Other mutations in this stock |
Total: 29 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700012B07Rik |
G |
T |
11: 109,684,980 (GRCm39) |
C172* |
probably null |
Het |
6820408C15Rik |
T |
C |
2: 152,282,790 (GRCm39) |
V215A |
probably damaging |
Het |
Abhd14a |
A |
T |
9: 106,321,065 (GRCm39) |
S97T |
possibly damaging |
Het |
Adamts2 |
T |
A |
11: 50,647,533 (GRCm39) |
I302N |
probably damaging |
Het |
Adgra2 |
G |
A |
8: 27,604,457 (GRCm39) |
A511T |
probably damaging |
Het |
Akap9 |
T |
C |
5: 4,117,924 (GRCm39) |
|
probably null |
Het |
Ccr6 |
G |
A |
17: 8,475,214 (GRCm39) |
V140I |
probably damaging |
Het |
Dlat |
A |
T |
9: 50,556,417 (GRCm39) |
|
probably null |
Het |
Gcg |
A |
G |
2: 62,306,148 (GRCm39) |
S150P |
probably damaging |
Het |
Gk5 |
C |
T |
9: 96,058,290 (GRCm39) |
Q424* |
probably null |
Het |
Insm2 |
T |
C |
12: 55,646,799 (GRCm39) |
I181T |
probably damaging |
Het |
Itgae |
A |
G |
11: 73,006,400 (GRCm39) |
E356G |
possibly damaging |
Het |
Kitl |
G |
A |
10: 99,912,768 (GRCm39) |
|
probably null |
Het |
Lgr6 |
C |
T |
1: 134,921,748 (GRCm39) |
A199T |
probably damaging |
Het |
Myo7a |
C |
T |
7: 97,714,997 (GRCm39) |
W1558* |
probably null |
Het |
Or1ak2 |
G |
A |
2: 36,827,241 (GRCm39) |
V37I |
probably benign |
Het |
Or5p81 |
T |
A |
7: 108,267,412 (GRCm39) |
V263E |
probably damaging |
Het |
Pgk1 |
C |
A |
X: 105,238,098 (GRCm39) |
L85I |
possibly damaging |
Het |
Pik3c2b |
G |
A |
1: 133,002,365 (GRCm39) |
|
probably null |
Het |
Plagl1 |
G |
A |
10: 13,003,490 (GRCm39) |
G253R |
probably damaging |
Het |
Ppp4r1 |
G |
A |
17: 66,121,343 (GRCm39) |
V268I |
possibly damaging |
Het |
Pramel27 |
T |
G |
4: 143,578,155 (GRCm39) |
H87Q |
possibly damaging |
Het |
Satl1 |
T |
C |
X: 111,315,613 (GRCm39) |
T281A |
probably benign |
Het |
Shroom3 |
G |
T |
5: 93,090,945 (GRCm39) |
V1151F |
probably damaging |
Het |
Spmap2 |
A |
G |
10: 79,420,589 (GRCm39) |
S159P |
probably damaging |
Het |
Synrg |
A |
G |
11: 83,915,126 (GRCm39) |
E1044G |
probably damaging |
Het |
Tbx5 |
T |
C |
5: 120,021,211 (GRCm39) |
S406P |
probably benign |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Vmn2r79 |
T |
A |
7: 86,653,319 (GRCm39) |
V528D |
possibly 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 |
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 |
|
R9334:Myo3b
|
UTSW |
2 |
70,047,360 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|