Other mutations in this stock |
Total: 107 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1500011B03Rik |
A |
T |
5: 114,947,334 (GRCm39) |
C64* |
probably null |
Het |
1700003H04Rik |
A |
C |
3: 124,368,985 (GRCm39) |
Y109D |
possibly damaging |
Het |
Abca15 |
A |
T |
7: 119,939,322 (GRCm39) |
I239F |
probably damaging |
Het |
Adgrv1 |
A |
G |
13: 81,741,167 (GRCm39) |
V99A |
probably damaging |
Het |
Adgrv1 |
A |
T |
13: 81,705,076 (GRCm39) |
I1578K |
probably damaging |
Het |
Ap4e1 |
G |
T |
2: 126,903,475 (GRCm39) |
K792N |
probably null |
Het |
Ap5b1 |
G |
A |
19: 5,619,892 (GRCm39) |
W437* |
probably null |
Het |
Arhgef17 |
A |
G |
7: 100,580,069 (GRCm39) |
L293P |
probably benign |
Het |
Arhgef33 |
A |
C |
17: 80,678,818 (GRCm39) |
M505L |
probably benign |
Het |
Arih1 |
T |
A |
9: 59,310,663 (GRCm39) |
R320S |
probably damaging |
Het |
Atp1b3 |
A |
T |
9: 96,246,206 (GRCm39) |
M1K |
probably null |
Het |
Bbs2 |
T |
C |
8: 94,816,472 (GRCm39) |
D130G |
possibly damaging |
Het |
Bscl2 |
G |
A |
19: 8,818,509 (GRCm39) |
R38H |
probably damaging |
Het |
Cad |
A |
G |
5: 31,226,106 (GRCm39) |
Y1102C |
probably damaging |
Het |
Cc2d1b |
G |
A |
4: 108,490,423 (GRCm39) |
R825Q |
probably damaging |
Het |
Ccdc39 |
A |
G |
3: 33,893,294 (GRCm39) |
V97A |
possibly damaging |
Het |
Ccr1 |
T |
C |
9: 123,764,510 (GRCm39) |
T7A |
probably benign |
Het |
Cd33 |
A |
G |
7: 43,181,618 (GRCm39) |
S181P |
probably damaging |
Het |
Cdc20 |
A |
C |
4: 118,290,304 (GRCm39) |
S452R |
probably damaging |
Het |
Cdk8 |
A |
T |
5: 146,233,188 (GRCm39) |
I229F |
possibly damaging |
Het |
Ces3a |
A |
T |
8: 105,776,909 (GRCm39) |
N131Y |
probably damaging |
Het |
Cgnl1 |
A |
G |
9: 71,631,872 (GRCm39) |
I493T |
probably benign |
Het |
Chia1 |
G |
A |
3: 106,039,220 (GRCm39) |
V437M |
probably benign |
Het |
Chrna2 |
G |
A |
14: 66,380,878 (GRCm39) |
R49H |
probably benign |
Het |
Clec12b |
A |
G |
6: 129,353,265 (GRCm39) |
C241R |
probably damaging |
Het |
Col11a1 |
A |
G |
3: 113,890,803 (GRCm39) |
D380G |
unknown |
Het |
Crebbp |
A |
G |
16: 3,933,749 (GRCm39) |
S948P |
probably damaging |
Het |
Dchs1 |
G |
A |
7: 105,421,278 (GRCm39) |
R381* |
probably null |
Het |
Defb19 |
A |
T |
2: 152,418,085 (GRCm39) |
*84R |
probably null |
Het |
Dnah8 |
T |
C |
17: 30,892,862 (GRCm39) |
F816L |
probably benign |
Het |
Dync2h1 |
T |
A |
9: 7,103,663 (GRCm39) |
I371F |
possibly damaging |
Het |
Ezhip |
GTCATCATCATCATC |
GTCATCATCATCATCATC |
X: 5,994,645 (GRCm39) |
|
probably benign |
Het |
Fggy |
T |
C |
4: 95,790,295 (GRCm39) |
|
probably benign |
Het |
Galnt12 |
G |
A |
4: 47,117,956 (GRCm39) |
C125Y |
probably damaging |
Het |
Gm4952 |
A |
T |
19: 12,602,039 (GRCm39) |
D149V |
probably damaging |
Het |
Gm6309 |
A |
T |
5: 146,107,393 (GRCm39) |
H37Q |
possibly damaging |
Het |
Gmnn |
A |
G |
13: 24,940,615 (GRCm39) |
L78P |
possibly damaging |
Het |
Golga4 |
C |
A |
9: 118,384,800 (GRCm39) |
Q613K |
probably benign |
Het |
Iqgap2 |
A |
T |
13: 95,766,518 (GRCm39) |
I1495K |
probably damaging |
Het |
Junb |
T |
C |
8: 85,704,758 (GRCm39) |
T101A |
probably damaging |
Het |
Kif21b |
T |
C |
1: 136,083,849 (GRCm39) |
Y699H |
probably damaging |
Het |
Klf17 |
T |
C |
4: 117,618,132 (GRCm39) |
E75G |
probably damaging |
Het |
Klra17 |
T |
C |
6: 129,849,277 (GRCm39) |
E99G |
possibly damaging |
Het |
Knop1 |
CTCTTCTTCTTCTTCTTCTTCTTC |
CTCTTCTTCTTCTTCTTCTTC |
7: 118,451,672 (GRCm39) |
|
probably benign |
Het |
Krt87 |
C |
T |
15: 101,387,538 (GRCm39) |
V167M |
probably benign |
Het |
Lce1m |
A |
G |
3: 92,925,932 (GRCm39) |
|
probably benign |
Het |
Lpin3 |
A |
T |
2: 160,746,468 (GRCm39) |
Y709F |
probably damaging |
Het |
Ltbp2 |
T |
A |
12: 84,838,718 (GRCm39) |
D1080V |
probably damaging |
Het |
Mycbp2 |
G |
A |
14: 103,441,825 (GRCm39) |
T1980I |
probably damaging |
Het |
Myo1g |
T |
A |
11: 6,465,140 (GRCm39) |
K435M |
probably damaging |
Het |
Mypn |
T |
A |
10: 63,005,147 (GRCm39) |
N320I |
probably damaging |
Het |
Naip5 |
A |
T |
13: 100,358,714 (GRCm39) |
W841R |
probably benign |
Het |
Ncapd2 |
A |
T |
6: 125,147,955 (GRCm39) |
M1124K |
probably damaging |
Het |
Ncf4 |
A |
G |
15: 78,146,560 (GRCm39) |
D330G |
probably benign |
Het |
Ndst3 |
C |
T |
3: 123,395,104 (GRCm39) |
V509M |
possibly damaging |
Het |
Neb |
A |
T |
2: 52,117,256 (GRCm39) |
D4105E |
probably damaging |
Het |
Nfix |
G |
A |
8: 85,453,155 (GRCm39) |
R300C |
probably damaging |
Het |
Nsrp1 |
A |
T |
11: 76,937,445 (GRCm39) |
F250L |
probably benign |
Het |
Or11g7 |
A |
G |
14: 50,691,138 (GRCm39) |
I210V |
probably benign |
Het |
Or4l15 |
T |
C |
14: 50,198,558 (GRCm39) |
|
probably null |
Het |
Or52d1 |
C |
T |
7: 103,755,671 (GRCm39) |
L62F |
probably benign |
Het |
Or52k2 |
G |
T |
7: 102,254,509 (GRCm39) |
G316V |
probably benign |
Het |
Or5m12 |
A |
T |
2: 85,735,015 (GRCm39) |
Y128N |
probably damaging |
Het |
Or8k3b |
C |
T |
2: 86,521,141 (GRCm39) |
M59I |
possibly damaging |
Het |
Oxr1 |
A |
G |
15: 41,660,870 (GRCm39) |
D67G |
probably damaging |
Het |
P2ry12 |
A |
T |
3: 59,125,498 (GRCm39) |
I59N |
probably damaging |
Het |
Pcdhb12 |
G |
T |
18: 37,570,111 (GRCm39) |
G419V |
probably damaging |
Het |
Pdzd2 |
G |
T |
15: 12,373,915 (GRCm39) |
S2073R |
possibly damaging |
Het |
Plaur |
A |
G |
7: 24,172,016 (GRCm39) |
D163G |
probably benign |
Het |
Plk2 |
A |
G |
13: 110,536,622 (GRCm39) |
Y638C |
probably benign |
Het |
Ppp1r15b |
A |
G |
1: 133,061,088 (GRCm39) |
N535S |
probably benign |
Het |
Ppp2r1b |
T |
C |
9: 50,781,445 (GRCm39) |
L21P |
probably damaging |
Het |
Prkar2a |
G |
A |
9: 108,605,469 (GRCm39) |
V176I |
possibly damaging |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Rag1 |
A |
G |
2: 101,473,336 (GRCm39) |
M602T |
possibly damaging |
Het |
Rb1 |
A |
G |
14: 73,559,524 (GRCm39) |
V60A |
probably benign |
Het |
Rgs20 |
T |
A |
1: 4,982,560 (GRCm39) |
I303F |
probably damaging |
Het |
Rnf43 |
T |
A |
11: 87,620,257 (GRCm39) |
I240N |
probably damaging |
Het |
Romo1 |
G |
A |
2: 155,986,433 (GRCm39) |
V19M |
probably benign |
Het |
Ryr1 |
A |
G |
7: 28,770,046 (GRCm39) |
S2676P |
probably damaging |
Het |
Ryr3 |
G |
A |
2: 112,539,542 (GRCm39) |
Q3233* |
probably null |
Het |
Skic2 |
G |
T |
17: 35,066,420 (GRCm39) |
P188T |
probably damaging |
Het |
Slc26a6 |
A |
G |
9: 108,733,035 (GRCm39) |
R5G |
probably benign |
Het |
Slc33a1 |
A |
G |
3: 63,871,376 (GRCm39) |
L79P |
probably damaging |
Het |
Snx31 |
G |
A |
15: 36,545,745 (GRCm39) |
R91C |
probably damaging |
Het |
Tecpr2 |
T |
C |
12: 110,921,234 (GRCm39) |
I1269T |
possibly damaging |
Het |
Tjap1 |
G |
T |
17: 46,572,368 (GRCm39) |
D89E |
probably benign |
Het |
Tmem53 |
A |
T |
4: 117,123,090 (GRCm39) |
Q39L |
probably damaging |
Het |
Tmod1 |
G |
T |
4: 46,083,549 (GRCm39) |
V95F |
possibly damaging |
Het |
Trim30c |
A |
C |
7: 104,031,896 (GRCm39) |
H306Q |
probably benign |
Het |
Trpm3 |
A |
T |
19: 22,964,236 (GRCm39) |
M1244L |
possibly damaging |
Het |
Tspan32 |
A |
G |
7: 142,558,886 (GRCm39) |
I14V |
probably null |
Het |
Ube4b |
A |
G |
4: 149,436,035 (GRCm39) |
V695A |
probably benign |
Het |
Ubxn11 |
G |
A |
4: 133,851,452 (GRCm39) |
|
probably null |
Het |
Ugt3a1 |
A |
G |
15: 9,361,610 (GRCm39) |
I129V |
probably benign |
Het |
Vmn1r45 |
A |
G |
6: 89,910,058 (GRCm39) |
V304A |
probably damaging |
Het |
Vmn2r124 |
A |
T |
17: 18,283,535 (GRCm39) |
S410C |
probably damaging |
Het |
Vmn2r15 |
T |
A |
5: 109,441,195 (GRCm39) |
D221V |
probably damaging |
Het |
Vmn2r79 |
G |
A |
7: 86,686,652 (GRCm39) |
V678I |
probably benign |
Het |
Vps13b |
A |
T |
15: 35,438,876 (GRCm39) |
R319* |
probably null |
Het |
Wdr95 |
G |
A |
5: 149,522,759 (GRCm39) |
R639Q |
probably benign |
Het |
Xirp2 |
A |
G |
2: 67,341,874 (GRCm39) |
I1372V |
probably benign |
Het |
Xpo5 |
T |
A |
17: 46,537,906 (GRCm39) |
M611K |
probably benign |
Het |
Zfat |
A |
G |
15: 68,084,529 (GRCm39) |
C121R |
probably damaging |
Het |
Zfp382 |
A |
T |
7: 29,832,721 (GRCm39) |
Y124F |
probably benign |
Het |
Zfp512b |
A |
G |
2: 181,230,982 (GRCm39) |
F371S |
probably benign |
Het |
Zfy2 |
A |
G |
Y: 2,116,185 (GRCm39) |
V285A |
probably benign |
Het |
|
Other mutations in Pex5l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01397:Pex5l
|
APN |
3 |
33,006,746 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01621:Pex5l
|
APN |
3 |
33,069,110 (GRCm39) |
splice site |
probably null |
|
IGL01813:Pex5l
|
APN |
3 |
33,136,204 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02313:Pex5l
|
APN |
3 |
33,047,141 (GRCm39) |
missense |
probably benign |
0.22 |
IGL02508:Pex5l
|
APN |
3 |
33,047,051 (GRCm39) |
splice site |
probably benign |
|
IGL02997:Pex5l
|
APN |
3 |
33,009,991 (GRCm39) |
splice site |
probably benign |
|
R0195:Pex5l
|
UTSW |
3 |
33,047,102 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0674:Pex5l
|
UTSW |
3 |
33,006,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R0729:Pex5l
|
UTSW |
3 |
33,008,685 (GRCm39) |
splice site |
probably benign |
|
R1500:Pex5l
|
UTSW |
3 |
33,069,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R1695:Pex5l
|
UTSW |
3 |
33,008,531 (GRCm39) |
missense |
probably benign |
0.28 |
R1850:Pex5l
|
UTSW |
3 |
33,005,025 (GRCm39) |
splice site |
probably null |
|
R2165:Pex5l
|
UTSW |
3 |
33,007,281 (GRCm39) |
splice site |
probably null |
|
R2679:Pex5l
|
UTSW |
3 |
33,136,201 (GRCm39) |
missense |
probably benign |
0.02 |
R2880:Pex5l
|
UTSW |
3 |
33,047,152 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2881:Pex5l
|
UTSW |
3 |
33,047,152 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3766:Pex5l
|
UTSW |
3 |
33,061,327 (GRCm39) |
missense |
probably benign |
0.01 |
R3780:Pex5l
|
UTSW |
3 |
33,004,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R3934:Pex5l
|
UTSW |
3 |
33,061,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R3975:Pex5l
|
UTSW |
3 |
33,069,164 (GRCm39) |
missense |
probably damaging |
0.99 |
R4285:Pex5l
|
UTSW |
3 |
33,061,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R4825:Pex5l
|
UTSW |
3 |
33,047,134 (GRCm39) |
missense |
probably damaging |
0.99 |
R4855:Pex5l
|
UTSW |
3 |
33,196,989 (GRCm39) |
splice site |
probably benign |
|
R4868:Pex5l
|
UTSW |
3 |
33,006,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5135:Pex5l
|
UTSW |
3 |
33,009,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R5217:Pex5l
|
UTSW |
3 |
33,061,477 (GRCm39) |
splice site |
probably null |
|
R5223:Pex5l
|
UTSW |
3 |
33,012,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R5362:Pex5l
|
UTSW |
3 |
33,047,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R5398:Pex5l
|
UTSW |
3 |
33,006,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5829:Pex5l
|
UTSW |
3 |
33,060,139 (GRCm39) |
missense |
probably benign |
0.00 |
R6731:Pex5l
|
UTSW |
3 |
33,012,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R7180:Pex5l
|
UTSW |
3 |
33,078,840 (GRCm39) |
splice site |
probably null |
|
R7452:Pex5l
|
UTSW |
3 |
33,058,467 (GRCm39) |
missense |
probably benign |
0.02 |
R7549:Pex5l
|
UTSW |
3 |
33,136,184 (GRCm39) |
missense |
probably benign |
0.04 |
R7563:Pex5l
|
UTSW |
3 |
33,008,625 (GRCm39) |
missense |
probably damaging |
0.98 |
R7757:Pex5l
|
UTSW |
3 |
33,136,300 (GRCm39) |
start gained |
probably benign |
|
R8030:Pex5l
|
UTSW |
3 |
33,008,568 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8143:Pex5l
|
UTSW |
3 |
33,136,658 (GRCm39) |
start gained |
probably benign |
|
R8242:Pex5l
|
UTSW |
3 |
33,060,184 (GRCm39) |
missense |
probably benign |
0.01 |
R8919:Pex5l
|
UTSW |
3 |
33,007,333 (GRCm39) |
missense |
probably damaging |
1.00 |
R9034:Pex5l
|
UTSW |
3 |
33,006,683 (GRCm39) |
missense |
probably damaging |
0.99 |
R9422:Pex5l
|
UTSW |
3 |
33,136,401 (GRCm39) |
start gained |
probably benign |
|
R9585:Pex5l
|
UTSW |
3 |
33,060,091 (GRCm39) |
missense |
probably benign |
|
R9654:Pex5l
|
UTSW |
3 |
33,010,827 (GRCm39) |
missense |
probably benign |
0.08 |
R9711:Pex5l
|
UTSW |
3 |
33,136,204 (GRCm39) |
missense |
probably benign |
0.02 |
Z1177:Pex5l
|
UTSW |
3 |
33,061,308 (GRCm39) |
missense |
probably damaging |
0.98 |
|