Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
A |
G |
6: 121,616,270 (GRCm39) |
S133G |
possibly damaging |
Het |
Agps |
A |
G |
2: 75,735,256 (GRCm39) |
E567G |
possibly damaging |
Het |
Ak9 |
T |
C |
10: 41,285,068 (GRCm39) |
I1381T |
unknown |
Het |
Apcdd1 |
C |
T |
18: 63,055,731 (GRCm39) |
|
probably benign |
Het |
Arrb1 |
T |
A |
7: 99,238,891 (GRCm39) |
C150S |
probably damaging |
Het |
Asz1 |
T |
C |
6: 18,051,330 (GRCm39) |
I450V |
probably benign |
Het |
Atp10b |
A |
G |
11: 43,063,608 (GRCm39) |
N181S |
probably damaging |
Het |
Bptf |
A |
C |
11: 106,965,134 (GRCm39) |
D1353E |
probably benign |
Het |
Cacna2d1 |
T |
C |
5: 16,140,013 (GRCm39) |
M1T |
probably null |
Het |
Ccdc106 |
T |
A |
7: 5,059,200 (GRCm39) |
I6N |
possibly damaging |
Het |
Celf6 |
A |
T |
9: 59,510,525 (GRCm39) |
Q252L |
probably benign |
Het |
Colgalt2 |
A |
T |
1: 152,360,598 (GRCm39) |
K212* |
probably null |
Het |
Cryba4 |
T |
C |
5: 112,394,632 (GRCm39) |
S166G |
probably benign |
Het |
Cyp2w1 |
A |
G |
5: 139,342,035 (GRCm39) |
E123G |
probably benign |
Het |
Cyp4a10 |
G |
C |
4: 115,382,566 (GRCm39) |
K285N |
probably damaging |
Het |
Cyth1 |
G |
T |
11: 118,074,710 (GRCm39) |
T197K |
probably benign |
Het |
Ddhd1 |
A |
G |
14: 45,894,685 (GRCm39) |
W262R |
probably damaging |
Het |
Dnah8 |
T |
A |
17: 30,872,361 (GRCm39) |
V450D |
possibly damaging |
Het |
Eml5 |
C |
T |
12: 98,842,433 (GRCm39) |
V222I |
probably benign |
Het |
Fbxw19 |
A |
G |
9: 109,324,873 (GRCm39) |
S15P |
probably damaging |
Het |
Fhip2b |
G |
A |
14: 70,831,463 (GRCm39) |
Q24* |
probably null |
Het |
Fignl2 |
C |
A |
15: 100,951,466 (GRCm39) |
R272L |
unknown |
Het |
Gm10842 |
A |
T |
11: 105,037,885 (GRCm39) |
D56V |
unknown |
Het |
Gmps |
T |
A |
3: 63,900,640 (GRCm39) |
N305K |
probably benign |
Het |
Gnai1 |
A |
T |
5: 18,565,055 (GRCm39) |
L38Q |
|
Het |
Golim4 |
A |
T |
3: 75,785,464 (GRCm39) |
D642E |
probably benign |
Het |
Gp1ba |
A |
T |
11: 70,531,293 (GRCm39) |
Q353L |
unknown |
Het |
Gpnmb |
T |
C |
6: 49,024,996 (GRCm39) |
S343P |
possibly damaging |
Het |
Hexb |
G |
A |
13: 97,313,336 (GRCm39) |
R507* |
probably null |
Het |
Ifitm10 |
A |
T |
7: 141,924,704 (GRCm39) |
V45D |
probably damaging |
Het |
Kif21a |
A |
T |
15: 90,853,981 (GRCm39) |
D795E |
probably benign |
Het |
Klkb1 |
A |
T |
8: 45,729,392 (GRCm39) |
V309E |
probably benign |
Het |
Krtap9-1 |
C |
A |
11: 99,764,664 (GRCm39) |
C133* |
probably null |
Het |
Krtcap2 |
T |
C |
3: 89,153,578 (GRCm39) |
|
probably benign |
Het |
Lilra5 |
T |
C |
7: 4,240,758 (GRCm39) |
M1T |
probably null |
Het |
Magi1 |
G |
A |
6: 93,659,890 (GRCm39) |
T1019I |
probably benign |
Het |
Mdn1 |
T |
A |
4: 32,713,825 (GRCm39) |
H1967Q |
|
Het |
Mgat4f |
A |
G |
1: 134,318,596 (GRCm39) |
D456G |
probably benign |
Het |
Mroh2b |
A |
T |
15: 4,980,666 (GRCm39) |
T1412S |
probably benign |
Het |
Myh13 |
A |
T |
11: 67,242,894 (GRCm39) |
M936L |
probably benign |
Het |
Nalf2 |
C |
T |
X: 98,889,097 (GRCm39) |
R321W |
probably damaging |
Het |
Ncapd3 |
A |
G |
9: 26,962,682 (GRCm39) |
T373A |
possibly damaging |
Het |
Noc2l |
T |
C |
4: 156,320,784 (GRCm39) |
|
probably null |
Het |
Nrg4 |
C |
T |
9: 55,149,420 (GRCm39) |
S59N |
probably benign |
Het |
Nrip1 |
A |
G |
16: 76,091,353 (GRCm39) |
V68A |
probably benign |
Het |
Or11g24 |
T |
C |
14: 50,662,255 (GRCm39) |
V93A |
probably benign |
Het |
Or9k2 |
T |
C |
10: 129,999,016 (GRCm39) |
T60A |
probably benign |
Het |
Pcdhga6 |
G |
T |
18: 37,840,212 (GRCm39) |
|
probably benign |
Het |
Phf20l1 |
A |
G |
15: 66,475,955 (GRCm39) |
N196S |
probably damaging |
Het |
Ppp4r4 |
T |
A |
12: 103,571,296 (GRCm39) |
Y787* |
probably null |
Het |
Psma8 |
G |
A |
18: 14,839,298 (GRCm39) |
R4Q |
probably null |
Het |
Reg4 |
A |
G |
3: 98,137,168 (GRCm39) |
K46E |
probably benign |
Het |
Rnf14 |
T |
A |
18: 38,442,680 (GRCm39) |
M327K |
possibly damaging |
Het |
Rtn1 |
A |
T |
12: 72,263,586 (GRCm39) |
Y753* |
probably null |
Het |
Slc26a11 |
A |
G |
11: 119,259,627 (GRCm39) |
R275G |
probably benign |
Het |
Stard9 |
A |
G |
2: 120,518,656 (GRCm39) |
T527A |
possibly damaging |
Het |
Stk26 |
C |
T |
X: 49,930,618 (GRCm39) |
|
probably benign |
Het |
Tas1r1 |
C |
T |
4: 152,116,413 (GRCm39) |
C407Y |
probably damaging |
Het |
Tcstv1b |
A |
T |
13: 120,634,958 (GRCm39) |
Y80F |
probably benign |
Het |
Tenm3 |
A |
G |
8: 49,127,559 (GRCm39) |
S40P |
probably damaging |
Het |
Tespa1 |
T |
A |
10: 130,183,066 (GRCm39) |
S4T |
probably damaging |
Het |
Tlr11 |
A |
G |
14: 50,599,547 (GRCm39) |
N511S |
probably benign |
Het |
Tmprss15 |
A |
G |
16: 78,754,211 (GRCm39) |
I1014T |
probably benign |
Het |
Tpte |
T |
A |
8: 22,774,990 (GRCm39) |
M20K |
probably benign |
Het |
Ttn |
A |
G |
2: 76,612,390 (GRCm39) |
V17199A |
possibly damaging |
Het |
Tubgcp3 |
A |
G |
8: 12,703,411 (GRCm39) |
Y305H |
probably damaging |
Het |
Ubr4 |
T |
A |
4: 139,212,613 (GRCm39) |
V5081E |
unknown |
Het |
Unkl |
T |
C |
17: 25,448,392 (GRCm39) |
S322P |
probably damaging |
Het |
Uqcc6 |
A |
G |
10: 82,458,475 (GRCm39) |
S59P |
unknown |
Het |
Vav3 |
T |
A |
3: 109,485,682 (GRCm39) |
|
probably null |
Het |
Vmn1r76 |
A |
G |
7: 11,664,765 (GRCm39) |
S150P |
probably benign |
Het |
Xpot |
A |
G |
10: 121,445,600 (GRCm39) |
|
probably null |
Het |
Xylt1 |
A |
G |
7: 117,242,906 (GRCm39) |
I650V |
probably benign |
Het |
Zan |
C |
A |
5: 137,403,682 (GRCm39) |
A3955S |
unknown |
Het |
|
Other mutations in Khsrp |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00569:Khsrp
|
APN |
17 |
57,330,092 (GRCm39) |
missense |
possibly damaging |
0.49 |
R0973:Khsrp
|
UTSW |
17 |
57,332,576 (GRCm39) |
missense |
probably benign |
|
R0973:Khsrp
|
UTSW |
17 |
57,332,576 (GRCm39) |
missense |
probably benign |
|
R0974:Khsrp
|
UTSW |
17 |
57,332,576 (GRCm39) |
missense |
probably benign |
|
R0975:Khsrp
|
UTSW |
17 |
57,334,066 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1080:Khsrp
|
UTSW |
17 |
57,331,410 (GRCm39) |
frame shift |
probably null |
|
R1561:Khsrp
|
UTSW |
17 |
57,332,639 (GRCm39) |
missense |
probably benign |
0.01 |
R1686:Khsrp
|
UTSW |
17 |
57,332,597 (GRCm39) |
missense |
probably benign |
0.32 |
R2133:Khsrp
|
UTSW |
17 |
57,334,832 (GRCm39) |
missense |
probably benign |
0.17 |
R2134:Khsrp
|
UTSW |
17 |
57,331,410 (GRCm39) |
frame shift |
probably null |
|
R4133:Khsrp
|
UTSW |
17 |
57,332,605 (GRCm39) |
missense |
probably benign |
0.00 |
R4819:Khsrp
|
UTSW |
17 |
57,330,360 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5213:Khsrp
|
UTSW |
17 |
57,331,366 (GRCm39) |
missense |
probably benign |
0.17 |
R5372:Khsrp
|
UTSW |
17 |
57,331,292 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6246:Khsrp
|
UTSW |
17 |
57,332,324 (GRCm39) |
missense |
possibly damaging |
0.45 |
R6528:Khsrp
|
UTSW |
17 |
57,330,543 (GRCm39) |
missense |
probably damaging |
0.99 |
R7071:Khsrp
|
UTSW |
17 |
57,332,386 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7141:Khsrp
|
UTSW |
17 |
57,332,602 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8282:Khsrp
|
UTSW |
17 |
57,331,123 (GRCm39) |
missense |
probably damaging |
0.98 |
R9759:Khsrp
|
UTSW |
17 |
57,332,925 (GRCm39) |
missense |
probably benign |
0.25 |
Z1088:Khsrp
|
UTSW |
17 |
57,331,249 (GRCm39) |
missense |
probably damaging |
0.96 |
|