Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A330070K13Rik |
T |
C |
5: 130,407,876 (GRCm39) |
I112V |
unknown |
Het |
Aars2 |
A |
G |
17: 45,818,002 (GRCm39) |
N75D |
possibly damaging |
Het |
Abcf2 |
G |
A |
5: 24,778,475 (GRCm39) |
R228C |
probably benign |
Het |
Agfg2 |
A |
G |
5: 137,652,114 (GRCm39) |
L415P |
probably benign |
Het |
Alpi |
A |
G |
1: 87,026,386 (GRCm39) |
L535P |
unknown |
Het |
Anxa9 |
T |
G |
3: 95,210,359 (GRCm39) |
T69P |
probably damaging |
Het |
Arrb2 |
T |
A |
11: 70,327,463 (GRCm39) |
D79E |
probably benign |
Het |
Bcat1 |
A |
G |
6: 144,994,332 (GRCm39) |
V55A |
probably benign |
Het |
Cacna1c |
A |
G |
6: 119,034,335 (GRCm39) |
L64P |
|
Het |
Cd247 |
A |
T |
1: 165,682,759 (GRCm39) |
D28V |
probably damaging |
Het |
Celsr2 |
T |
A |
3: 108,320,442 (GRCm39) |
N790I |
probably damaging |
Het |
Clrn1 |
C |
T |
3: 58,792,251 (GRCm39) |
V71I |
probably benign |
Het |
Cmtr2 |
T |
C |
8: 110,949,078 (GRCm39) |
Y463H |
possibly damaging |
Het |
Col6a6 |
T |
C |
9: 105,663,172 (GRCm39) |
T122A |
probably benign |
Het |
Cubn |
T |
A |
2: 13,463,767 (GRCm39) |
D646V |
probably damaging |
Het |
Dab2ip |
T |
A |
2: 35,613,105 (GRCm39) |
L1062Q |
possibly damaging |
Het |
Dnajb4 |
T |
C |
3: 151,892,272 (GRCm39) |
N187S |
probably benign |
Het |
Dock10 |
A |
T |
1: 80,570,360 (GRCm39) |
F365L |
probably benign |
Het |
Ext1 |
T |
C |
15: 53,208,524 (GRCm39) |
H79R |
probably benign |
Het |
Fam187b |
T |
A |
7: 30,677,185 (GRCm39) |
C231* |
probably null |
Het |
Fbh1 |
T |
C |
2: 11,754,414 (GRCm39) |
I775V |
probably benign |
Het |
Fbxo15 |
T |
A |
18: 84,983,609 (GRCm39) |
M319K |
unknown |
Het |
Fbxo9 |
A |
T |
9: 78,002,520 (GRCm39) |
M187K |
possibly damaging |
Het |
Fer1l4 |
T |
C |
2: 155,877,196 (GRCm39) |
D1113G |
probably benign |
Het |
Fsip2 |
A |
T |
2: 82,818,747 (GRCm39) |
T4827S |
possibly damaging |
Het |
Gm49398 |
A |
T |
13: 61,435,478 (GRCm39) |
L7Q |
probably damaging |
Het |
H2-M10.4 |
A |
T |
17: 36,771,285 (GRCm39) |
W298R |
probably damaging |
Het |
Hoxd10 |
A |
G |
2: 74,522,982 (GRCm39) |
E220G |
probably benign |
Het |
Hrh2 |
T |
G |
13: 54,368,222 (GRCm39) |
L66R |
probably damaging |
Het |
Igf1r |
A |
G |
7: 67,844,746 (GRCm39) |
T840A |
probably benign |
Het |
Iqca1 |
A |
G |
1: 90,072,688 (GRCm39) |
V64A |
probably damaging |
Het |
Klc2 |
A |
G |
19: 5,158,659 (GRCm39) |
S612P |
probably benign |
Het |
Klf15 |
A |
G |
6: 90,443,851 (GRCm39) |
E142G |
probably damaging |
Het |
Krt40 |
T |
A |
11: 99,429,579 (GRCm39) |
T332S |
probably damaging |
Het |
Lrrc9 |
T |
C |
12: 72,506,767 (GRCm39) |
F348S |
probably damaging |
Het |
Lrrn4 |
T |
C |
2: 132,712,290 (GRCm39) |
D511G |
probably benign |
Het |
Lrtm2 |
T |
C |
6: 119,297,934 (GRCm39) |
I36V |
probably benign |
Het |
Lsm10 |
T |
C |
4: 125,991,860 (GRCm39) |
L72P |
probably damaging |
Het |
Mab21l3 |
T |
A |
3: 101,742,519 (GRCm39) |
S14C |
possibly damaging |
Het |
Map2k4 |
T |
C |
11: 65,581,569 (GRCm39) |
K381R |
probably benign |
Het |
Mcidas |
A |
G |
13: 113,130,915 (GRCm39) |
D80G |
probably damaging |
Het |
Med23 |
A |
G |
10: 24,750,469 (GRCm39) |
M99V |
probably benign |
Het |
Mga |
A |
G |
2: 119,778,656 (GRCm39) |
D2067G |
probably benign |
Het |
Ms4a19 |
T |
A |
19: 11,119,775 (GRCm39) |
T52S |
possibly damaging |
Het |
Msc |
G |
T |
1: 14,825,707 (GRCm39) |
P89Q |
probably benign |
Het |
Nalf1 |
C |
A |
8: 9,821,006 (GRCm39) |
A5S |
probably damaging |
Het |
Or14c44 |
A |
G |
7: 86,062,430 (GRCm39) |
I287V |
probably benign |
Het |
Or2d3c |
A |
T |
7: 106,526,564 (GRCm39) |
I34N |
possibly damaging |
Het |
Or5t7 |
A |
T |
2: 86,507,494 (GRCm39) |
L61Q |
probably damaging |
Het |
Plekhg6 |
T |
C |
6: 125,340,023 (GRCm39) |
D779G |
probably damaging |
Het |
Pnpla2 |
C |
A |
7: 141,035,331 (GRCm39) |
Y44* |
probably null |
Het |
Ppp1r17 |
T |
A |
6: 56,003,524 (GRCm39) |
D112E |
probably damaging |
Het |
Prdm2 |
A |
G |
4: 142,861,478 (GRCm39) |
I604T |
probably damaging |
Het |
Prkce |
A |
G |
17: 86,781,877 (GRCm39) |
Y182C |
probably damaging |
Het |
Prokr2 |
G |
A |
2: 132,182,790 (GRCm39) |
S189F |
possibly damaging |
Het |
Qser1 |
A |
T |
2: 104,618,164 (GRCm39) |
S793T |
probably benign |
Het |
Reck |
T |
C |
4: 43,943,301 (GRCm39) |
F951S |
probably benign |
Het |
Rev3l |
T |
C |
10: 39,697,458 (GRCm39) |
S652P |
probably benign |
Het |
Rtl1 |
A |
C |
12: 109,558,884 (GRCm39) |
L985R |
probably damaging |
Het |
Sardh |
T |
C |
2: 27,120,869 (GRCm39) |
E385G |
possibly damaging |
Het |
Sfmbt1 |
G |
T |
14: 30,519,599 (GRCm39) |
W440L |
possibly damaging |
Het |
Slc4a7 |
T |
A |
14: 14,772,541 (GRCm38) |
C683* |
probably null |
Het |
Slc51a |
A |
G |
16: 32,298,517 (GRCm39) |
L80P |
possibly damaging |
Het |
Slco3a1 |
C |
A |
7: 74,154,037 (GRCm39) |
L178F |
probably damaging |
Het |
Spata6 |
T |
A |
4: 111,636,389 (GRCm39) |
C227S |
possibly damaging |
Het |
Tbc1d30 |
A |
T |
10: 121,103,366 (GRCm39) |
Y555* |
probably null |
Het |
Tcf7l2 |
A |
G |
19: 55,731,517 (GRCm39) |
Q90R |
probably benign |
Het |
Tff3 |
A |
C |
17: 31,346,423 (GRCm39) |
S50A |
probably benign |
Het |
Tnrc6c |
T |
C |
11: 117,630,720 (GRCm39) |
M1027T |
probably benign |
Het |
Ttc12 |
A |
G |
9: 49,351,680 (GRCm39) |
F606L |
probably benign |
Het |
Uqcc3 |
G |
A |
19: 8,858,090 (GRCm39) |
Q34* |
probably null |
Het |
Veph1 |
T |
A |
3: 66,151,959 (GRCm39) |
I157F |
probably damaging |
Het |
Vmn2r14 |
G |
A |
5: 109,368,428 (GRCm39) |
T188I |
probably damaging |
Het |
Vmn2r67 |
A |
G |
7: 84,785,788 (GRCm39) |
I739T |
probably benign |
Het |
Vmn2r68 |
A |
G |
7: 84,882,993 (GRCm39) |
F253S |
probably benign |
Het |
Vmn2r74 |
T |
C |
7: 85,606,624 (GRCm39) |
I241V |
probably benign |
Het |
Vmn2r97 |
A |
G |
17: 19,149,368 (GRCm39) |
E252G |
probably benign |
Het |
Vps13b |
T |
C |
15: 35,455,200 (GRCm39) |
V703A |
possibly damaging |
Het |
Vps25 |
T |
A |
11: 101,149,623 (GRCm39) |
L149Q |
probably damaging |
Het |
Xirp1 |
T |
C |
9: 119,845,950 (GRCm39) |
T978A |
probably benign |
Het |
Xpnpep1 |
T |
A |
19: 52,993,248 (GRCm39) |
I360F |
probably benign |
Het |
Zfpm1 |
C |
T |
8: 123,061,308 (GRCm39) |
T291M |
probably benign |
Het |
Zkscan8 |
A |
G |
13: 21,710,702 (GRCm39) |
V136A |
probably benign |
Het |
Zscan18 |
A |
G |
7: 12,505,612 (GRCm39) |
Y592H |
probably damaging |
Het |
|
Other mutations in Erich6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00583:Erich6
|
APN |
3 |
58,544,464 (GRCm39) |
missense |
unknown |
|
IGL01352:Erich6
|
APN |
3 |
58,529,781 (GRCm39) |
splice site |
probably null |
|
IGL01362:Erich6
|
APN |
3 |
58,529,781 (GRCm39) |
splice site |
probably null |
|
IGL01928:Erich6
|
APN |
3 |
58,528,692 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02930:Erich6
|
APN |
3 |
58,529,775 (GRCm39) |
splice site |
probably benign |
|
IGL03125:Erich6
|
APN |
3 |
58,531,727 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4243001:Erich6
|
UTSW |
3 |
58,537,300 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0081:Erich6
|
UTSW |
3 |
58,543,547 (GRCm39) |
splice site |
probably benign |
|
R0129:Erich6
|
UTSW |
3 |
58,531,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R0308:Erich6
|
UTSW |
3 |
58,543,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R0682:Erich6
|
UTSW |
3 |
58,544,232 (GRCm39) |
missense |
probably benign |
0.39 |
R0734:Erich6
|
UTSW |
3 |
58,536,809 (GRCm39) |
splice site |
probably benign |
|
R0744:Erich6
|
UTSW |
3 |
58,543,543 (GRCm39) |
splice site |
probably benign |
|
R0833:Erich6
|
UTSW |
3 |
58,526,365 (GRCm39) |
splice site |
probably benign |
|
R0836:Erich6
|
UTSW |
3 |
58,526,365 (GRCm39) |
splice site |
probably benign |
|
R1385:Erich6
|
UTSW |
3 |
58,544,251 (GRCm39) |
missense |
probably benign |
0.00 |
R1536:Erich6
|
UTSW |
3 |
58,534,019 (GRCm39) |
missense |
probably benign |
0.01 |
R1570:Erich6
|
UTSW |
3 |
58,538,080 (GRCm39) |
critical splice donor site |
probably null |
|
R1708:Erich6
|
UTSW |
3 |
58,523,868 (GRCm39) |
missense |
probably benign |
0.21 |
R2187:Erich6
|
UTSW |
3 |
58,537,266 (GRCm39) |
critical splice donor site |
probably null |
|
R2268:Erich6
|
UTSW |
3 |
58,526,260 (GRCm39) |
missense |
probably benign |
0.03 |
R2441:Erich6
|
UTSW |
3 |
58,526,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R3803:Erich6
|
UTSW |
3 |
58,528,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R3981:Erich6
|
UTSW |
3 |
58,544,125 (GRCm39) |
missense |
probably benign |
0.41 |
R4166:Erich6
|
UTSW |
3 |
58,526,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R4298:Erich6
|
UTSW |
3 |
58,531,712 (GRCm39) |
missense |
probably benign |
0.09 |
R4729:Erich6
|
UTSW |
3 |
58,543,480 (GRCm39) |
critical splice donor site |
probably null |
|
R4838:Erich6
|
UTSW |
3 |
58,544,251 (GRCm39) |
missense |
probably benign |
0.00 |
R5117:Erich6
|
UTSW |
3 |
58,530,626 (GRCm39) |
missense |
probably benign |
0.00 |
R5305:Erich6
|
UTSW |
3 |
58,532,537 (GRCm39) |
missense |
probably benign |
0.21 |
R5546:Erich6
|
UTSW |
3 |
58,526,218 (GRCm39) |
missense |
probably benign |
0.39 |
R5605:Erich6
|
UTSW |
3 |
58,532,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R6033:Erich6
|
UTSW |
3 |
58,530,622 (GRCm39) |
missense |
probably benign |
0.16 |
R6033:Erich6
|
UTSW |
3 |
58,530,622 (GRCm39) |
missense |
probably benign |
0.16 |
R6378:Erich6
|
UTSW |
3 |
58,529,780 (GRCm39) |
splice site |
probably null |
|
R6606:Erich6
|
UTSW |
3 |
58,523,921 (GRCm39) |
missense |
probably damaging |
1.00 |
R6736:Erich6
|
UTSW |
3 |
58,532,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R6746:Erich6
|
UTSW |
3 |
58,523,987 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6974:Erich6
|
UTSW |
3 |
58,526,220 (GRCm39) |
missense |
probably benign |
0.06 |
R6996:Erich6
|
UTSW |
3 |
58,543,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R7317:Erich6
|
UTSW |
3 |
58,544,305 (GRCm39) |
missense |
probably benign |
0.26 |
R7484:Erich6
|
UTSW |
3 |
58,534,112 (GRCm39) |
splice site |
probably null |
|
R7526:Erich6
|
UTSW |
3 |
58,538,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R7747:Erich6
|
UTSW |
3 |
58,526,349 (GRCm39) |
missense |
probably damaging |
1.00 |
R7947:Erich6
|
UTSW |
3 |
58,528,699 (GRCm39) |
missense |
possibly damaging |
0.63 |
R8358:Erich6
|
UTSW |
3 |
58,544,449 (GRCm39) |
nonsense |
probably null |
|
R8944:Erich6
|
UTSW |
3 |
58,537,275 (GRCm39) |
missense |
probably benign |
0.16 |
R8965:Erich6
|
UTSW |
3 |
58,531,738 (GRCm39) |
missense |
probably benign |
0.02 |
R9429:Erich6
|
UTSW |
3 |
58,536,935 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9622:Erich6
|
UTSW |
3 |
58,544,162 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9624:Erich6
|
UTSW |
3 |
58,536,766 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9633:Erich6
|
UTSW |
3 |
58,537,277 (GRCm39) |
missense |
probably benign |
0.27 |
|