Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931406B18Rik |
G |
A |
7: 43,150,571 (GRCm39) |
T67I |
possibly damaging |
Het |
Abca5 |
A |
T |
11: 110,197,106 (GRCm39) |
M524K |
probably benign |
Het |
Aco2 |
G |
A |
15: 81,779,597 (GRCm39) |
V134I |
probably benign |
Het |
Acsf2 |
C |
T |
11: 94,461,206 (GRCm39) |
M323I |
probably benign |
Het |
Acvr1 |
T |
C |
2: 58,337,585 (GRCm39) |
D499G |
probably benign |
Het |
Armc5 |
G |
A |
7: 127,839,597 (GRCm39) |
C305Y |
probably damaging |
Het |
Astl |
T |
C |
2: 127,198,306 (GRCm39) |
I286T |
probably benign |
Het |
Atp8a2 |
G |
A |
14: 60,249,859 (GRCm39) |
S544L |
probably benign |
Het |
Bbs7 |
G |
T |
3: 36,659,853 (GRCm39) |
A194E |
probably benign |
Het |
Brca2 |
A |
G |
5: 150,465,207 (GRCm39) |
D1657G |
probably damaging |
Het |
Cfap46 |
G |
A |
7: 139,219,616 (GRCm39) |
S1283L |
probably benign |
Het |
Creld2 |
T |
C |
15: 88,704,200 (GRCm39) |
S64P |
probably damaging |
Het |
Crtc1 |
T |
C |
8: 70,850,961 (GRCm39) |
E217G |
probably damaging |
Het |
Cyp2d26 |
C |
T |
15: 82,675,320 (GRCm39) |
V345M |
probably benign |
Het |
Cyp2j11 |
T |
C |
4: 96,183,108 (GRCm39) |
M487V |
probably benign |
Het |
Dnah12 |
T |
C |
14: 26,600,036 (GRCm39) |
I3692T |
probably damaging |
Het |
Dnah14 |
A |
T |
1: 181,577,748 (GRCm39) |
T3022S |
possibly damaging |
Het |
Dtnb |
A |
T |
12: 3,698,221 (GRCm39) |
|
probably null |
Het |
Erf |
T |
C |
7: 24,944,003 (GRCm39) |
T443A |
possibly damaging |
Het |
Ermp1 |
T |
A |
19: 29,594,011 (GRCm39) |
I720F |
probably benign |
Het |
Fam83b |
T |
A |
9: 76,398,214 (GRCm39) |
E963V |
probably damaging |
Het |
Fat1 |
T |
A |
8: 45,504,060 (GRCm39) |
S4463T |
probably benign |
Het |
Fbxw27 |
T |
A |
9: 109,617,148 (GRCm39) |
K118* |
probably null |
Het |
Fcgbp |
A |
T |
7: 27,789,129 (GRCm39) |
Y565F |
probably benign |
Het |
Garre1 |
A |
G |
7: 33,945,093 (GRCm39) |
S384P |
probably benign |
Het |
Gm128 |
A |
T |
3: 95,147,740 (GRCm39) |
S185T |
probably benign |
Het |
Gm6309 |
C |
T |
5: 146,105,640 (GRCm39) |
E175K |
probably damaging |
Het |
Gpatch2l |
G |
A |
12: 86,290,958 (GRCm39) |
R47H |
probably damaging |
Het |
Gprin2 |
T |
C |
14: 33,916,597 (GRCm39) |
Y391C |
probably damaging |
Het |
Hexa |
T |
C |
9: 59,447,221 (GRCm39) |
L72P |
probably damaging |
Het |
Il31ra |
T |
A |
13: 112,685,998 (GRCm39) |
D124V |
probably damaging |
Het |
Kdm2a |
C |
T |
19: 4,372,529 (GRCm39) |
A939T |
probably benign |
Het |
Kif16b |
A |
G |
2: 142,542,019 (GRCm39) |
|
probably benign |
Het |
Kndc1 |
A |
T |
7: 139,490,194 (GRCm39) |
D232V |
probably damaging |
Het |
Lrrc37a |
T |
G |
11: 103,348,369 (GRCm39) |
R2775S |
unknown |
Het |
Luc7l3 |
C |
T |
11: 94,200,462 (GRCm39) |
R52H |
probably damaging |
Het |
Mapk15 |
A |
T |
15: 75,865,747 (GRCm39) |
R13S |
probably damaging |
Het |
Mdga2 |
G |
T |
12: 66,552,889 (GRCm39) |
Q187K |
probably benign |
Het |
Mfsd2b |
G |
A |
12: 4,920,611 (GRCm39) |
Q69* |
probably null |
Het |
Mlph |
A |
T |
1: 90,873,342 (GRCm39) |
D551V |
probably damaging |
Het |
Mup5 |
A |
T |
4: 61,752,806 (GRCm39) |
F72L |
probably benign |
Het |
Ncapg2 |
A |
G |
12: 116,390,202 (GRCm39) |
I384V |
probably benign |
Het |
Neo1 |
T |
C |
9: 58,824,335 (GRCm39) |
T698A |
probably benign |
Het |
Nox3 |
A |
G |
17: 3,736,198 (GRCm39) |
S143P |
probably damaging |
Het |
Nrros |
T |
C |
16: 31,981,057 (GRCm39) |
R24G |
probably null |
Het |
Or10ak9 |
T |
A |
4: 118,726,335 (GRCm39) |
M119K |
probably damaging |
Het |
Or6b1 |
T |
C |
6: 42,815,736 (GRCm39) |
V307A |
probably benign |
Het |
Pde9a |
T |
C |
17: 31,685,386 (GRCm39) |
S347P |
possibly damaging |
Het |
Pitpnm3 |
T |
C |
11: 71,961,222 (GRCm39) |
D315G |
probably benign |
Het |
Plaat5 |
A |
G |
19: 7,616,830 (GRCm39) |
|
probably benign |
Het |
Plekha6 |
C |
T |
1: 133,200,273 (GRCm39) |
A284V |
probably benign |
Het |
Plekhg2 |
A |
G |
7: 28,059,684 (GRCm39) |
V1215A |
probably benign |
Het |
Ppif |
C |
A |
14: 25,698,711 (GRCm39) |
A144E |
probably damaging |
Het |
Ppp1r10 |
T |
C |
17: 36,240,453 (GRCm39) |
V581A |
possibly damaging |
Het |
Prr12 |
A |
G |
7: 44,698,269 (GRCm39) |
|
probably benign |
Het |
Rfx6 |
T |
C |
10: 51,599,949 (GRCm39) |
V565A |
probably benign |
Het |
Rsrc1 |
C |
T |
3: 66,901,982 (GRCm39) |
P44L |
unknown |
Het |
Saxo2 |
A |
G |
7: 82,284,402 (GRCm39) |
V152A |
possibly damaging |
Het |
Sdk2 |
T |
C |
11: 113,793,946 (GRCm39) |
D86G |
probably benign |
Het |
Shroom3 |
A |
T |
5: 93,090,876 (GRCm39) |
M1128L |
probably benign |
Het |
Smok2a |
C |
A |
17: 13,444,543 (GRCm39) |
T40K |
probably benign |
Het |
Tatdn1 |
C |
T |
15: 58,793,118 (GRCm39) |
|
probably null |
Het |
Tbc1d2 |
C |
A |
4: 46,649,712 (GRCm39) |
G108V |
probably damaging |
Het |
Tbck |
T |
C |
3: 132,392,703 (GRCm39) |
I48T |
possibly damaging |
Het |
Tm7sf3 |
A |
G |
6: 146,527,601 (GRCm39) |
F75S |
possibly damaging |
Het |
Tmx4 |
T |
C |
2: 134,440,719 (GRCm39) |
D245G |
probably benign |
Het |
Trim68 |
A |
T |
7: 102,333,675 (GRCm39) |
D2E |
probably damaging |
Het |
Trps1 |
T |
A |
15: 50,685,694 (GRCm39) |
Q157L |
possibly damaging |
Het |
Ttc22 |
A |
G |
4: 106,495,800 (GRCm39) |
T385A |
probably benign |
Het |
Ubap2l |
A |
T |
3: 89,946,155 (GRCm39) |
F150I |
possibly damaging |
Het |
Ube2u |
C |
T |
4: 100,389,352 (GRCm39) |
R105W |
probably damaging |
Het |
Ubr4 |
G |
A |
4: 139,185,545 (GRCm39) |
|
probably null |
Het |
Unc5b |
A |
G |
10: 60,666,871 (GRCm39) |
L25P |
probably benign |
Het |
Usp38 |
A |
G |
8: 81,719,958 (GRCm39) |
S424P |
probably damaging |
Het |
Vmn1r222 |
T |
A |
13: 23,416,374 (GRCm39) |
S280C |
probably benign |
Het |
Vmn1r59 |
A |
T |
7: 5,457,599 (GRCm39) |
F54I |
probably benign |
Het |
Vmn2r-ps117 |
T |
A |
17: 19,047,464 (GRCm39) |
C536S |
probably damaging |
Het |
Zkscan2 |
A |
C |
7: 123,099,196 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Narf |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00402:Narf
|
APN |
11 |
121,129,344 (GRCm39) |
critical splice donor site |
probably null |
|
R0128:Narf
|
UTSW |
11 |
121,141,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R0542:Narf
|
UTSW |
11 |
121,143,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R1326:Narf
|
UTSW |
11 |
121,133,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R2035:Narf
|
UTSW |
11 |
121,129,326 (GRCm39) |
missense |
probably benign |
0.00 |
R2049:Narf
|
UTSW |
11 |
121,141,195 (GRCm39) |
nonsense |
probably null |
|
R2078:Narf
|
UTSW |
11 |
121,136,220 (GRCm39) |
missense |
probably benign |
0.03 |
R3711:Narf
|
UTSW |
11 |
121,137,764 (GRCm39) |
nonsense |
probably null |
|
R3967:Narf
|
UTSW |
11 |
121,129,247 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3968:Narf
|
UTSW |
11 |
121,129,247 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3970:Narf
|
UTSW |
11 |
121,129,247 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4128:Narf
|
UTSW |
11 |
121,141,261 (GRCm39) |
splice site |
probably null |
|
R4913:Narf
|
UTSW |
11 |
121,135,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R4928:Narf
|
UTSW |
11 |
121,135,765 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4946:Narf
|
UTSW |
11 |
121,141,179 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5404:Narf
|
UTSW |
11 |
121,133,452 (GRCm39) |
missense |
probably benign |
0.00 |
R5799:Narf
|
UTSW |
11 |
121,135,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R6753:Narf
|
UTSW |
11 |
121,133,452 (GRCm39) |
missense |
probably benign |
0.00 |
R7311:Narf
|
UTSW |
11 |
121,139,976 (GRCm39) |
missense |
probably benign |
0.31 |
R8056:Narf
|
UTSW |
11 |
121,136,170 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8559:Narf
|
UTSW |
11 |
121,141,258 (GRCm39) |
critical splice donor site |
probably null |
|
R9021:Narf
|
UTSW |
11 |
121,136,209 (GRCm39) |
missense |
probably damaging |
0.98 |
X0011:Narf
|
UTSW |
11 |
121,141,698 (GRCm39) |
missense |
probably damaging |
1.00 |
|