Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam18 |
C |
G |
8: 25,140,893 (GRCm39) |
G286A |
probably damaging |
Het |
Adcy1 |
G |
A |
11: 7,089,142 (GRCm39) |
A519T |
probably benign |
Het |
Anxa2 |
T |
A |
9: 69,371,762 (GRCm39) |
S2T |
possibly damaging |
Het |
Ap3m1 |
G |
A |
14: 21,089,217 (GRCm39) |
S261L |
possibly damaging |
Het |
Baz2b |
A |
T |
2: 59,743,067 (GRCm39) |
|
probably benign |
Het |
Brdt |
T |
A |
5: 107,507,090 (GRCm39) |
S497T |
probably benign |
Het |
Cdh11 |
A |
G |
8: 103,406,404 (GRCm39) |
F23S |
probably benign |
Het |
Cdh16 |
A |
C |
8: 105,344,434 (GRCm39) |
L540R |
probably damaging |
Het |
Ces5a |
A |
T |
8: 94,261,205 (GRCm39) |
L74Q |
probably damaging |
Het |
Cfap69 |
A |
G |
5: 5,654,306 (GRCm39) |
S543P |
probably damaging |
Het |
Cfap74 |
T |
C |
4: 155,526,538 (GRCm39) |
I763T |
possibly damaging |
Het |
Cma1 |
T |
A |
14: 56,181,191 (GRCm39) |
R58S |
possibly damaging |
Het |
Csmd3 |
C |
T |
15: 47,701,975 (GRCm39) |
D1599N |
probably damaging |
Het |
Cyld |
A |
G |
8: 89,471,940 (GRCm39) |
K857R |
probably benign |
Het |
Cyp3a16 |
T |
C |
5: 145,388,667 (GRCm39) |
D270G |
probably damaging |
Het |
D1Pas1 |
T |
C |
1: 186,700,286 (GRCm39) |
S72P |
possibly damaging |
Het |
Ddx3y |
T |
C |
Y: 1,266,389 (GRCm39) |
E331G |
probably benign |
Het |
Degs1l |
T |
A |
1: 180,882,496 (GRCm39) |
I86K |
probably benign |
Het |
Dis3l2 |
T |
C |
1: 86,782,189 (GRCm39) |
|
probably benign |
Het |
Dop1a |
G |
T |
9: 86,403,418 (GRCm39) |
W1539C |
probably damaging |
Het |
Dop1b |
A |
G |
16: 93,566,323 (GRCm39) |
K917E |
probably benign |
Het |
Ecpas |
G |
A |
4: 58,844,165 (GRCm39) |
R534* |
probably null |
Het |
Efcab3 |
T |
C |
11: 104,990,851 (GRCm39) |
I5462T |
probably damaging |
Het |
Eif1ad15 |
A |
T |
12: 88,288,191 (GRCm39) |
S21T |
unknown |
Het |
Epo |
A |
G |
5: 137,483,447 (GRCm39) |
|
probably benign |
Het |
Figla |
T |
A |
6: 85,997,624 (GRCm39) |
|
probably benign |
Het |
Flvcr1 |
T |
C |
1: 190,753,353 (GRCm39) |
D273G |
probably benign |
Het |
Fryl |
T |
A |
5: 73,179,465 (GRCm39) |
R304* |
probably null |
Het |
Gcm1 |
T |
G |
9: 77,972,326 (GRCm39) |
D422E |
possibly damaging |
Het |
Get3 |
A |
T |
8: 85,746,403 (GRCm39) |
Y148* |
probably null |
Het |
Ggt6 |
A |
G |
11: 72,328,367 (GRCm39) |
D251G |
possibly damaging |
Het |
Git2 |
A |
G |
5: 114,904,511 (GRCm39) |
|
probably null |
Het |
Gm18856 |
A |
T |
13: 14,139,376 (GRCm39) |
|
probably benign |
Het |
Gm20939 |
T |
A |
17: 95,183,252 (GRCm39) |
|
probably benign |
Het |
Gpr176 |
A |
G |
2: 118,109,913 (GRCm39) |
Y449H |
probably benign |
Het |
H2-Eb1 |
A |
G |
17: 34,533,366 (GRCm39) |
E196G |
probably damaging |
Het |
H2-M10.6 |
A |
G |
17: 37,124,799 (GRCm39) |
T239A |
possibly damaging |
Het |
Haus5 |
T |
C |
7: 30,358,825 (GRCm39) |
N237S |
possibly damaging |
Het |
Hectd3 |
T |
C |
4: 116,857,882 (GRCm39) |
M605T |
probably damaging |
Het |
Hps3 |
T |
C |
3: 20,084,691 (GRCm39) |
I166V |
probably benign |
Het |
Ighv5-21 |
A |
T |
12: 114,286,434 (GRCm39) |
|
probably benign |
Het |
Kdm6b |
C |
T |
11: 69,294,418 (GRCm39) |
G1218D |
unknown |
Het |
Klhl30 |
A |
G |
1: 91,285,636 (GRCm39) |
|
probably null |
Het |
Kmt2a |
A |
T |
9: 44,729,747 (GRCm39) |
S3523R |
probably benign |
Het |
Lnpep |
A |
T |
17: 17,788,661 (GRCm39) |
N481K |
probably damaging |
Het |
Lrp1b |
T |
C |
2: 41,231,861 (GRCm39) |
H1203R |
probably benign |
Het |
Lrrc8a |
C |
T |
2: 30,146,661 (GRCm39) |
R492W |
probably damaging |
Het |
Magel2 |
T |
A |
7: 62,030,342 (GRCm39) |
V1082D |
unknown |
Het |
Memo1 |
A |
C |
17: 74,552,049 (GRCm39) |
H82Q |
probably null |
Het |
Myh13 |
A |
T |
11: 67,252,115 (GRCm39) |
T1408S |
probably benign |
Het |
Myh2 |
A |
T |
11: 67,085,451 (GRCm39) |
N1792Y |
possibly damaging |
Het |
Myo5c |
T |
C |
9: 75,196,337 (GRCm39) |
|
probably benign |
Het |
Or11l3 |
T |
A |
11: 58,516,319 (GRCm39) |
L184F |
probably damaging |
Het |
Or1e19 |
A |
G |
11: 73,316,188 (GRCm39) |
V207A |
probably benign |
Het |
Or2d2b |
T |
C |
7: 106,705,643 (GRCm39) |
I142V |
probably benign |
Het |
Or4c11c |
T |
A |
2: 88,661,749 (GRCm39) |
M96K |
possibly damaging |
Het |
Or51g1 |
T |
A |
7: 102,633,478 (GRCm39) |
T298S |
probably damaging |
Het |
Or52e3 |
T |
C |
7: 102,868,967 (GRCm39) |
F14S |
probably damaging |
Het |
Parp2 |
C |
T |
14: 51,047,543 (GRCm39) |
A18V |
probably benign |
Het |
Peli1 |
T |
A |
11: 21,098,110 (GRCm39) |
C282S |
probably damaging |
Het |
Phf8-ps |
G |
T |
17: 33,286,598 (GRCm39) |
S68* |
probably null |
Het |
Piezo2 |
T |
C |
18: 63,252,006 (GRCm39) |
M404V |
possibly damaging |
Het |
Pkn1 |
T |
A |
8: 84,404,592 (GRCm39) |
Q496L |
possibly damaging |
Het |
Pla2r1 |
A |
T |
2: 60,262,317 (GRCm39) |
F1093L |
probably damaging |
Het |
Ppp2r3d |
A |
G |
9: 101,022,680 (GRCm39) |
V323A |
probably damaging |
Het |
Pramel16 |
T |
A |
4: 143,676,453 (GRCm39) |
Y217F |
probably benign |
Het |
Prg2 |
C |
T |
2: 84,812,342 (GRCm39) |
|
probably benign |
Het |
Ptprb |
G |
A |
10: 116,182,958 (GRCm39) |
G1545S |
probably benign |
Het |
Rbm19 |
A |
G |
5: 120,258,307 (GRCm39) |
D174G |
possibly damaging |
Het |
Rhbdf2 |
T |
A |
11: 116,491,974 (GRCm39) |
T526S |
probably damaging |
Het |
Rpusd4 |
A |
G |
9: 35,179,310 (GRCm39) |
N42S |
probably benign |
Het |
Ryr3 |
T |
A |
2: 112,477,361 (GRCm39) |
Q4455L |
possibly damaging |
Het |
Sema4a |
G |
T |
3: 88,358,668 (GRCm39) |
H30Q |
probably damaging |
Het |
Skint1 |
G |
A |
4: 111,878,653 (GRCm39) |
|
probably null |
Het |
Slc1a3 |
A |
G |
15: 8,675,153 (GRCm39) |
V284A |
probably benign |
Het |
Slc30a9 |
A |
T |
5: 67,497,318 (GRCm39) |
K288* |
probably null |
Het |
Slc36a1 |
G |
T |
11: 55,119,164 (GRCm39) |
A380S |
probably benign |
Het |
Slc47a1 |
G |
A |
11: 61,268,833 (GRCm39) |
|
probably benign |
Het |
Snx19 |
A |
T |
9: 30,340,296 (GRCm39) |
E478V |
probably benign |
Het |
Spag6 |
T |
C |
2: 18,738,916 (GRCm39) |
|
probably benign |
Het |
Stag1 |
A |
T |
9: 100,668,740 (GRCm39) |
T223S |
probably damaging |
Het |
Terb1 |
A |
T |
8: 105,224,732 (GRCm39) |
|
probably benign |
Het |
Terf1 |
A |
G |
1: 15,876,170 (GRCm39) |
D90G |
possibly damaging |
Het |
Tex15 |
A |
G |
8: 34,061,302 (GRCm39) |
D518G |
probably damaging |
Het |
Tmem174 |
T |
A |
13: 98,773,546 (GRCm39) |
M95L |
possibly damaging |
Het |
Tnnt3 |
GTCCAGGCATCTC |
GTC |
7: 142,066,364 (GRCm39) |
|
probably benign |
Het |
Usp28 |
A |
G |
9: 48,896,803 (GRCm39) |
D8G |
probably benign |
Het |
Vmn2r105 |
T |
C |
17: 20,444,840 (GRCm39) |
T551A |
probably damaging |
Het |
Vmn2r107 |
A |
G |
17: 20,595,549 (GRCm39) |
I701V |
probably benign |
Het |
Vmn2r13 |
A |
C |
5: 109,339,943 (GRCm39) |
F11V |
probably benign |
Het |
Vmn2r85 |
G |
C |
10: 130,261,443 (GRCm39) |
S298* |
probably null |
Het |
Wdr6 |
C |
G |
9: 108,452,554 (GRCm39) |
W443S |
probably damaging |
Het |
Wipi1 |
A |
G |
11: 109,474,016 (GRCm39) |
V210A |
probably damaging |
Het |
Zfp317 |
A |
G |
9: 19,556,532 (GRCm39) |
T47A |
probably benign |
Het |
Zfp61 |
T |
C |
7: 23,991,714 (GRCm39) |
T146A |
probably benign |
Het |
Zfp964 |
A |
G |
8: 70,116,567 (GRCm39) |
E389G |
unknown |
Het |
Zfyve16 |
T |
C |
13: 92,640,985 (GRCm39) |
D1253G |
probably damaging |
Het |
Zpld2 |
T |
C |
4: 133,929,669 (GRCm39) |
K212R |
possibly damaging |
Het |
Zswim7 |
G |
A |
11: 62,158,299 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Myo1e |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00817:Myo1e
|
APN |
9 |
70,249,430 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00833:Myo1e
|
APN |
9 |
70,246,060 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00973:Myo1e
|
APN |
9 |
70,246,069 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01011:Myo1e
|
APN |
9 |
70,223,871 (GRCm39) |
splice site |
probably benign |
|
IGL01401:Myo1e
|
APN |
9 |
70,234,448 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01402:Myo1e
|
APN |
9 |
70,245,048 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01404:Myo1e
|
APN |
9 |
70,245,048 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01613:Myo1e
|
APN |
9 |
70,248,555 (GRCm39) |
splice site |
probably benign |
|
IGL01738:Myo1e
|
APN |
9 |
70,266,652 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01819:Myo1e
|
APN |
9 |
70,250,322 (GRCm39) |
splice site |
probably benign |
|
IGL02233:Myo1e
|
APN |
9 |
70,291,081 (GRCm39) |
splice site |
probably benign |
|
IGL02244:Myo1e
|
APN |
9 |
70,274,971 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02440:Myo1e
|
APN |
9 |
70,254,022 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02806:Myo1e
|
APN |
9 |
70,269,552 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02886:Myo1e
|
APN |
9 |
70,276,055 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03178:Myo1e
|
APN |
9 |
70,194,231 (GRCm39) |
missense |
possibly damaging |
0.47 |
I2288:Myo1e
|
UTSW |
9 |
70,249,379 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0036:Myo1e
|
UTSW |
9 |
70,248,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R0238:Myo1e
|
UTSW |
9 |
70,249,408 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0238:Myo1e
|
UTSW |
9 |
70,249,408 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0399:Myo1e
|
UTSW |
9 |
70,209,075 (GRCm39) |
splice site |
probably benign |
|
R0526:Myo1e
|
UTSW |
9 |
70,229,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R0599:Myo1e
|
UTSW |
9 |
70,283,942 (GRCm39) |
splice site |
probably benign |
|
R0656:Myo1e
|
UTSW |
9 |
70,274,956 (GRCm39) |
missense |
probably damaging |
1.00 |
R1078:Myo1e
|
UTSW |
9 |
70,291,281 (GRCm39) |
missense |
probably benign |
|
R1278:Myo1e
|
UTSW |
9 |
70,306,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R1300:Myo1e
|
UTSW |
9 |
70,209,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R1329:Myo1e
|
UTSW |
9 |
70,246,020 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1349:Myo1e
|
UTSW |
9 |
70,194,351 (GRCm39) |
splice site |
probably benign |
|
R1463:Myo1e
|
UTSW |
9 |
70,246,038 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1656:Myo1e
|
UTSW |
9 |
70,303,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R1727:Myo1e
|
UTSW |
9 |
70,283,806 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1789:Myo1e
|
UTSW |
9 |
70,246,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R1970:Myo1e
|
UTSW |
9 |
70,276,055 (GRCm39) |
missense |
probably benign |
0.00 |
R2029:Myo1e
|
UTSW |
9 |
70,275,969 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2039:Myo1e
|
UTSW |
9 |
70,227,415 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2076:Myo1e
|
UTSW |
9 |
70,291,159 (GRCm39) |
missense |
probably benign |
|
R2256:Myo1e
|
UTSW |
9 |
70,285,655 (GRCm39) |
splice site |
probably null |
|
R2257:Myo1e
|
UTSW |
9 |
70,285,655 (GRCm39) |
splice site |
probably null |
|
R2323:Myo1e
|
UTSW |
9 |
70,286,040 (GRCm39) |
nonsense |
probably null |
|
R2443:Myo1e
|
UTSW |
9 |
70,234,454 (GRCm39) |
missense |
probably benign |
|
R4023:Myo1e
|
UTSW |
9 |
70,232,157 (GRCm39) |
missense |
probably benign |
|
R4024:Myo1e
|
UTSW |
9 |
70,232,157 (GRCm39) |
missense |
probably benign |
|
R4025:Myo1e
|
UTSW |
9 |
70,232,157 (GRCm39) |
missense |
probably benign |
|
R4026:Myo1e
|
UTSW |
9 |
70,232,157 (GRCm39) |
missense |
probably benign |
|
R4151:Myo1e
|
UTSW |
9 |
70,204,633 (GRCm39) |
nonsense |
probably null |
|
R4764:Myo1e
|
UTSW |
9 |
70,250,417 (GRCm39) |
splice site |
probably null |
|
R4768:Myo1e
|
UTSW |
9 |
70,277,751 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4911:Myo1e
|
UTSW |
9 |
70,250,378 (GRCm39) |
missense |
probably benign |
|
R4995:Myo1e
|
UTSW |
9 |
70,260,554 (GRCm39) |
missense |
probably benign |
0.01 |
R4999:Myo1e
|
UTSW |
9 |
70,260,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R5228:Myo1e
|
UTSW |
9 |
70,229,640 (GRCm39) |
splice site |
probably null |
|
R5414:Myo1e
|
UTSW |
9 |
70,229,640 (GRCm39) |
splice site |
probably null |
|
R5577:Myo1e
|
UTSW |
9 |
70,277,753 (GRCm39) |
missense |
probably benign |
0.31 |
R5851:Myo1e
|
UTSW |
9 |
70,291,086 (GRCm39) |
missense |
probably benign |
0.17 |
R6208:Myo1e
|
UTSW |
9 |
70,283,887 (GRCm39) |
missense |
probably damaging |
0.99 |
R6907:Myo1e
|
UTSW |
9 |
70,234,437 (GRCm39) |
missense |
probably benign |
|
R7084:Myo1e
|
UTSW |
9 |
70,245,083 (GRCm39) |
missense |
probably damaging |
0.96 |
R7313:Myo1e
|
UTSW |
9 |
70,266,667 (GRCm39) |
critical splice donor site |
probably null |
|
R7383:Myo1e
|
UTSW |
9 |
70,204,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R7811:Myo1e
|
UTSW |
9 |
70,234,544 (GRCm39) |
missense |
probably damaging |
0.96 |
R7962:Myo1e
|
UTSW |
9 |
70,242,501 (GRCm39) |
missense |
possibly damaging |
0.64 |
R8309:Myo1e
|
UTSW |
9 |
70,254,045 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8510:Myo1e
|
UTSW |
9 |
70,242,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R8513:Myo1e
|
UTSW |
9 |
70,227,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R8694:Myo1e
|
UTSW |
9 |
70,291,172 (GRCm39) |
missense |
probably benign |
|
R8720:Myo1e
|
UTSW |
9 |
70,204,570 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9112:Myo1e
|
UTSW |
9 |
70,274,983 (GRCm39) |
missense |
probably benign |
0.25 |
R9148:Myo1e
|
UTSW |
9 |
70,283,830 (GRCm39) |
missense |
probably damaging |
0.98 |
R9156:Myo1e
|
UTSW |
9 |
70,266,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R9251:Myo1e
|
UTSW |
9 |
70,276,076 (GRCm39) |
missense |
probably benign |
0.00 |
R9541:Myo1e
|
UTSW |
9 |
70,204,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R9624:Myo1e
|
UTSW |
9 |
70,303,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R9660:Myo1e
|
UTSW |
9 |
70,223,924 (GRCm39) |
missense |
probably damaging |
1.00 |
R9728:Myo1e
|
UTSW |
9 |
70,223,924 (GRCm39) |
missense |
probably damaging |
1.00 |
X0021:Myo1e
|
UTSW |
9 |
70,285,555 (GRCm39) |
missense |
probably damaging |
0.99 |
X0065:Myo1e
|
UTSW |
9 |
70,285,576 (GRCm39) |
missense |
possibly damaging |
0.94 |
|