Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930550C14Rik |
A |
T |
9: 53,336,830 (GRCm39) |
M45L |
probably benign |
Het |
Acss2 |
T |
C |
2: 155,403,063 (GRCm39) |
F627L |
probably damaging |
Het |
Akap8 |
A |
G |
17: 32,535,184 (GRCm39) |
S277P |
probably damaging |
Het |
Akap9 |
T |
A |
5: 4,051,418 (GRCm39) |
M1395K |
probably damaging |
Het |
Ank1 |
A |
G |
8: 23,612,893 (GRCm39) |
D1468G |
probably benign |
Het |
Apoe |
A |
G |
7: 19,430,846 (GRCm39) |
V121A |
probably benign |
Het |
Aqp9 |
A |
T |
9: 71,070,331 (GRCm39) |
L12H |
probably damaging |
Het |
Atp2b4 |
G |
A |
1: 133,639,529 (GRCm39) |
A1115V |
probably benign |
Het |
Atp2b4 |
G |
A |
1: 133,667,134 (GRCm39) |
P139L |
probably benign |
Het |
B430218F22Rik |
T |
C |
13: 118,523,980 (GRCm39) |
|
probably benign |
Het |
Bltp2 |
T |
A |
11: 78,154,854 (GRCm39) |
L122H |
probably damaging |
Het |
Brsk1 |
A |
G |
7: 4,711,866 (GRCm39) |
E572G |
possibly damaging |
Het |
C6 |
T |
C |
15: 4,811,394 (GRCm39) |
I414T |
probably benign |
Het |
C8b |
T |
A |
4: 104,644,083 (GRCm39) |
M250K |
probably benign |
Het |
Camk1g |
T |
A |
1: 193,044,393 (GRCm39) |
E7V |
probably benign |
Het |
Clcc1 |
A |
G |
3: 108,580,236 (GRCm39) |
|
probably null |
Het |
Col4a3 |
G |
T |
1: 82,694,018 (GRCm39) |
|
probably null |
Het |
Cox5b |
T |
A |
1: 36,732,310 (GRCm39) |
W104R |
probably damaging |
Het |
Cyp2c55 |
A |
C |
19: 39,019,815 (GRCm39) |
H251P |
probably damaging |
Het |
Cyp2c67 |
G |
A |
19: 39,632,188 (GRCm39) |
T60I |
probably benign |
Het |
Defb42 |
T |
A |
14: 63,285,824 (GRCm39) |
V68E |
probably benign |
Het |
Ercc4 |
T |
A |
16: 12,941,287 (GRCm39) |
I225N |
probably damaging |
Het |
Fam120b |
G |
T |
17: 15,622,658 (GRCm39) |
C212F |
probably damaging |
Het |
Fgf10 |
T |
C |
13: 118,918,045 (GRCm39) |
V111A |
probably benign |
Het |
Fn1 |
G |
T |
1: 71,629,967 (GRCm39) |
T2186K |
probably damaging |
Het |
Fras1 |
T |
C |
5: 96,929,518 (GRCm39) |
V3974A |
probably benign |
Het |
Galnt4 |
T |
C |
10: 98,944,362 (GRCm39) |
V29A |
probably benign |
Het |
Heatr9 |
A |
T |
11: 83,407,475 (GRCm39) |
L236Q |
probably damaging |
Het |
Hivep3 |
C |
A |
4: 119,955,020 (GRCm39) |
P1112H |
probably damaging |
Het |
Hnf4g |
A |
G |
3: 3,708,069 (GRCm39) |
Y106C |
possibly damaging |
Het |
Hnrnpdl |
A |
T |
5: 100,185,783 (GRCm39) |
Y69* |
probably null |
Het |
Itgb1 |
G |
A |
8: 129,443,703 (GRCm39) |
A320T |
probably damaging |
Het |
Kcna2 |
T |
C |
3: 107,012,733 (GRCm39) |
I438T |
probably benign |
Het |
Kif24 |
A |
G |
4: 41,397,545 (GRCm39) |
|
probably null |
Het |
Klhl1 |
G |
A |
14: 96,389,402 (GRCm39) |
T584I |
probably benign |
Het |
Ltbp1 |
A |
G |
17: 75,532,199 (GRCm39) |
D91G |
probably damaging |
Het |
Mdga2 |
T |
C |
12: 66,844,427 (GRCm39) |
I190M |
probably damaging |
Het |
Meis2 |
G |
A |
2: 115,830,686 (GRCm39) |
R276C |
probably damaging |
Het |
Mob4 |
C |
T |
1: 55,191,855 (GRCm39) |
R190W |
probably damaging |
Het |
Mrgpra2a |
A |
G |
7: 47,077,114 (GRCm39) |
I48T |
possibly damaging |
Het |
Mst1 |
T |
C |
9: 107,960,826 (GRCm39) |
V481A |
probably benign |
Het |
Mttp |
A |
T |
3: 137,821,832 (GRCm39) |
V245E |
possibly damaging |
Het |
Nbn |
T |
A |
4: 15,981,470 (GRCm39) |
S521T |
probably benign |
Het |
Neb |
G |
T |
2: 52,083,243 (GRCm39) |
T5654N |
probably damaging |
Het |
Nlrp9a |
A |
T |
7: 26,256,866 (GRCm39) |
K161N |
probably damaging |
Het |
Nod2 |
T |
G |
8: 89,390,902 (GRCm39) |
F388C |
possibly damaging |
Het |
Or3a1 |
G |
T |
11: 74,225,402 (GRCm39) |
F218L |
probably benign |
Het |
Or4a75 |
G |
T |
2: 89,447,814 (GRCm39) |
H241N |
possibly damaging |
Het |
Or4f58 |
A |
G |
2: 111,851,332 (GRCm39) |
F289S |
possibly damaging |
Het |
Or52e2 |
A |
T |
7: 102,804,332 (GRCm39) |
N207K |
probably benign |
Het |
Or7a38 |
T |
A |
10: 78,753,361 (GRCm39) |
I229N |
probably damaging |
Het |
Or7g25 |
G |
A |
9: 19,160,153 (GRCm39) |
L181F |
possibly damaging |
Het |
P2ry1 |
A |
G |
3: 60,911,898 (GRCm39) |
S346G |
probably benign |
Het |
Polr1f |
T |
A |
12: 33,487,679 (GRCm39) |
|
probably null |
Het |
Prkcd |
A |
G |
14: 30,321,623 (GRCm39) |
F524L |
probably benign |
Het |
Qrfprl |
T |
C |
6: 65,429,898 (GRCm39) |
I198T |
probably benign |
Het |
Ramp3 |
A |
T |
11: 6,624,843 (GRCm39) |
M46L |
probably benign |
Het |
Rint1 |
T |
C |
5: 24,014,791 (GRCm39) |
Y278H |
probably damaging |
Het |
Skint11 |
C |
T |
4: 114,051,874 (GRCm39) |
T74I |
probably benign |
Het |
Slc10a7 |
T |
C |
8: 79,433,579 (GRCm39) |
|
probably null |
Het |
Slc45a2 |
T |
A |
15: 11,028,016 (GRCm39) |
Y528* |
probably null |
Het |
Slit1 |
A |
G |
19: 41,637,452 (GRCm39) |
F329L |
probably damaging |
Het |
Sltm |
A |
T |
9: 70,498,892 (GRCm39) |
M989L |
possibly damaging |
Het |
Smad9 |
A |
T |
3: 54,701,874 (GRCm39) |
T372S |
possibly damaging |
Het |
Snrpc |
T |
A |
17: 28,061,306 (GRCm39) |
Y38* |
probably null |
Het |
Spag17 |
A |
G |
3: 100,010,701 (GRCm39) |
K2065R |
possibly damaging |
Het |
Stxbp4 |
T |
A |
11: 90,498,197 (GRCm39) |
K87N |
probably damaging |
Het |
Tbc1d23 |
AT |
ATT |
16: 57,019,258 (GRCm39) |
|
probably null |
Het |
Tgfb1i1 |
A |
T |
7: 127,848,571 (GRCm39) |
M96L |
probably damaging |
Het |
Tnc |
T |
A |
4: 63,885,580 (GRCm39) |
I1841F |
probably damaging |
Het |
Ubap2 |
G |
T |
4: 41,211,771 (GRCm39) |
H63Q |
probably damaging |
Het |
Vps13a |
T |
C |
19: 16,632,580 (GRCm39) |
N2592S |
probably benign |
Het |
Xdh |
G |
A |
17: 74,193,381 (GRCm39) |
P1305L |
probably benign |
Het |
Xrn1 |
G |
A |
9: 95,921,862 (GRCm39) |
R1425K |
probably benign |
Het |
Zfp418 |
G |
A |
7: 7,185,762 (GRCm39) |
R575Q |
possibly damaging |
Het |
Zfp608 |
T |
A |
18: 55,027,544 (GRCm39) |
Q1424H |
probably damaging |
Het |
Zfp839 |
C |
A |
12: 110,821,635 (GRCm39) |
L150I |
possibly damaging |
Het |
|
Other mutations in Gpr26 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01065:Gpr26
|
APN |
7 |
131,569,230 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01345:Gpr26
|
APN |
7 |
131,569,161 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01658:Gpr26
|
APN |
7 |
131,585,834 (GRCm39) |
missense |
probably benign |
|
IGL02724:Gpr26
|
APN |
7 |
131,576,121 (GRCm39) |
critical splice donor site |
probably null |
|
R0408:Gpr26
|
UTSW |
7 |
131,576,001 (GRCm39) |
splice site |
probably null |
|
R0408:Gpr26
|
UTSW |
7 |
131,569,249 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0547:Gpr26
|
UTSW |
7 |
131,586,026 (GRCm39) |
missense |
probably benign |
0.01 |
R2508:Gpr26
|
UTSW |
7 |
131,568,823 (GRCm39) |
missense |
probably damaging |
0.98 |
R4088:Gpr26
|
UTSW |
7 |
131,568,805 (GRCm39) |
missense |
probably benign |
0.00 |
R4630:Gpr26
|
UTSW |
7 |
131,568,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R4680:Gpr26
|
UTSW |
7 |
131,576,082 (GRCm39) |
missense |
probably benign |
0.34 |
R5229:Gpr26
|
UTSW |
7 |
131,585,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R5610:Gpr26
|
UTSW |
7 |
131,568,694 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6605:Gpr26
|
UTSW |
7 |
131,585,893 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6653:Gpr26
|
UTSW |
7 |
131,585,830 (GRCm39) |
missense |
probably benign |
0.00 |
R7213:Gpr26
|
UTSW |
7 |
131,569,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R7351:Gpr26
|
UTSW |
7 |
131,576,094 (GRCm39) |
missense |
probably damaging |
1.00 |
R7768:Gpr26
|
UTSW |
7 |
131,576,077 (GRCm39) |
missense |
probably damaging |
0.99 |
R7887:Gpr26
|
UTSW |
7 |
131,568,702 (GRCm39) |
missense |
probably benign |
|
R8822:Gpr26
|
UTSW |
7 |
131,568,997 (GRCm39) |
missense |
probably damaging |
0.98 |
R9382:Gpr26
|
UTSW |
7 |
131,568,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R9508:Gpr26
|
UTSW |
7 |
131,585,830 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Gpr26
|
UTSW |
7 |
131,585,823 (GRCm39) |
frame shift |
probably null |
|
Z1176:Gpr26
|
UTSW |
7 |
131,568,954 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Gpr26
|
UTSW |
7 |
131,568,777 (GRCm39) |
missense |
probably damaging |
1.00 |
|