Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actr1b |
A |
T |
1: 36,739,251 (GRCm39) |
I346N |
probably damaging |
Het |
Adam6b |
A |
C |
12: 113,454,768 (GRCm39) |
E528D |
probably damaging |
Het |
Ang |
A |
G |
14: 51,339,017 (GRCm39) |
M53V |
possibly damaging |
Het |
Ankrd26 |
G |
A |
6: 118,509,262 (GRCm39) |
A601V |
probably benign |
Het |
Atp6v0d2 |
A |
G |
4: 19,890,695 (GRCm39) |
L155P |
probably damaging |
Het |
Cacna1a |
T |
C |
8: 85,296,594 (GRCm39) |
V1204A |
probably damaging |
Het |
Car4 |
A |
G |
11: 84,855,415 (GRCm39) |
I183V |
probably benign |
Het |
Ccdc149 |
G |
T |
5: 52,578,171 (GRCm39) |
A87E |
possibly damaging |
Het |
Ccdc88b |
A |
G |
19: 6,833,541 (GRCm39) |
M208T |
possibly damaging |
Het |
Ccnt2 |
T |
C |
1: 127,723,046 (GRCm39) |
L162S |
probably damaging |
Het |
Cd27 |
A |
G |
6: 125,213,718 (GRCm39) |
|
probably null |
Het |
Cfap44 |
C |
A |
16: 44,239,654 (GRCm39) |
T567K |
probably damaging |
Het |
Cpne5 |
C |
T |
17: 29,423,673 (GRCm39) |
V152M |
probably benign |
Het |
Cyp2u1 |
C |
T |
3: 131,092,065 (GRCm39) |
V152M |
probably damaging |
Het |
Dnajc13 |
A |
T |
9: 104,051,659 (GRCm39) |
F1733I |
probably benign |
Het |
Dop1a |
A |
G |
9: 86,403,027 (GRCm39) |
Y1409C |
probably damaging |
Het |
Ecm2 |
T |
C |
13: 49,677,815 (GRCm39) |
M367T |
probably benign |
Het |
Eif4g2 |
A |
G |
7: 110,674,031 (GRCm39) |
S658P |
possibly damaging |
Het |
Exoc3l4 |
T |
C |
12: 111,397,117 (GRCm39) |
L666P |
probably damaging |
Het |
Fbxl4 |
G |
A |
4: 22,376,778 (GRCm39) |
M71I |
probably damaging |
Het |
Fbxw10 |
T |
C |
11: 62,765,910 (GRCm39) |
S727P |
possibly damaging |
Het |
Fem1b |
A |
T |
9: 62,703,604 (GRCm39) |
L552* |
probably null |
Het |
Filip1 |
A |
T |
9: 79,725,739 (GRCm39) |
V960D |
probably benign |
Het |
Glipr1l3 |
A |
T |
10: 111,979,948 (GRCm39) |
M198K |
probably benign |
Het |
Gm19410 |
T |
A |
8: 36,270,722 (GRCm39) |
C1216* |
probably null |
Het |
Gmps |
T |
A |
3: 63,889,864 (GRCm39) |
V81E |
probably damaging |
Het |
Gpr150 |
G |
T |
13: 76,204,103 (GRCm39) |
Q281K |
probably benign |
Het |
Grsf1 |
A |
G |
5: 88,820,469 (GRCm39) |
V221A |
probably damaging |
Het |
Gsc |
T |
A |
12: 104,439,353 (GRCm39) |
I8F |
probably damaging |
Het |
Homer2 |
A |
T |
7: 81,261,078 (GRCm39) |
C284* |
probably null |
Het |
Hrg |
T |
A |
16: 22,780,061 (GRCm39) |
H446Q |
unknown |
Het |
Jag1 |
C |
T |
2: 136,943,593 (GRCm39) |
R201H |
probably damaging |
Het |
Kctd15 |
C |
T |
7: 34,341,483 (GRCm39) |
R148H |
possibly damaging |
Het |
Klhdc7a |
G |
A |
4: 139,693,493 (GRCm39) |
R485C |
probably benign |
Het |
Ldhd |
T |
A |
8: 112,353,980 (GRCm39) |
I407F |
probably benign |
Het |
Lgals12 |
G |
A |
19: 7,578,086 (GRCm39) |
R192C |
probably benign |
Het |
Lmf2 |
G |
A |
15: 89,239,577 (GRCm39) |
L26F |
probably damaging |
Het |
Lum |
A |
T |
10: 97,404,347 (GRCm39) |
I81F |
probably damaging |
Het |
Map1b |
G |
T |
13: 99,568,148 (GRCm39) |
D1524E |
unknown |
Het |
Marveld3 |
A |
G |
8: 110,675,036 (GRCm39) |
L260S |
probably damaging |
Het |
Mms19 |
C |
T |
19: 41,942,203 (GRCm39) |
R555H |
probably benign |
Het |
Mrpl37 |
G |
A |
4: 106,921,605 (GRCm39) |
T208I |
probably benign |
Het |
Mug1 |
A |
T |
6: 121,838,490 (GRCm39) |
T498S |
probably benign |
Het |
Myo7a |
A |
T |
7: 97,716,369 (GRCm39) |
F1459Y |
probably damaging |
Het |
Neurl4 |
C |
A |
11: 69,796,792 (GRCm39) |
R518S |
probably damaging |
Het |
Nmnat2 |
T |
G |
1: 152,949,585 (GRCm39) |
V43G |
probably damaging |
Het |
Or2b11 |
T |
C |
11: 59,462,272 (GRCm39) |
Y98C |
probably damaging |
Het |
Or2n1b |
T |
A |
17: 38,459,840 (GRCm39) |
F120L |
probably benign |
Het |
Or6c6c |
A |
G |
10: 129,541,683 (GRCm39) |
N312S |
probably benign |
Het |
Otog |
A |
G |
7: 45,909,353 (GRCm39) |
T608A |
possibly damaging |
Het |
Pck2 |
G |
A |
14: 55,785,283 (GRCm39) |
R482Q |
probably damaging |
Het |
Pcx |
G |
A |
19: 4,670,532 (GRCm39) |
M1013I |
probably benign |
Het |
Pex13 |
A |
G |
11: 23,605,630 (GRCm39) |
M200T |
probably benign |
Het |
Pigt |
CCGTGCCCGTGGTGTGCCCCCTCTCTAGTCCGGCGTGCCCGTGGTGTACCCCCTCTCTAGTCCTGTGAGCCCGTGGTGTACCCCCTCTCTAGTCCGGCGCGCCCGTGGTGTGCCCCCTCTCTAGTCCGGCGCGCCCGTGGTGTGCCCCCTCTCTAGTCCGGCGAGCCCGTGGTGTGCCCCCTCTCTAGTCCGGCGAGCCCGTGGTGTGCCCCCTCTCTAGTCCGGCGTGCCCGTGGTGTACCCCCTCTCTAGTCCTGTGAGCCCGTGGTGTACCCCCTCTCTAGTCCGGCGCGCCCGTGGTGTGCCCCCTCTCTAGTCCGGCGCTCCCATGGTGTGCCCCCTCTCTAGTCCGGCGCTCCCGTGGTGTGCCCCCTCTCTAGTCCGGCGAGCCCGTGGTGTGCCCCCTCTCTAGTCC |
CCGTGCCCGTGGTGTACCCCCTCTCTAGTCCTGTGAGCCCGTGGTGTACCCCCTCTCTAGTCCGGCGCGCCCGTGGTGTGCCCCCTCTCTAGTCCGGCGCGCCCGTGGTGTGCCCCCTCTCTAGTCCGGCGAGCCCGTGGTGTGCCCCCTCTCTAGTCCGGCGAGCCCGTGGTGTGCCCCCTCTCTAGTCCGGCGTGCCCGTGGTGTACCCCCTCTCTAGTCCTGTGAGCCCGTGGTGTACCCCCTCTCTAGTCCGGCGCGCCCGTGGTGTGCCCCCTCTCTAGTCCGGCGCTCCCATGGTGTGCCCCCTCTCTAGTCCGGCGCTCCCGTGGTGTGCCCCCTCTCTAGTCCGGCGAGCCCGTGGTGTGCCCCCTCTCTAGTCC |
2: 164,349,420 (GRCm39) |
|
probably null |
Het |
Pramel32 |
A |
T |
4: 88,548,186 (GRCm39) |
I73K |
probably damaging |
Het |
Ptpn4 |
T |
C |
1: 119,730,114 (GRCm39) |
H26R |
probably benign |
Het |
Ralgps2 |
T |
A |
1: 156,715,599 (GRCm39) |
E72V |
probably damaging |
Het |
Relch |
T |
A |
1: 105,654,179 (GRCm39) |
F873L |
possibly damaging |
Het |
Scube1 |
A |
T |
15: 83,512,264 (GRCm39) |
C396S |
possibly damaging |
Het |
Sec23b |
T |
A |
2: 144,410,550 (GRCm39) |
N283K |
possibly damaging |
Het |
Setx |
T |
A |
2: 29,044,032 (GRCm39) |
Y1800* |
probably null |
Het |
Sgce |
G |
T |
6: 4,707,205 (GRCm39) |
S213R |
probably damaging |
Het |
Skic3 |
C |
A |
13: 76,281,076 (GRCm39) |
T704N |
possibly damaging |
Het |
Slc36a2 |
T |
C |
11: 55,075,865 (GRCm39) |
|
probably benign |
Het |
Sult5a1 |
A |
T |
8: 123,875,146 (GRCm39) |
D129E |
probably damaging |
Het |
Tacr1 |
A |
T |
6: 82,380,913 (GRCm39) |
H108L |
probably damaging |
Het |
Tnfsf10 |
T |
A |
3: 27,389,496 (GRCm39) |
Y186N |
probably damaging |
Het |
Unc80 |
T |
C |
1: 66,688,919 (GRCm39) |
S2428P |
possibly damaging |
Het |
Vwf |
G |
A |
6: 125,654,909 (GRCm39) |
R2535H |
|
Het |
Zfp532 |
A |
G |
18: 65,756,128 (GRCm39) |
I20M |
probably damaging |
Het |
|
Other mutations in Myo3b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00736:Myo3b
|
APN |
2 |
69,935,989 (GRCm39) |
splice site |
probably benign |
|
IGL00959:Myo3b
|
APN |
2 |
70,144,636 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01069:Myo3b
|
APN |
2 |
70,075,735 (GRCm39) |
missense |
probably benign |
0.22 |
IGL01116:Myo3b
|
APN |
2 |
70,119,730 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02097:Myo3b
|
APN |
2 |
70,069,173 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02220:Myo3b
|
APN |
2 |
70,119,923 (GRCm39) |
splice site |
probably benign |
|
IGL02553:Myo3b
|
APN |
2 |
69,925,568 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02557:Myo3b
|
APN |
2 |
70,085,663 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02648:Myo3b
|
APN |
2 |
69,935,716 (GRCm39) |
splice site |
probably benign |
|
IGL02902:Myo3b
|
APN |
2 |
70,119,745 (GRCm39) |
missense |
probably benign |
0.36 |
IGL02981:Myo3b
|
APN |
2 |
69,938,969 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03030:Myo3b
|
APN |
2 |
70,257,160 (GRCm39) |
splice site |
probably benign |
|
IGL03031:Myo3b
|
APN |
2 |
70,085,721 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL03068:Myo3b
|
APN |
2 |
70,257,160 (GRCm39) |
splice site |
probably benign |
|
IGL03078:Myo3b
|
APN |
2 |
70,117,335 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03224:Myo3b
|
APN |
2 |
70,180,283 (GRCm39) |
missense |
probably benign |
|
IGL03329:Myo3b
|
APN |
2 |
70,084,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R0079:Myo3b
|
UTSW |
2 |
69,925,502 (GRCm39) |
missense |
possibly damaging |
0.58 |
R0226:Myo3b
|
UTSW |
2 |
70,047,510 (GRCm39) |
missense |
probably benign |
0.00 |
R0238:Myo3b
|
UTSW |
2 |
69,935,769 (GRCm39) |
missense |
probably benign |
0.00 |
R0238:Myo3b
|
UTSW |
2 |
69,935,769 (GRCm39) |
missense |
probably benign |
0.00 |
R0239:Myo3b
|
UTSW |
2 |
69,935,769 (GRCm39) |
missense |
probably benign |
0.00 |
R0239:Myo3b
|
UTSW |
2 |
69,935,769 (GRCm39) |
missense |
probably benign |
0.00 |
R0313:Myo3b
|
UTSW |
2 |
70,179,303 (GRCm39) |
nonsense |
probably null |
|
R0331:Myo3b
|
UTSW |
2 |
69,925,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R0371:Myo3b
|
UTSW |
2 |
70,083,304 (GRCm39) |
splice site |
probably benign |
|
R0442:Myo3b
|
UTSW |
2 |
70,069,305 (GRCm39) |
critical splice donor site |
probably null |
|
R0964:Myo3b
|
UTSW |
2 |
70,257,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R1217:Myo3b
|
UTSW |
2 |
70,161,224 (GRCm39) |
missense |
probably benign |
0.02 |
R1429:Myo3b
|
UTSW |
2 |
70,083,351 (GRCm39) |
missense |
probably damaging |
0.97 |
R1460:Myo3b
|
UTSW |
2 |
70,062,798 (GRCm39) |
missense |
probably benign |
0.31 |
R1617:Myo3b
|
UTSW |
2 |
70,111,562 (GRCm39) |
missense |
probably benign |
0.00 |
R1628:Myo3b
|
UTSW |
2 |
70,117,306 (GRCm39) |
missense |
probably benign |
0.01 |
R1708:Myo3b
|
UTSW |
2 |
70,075,729 (GRCm39) |
nonsense |
probably null |
|
R1940:Myo3b
|
UTSW |
2 |
70,088,419 (GRCm39) |
missense |
probably benign |
0.01 |
R2407:Myo3b
|
UTSW |
2 |
70,085,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R3081:Myo3b
|
UTSW |
2 |
70,086,927 (GRCm39) |
splice site |
probably benign |
|
R3687:Myo3b
|
UTSW |
2 |
70,075,658 (GRCm39) |
missense |
probably benign |
|
R3745:Myo3b
|
UTSW |
2 |
70,064,829 (GRCm39) |
splice site |
probably benign |
|
R4011:Myo3b
|
UTSW |
2 |
69,926,720 (GRCm39) |
missense |
probably benign |
0.15 |
R4074:Myo3b
|
UTSW |
2 |
70,119,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R4419:Myo3b
|
UTSW |
2 |
69,926,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R4496:Myo3b
|
UTSW |
2 |
70,084,748 (GRCm39) |
missense |
probably benign |
|
R4539:Myo3b
|
UTSW |
2 |
69,869,491 (GRCm39) |
start codon destroyed |
probably null |
0.00 |
R4643:Myo3b
|
UTSW |
2 |
70,069,186 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4657:Myo3b
|
UTSW |
2 |
70,069,243 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4807:Myo3b
|
UTSW |
2 |
69,936,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R4849:Myo3b
|
UTSW |
2 |
70,075,253 (GRCm39) |
missense |
probably damaging |
0.98 |
R4997:Myo3b
|
UTSW |
2 |
70,088,427 (GRCm39) |
missense |
possibly damaging |
0.49 |
R5008:Myo3b
|
UTSW |
2 |
70,088,412 (GRCm39) |
missense |
probably damaging |
0.99 |
R5070:Myo3b
|
UTSW |
2 |
70,083,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R5072:Myo3b
|
UTSW |
2 |
69,925,593 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5082:Myo3b
|
UTSW |
2 |
70,088,374 (GRCm39) |
missense |
probably benign |
0.01 |
R5103:Myo3b
|
UTSW |
2 |
69,926,747 (GRCm39) |
missense |
probably benign |
0.08 |
R5109:Myo3b
|
UTSW |
2 |
69,925,637 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5304:Myo3b
|
UTSW |
2 |
70,257,232 (GRCm39) |
missense |
probably damaging |
0.97 |
R5396:Myo3b
|
UTSW |
2 |
69,957,329 (GRCm39) |
missense |
probably damaging |
0.99 |
R5400:Myo3b
|
UTSW |
2 |
69,935,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R5468:Myo3b
|
UTSW |
2 |
70,064,785 (GRCm39) |
missense |
probably benign |
0.00 |
R5620:Myo3b
|
UTSW |
2 |
70,069,254 (GRCm39) |
missense |
probably benign |
0.04 |
R5646:Myo3b
|
UTSW |
2 |
70,144,774 (GRCm39) |
missense |
probably damaging |
0.97 |
R5729:Myo3b
|
UTSW |
2 |
69,936,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R5943:Myo3b
|
UTSW |
2 |
70,117,285 (GRCm39) |
missense |
probably benign |
0.03 |
R5971:Myo3b
|
UTSW |
2 |
70,069,243 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6091:Myo3b
|
UTSW |
2 |
70,069,113 (GRCm39) |
missense |
probably benign |
0.00 |
R6138:Myo3b
|
UTSW |
2 |
70,069,243 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6164:Myo3b
|
UTSW |
2 |
70,075,754 (GRCm39) |
critical splice donor site |
probably null |
|
R6177:Myo3b
|
UTSW |
2 |
70,143,707 (GRCm39) |
missense |
probably benign |
0.00 |
R6421:Myo3b
|
UTSW |
2 |
70,143,700 (GRCm39) |
missense |
probably benign |
0.02 |
R6478:Myo3b
|
UTSW |
2 |
70,179,304 (GRCm39) |
missense |
probably benign |
|
R6606:Myo3b
|
UTSW |
2 |
70,062,829 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6752:Myo3b
|
UTSW |
2 |
70,119,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R6982:Myo3b
|
UTSW |
2 |
70,256,409 (GRCm39) |
missense |
probably benign |
0.02 |
R6997:Myo3b
|
UTSW |
2 |
69,957,329 (GRCm39) |
missense |
probably damaging |
0.99 |
R7032:Myo3b
|
UTSW |
2 |
69,925,608 (GRCm39) |
missense |
probably damaging |
0.98 |
R7038:Myo3b
|
UTSW |
2 |
69,925,552 (GRCm39) |
missense |
probably benign |
0.00 |
R7062:Myo3b
|
UTSW |
2 |
70,047,501 (GRCm39) |
missense |
probably benign |
0.00 |
R7537:Myo3b
|
UTSW |
2 |
70,047,513 (GRCm39) |
missense |
probably benign |
0.01 |
R7861:Myo3b
|
UTSW |
2 |
69,939,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R7955:Myo3b
|
UTSW |
2 |
69,925,623 (GRCm39) |
missense |
probably benign |
0.37 |
R7977:Myo3b
|
UTSW |
2 |
70,161,277 (GRCm39) |
missense |
probably benign |
|
R7978:Myo3b
|
UTSW |
2 |
70,083,458 (GRCm39) |
missense |
probably damaging |
1.00 |
R7987:Myo3b
|
UTSW |
2 |
70,161,277 (GRCm39) |
missense |
probably benign |
|
R8803:Myo3b
|
UTSW |
2 |
70,083,338 (GRCm39) |
missense |
probably benign |
|
R8843:Myo3b
|
UTSW |
2 |
70,088,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R8896:Myo3b
|
UTSW |
2 |
70,069,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R8904:Myo3b
|
UTSW |
2 |
70,257,252 (GRCm39) |
missense |
probably benign |
0.07 |
R8909:Myo3b
|
UTSW |
2 |
70,083,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R9031:Myo3b
|
UTSW |
2 |
70,082,094 (GRCm39) |
missense |
probably damaging |
0.99 |
R9052:Myo3b
|
UTSW |
2 |
70,062,747 (GRCm39) |
missense |
probably benign |
0.00 |
R9251:Myo3b
|
UTSW |
2 |
70,088,425 (GRCm39) |
nonsense |
probably null |
|
R9268:Myo3b
|
UTSW |
2 |
70,257,305 (GRCm39) |
makesense |
probably null |
|
R9377:Myo3b
|
UTSW |
2 |
70,069,242 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9457:Myo3b
|
UTSW |
2 |
69,925,553 (GRCm39) |
missense |
probably benign |
0.01 |
R9520:Myo3b
|
UTSW |
2 |
70,062,753 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9593:Myo3b
|
UTSW |
2 |
70,075,648 (GRCm39) |
missense |
probably benign |
0.43 |
R9671:Myo3b
|
UTSW |
2 |
70,086,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R9790:Myo3b
|
UTSW |
2 |
70,180,287 (GRCm39) |
missense |
probably benign |
0.35 |
R9791:Myo3b
|
UTSW |
2 |
70,180,287 (GRCm39) |
missense |
probably benign |
0.35 |
U15987:Myo3b
|
UTSW |
2 |
70,069,243 (GRCm39) |
missense |
possibly damaging |
0.95 |
X0025:Myo3b
|
UTSW |
2 |
70,062,747 (GRCm39) |
missense |
probably benign |
0.00 |
X0065:Myo3b
|
UTSW |
2 |
70,088,313 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Myo3b
|
UTSW |
2 |
70,088,371 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Myo3b
|
UTSW |
2 |
69,926,705 (GRCm39) |
missense |
probably damaging |
1.00 |
|