Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610008E11Rik |
A |
C |
10: 78,903,573 (GRCm39) |
C248G |
probably damaging |
Het |
4933427D14Rik |
A |
T |
11: 72,059,612 (GRCm39) |
V693E |
possibly damaging |
Het |
Abcc10 |
G |
T |
17: 46,638,735 (GRCm39) |
L42I |
probably damaging |
Het |
Alb |
A |
G |
5: 90,616,449 (GRCm39) |
E318G |
probably benign |
Het |
Alkal2 |
G |
T |
12: 30,934,850 (GRCm39) |
G23V |
probably damaging |
Het |
Aox4 |
T |
A |
1: 58,293,470 (GRCm39) |
C941S |
possibly damaging |
Het |
Aqp9 |
A |
G |
9: 71,045,495 (GRCm39) |
V38A |
probably benign |
Het |
AW209491 |
A |
G |
13: 14,812,349 (GRCm39) |
T401A |
probably damaging |
Het |
Ccdc57 |
C |
T |
11: 120,776,742 (GRCm39) |
A553T |
probably damaging |
Het |
Celf2 |
C |
T |
2: 6,551,914 (GRCm39) |
D522N |
probably benign |
Het |
Cfap210 |
A |
G |
2: 69,612,287 (GRCm39) |
|
probably null |
Het |
Cmpk2 |
A |
G |
12: 26,524,136 (GRCm39) |
N311S |
probably damaging |
Het |
Dcn |
T |
C |
10: 97,330,939 (GRCm39) |
I91T |
probably damaging |
Het |
Defa30 |
G |
A |
8: 21,624,709 (GRCm39) |
V11I |
probably benign |
Het |
Dnmt3a |
T |
A |
12: 3,946,965 (GRCm39) |
V397E |
probably benign |
Het |
Ehhadh |
G |
A |
16: 21,585,053 (GRCm39) |
A276V |
probably benign |
Het |
Fibcd1 |
T |
C |
2: 31,723,791 (GRCm39) |
|
probably benign |
Het |
H2-T5 |
A |
G |
17: 36,479,154 (GRCm39) |
S32P |
unknown |
Het |
Invs |
G |
T |
4: 48,426,199 (GRCm39) |
R995S |
possibly damaging |
Het |
Itpr3 |
T |
C |
17: 27,325,199 (GRCm39) |
M1264T |
possibly damaging |
Het |
Lzic |
C |
T |
4: 149,572,527 (GRCm39) |
A39V |
probably benign |
Het |
Marchf6 |
A |
G |
15: 31,482,650 (GRCm39) |
L516P |
possibly damaging |
Het |
Mecom |
C |
T |
3: 30,011,529 (GRCm39) |
E591K |
probably benign |
Het |
Mical3 |
T |
C |
6: 120,911,944 (GRCm39) |
D1916G |
probably damaging |
Het |
Mms22l |
T |
C |
4: 24,578,855 (GRCm39) |
I738T |
probably damaging |
Het |
Mroh2b |
G |
A |
15: 4,980,746 (GRCm39) |
W1438* |
probably null |
Het |
Mroh8 |
G |
T |
2: 157,071,879 (GRCm39) |
T542K |
possibly damaging |
Het |
Msl1 |
A |
T |
11: 98,691,074 (GRCm39) |
K416I |
probably damaging |
Het |
Myh15 |
C |
A |
16: 48,940,381 (GRCm39) |
T777N |
probably damaging |
Het |
Or51a10 |
A |
T |
7: 103,698,829 (GRCm39) |
V244E |
probably damaging |
Het |
Or5p5 |
G |
T |
7: 107,414,030 (GRCm39) |
V82F |
possibly damaging |
Het |
Or5p58 |
A |
G |
7: 107,694,450 (GRCm39) |
F109S |
probably benign |
Het |
Or6c70 |
A |
G |
10: 129,709,891 (GRCm39) |
V245A |
probably damaging |
Het |
Pdzk1ip1 |
T |
A |
4: 114,946,323 (GRCm39) |
V61D |
probably benign |
Het |
Plcxd1 |
A |
T |
5: 110,250,180 (GRCm39) |
M212L |
probably benign |
Het |
Pld1 |
A |
G |
3: 28,078,361 (GRCm39) |
T7A |
probably benign |
Het |
Ppm1n |
T |
C |
7: 19,012,302 (GRCm39) |
D310G |
probably damaging |
Het |
Prpf8 |
A |
G |
11: 75,390,641 (GRCm39) |
N1264S |
possibly damaging |
Het |
Pum2 |
T |
A |
12: 8,763,456 (GRCm39) |
N204K |
possibly damaging |
Het |
Recql5 |
G |
A |
11: 115,784,861 (GRCm39) |
T822I |
possibly damaging |
Het |
Rfc1 |
T |
C |
5: 65,436,077 (GRCm39) |
T656A |
probably benign |
Het |
Sacs |
T |
C |
14: 61,427,068 (GRCm39) |
Y159H |
possibly damaging |
Het |
Septin14 |
A |
G |
5: 129,773,194 (GRCm39) |
S148P |
probably damaging |
Het |
Slco1c1 |
T |
A |
6: 141,492,640 (GRCm39) |
M341K |
probably benign |
Het |
Smok2a |
T |
C |
17: 13,445,160 (GRCm39) |
S246P |
probably damaging |
Het |
Spata9 |
C |
A |
13: 76,125,890 (GRCm39) |
S124R |
possibly damaging |
Het |
Sri |
A |
G |
5: 8,113,317 (GRCm39) |
N103D |
probably damaging |
Het |
Sspo |
G |
A |
6: 48,459,622 (GRCm39) |
C3327Y |
probably damaging |
Het |
Trank1 |
A |
G |
9: 111,178,370 (GRCm39) |
M353V |
probably benign |
Het |
Trim80 |
A |
T |
11: 115,332,006 (GRCm39) |
E66V |
probably damaging |
Het |
Txndc16 |
A |
G |
14: 45,448,641 (GRCm39) |
L73P |
probably damaging |
Het |
Ugt2b34 |
T |
A |
5: 87,039,249 (GRCm39) |
M471L |
probably damaging |
Het |
Ush2a |
G |
T |
1: 188,178,899 (GRCm39) |
V1357L |
probably benign |
Het |
Usp15 |
G |
T |
10: 122,959,848 (GRCm39) |
P855T |
|
Het |
Uspl1 |
C |
T |
5: 149,135,491 (GRCm39) |
T290I |
possibly damaging |
Het |
Zbtb2 |
A |
C |
10: 4,319,084 (GRCm39) |
M314R |
probably benign |
Het |
Zcchc2 |
A |
G |
1: 105,959,844 (GRCm39) |
Y1151C |
probably damaging |
Het |
Zmat3 |
T |
C |
3: 32,395,670 (GRCm39) |
Y279C |
probably damaging |
Het |
|
Other mutations in Gpr156 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00943:Gpr156
|
APN |
16 |
37,808,938 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01615:Gpr156
|
APN |
16 |
37,808,953 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01976:Gpr156
|
APN |
16 |
37,799,395 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02217:Gpr156
|
APN |
16 |
37,825,673 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02515:Gpr156
|
APN |
16 |
37,826,041 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02596:Gpr156
|
APN |
16 |
37,799,086 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03068:Gpr156
|
APN |
16 |
37,812,491 (GRCm39) |
missense |
probably damaging |
0.99 |
R0690:Gpr156
|
UTSW |
16 |
37,812,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R1034:Gpr156
|
UTSW |
16 |
37,825,088 (GRCm39) |
missense |
probably benign |
|
R1133:Gpr156
|
UTSW |
16 |
37,825,683 (GRCm39) |
missense |
probably benign |
0.10 |
R1317:Gpr156
|
UTSW |
16 |
37,807,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R1437:Gpr156
|
UTSW |
16 |
37,808,904 (GRCm39) |
missense |
probably damaging |
0.99 |
R1484:Gpr156
|
UTSW |
16 |
37,812,558 (GRCm39) |
missense |
probably damaging |
0.99 |
R1759:Gpr156
|
UTSW |
16 |
37,768,583 (GRCm39) |
missense |
probably damaging |
0.96 |
R1761:Gpr156
|
UTSW |
16 |
37,807,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R1998:Gpr156
|
UTSW |
16 |
37,818,270 (GRCm39) |
missense |
possibly damaging |
0.57 |
R2067:Gpr156
|
UTSW |
16 |
37,799,113 (GRCm39) |
missense |
probably benign |
0.02 |
R2111:Gpr156
|
UTSW |
16 |
37,799,113 (GRCm39) |
missense |
probably benign |
0.02 |
R2509:Gpr156
|
UTSW |
16 |
37,768,149 (GRCm39) |
missense |
probably benign |
0.04 |
R2872:Gpr156
|
UTSW |
16 |
37,812,585 (GRCm39) |
missense |
probably damaging |
0.99 |
R2872:Gpr156
|
UTSW |
16 |
37,812,585 (GRCm39) |
missense |
probably damaging |
0.99 |
R3839:Gpr156
|
UTSW |
16 |
37,808,962 (GRCm39) |
missense |
probably damaging |
0.99 |
R4492:Gpr156
|
UTSW |
16 |
37,812,468 (GRCm39) |
missense |
probably damaging |
0.99 |
R4988:Gpr156
|
UTSW |
16 |
37,768,577 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5329:Gpr156
|
UTSW |
16 |
37,825,810 (GRCm39) |
missense |
probably benign |
0.00 |
R5361:Gpr156
|
UTSW |
16 |
37,826,087 (GRCm39) |
missense |
probably damaging |
0.99 |
R5386:Gpr156
|
UTSW |
16 |
37,768,671 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5531:Gpr156
|
UTSW |
16 |
37,825,619 (GRCm39) |
missense |
probably benign |
0.01 |
R5886:Gpr156
|
UTSW |
16 |
37,799,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R5942:Gpr156
|
UTSW |
16 |
37,825,264 (GRCm39) |
missense |
probably benign |
0.04 |
R6345:Gpr156
|
UTSW |
16 |
37,807,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R7247:Gpr156
|
UTSW |
16 |
37,768,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R7353:Gpr156
|
UTSW |
16 |
37,812,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R7954:Gpr156
|
UTSW |
16 |
37,807,920 (GRCm39) |
missense |
probably damaging |
0.97 |
R8333:Gpr156
|
UTSW |
16 |
37,812,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R8507:Gpr156
|
UTSW |
16 |
37,768,598 (GRCm39) |
missense |
probably benign |
|
R8770:Gpr156
|
UTSW |
16 |
37,824,974 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9237:Gpr156
|
UTSW |
16 |
37,825,648 (GRCm39) |
nonsense |
probably null |
|
R9491:Gpr156
|
UTSW |
16 |
37,825,704 (GRCm39) |
missense |
probably benign |
0.03 |
R9767:Gpr156
|
UTSW |
16 |
37,818,297 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Gpr156
|
UTSW |
16 |
37,825,225 (GRCm39) |
missense |
probably benign |
0.22 |
|