Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310003L06Rik |
T |
A |
5: 88,120,438 (GRCm39) |
D398E |
possibly damaging |
Het |
Adam34 |
T |
C |
8: 44,105,303 (GRCm39) |
Y114C |
probably damaging |
Het |
Akap9 |
T |
A |
5: 4,004,896 (GRCm39) |
D156E |
probably benign |
Het |
Apba1 |
T |
A |
19: 23,889,825 (GRCm39) |
S408T |
probably benign |
Het |
Asb14 |
C |
T |
14: 26,625,412 (GRCm39) |
H256Y |
probably benign |
Het |
Atf6 |
A |
T |
1: 170,627,181 (GRCm39) |
|
probably null |
Het |
Atp6v1b2 |
T |
A |
8: 69,541,548 (GRCm39) |
V35E |
probably benign |
Het |
Atp8a2 |
T |
C |
14: 60,255,289 (GRCm39) |
|
probably null |
Het |
Ccdc170 |
C |
A |
10: 4,432,597 (GRCm39) |
P12Q |
unknown |
Het |
Cdh23 |
C |
T |
10: 60,167,567 (GRCm39) |
E1810K |
probably damaging |
Het |
Cdo1 |
A |
T |
18: 46,853,475 (GRCm39) |
F94L |
probably damaging |
Het |
Cfap96 |
T |
G |
8: 46,409,474 (GRCm39) |
S282R |
probably damaging |
Het |
Chdh |
C |
T |
14: 29,758,809 (GRCm39) |
P585S |
possibly damaging |
Het |
Clasp2 |
A |
G |
9: 113,683,391 (GRCm39) |
N407S |
probably benign |
Het |
Clca3a1 |
T |
A |
3: 144,453,329 (GRCm39) |
S465C |
probably benign |
Het |
Clip2 |
C |
A |
5: 134,551,484 (GRCm39) |
V213L |
probably damaging |
Het |
Col6a6 |
A |
G |
9: 105,644,707 (GRCm39) |
S1194P |
probably damaging |
Het |
Cyp7a1 |
T |
C |
4: 6,268,463 (GRCm39) |
T421A |
possibly damaging |
Het |
Dhh |
C |
T |
15: 98,791,907 (GRCm39) |
G367E |
possibly damaging |
Het |
Dnah5 |
A |
G |
15: 28,326,796 (GRCm39) |
N2002D |
probably damaging |
Het |
Epn2 |
T |
A |
11: 61,437,528 (GRCm39) |
N15Y |
probably damaging |
Het |
Evi5 |
A |
C |
5: 107,936,147 (GRCm39) |
V647G |
probably benign |
Het |
Eya1 |
T |
C |
1: 14,353,424 (GRCm39) |
|
probably null |
Het |
Fam120a |
A |
G |
13: 49,102,589 (GRCm39) |
V222A |
probably benign |
Het |
Fastkd5 |
A |
T |
2: 130,457,864 (GRCm39) |
I242K |
possibly damaging |
Het |
Hnrnpul1 |
A |
G |
7: 25,450,319 (GRCm39) |
M131T |
probably benign |
Het |
Ice1 |
T |
C |
13: 70,744,283 (GRCm39) |
N2100S |
probably damaging |
Het |
Ifi205 |
T |
A |
1: 173,855,916 (GRCm39) |
D38V |
possibly damaging |
Het |
Klhl9 |
G |
A |
4: 88,639,843 (GRCm39) |
Q133* |
probably null |
Het |
Krt84 |
T |
C |
15: 101,436,924 (GRCm39) |
E370G |
probably benign |
Het |
Lrrc4c |
T |
C |
2: 97,459,410 (GRCm39) |
I12T |
probably benign |
Het |
Lrriq4 |
T |
A |
3: 30,709,850 (GRCm39) |
L398* |
probably null |
Het |
Ltf |
G |
A |
9: 110,855,198 (GRCm39) |
|
probably null |
Het |
Macf1 |
C |
T |
4: 123,366,101 (GRCm39) |
V1322I |
probably benign |
Het |
Mark2 |
T |
A |
19: 7,264,698 (GRCm39) |
I112L |
probably damaging |
Het |
Mettl25b |
A |
G |
3: 87,831,649 (GRCm39) |
|
probably null |
Het |
Mterf2 |
A |
T |
10: 84,956,527 (GRCm39) |
C32* |
probably null |
Het |
Nsun7 |
A |
C |
5: 66,421,378 (GRCm39) |
I115L |
probably benign |
Het |
Olfm3 |
G |
A |
3: 114,883,805 (GRCm39) |
V36M |
probably damaging |
Het |
Or1p1c |
T |
C |
11: 74,160,428 (GRCm39) |
I71T |
possibly damaging |
Het |
Or5d44 |
T |
C |
2: 88,141,373 (GRCm39) |
T256A |
probably benign |
Het |
Or8b3 |
A |
T |
9: 38,314,965 (GRCm39) |
Y262F |
possibly damaging |
Het |
Or8g18 |
A |
T |
9: 39,148,983 (GRCm39) |
S246T |
possibly damaging |
Het |
Pcdhgb8 |
A |
T |
18: 37,896,962 (GRCm39) |
R677S |
probably benign |
Het |
Prrt4 |
A |
C |
6: 29,170,538 (GRCm39) |
L638R |
possibly damaging |
Het |
Ptk2 |
G |
A |
15: 73,093,658 (GRCm39) |
P854S |
possibly damaging |
Het |
Rab44 |
T |
C |
17: 29,359,438 (GRCm39) |
F542S |
unknown |
Het |
Rhobtb3 |
T |
A |
13: 76,020,513 (GRCm39) |
E596D |
probably benign |
Het |
Rpl36 |
T |
C |
17: 56,920,944 (GRCm39) |
I44T |
probably benign |
Het |
Rptor |
A |
G |
11: 119,737,762 (GRCm39) |
I112V |
probably benign |
Het |
Rxfp2 |
T |
C |
5: 149,993,813 (GRCm39) |
I611T |
probably damaging |
Het |
Slc12a4 |
G |
T |
8: 106,675,865 (GRCm39) |
N553K |
probably damaging |
Het |
Spata31d1d |
T |
A |
13: 59,876,046 (GRCm39) |
R496S |
probably benign |
Het |
Strbp |
T |
C |
2: 37,493,125 (GRCm39) |
D387G |
possibly damaging |
Het |
Tas2r107 |
A |
T |
6: 131,636,153 (GRCm39) |
C299S |
possibly damaging |
Het |
Tbc1d21 |
A |
T |
9: 58,274,134 (GRCm39) |
|
probably null |
Het |
Tdrd12 |
A |
T |
7: 35,180,471 (GRCm39) |
Y847* |
probably null |
Het |
Tlr2 |
A |
T |
3: 83,745,212 (GRCm39) |
N290K |
probably benign |
Het |
Tmppe |
A |
G |
9: 114,234,858 (GRCm39) |
T386A |
probably damaging |
Het |
Tnks1bp1 |
C |
A |
2: 84,892,297 (GRCm39) |
H741Q |
probably benign |
Het |
Trpc6 |
G |
A |
9: 8,609,951 (GRCm39) |
V140M |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,641,932 (GRCm39) |
D13427G |
probably damaging |
Het |
Uba7 |
C |
A |
9: 107,853,371 (GRCm39) |
L106I |
possibly damaging |
Het |
Unc5b |
T |
G |
10: 60,614,587 (GRCm39) |
T237P |
probably damaging |
Het |
Vit |
A |
C |
17: 78,932,294 (GRCm39) |
D467A |
probably damaging |
Het |
Vmn1r103 |
T |
C |
7: 20,243,780 (GRCm39) |
Y227C |
possibly damaging |
Het |
Vmn1r77 |
T |
A |
7: 11,776,017 (GRCm39) |
Y196* |
probably null |
Het |
Zhx3 |
A |
G |
2: 160,622,898 (GRCm39) |
V423A |
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 |
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 |
|