Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acoxl |
C |
A |
2: 127,965,028 (GRCm39) |
A624E |
probably benign |
Het |
Adnp |
A |
G |
2: 168,024,287 (GRCm39) |
S1003P |
probably benign |
Het |
Akap8l |
T |
C |
17: 32,557,386 (GRCm39) |
D75G |
probably damaging |
Het |
Ap4e1 |
A |
T |
2: 126,905,238 (GRCm39) |
T970S |
possibly damaging |
Het |
Asb3 |
T |
A |
11: 30,979,029 (GRCm39) |
N106K |
probably damaging |
Het |
Atp1a3 |
T |
C |
7: 24,678,390 (GRCm39) |
I988V |
probably benign |
Het |
Camta1 |
A |
G |
4: 151,169,157 (GRCm39) |
L198S |
possibly damaging |
Het |
Ccdc77 |
A |
G |
6: 120,327,193 (GRCm39) |
L84P |
probably damaging |
Het |
Ccne1 |
C |
T |
7: 37,798,726 (GRCm39) |
A298T |
probably damaging |
Het |
Clasp2 |
G |
A |
9: 113,615,467 (GRCm39) |
|
probably null |
Het |
Cntnap5b |
C |
A |
1: 100,003,887 (GRCm39) |
T289N |
possibly damaging |
Het |
Dcun1d4 |
A |
G |
5: 73,648,538 (GRCm39) |
|
probably null |
Het |
Dnah14 |
A |
G |
1: 181,532,100 (GRCm39) |
T2296A |
probably benign |
Het |
Dnaja4 |
A |
T |
9: 54,616,516 (GRCm39) |
Q173L |
probably damaging |
Het |
Dync2h1 |
G |
A |
9: 7,050,479 (GRCm39) |
A3190V |
probably benign |
Het |
Frrs1 |
T |
A |
3: 116,671,920 (GRCm39) |
I6N |
probably benign |
Het |
Fscn1 |
T |
C |
5: 142,957,801 (GRCm39) |
V477A |
probably benign |
Het |
Fsip2 |
G |
A |
2: 82,811,541 (GRCm39) |
G2620E |
possibly damaging |
Het |
Glp1r |
C |
T |
17: 31,128,297 (GRCm39) |
A92V |
probably benign |
Het |
Gpr137b |
A |
T |
13: 13,542,205 (GRCm39) |
M204K |
probably damaging |
Het |
Gstm1 |
A |
G |
3: 107,923,693 (GRCm39) |
V104A |
probably benign |
Het |
Gtf2e1 |
A |
T |
16: 37,356,228 (GRCm39) |
N101K |
probably damaging |
Het |
Igsf9b |
T |
C |
9: 27,245,536 (GRCm39) |
F1168L |
probably benign |
Het |
Itpr2 |
A |
T |
6: 146,195,589 (GRCm39) |
V1629E |
probably damaging |
Het |
Kat14 |
A |
G |
2: 144,235,918 (GRCm39) |
T428A |
probably benign |
Het |
Kif21b |
T |
C |
1: 136,077,186 (GRCm39) |
Y403H |
probably damaging |
Het |
Lpcat1 |
G |
C |
13: 73,662,649 (GRCm39) |
A533P |
probably benign |
Het |
Lrp2 |
A |
T |
2: 69,336,917 (GRCm39) |
I1285N |
probably damaging |
Het |
Mboat1 |
A |
T |
13: 30,408,398 (GRCm39) |
Y187F |
probably damaging |
Het |
Mkx |
T |
C |
18: 7,002,525 (GRCm39) |
N7S |
probably damaging |
Het |
Mrps27 |
A |
T |
13: 99,551,307 (GRCm39) |
T357S |
possibly damaging |
Het |
Muc21 |
A |
G |
17: 35,932,870 (GRCm39) |
S439P |
unknown |
Het |
Naa35 |
A |
G |
13: 59,733,997 (GRCm39) |
D9G |
probably benign |
Het |
Ncoa4 |
T |
A |
14: 31,897,940 (GRCm39) |
N253K |
probably damaging |
Het |
Neb |
A |
G |
2: 52,160,318 (GRCm39) |
Y2232H |
probably damaging |
Het |
Nlk |
G |
A |
11: 78,481,793 (GRCm39) |
Q223* |
probably null |
Het |
Npas2 |
T |
A |
1: 39,331,798 (GRCm39) |
I71N |
possibly damaging |
Het |
Nup107 |
T |
A |
10: 117,609,267 (GRCm39) |
Q364L |
probably damaging |
Het |
Or8g17 |
T |
A |
9: 38,934,566 (GRCm39) |
|
probably benign |
Het |
Otof |
C |
T |
5: 30,532,964 (GRCm39) |
G1593S |
probably damaging |
Het |
Panx3 |
G |
T |
9: 37,575,381 (GRCm39) |
H160Q |
probably damaging |
Het |
Pappa |
T |
A |
4: 65,180,110 (GRCm39) |
H990Q |
probably damaging |
Het |
Pax4 |
G |
A |
6: 28,446,136 (GRCm39) |
P119L |
probably damaging |
Het |
Pcdhb20 |
T |
A |
18: 37,638,123 (GRCm39) |
D216E |
probably damaging |
Het |
Pcdhgb8 |
T |
A |
18: 37,896,231 (GRCm39) |
S434T |
possibly damaging |
Het |
Pf4 |
T |
C |
5: 90,920,448 (GRCm39) |
V3A |
probably benign |
Het |
Phf24 |
T |
C |
4: 42,938,325 (GRCm39) |
S229P |
probably benign |
Het |
Plcd3 |
A |
G |
11: 102,970,439 (GRCm39) |
F200S |
probably damaging |
Het |
Ppp1r16a |
A |
G |
15: 76,575,104 (GRCm39) |
H4R |
probably damaging |
Het |
Pramel15 |
A |
G |
4: 144,099,389 (GRCm39) |
C459R |
probably damaging |
Het |
Prdm10 |
A |
G |
9: 31,227,738 (GRCm39) |
|
probably null |
Het |
Prim2 |
A |
G |
1: 33,667,474 (GRCm39) |
|
probably null |
Het |
Prkg1 |
T |
A |
19: 30,562,599 (GRCm39) |
H550L |
probably damaging |
Het |
Prrc2c |
G |
T |
1: 162,501,086 (GRCm39) |
T2809N |
possibly damaging |
Het |
Ptx3 |
A |
G |
3: 66,132,391 (GRCm39) |
E304G |
probably benign |
Het |
Ralgps2 |
A |
G |
1: 156,655,818 (GRCm39) |
F369L |
probably benign |
Het |
Rasgrp1 |
G |
A |
2: 117,168,885 (GRCm39) |
T31I |
probably benign |
Het |
Rbsn |
A |
T |
6: 92,168,315 (GRCm39) |
M373K |
probably benign |
Het |
Rnf168 |
C |
G |
16: 32,101,179 (GRCm39) |
R120G |
probably benign |
Het |
Rp1 |
A |
G |
1: 4,420,140 (GRCm39) |
I324T |
probably damaging |
Het |
Samd11 |
T |
C |
4: 156,336,747 (GRCm39) |
S31G |
probably benign |
Het |
Sart3 |
A |
T |
5: 113,884,056 (GRCm39) |
L652Q |
probably benign |
Het |
Scrn2 |
A |
G |
11: 96,924,634 (GRCm39) |
E421G |
probably benign |
Het |
Sik2 |
A |
T |
9: 50,828,397 (GRCm39) |
L215Q |
probably damaging |
Het |
Speer4a3 |
AACT |
A |
5: 26,155,849 (GRCm39) |
|
probably benign |
Het |
Stard9 |
A |
T |
2: 120,534,639 (GRCm39) |
K3632M |
probably damaging |
Het |
Swt1 |
A |
T |
1: 151,264,428 (GRCm39) |
D695E |
probably damaging |
Het |
Tead3 |
T |
A |
17: 28,552,228 (GRCm39) |
M357L |
probably benign |
Het |
Tgfbi |
A |
T |
13: 56,775,829 (GRCm39) |
T292S |
probably damaging |
Het |
Tmc7 |
T |
C |
7: 118,155,157 (GRCm39) |
H247R |
probably benign |
Het |
Trmt10b |
T |
A |
4: 45,308,549 (GRCm39) |
D236E |
probably damaging |
Het |
Tshz1 |
C |
A |
18: 84,034,052 (GRCm39) |
V119L |
probably damaging |
Het |
Ttn |
A |
C |
2: 76,658,258 (GRCm39) |
V12374G |
unknown |
Het |
Tubgcp2 |
A |
G |
7: 139,585,274 (GRCm39) |
Y484H |
probably damaging |
Het |
Ubr4 |
G |
C |
4: 139,177,824 (GRCm39) |
A1947P |
|
Het |
Uggt1 |
A |
C |
1: 36,194,188 (GRCm39) |
V1350G |
probably benign |
Het |
Vmn1r173 |
A |
T |
7: 23,402,076 (GRCm39) |
M104L |
probably benign |
Het |
Xirp1 |
A |
T |
9: 119,848,113 (GRCm39) |
C257S |
probably damaging |
Het |
Zfyve26 |
A |
G |
12: 79,327,179 (GRCm39) |
S724P |
probably damaging |
Het |
Zmpste24 |
A |
T |
4: 120,940,091 (GRCm39) |
L185Q |
probably null |
Het |
Zpld1 |
G |
A |
16: 55,052,594 (GRCm39) |
A340V |
probably benign |
Het |
|
Other mutations in Cdc42bpb |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01335:Cdc42bpb
|
APN |
12 |
111,260,530 (GRCm39) |
unclassified |
probably benign |
|
IGL01360:Cdc42bpb
|
APN |
12 |
111,308,509 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01577:Cdc42bpb
|
APN |
12 |
111,268,477 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01909:Cdc42bpb
|
APN |
12 |
111,289,576 (GRCm39) |
missense |
probably benign |
|
IGL01924:Cdc42bpb
|
APN |
12 |
111,283,887 (GRCm39) |
unclassified |
probably benign |
|
IGL02428:Cdc42bpb
|
APN |
12 |
111,289,561 (GRCm39) |
missense |
probably benign |
|
IGL02678:Cdc42bpb
|
APN |
12 |
111,292,530 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02792:Cdc42bpb
|
APN |
12 |
111,265,995 (GRCm39) |
missense |
probably benign |
|
IGL03367:Cdc42bpb
|
APN |
12 |
111,302,593 (GRCm39) |
missense |
probably damaging |
1.00 |
F5770:Cdc42bpb
|
UTSW |
12 |
111,262,825 (GRCm39) |
missense |
probably benign |
0.28 |
PIT4585001:Cdc42bpb
|
UTSW |
12 |
111,271,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R0129:Cdc42bpb
|
UTSW |
12 |
111,271,393 (GRCm39) |
intron |
probably benign |
|
R0633:Cdc42bpb
|
UTSW |
12 |
111,311,989 (GRCm39) |
missense |
probably damaging |
0.99 |
R1054:Cdc42bpb
|
UTSW |
12 |
111,279,787 (GRCm39) |
missense |
probably benign |
0.00 |
R1335:Cdc42bpb
|
UTSW |
12 |
111,262,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R1459:Cdc42bpb
|
UTSW |
12 |
111,262,734 (GRCm39) |
unclassified |
probably benign |
|
R1780:Cdc42bpb
|
UTSW |
12 |
111,289,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R1823:Cdc42bpb
|
UTSW |
12 |
111,293,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R1843:Cdc42bpb
|
UTSW |
12 |
111,289,255 (GRCm39) |
missense |
probably benign |
|
R1902:Cdc42bpb
|
UTSW |
12 |
111,292,450 (GRCm39) |
missense |
probably damaging |
1.00 |
R1945:Cdc42bpb
|
UTSW |
12 |
111,265,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R2077:Cdc42bpb
|
UTSW |
12 |
111,265,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R2184:Cdc42bpb
|
UTSW |
12 |
111,262,478 (GRCm39) |
missense |
probably damaging |
0.99 |
R2208:Cdc42bpb
|
UTSW |
12 |
111,302,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R2211:Cdc42bpb
|
UTSW |
12 |
111,268,288 (GRCm39) |
missense |
probably benign |
0.11 |
R2273:Cdc42bpb
|
UTSW |
12 |
111,268,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R2406:Cdc42bpb
|
UTSW |
12 |
111,268,558 (GRCm39) |
missense |
probably benign |
0.00 |
R3080:Cdc42bpb
|
UTSW |
12 |
111,262,252 (GRCm39) |
missense |
probably damaging |
0.99 |
R3612:Cdc42bpb
|
UTSW |
12 |
111,270,256 (GRCm39) |
intron |
probably benign |
|
R4106:Cdc42bpb
|
UTSW |
12 |
111,261,579 (GRCm39) |
missense |
probably benign |
0.01 |
R4133:Cdc42bpb
|
UTSW |
12 |
111,287,976 (GRCm39) |
missense |
probably benign |
0.00 |
R4156:Cdc42bpb
|
UTSW |
12 |
111,260,573 (GRCm39) |
missense |
probably benign |
0.17 |
R4202:Cdc42bpb
|
UTSW |
12 |
111,260,573 (GRCm39) |
missense |
probably benign |
0.17 |
R4573:Cdc42bpb
|
UTSW |
12 |
111,289,575 (GRCm39) |
missense |
probably benign |
0.00 |
R4659:Cdc42bpb
|
UTSW |
12 |
111,306,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R5101:Cdc42bpb
|
UTSW |
12 |
111,265,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R5591:Cdc42bpb
|
UTSW |
12 |
111,289,521 (GRCm39) |
missense |
probably benign |
0.01 |
R5669:Cdc42bpb
|
UTSW |
12 |
111,268,447 (GRCm39) |
critical splice donor site |
probably null |
|
R5830:Cdc42bpb
|
UTSW |
12 |
111,312,016 (GRCm39) |
nonsense |
probably null |
|
R5872:Cdc42bpb
|
UTSW |
12 |
111,292,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R6748:Cdc42bpb
|
UTSW |
12 |
111,261,273 (GRCm39) |
unclassified |
probably benign |
|
R6813:Cdc42bpb
|
UTSW |
12 |
111,294,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R7024:Cdc42bpb
|
UTSW |
12 |
111,292,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R7228:Cdc42bpb
|
UTSW |
12 |
111,271,527 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7258:Cdc42bpb
|
UTSW |
12 |
111,292,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R7352:Cdc42bpb
|
UTSW |
12 |
111,265,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R7361:Cdc42bpb
|
UTSW |
12 |
111,312,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R7399:Cdc42bpb
|
UTSW |
12 |
111,272,101 (GRCm39) |
missense |
probably benign |
0.00 |
R7468:Cdc42bpb
|
UTSW |
12 |
111,306,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R7622:Cdc42bpb
|
UTSW |
12 |
111,261,206 (GRCm39) |
missense |
unknown |
|
R7648:Cdc42bpb
|
UTSW |
12 |
111,343,587 (GRCm39) |
missense |
probably damaging |
1.00 |
R7734:Cdc42bpb
|
UTSW |
12 |
111,295,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R7783:Cdc42bpb
|
UTSW |
12 |
111,302,459 (GRCm39) |
critical splice donor site |
probably null |
|
R8738:Cdc42bpb
|
UTSW |
12 |
111,274,221 (GRCm39) |
missense |
probably benign |
0.42 |
R9111:Cdc42bpb
|
UTSW |
12 |
111,284,903 (GRCm39) |
missense |
probably benign |
|
R9168:Cdc42bpb
|
UTSW |
12 |
111,286,517 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9506:Cdc42bpb
|
UTSW |
12 |
111,261,372 (GRCm39) |
missense |
probably benign |
0.00 |
R9510:Cdc42bpb
|
UTSW |
12 |
111,261,372 (GRCm39) |
missense |
probably benign |
0.00 |
R9511:Cdc42bpb
|
UTSW |
12 |
111,261,372 (GRCm39) |
missense |
probably benign |
0.00 |
R9542:Cdc42bpb
|
UTSW |
12 |
111,268,508 (GRCm39) |
nonsense |
probably null |
|
R9563:Cdc42bpb
|
UTSW |
12 |
111,265,762 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9758:Cdc42bpb
|
UTSW |
12 |
111,265,783 (GRCm39) |
missense |
possibly damaging |
0.65 |
V7582:Cdc42bpb
|
UTSW |
12 |
111,262,825 (GRCm39) |
missense |
probably benign |
0.28 |
V7583:Cdc42bpb
|
UTSW |
12 |
111,262,825 (GRCm39) |
missense |
probably benign |
0.28 |
X0023:Cdc42bpb
|
UTSW |
12 |
111,292,512 (GRCm39) |
missense |
probably damaging |
1.00 |
|