S |
probably damaging |
Het |
Sftpd |
C |
A |
14: 40,894,384 (GRCm39) |
G345V |
probably damaging |
Het |
Slc41a1 |
T |
A |
1: 131,774,319 (GRCm39) |
M462K |
probably damaging |
Het |
Slc44a2 |
A |
G |
9: 21,264,990 (GRCm39) |
E676G |
probably damaging |
Het |
Sox6 |
T |
A |
7: 115,300,926 (GRCm39) |
|
probably benign |
Het |
Spdye4b |
G |
A |
5: 143,181,472 (GRCm39) |
R109Q |
probably damaging |
Het |
Spef1l |
C |
A |
7: 139,556,555 (GRCm39) |
R144L |
probably benign |
Het |
Spink8 |
A |
T |
9: 109,649,706 (GRCm39) |
I63L |
probably damaging |
Het |
St3gal3 |
A |
G |
4: 117,871,983 (GRCm39) |
L73P |
probably damaging |
Het |
Stab1 |
A |
G |
14: 30,871,818 (GRCm39) |
L1247P |
probably benign |
Het |
Tat |
A |
G |
8: 110,718,195 (GRCm39) |
R27G |
probably benign |
Het |
Tcerg1l |
C |
T |
7: 137,881,804 (GRCm39) |
R295H |
probably damaging |
Het |
Tfrc |
T |
C |
16: 32,445,467 (GRCm39) |
V596A |
probably damaging |
Het |
Tgfb3 |
C |
T |
12: 86,116,120 (GRCm39) |
|
probably null |
Het |
Tmed5 |
A |
T |
5: 108,280,248 (GRCm39) |
S15T |
probably benign |
Het |
Tph1 |
A |
T |
7: 46,303,286 (GRCm39) |
S231T |
probably benign |
Het |
Trim30d |
G |
A |
7: 104,121,701 (GRCm39) |
S198L |
probably damaging |
Het |
Trpm6 |
T |
C |
19: 18,773,859 (GRCm39) |
M412T |
probably benign |
Het |
Ttn |
G |
T |
2: 76,612,589 (GRCm39) |
D15417E |
probably benign |
Het |
U2surp |
A |
G |
9: 95,375,251 (GRCm39) |
I157T |
possibly damaging |
Het |
Ubr4 |
A |
G |
4: 139,156,890 (GRCm39) |
D2305G |
probably damaging |
Het |
Uvssa |
A |
G |
5: 33,546,165 (GRCm39) |
K179E |
probably benign |
Het |
Vps35l |
T |
C |
7: 118,359,436 (GRCm39) |
F230S |
probably damaging |
Het |
Xirp2 |
A |
G |
2: 67,355,411 (GRCm39) |
K3391E |
probably benign |
Het |
Xpo7 |
T |
A |
14: 70,936,473 (GRCm39) |
H170L |
probably benign |
Het |
Zrsr2-ps1 |
T |
C |
11: 22,924,404 (GRCm39) |
W393R |
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 |
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 |
|
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'- GCTGTGACCAAGACTCAAGCCAATG -3'
(R):5'- TTGTGCCCGAGCAGAGTAAAGAC -3'
Sequencing Primer
(F):5'- CAAGAAGAGTCACTGTCTGTCTG -3'
(R):5'- CCGAGCAGAGTAAAGACAACAG -3'
|
Posted On |
2014-03-28 |