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 |
Pex5l |
C |
A |
3: 33,069,162 (GRCm39) |
E112* |
probably null |
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 |
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 Zfat |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00542:Zfat
|
APN |
15 |
68,042,071 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL00862:Zfat
|
APN |
15 |
68,130,512 (GRCm39) |
splice site |
probably null |
|
IGL01021:Zfat
|
APN |
15 |
68,042,015 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL01152:Zfat
|
APN |
15 |
67,982,353 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01733:Zfat
|
APN |
15 |
68,052,579 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01873:Zfat
|
APN |
15 |
68,096,744 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01990:Zfat
|
APN |
15 |
68,096,666 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02066:Zfat
|
APN |
15 |
68,052,678 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02664:Zfat
|
APN |
15 |
68,052,570 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02955:Zfat
|
APN |
15 |
68,052,963 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03201:Zfat
|
APN |
15 |
68,037,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R0145:Zfat
|
UTSW |
15 |
68,058,948 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0408:Zfat
|
UTSW |
15 |
68,052,141 (GRCm39) |
missense |
probably benign |
0.10 |
R0633:Zfat
|
UTSW |
15 |
68,052,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R1147:Zfat
|
UTSW |
15 |
68,084,432 (GRCm39) |
splice site |
probably benign |
|
R1508:Zfat
|
UTSW |
15 |
68,050,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R1641:Zfat
|
UTSW |
15 |
68,051,959 (GRCm39) |
missense |
probably benign |
0.19 |
R1889:Zfat
|
UTSW |
15 |
67,973,388 (GRCm39) |
missense |
probably benign |
0.00 |
R1959:Zfat
|
UTSW |
15 |
68,018,392 (GRCm39) |
missense |
probably benign |
0.32 |
R2030:Zfat
|
UTSW |
15 |
67,990,783 (GRCm39) |
critical splice donor site |
probably null |
|
R2202:Zfat
|
UTSW |
15 |
68,051,709 (GRCm39) |
missense |
probably benign |
0.36 |
R2340:Zfat
|
UTSW |
15 |
67,973,390 (GRCm39) |
missense |
probably damaging |
0.99 |
R3440:Zfat
|
UTSW |
15 |
67,956,402 (GRCm39) |
missense |
probably benign |
0.00 |
R3442:Zfat
|
UTSW |
15 |
67,973,430 (GRCm39) |
missense |
probably damaging |
0.99 |
R3442:Zfat
|
UTSW |
15 |
67,956,402 (GRCm39) |
missense |
probably benign |
0.00 |
R4406:Zfat
|
UTSW |
15 |
68,052,040 (GRCm39) |
missense |
probably benign |
0.00 |
R4649:Zfat
|
UTSW |
15 |
68,056,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R4710:Zfat
|
UTSW |
15 |
68,052,131 (GRCm39) |
missense |
probably benign |
|
R4712:Zfat
|
UTSW |
15 |
67,982,324 (GRCm39) |
critical splice donor site |
probably null |
|
R4745:Zfat
|
UTSW |
15 |
68,052,223 (GRCm39) |
missense |
probably benign |
0.09 |
R4862:Zfat
|
UTSW |
15 |
68,051,959 (GRCm39) |
missense |
probably benign |
0.02 |
R5015:Zfat
|
UTSW |
15 |
68,050,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R5075:Zfat
|
UTSW |
15 |
68,052,079 (GRCm39) |
missense |
probably benign |
|
R5208:Zfat
|
UTSW |
15 |
68,052,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R5277:Zfat
|
UTSW |
15 |
68,037,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R5303:Zfat
|
UTSW |
15 |
67,982,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R5328:Zfat
|
UTSW |
15 |
68,051,677 (GRCm39) |
missense |
probably damaging |
0.99 |
R5642:Zfat
|
UTSW |
15 |
68,052,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R5659:Zfat
|
UTSW |
15 |
67,990,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R5947:Zfat
|
UTSW |
15 |
68,051,806 (GRCm39) |
missense |
probably benign |
|
R6046:Zfat
|
UTSW |
15 |
68,052,626 (GRCm39) |
missense |
probably damaging |
0.99 |
R6315:Zfat
|
UTSW |
15 |
67,956,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R6342:Zfat
|
UTSW |
15 |
68,052,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R6573:Zfat
|
UTSW |
15 |
68,037,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R6789:Zfat
|
UTSW |
15 |
67,956,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R7028:Zfat
|
UTSW |
15 |
68,052,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R7033:Zfat
|
UTSW |
15 |
68,052,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R7039:Zfat
|
UTSW |
15 |
68,052,211 (GRCm39) |
missense |
probably benign |
|
R7065:Zfat
|
UTSW |
15 |
68,052,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R7144:Zfat
|
UTSW |
15 |
68,050,631 (GRCm39) |
missense |
probably benign |
0.12 |
R7208:Zfat
|
UTSW |
15 |
68,051,856 (GRCm39) |
missense |
probably benign |
0.39 |
R7330:Zfat
|
UTSW |
15 |
68,084,600 (GRCm39) |
missense |
probably benign |
0.00 |
R7345:Zfat
|
UTSW |
15 |
67,976,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R7378:Zfat
|
UTSW |
15 |
68,052,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R7405:Zfat
|
UTSW |
15 |
68,056,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R7481:Zfat
|
UTSW |
15 |
68,050,715 (GRCm39) |
nonsense |
probably null |
|
R7672:Zfat
|
UTSW |
15 |
68,130,535 (GRCm39) |
start codon destroyed |
probably null |
0.39 |
R7676:Zfat
|
UTSW |
15 |
68,096,693 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7701:Zfat
|
UTSW |
15 |
68,052,757 (GRCm39) |
nonsense |
probably null |
|
R7825:Zfat
|
UTSW |
15 |
68,051,769 (GRCm39) |
missense |
probably benign |
0.01 |
R8152:Zfat
|
UTSW |
15 |
67,973,355 (GRCm39) |
missense |
probably benign |
0.23 |
R8404:Zfat
|
UTSW |
15 |
67,976,916 (GRCm39) |
missense |
probably benign |
0.00 |
R8405:Zfat
|
UTSW |
15 |
68,018,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R8502:Zfat
|
UTSW |
15 |
67,976,916 (GRCm39) |
missense |
probably benign |
0.00 |
R8534:Zfat
|
UTSW |
15 |
68,037,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R8708:Zfat
|
UTSW |
15 |
67,956,278 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8887:Zfat
|
UTSW |
15 |
68,056,315 (GRCm39) |
missense |
probably damaging |
1.00 |
R8896:Zfat
|
UTSW |
15 |
68,052,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R8906:Zfat
|
UTSW |
15 |
67,956,404 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9117:Zfat
|
UTSW |
15 |
68,058,918 (GRCm39) |
missense |
probably damaging |
0.98 |
R9137:Zfat
|
UTSW |
15 |
68,051,794 (GRCm39) |
missense |
probably benign |
0.00 |
R9310:Zfat
|
UTSW |
15 |
67,956,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R9482:Zfat
|
UTSW |
15 |
68,084,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R9610:Zfat
|
UTSW |
15 |
68,051,655 (GRCm39) |
missense |
possibly damaging |
0.58 |
R9611:Zfat
|
UTSW |
15 |
68,051,655 (GRCm39) |
missense |
possibly damaging |
0.58 |
R9630:Zfat
|
UTSW |
15 |
67,990,793 (GRCm39) |
missense |
probably benign |
0.37 |
Z1088:Zfat
|
UTSW |
15 |
68,058,950 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Zfat
|
UTSW |
15 |
68,051,677 (GRCm39) |
missense |
probably damaging |
0.99 |
|