Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alg6 |
A |
T |
4: 99,634,564 (GRCm39) |
D273V |
probably damaging |
Het |
Ankk1 |
T |
A |
9: 49,327,097 (GRCm39) |
H694L |
possibly damaging |
Het |
Asb7 |
G |
T |
7: 66,309,696 (GRCm39) |
N173K |
probably benign |
Het |
Atp10b |
A |
T |
11: 43,092,949 (GRCm39) |
Q428L |
probably damaging |
Het |
Bag3 |
A |
G |
7: 128,147,612 (GRCm39) |
E409G |
possibly damaging |
Het |
Bltp1 |
T |
C |
3: 37,052,416 (GRCm39) |
S3039P |
probably damaging |
Het |
Bpifb2 |
T |
A |
2: 153,733,232 (GRCm39) |
V398E |
probably damaging |
Het |
Btf3l4b |
A |
T |
13: 96,217,649 (GRCm39) |
D63E |
probably benign |
Het |
Ccr6 |
T |
C |
17: 8,474,945 (GRCm39) |
V50A |
probably benign |
Het |
Cdcp3 |
G |
T |
7: 130,898,045 (GRCm39) |
V2088L |
unknown |
Het |
Cdx1 |
T |
C |
18: 61,152,995 (GRCm39) |
N204D |
probably damaging |
Het |
Ciao1 |
T |
C |
2: 127,087,726 (GRCm39) |
D203G |
possibly damaging |
Het |
Cldn7 |
A |
T |
11: 69,856,892 (GRCm39) |
Y47F |
possibly damaging |
Het |
Col6a1 |
A |
T |
10: 76,559,305 (GRCm39) |
D110E |
possibly damaging |
Het |
Cpne6 |
C |
A |
14: 55,752,025 (GRCm39) |
Q261K |
probably benign |
Het |
Crebbp |
T |
C |
16: 3,946,389 (GRCm39) |
T497A |
probably benign |
Het |
Cyp2s1 |
A |
G |
7: 25,507,467 (GRCm39) |
|
probably null |
Het |
Ddx42 |
A |
T |
11: 106,130,887 (GRCm39) |
I454F |
possibly damaging |
Het |
Ddx5 |
G |
T |
11: 106,672,911 (GRCm39) |
A538E |
probably benign |
Het |
Dnajb1 |
T |
A |
8: 84,336,944 (GRCm39) |
V238D |
probably damaging |
Het |
Dntt |
A |
G |
19: 41,044,224 (GRCm39) |
Y463C |
probably damaging |
Het |
Eif4b |
A |
G |
15: 102,001,423 (GRCm39) |
T437A |
unknown |
Het |
Eppk1 |
T |
C |
15: 75,990,900 (GRCm39) |
T1994A |
possibly damaging |
Het |
Fbxw15 |
A |
T |
9: 109,384,658 (GRCm39) |
C381S |
probably benign |
Het |
Fosl2 |
T |
A |
5: 32,310,412 (GRCm39) |
V287D |
probably damaging |
Het |
Gdpd4 |
A |
G |
7: 97,690,077 (GRCm39) |
T590A |
probably benign |
Het |
Gm49368 |
A |
G |
7: 127,712,487 (GRCm39) |
E877G |
probably null |
Het |
Grin2b |
C |
T |
6: 135,709,497 (GRCm39) |
A1350T |
probably benign |
Het |
Gzmk |
A |
G |
13: 113,308,430 (GRCm39) |
L257P |
probably damaging |
Het |
Has2 |
T |
A |
15: 56,545,175 (GRCm39) |
K142N |
probably benign |
Het |
Hectd1 |
T |
C |
12: 51,831,016 (GRCm39) |
E944G |
possibly damaging |
Het |
Hmcn1 |
T |
C |
1: 150,629,411 (GRCm39) |
R949G |
probably benign |
Het |
Hmcn2 |
A |
G |
2: 31,313,117 (GRCm39) |
E3442G |
probably damaging |
Het |
Irf9 |
T |
A |
14: 55,843,255 (GRCm39) |
C152* |
probably null |
Het |
Itga3 |
A |
G |
11: 94,943,290 (GRCm39) |
W936R |
probably damaging |
Het |
Klhl11 |
G |
T |
11: 100,354,740 (GRCm39) |
D360E |
probably damaging |
Het |
Lnx1 |
G |
A |
5: 74,846,060 (GRCm39) |
T130I |
probably benign |
Het |
Lrrc36 |
C |
T |
8: 106,170,396 (GRCm39) |
P82L |
probably damaging |
Het |
Map4k4 |
T |
C |
1: 40,039,694 (GRCm39) |
C29R |
|
Het |
Mki67 |
T |
C |
7: 135,296,065 (GRCm39) |
K2990E |
probably benign |
Het |
Mnt |
G |
A |
11: 74,733,799 (GRCm39) |
A477T |
unknown |
Het |
Mroh9 |
A |
G |
1: 162,890,096 (GRCm39) |
S214P |
probably benign |
Het |
Mrps18b |
C |
A |
17: 36,225,293 (GRCm39) |
R94L |
possibly damaging |
Het |
Myh6 |
T |
A |
14: 55,191,382 (GRCm39) |
I820F |
probably benign |
Het |
Nphp3 |
A |
G |
9: 103,913,050 (GRCm39) |
T943A |
probably benign |
Het |
Or51a25 |
C |
A |
7: 102,372,937 (GRCm39) |
L253F |
probably damaging |
Het |
Or52b4i |
A |
G |
7: 102,191,830 (GRCm39) |
H229R |
probably benign |
Het |
Papolb |
T |
C |
5: 142,514,353 (GRCm39) |
D430G |
probably benign |
Het |
Pdzd2 |
T |
C |
15: 12,407,458 (GRCm39) |
H334R |
probably benign |
Het |
Pkd1l2 |
T |
A |
8: 117,781,742 (GRCm39) |
M768L |
probably benign |
Het |
Pklr |
G |
T |
3: 89,052,795 (GRCm39) |
R547L |
probably benign |
Het |
Pla2g4a |
T |
C |
1: 149,716,394 (GRCm39) |
Y697C |
probably benign |
Het |
Prkcd |
T |
C |
14: 30,324,019 (GRCm39) |
T435A |
probably benign |
Het |
Rfx1 |
C |
T |
8: 84,800,657 (GRCm39) |
P86L |
probably benign |
Het |
Rnf19b |
C |
A |
4: 128,977,862 (GRCm39) |
A693D |
probably benign |
Het |
Scn9a |
A |
G |
2: 66,317,754 (GRCm39) |
I1578T |
probably damaging |
Het |
Slamf9 |
A |
G |
1: 172,303,942 (GRCm39) |
S96G |
probably benign |
Het |
Slc17a8 |
T |
C |
10: 89,412,233 (GRCm39) |
D584G |
probably benign |
Het |
Slc1a7 |
G |
A |
4: 107,869,473 (GRCm39) |
V513M |
probably benign |
Het |
Slc2a7 |
C |
A |
4: 150,252,818 (GRCm39) |
T486K |
probably damaging |
Het |
Slc6a20a |
G |
A |
9: 123,466,065 (GRCm39) |
A592V |
probably damaging |
Het |
Sspo |
G |
A |
6: 48,444,683 (GRCm39) |
C2226Y |
possibly damaging |
Het |
Taf4b |
T |
G |
18: 14,963,085 (GRCm39) |
D608E |
probably damaging |
Het |
Tagap1 |
A |
T |
17: 7,223,526 (GRCm39) |
I390N |
probably damaging |
Het |
Tcp11l2 |
A |
G |
10: 84,444,480 (GRCm39) |
N430D |
probably damaging |
Het |
Thsd7b |
T |
C |
1: 129,688,036 (GRCm39) |
L649P |
probably damaging |
Het |
Tmprss15 |
C |
T |
16: 78,757,473 (GRCm39) |
G956R |
probably damaging |
Het |
Tnc |
G |
T |
4: 63,935,716 (GRCm39) |
Q407K |
probably benign |
Het |
Tti1 |
C |
A |
2: 157,849,509 (GRCm39) |
E577* |
probably null |
Het |
Vmn2r79 |
A |
T |
7: 86,686,862 (GRCm39) |
M748L |
probably benign |
Het |
Zbtb37 |
C |
T |
1: 160,847,654 (GRCm39) |
R451Q |
probably damaging |
Het |
Zfp1002 |
T |
C |
2: 150,096,455 (GRCm39) |
K325E |
probably benign |
Het |
Zfp566 |
A |
T |
7: 29,777,785 (GRCm39) |
I132N |
probably benign |
Het |
Zik1 |
C |
T |
7: 10,223,930 (GRCm39) |
G389E |
probably damaging |
Het |
Zzef1 |
A |
T |
11: 72,799,295 (GRCm39) |
K2382* |
probably null |
Het |
|
Other mutations in Spz1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01082:Spz1
|
APN |
13 |
92,712,029 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01473:Spz1
|
APN |
13 |
92,711,764 (GRCm39) |
nonsense |
probably null |
|
IGL01903:Spz1
|
APN |
13 |
92,711,407 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02312:Spz1
|
APN |
13 |
92,712,393 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02343:Spz1
|
APN |
13 |
92,712,054 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02969:Spz1
|
APN |
13 |
92,711,851 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1255:Spz1
|
UTSW |
13 |
92,712,138 (GRCm39) |
missense |
probably benign |
|
R1756:Spz1
|
UTSW |
13 |
92,711,633 (GRCm39) |
missense |
probably damaging |
0.96 |
R1992:Spz1
|
UTSW |
13 |
92,712,166 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3710:Spz1
|
UTSW |
13 |
92,711,631 (GRCm39) |
nonsense |
probably null |
|
R4431:Spz1
|
UTSW |
13 |
92,711,837 (GRCm39) |
missense |
probably damaging |
1.00 |
R5108:Spz1
|
UTSW |
13 |
92,711,554 (GRCm39) |
nonsense |
probably null |
|
R5922:Spz1
|
UTSW |
13 |
92,712,106 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6724:Spz1
|
UTSW |
13 |
92,711,992 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7166:Spz1
|
UTSW |
13 |
92,712,435 (GRCm39) |
missense |
probably benign |
0.00 |
R8945:Spz1
|
UTSW |
13 |
92,711,499 (GRCm39) |
missense |
possibly damaging |
0.89 |
|