Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
0610010F05Rik |
G |
T |
11: 23,576,764 (GRCm38) |
T696N |
probably benign |
Het |
Ankrd45 |
T |
C |
1: 161,151,319 (GRCm38) |
|
probably null |
Het |
Appl1 |
C |
A |
14: 26,927,794 (GRCm38) |
G592* |
probably null |
Het |
Arfgef2 |
T |
A |
2: 166,878,544 (GRCm38) |
M1501K |
probably benign |
Het |
Calcrl |
C |
T |
2: 84,339,339 (GRCm38) |
A333T |
probably damaging |
Het |
Cd200r3 |
T |
A |
16: 44,951,472 (GRCm38) |
I33N |
probably benign |
Het |
Ceacam15 |
A |
G |
7: 16,673,409 (GRCm38) |
L61P |
probably benign |
Het |
Cfap69 |
T |
A |
5: 5,582,515 (GRCm38) |
H827L |
possibly damaging |
Het |
Csmd3 |
T |
A |
15: 47,644,270 (GRCm38) |
E2780V |
probably damaging |
Het |
Cyp2u1 |
G |
A |
3: 131,293,654 (GRCm38) |
T426I |
probably damaging |
Het |
Eefsec |
A |
C |
6: 88,376,330 (GRCm38) |
I119S |
probably damaging |
Het |
Fem1b |
T |
C |
9: 62,796,268 (GRCm38) |
N570S |
probably damaging |
Het |
Fmo9 |
A |
G |
1: 166,663,526 (GRCm38) |
M461T |
probably benign |
Het |
Fryl |
A |
G |
5: 73,133,277 (GRCm38) |
Y95H |
probably benign |
Het |
Fsip2 |
T |
C |
2: 82,958,673 (GRCm38) |
I346T |
probably benign |
Het |
Fto |
T |
C |
8: 91,485,190 (GRCm38) |
F381S |
probably damaging |
Het |
Gabbr1 |
G |
C |
17: 37,048,583 (GRCm38) |
S150T |
probably benign |
Het |
Galnt9 |
G |
T |
5: 110,615,473 (GRCm38) |
W448L |
probably damaging |
Het |
Gcnt2 |
G |
T |
13: 40,917,722 (GRCm38) |
|
probably benign |
Het |
Gm10800 |
CAAGAAAACTGAAAATCAAAGAAAACTGAAAATCA |
CAAGAAAACTGAAAATCA |
2: 98,667,016 (GRCm38) |
|
probably null |
Het |
Gm17727 |
T |
C |
9: 35,778,033 (GRCm38) |
*84W |
probably null |
Het |
Gm8882 |
C |
T |
6: 132,361,568 (GRCm38) |
G229D |
unknown |
Het |
Gmcl1 |
G |
T |
6: 86,721,426 (GRCm38) |
A163E |
probably damaging |
Het |
Hectd4 |
A |
G |
5: 121,332,949 (GRCm38) |
Y2633C |
possibly damaging |
Het |
Hsd11b2 |
A |
G |
8: 105,522,634 (GRCm38) |
I214V |
probably damaging |
Het |
Hspa12a |
T |
A |
19: 58,821,013 (GRCm38) |
E217V |
possibly damaging |
Het |
Itih2 |
A |
G |
2: 10,097,137 (GRCm38) |
F845L |
probably damaging |
Het |
Kcnn3 |
T |
A |
3: 89,661,233 (GRCm38) |
L606H |
probably damaging |
Het |
Krt6b |
G |
A |
15: 101,680,142 (GRCm38) |
R28C |
probably damaging |
Het |
Lama2 |
T |
A |
10: 26,990,870 (GRCm38) |
D2876V |
probably damaging |
Het |
Lmbrd2 |
T |
C |
15: 9,175,192 (GRCm38) |
S397P |
probably damaging |
Het |
Lmf2 |
C |
T |
15: 89,352,358 (GRCm38) |
|
probably null |
Het |
Lrp2 |
A |
G |
2: 69,506,453 (GRCm38) |
I1325T |
probably benign |
Het |
Ltbp2 |
A |
T |
12: 84,803,902 (GRCm38) |
C879* |
probably null |
Het |
Map3k1 |
A |
G |
13: 111,755,313 (GRCm38) |
V1136A |
probably damaging |
Het |
Mettl3 |
G |
T |
14: 52,300,252 (GRCm38) |
H84N |
probably benign |
Het |
Mia2 |
A |
G |
12: 59,109,087 (GRCm38) |
|
probably null |
Het |
Mlip |
G |
T |
9: 77,239,579 (GRCm38) |
T92K |
probably damaging |
Het |
Nalcn |
T |
A |
14: 123,464,701 (GRCm38) |
Y466F |
probably benign |
Het |
Nbn |
T |
C |
4: 15,981,588 (GRCm38) |
V560A |
probably benign |
Het |
Ncln |
A |
T |
10: 81,493,153 (GRCm38) |
Y144N |
possibly damaging |
Het |
Nfe2l2 |
A |
C |
2: 75,679,421 (GRCm38) |
D18E |
probably benign |
Het |
Olfr102 |
A |
G |
17: 37,313,713 (GRCm38) |
F224L |
probably benign |
Het |
Olfr1131 |
T |
C |
2: 87,628,607 (GRCm38) |
I48T |
possibly damaging |
Het |
Olfr356 |
T |
C |
2: 36,937,709 (GRCm38) |
C197R |
possibly damaging |
Het |
Olfr432 |
G |
A |
1: 174,050,525 (GRCm38) |
A51T |
probably benign |
Het |
Otop3 |
A |
T |
11: 115,339,395 (GRCm38) |
M33L |
probably benign |
Het |
Pdzd2 |
G |
A |
15: 12,373,506 (GRCm38) |
S2181L |
probably benign |
Het |
Phf14 |
T |
C |
6: 11,953,423 (GRCm38) |
I387T |
possibly damaging |
Het |
Prdm9 |
T |
A |
17: 15,554,698 (GRCm38) |
N318Y |
probably damaging |
Het |
Proca1 |
A |
G |
11: 78,204,911 (GRCm38) |
D123G |
probably damaging |
Het |
Prune2 |
G |
A |
19: 17,120,719 (GRCm38) |
G1196S |
probably benign |
Het |
Psd3 |
T |
A |
8: 68,121,056 (GRCm38) |
S158C |
probably damaging |
Het |
Rps18 |
A |
G |
17: 33,955,136 (GRCm38) |
V15A |
probably benign |
Het |
Sharpin |
C |
A |
15: 76,347,765 (GRCm38) |
R271L |
possibly damaging |
Het |
Smad5 |
C |
A |
13: 56,723,888 (GRCm38) |
Q99K |
probably damaging |
Het |
Sox5 |
T |
C |
6: 144,116,474 (GRCm38) |
M151V |
possibly damaging |
Het |
Sphkap |
A |
T |
1: 83,278,771 (GRCm38) |
F419Y |
possibly damaging |
Het |
Tbx20 |
T |
A |
9: 24,725,525 (GRCm38) |
Y422F |
probably damaging |
Het |
Tcirg1 |
A |
C |
19: 3,899,099 (GRCm38) |
F397V |
probably damaging |
Het |
Tex36 |
G |
A |
7: 133,595,283 (GRCm38) |
S35F |
possibly damaging |
Het |
Tsen54 |
G |
T |
11: 115,814,934 (GRCm38) |
A26S |
unknown |
Het |
Usp50 |
T |
A |
2: 126,780,330 (GRCm38) |
|
probably null |
Het |
Vmn2r5 |
A |
T |
3: 64,491,288 (GRCm38) |
F757I |
probably benign |
Het |
Zbbx |
T |
C |
3: 75,155,442 (GRCm38) |
T3A |
possibly damaging |
Het |
Zfp28 |
T |
A |
7: 6,389,829 (GRCm38) |
M168K |
probably benign |
Het |
Zfp568 |
G |
T |
7: 30,023,126 (GRCm38) |
G499W |
probably damaging |
Het |
Zfp7 |
C |
G |
15: 76,890,931 (GRCm38) |
P391R |
possibly damaging |
Het |
|
Other mutations in Nav2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01097:Nav2
|
APN |
7 |
49,571,194 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01150:Nav2
|
APN |
7 |
49,452,521 (GRCm38) |
missense |
probably benign |
0.17 |
IGL01649:Nav2
|
APN |
7 |
49,575,729 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01662:Nav2
|
APN |
7 |
49,571,209 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02297:Nav2
|
APN |
7 |
49,594,229 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL02313:Nav2
|
APN |
7 |
49,558,773 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL02441:Nav2
|
APN |
7 |
49,452,512 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02472:Nav2
|
APN |
7 |
49,546,041 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02477:Nav2
|
APN |
7 |
49,582,875 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL02725:Nav2
|
APN |
7 |
49,565,095 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02944:Nav2
|
APN |
7 |
49,420,256 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL02953:Nav2
|
APN |
7 |
49,548,423 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03105:Nav2
|
APN |
7 |
49,464,879 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03234:Nav2
|
APN |
7 |
49,462,008 (GRCm38) |
missense |
possibly damaging |
0.94 |
IGL03274:Nav2
|
APN |
7 |
49,362,099 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03294:Nav2
|
APN |
7 |
49,491,457 (GRCm38) |
nonsense |
probably null |
|
R0006:Nav2
|
UTSW |
7 |
49,453,230 (GRCm38) |
missense |
possibly damaging |
0.50 |
R0070:Nav2
|
UTSW |
7 |
49,570,714 (GRCm38) |
missense |
probably damaging |
1.00 |
R0113:Nav2
|
UTSW |
7 |
49,535,953 (GRCm38) |
missense |
probably damaging |
1.00 |
R0306:Nav2
|
UTSW |
7 |
49,545,903 (GRCm38) |
missense |
probably benign |
0.01 |
R0346:Nav2
|
UTSW |
7 |
49,604,585 (GRCm38) |
missense |
probably benign |
0.11 |
R0539:Nav2
|
UTSW |
7 |
49,461,938 (GRCm38) |
missense |
probably damaging |
1.00 |
R0669:Nav2
|
UTSW |
7 |
49,408,683 (GRCm38) |
missense |
probably damaging |
1.00 |
R0785:Nav2
|
UTSW |
7 |
49,420,333 (GRCm38) |
missense |
probably benign |
0.06 |
R0970:Nav2
|
UTSW |
7 |
49,584,153 (GRCm38) |
missense |
probably damaging |
1.00 |
R1162:Nav2
|
UTSW |
7 |
49,536,040 (GRCm38) |
splice site |
probably benign |
|
R1274:Nav2
|
UTSW |
7 |
49,604,430 (GRCm38) |
nonsense |
probably null |
|
R1463:Nav2
|
UTSW |
7 |
49,535,962 (GRCm38) |
missense |
probably damaging |
1.00 |
R1464:Nav2
|
UTSW |
7 |
49,362,204 (GRCm38) |
missense |
probably damaging |
1.00 |
R1464:Nav2
|
UTSW |
7 |
49,362,204 (GRCm38) |
missense |
probably damaging |
1.00 |
R1536:Nav2
|
UTSW |
7 |
49,545,934 (GRCm38) |
missense |
probably damaging |
1.00 |
R1612:Nav2
|
UTSW |
7 |
49,571,211 (GRCm38) |
missense |
probably damaging |
1.00 |
R1638:Nav2
|
UTSW |
7 |
49,452,465 (GRCm38) |
missense |
probably benign |
|
R1731:Nav2
|
UTSW |
7 |
49,548,174 (GRCm38) |
missense |
probably damaging |
1.00 |
R1734:Nav2
|
UTSW |
7 |
49,575,720 (GRCm38) |
missense |
probably damaging |
1.00 |
R1865:Nav2
|
UTSW |
7 |
49,548,195 (GRCm38) |
missense |
possibly damaging |
0.95 |
R1945:Nav2
|
UTSW |
7 |
49,464,872 (GRCm38) |
missense |
probably damaging |
1.00 |
R1997:Nav2
|
UTSW |
7 |
49,548,471 (GRCm38) |
missense |
probably benign |
0.16 |
R2061:Nav2
|
UTSW |
7 |
49,598,897 (GRCm38) |
splice site |
probably benign |
|
R2117:Nav2
|
UTSW |
7 |
49,464,580 (GRCm38) |
missense |
probably benign |
0.00 |
R2174:Nav2
|
UTSW |
7 |
49,452,663 (GRCm38) |
missense |
probably damaging |
0.99 |
R2182:Nav2
|
UTSW |
7 |
49,597,254 (GRCm38) |
missense |
probably benign |
0.38 |
R2251:Nav2
|
UTSW |
7 |
49,453,277 (GRCm38) |
missense |
probably damaging |
1.00 |
R2283:Nav2
|
UTSW |
7 |
49,491,404 (GRCm38) |
missense |
probably damaging |
1.00 |
R2343:Nav2
|
UTSW |
7 |
49,598,817 (GRCm38) |
missense |
possibly damaging |
0.82 |
R2472:Nav2
|
UTSW |
7 |
49,408,884 (GRCm38) |
missense |
probably benign |
|
R2568:Nav2
|
UTSW |
7 |
49,597,564 (GRCm38) |
missense |
probably damaging |
1.00 |
R2656:Nav2
|
UTSW |
7 |
49,545,942 (GRCm38) |
missense |
probably damaging |
1.00 |
R2964:Nav2
|
UTSW |
7 |
49,557,032 (GRCm38) |
missense |
probably damaging |
1.00 |
R2966:Nav2
|
UTSW |
7 |
49,557,032 (GRCm38) |
missense |
probably damaging |
1.00 |
R3817:Nav2
|
UTSW |
7 |
49,464,562 (GRCm38) |
missense |
probably benign |
0.00 |
R3834:Nav2
|
UTSW |
7 |
49,545,858 (GRCm38) |
missense |
possibly damaging |
0.91 |
R4207:Nav2
|
UTSW |
7 |
49,597,231 (GRCm38) |
missense |
probably damaging |
1.00 |
R4207:Nav2
|
UTSW |
7 |
49,572,298 (GRCm38) |
splice site |
probably null |
|
R4411:Nav2
|
UTSW |
7 |
49,398,109 (GRCm38) |
missense |
probably benign |
0.37 |
R4413:Nav2
|
UTSW |
7 |
49,398,109 (GRCm38) |
missense |
probably benign |
0.37 |
R4440:Nav2
|
UTSW |
7 |
49,575,263 (GRCm38) |
splice site |
probably benign |
|
R4440:Nav2
|
UTSW |
7 |
49,552,037 (GRCm38) |
missense |
possibly damaging |
0.86 |
R4454:Nav2
|
UTSW |
7 |
49,548,544 (GRCm38) |
splice site |
probably null |
|
R4729:Nav2
|
UTSW |
7 |
49,452,819 (GRCm38) |
missense |
probably benign |
0.17 |
R4801:Nav2
|
UTSW |
7 |
49,545,852 (GRCm38) |
missense |
possibly damaging |
0.94 |
R4802:Nav2
|
UTSW |
7 |
49,545,852 (GRCm38) |
missense |
possibly damaging |
0.94 |
R4824:Nav2
|
UTSW |
7 |
49,409,001 (GRCm38) |
intron |
probably benign |
|
R4887:Nav2
|
UTSW |
7 |
49,548,434 (GRCm38) |
nonsense |
probably null |
|
R4908:Nav2
|
UTSW |
7 |
49,604,510 (GRCm38) |
missense |
probably damaging |
1.00 |
R4952:Nav2
|
UTSW |
7 |
49,304,540 (GRCm38) |
intron |
probably benign |
|
R4965:Nav2
|
UTSW |
7 |
49,552,877 (GRCm38) |
nonsense |
probably null |
|
R5169:Nav2
|
UTSW |
7 |
49,548,483 (GRCm38) |
nonsense |
probably null |
|
R5224:Nav2
|
UTSW |
7 |
49,551,725 (GRCm38) |
missense |
probably benign |
0.00 |
R5249:Nav2
|
UTSW |
7 |
49,535,913 (GRCm38) |
missense |
probably damaging |
1.00 |
R5285:Nav2
|
UTSW |
7 |
49,548,234 (GRCm38) |
missense |
probably damaging |
1.00 |
R5314:Nav2
|
UTSW |
7 |
49,408,692 (GRCm38) |
small deletion |
probably benign |
|
R5320:Nav2
|
UTSW |
7 |
49,491,373 (GRCm38) |
missense |
probably benign |
0.00 |
R5377:Nav2
|
UTSW |
7 |
49,589,160 (GRCm38) |
missense |
probably benign |
0.02 |
R5471:Nav2
|
UTSW |
7 |
49,548,169 (GRCm38) |
missense |
probably damaging |
1.00 |
R5754:Nav2
|
UTSW |
7 |
49,557,046 (GRCm38) |
missense |
probably damaging |
1.00 |
R5832:Nav2
|
UTSW |
7 |
49,548,069 (GRCm38) |
splice site |
probably null |
|
R5884:Nav2
|
UTSW |
7 |
49,597,169 (GRCm38) |
nonsense |
probably null |
|
R5921:Nav2
|
UTSW |
7 |
49,304,576 (GRCm38) |
intron |
probably benign |
|
R6180:Nav2
|
UTSW |
7 |
49,458,167 (GRCm38) |
missense |
probably benign |
0.39 |
R6208:Nav2
|
UTSW |
7 |
49,564,103 (GRCm38) |
missense |
probably damaging |
0.99 |
R6373:Nav2
|
UTSW |
7 |
49,453,175 (GRCm38) |
missense |
probably damaging |
1.00 |
R6450:Nav2
|
UTSW |
7 |
49,594,366 (GRCm38) |
missense |
probably damaging |
1.00 |
R6522:Nav2
|
UTSW |
7 |
49,597,533 (GRCm38) |
missense |
probably damaging |
1.00 |
R6626:Nav2
|
UTSW |
7 |
49,594,352 (GRCm38) |
missense |
probably damaging |
1.00 |
R6695:Nav2
|
UTSW |
7 |
49,464,904 (GRCm38) |
missense |
probably benign |
0.04 |
R6705:Nav2
|
UTSW |
7 |
49,551,916 (GRCm38) |
missense |
probably damaging |
1.00 |
R6842:Nav2
|
UTSW |
7 |
49,458,169 (GRCm38) |
missense |
possibly damaging |
0.91 |
R6847:Nav2
|
UTSW |
7 |
49,491,456 (GRCm38) |
missense |
probably benign |
0.14 |
R7287:Nav2
|
UTSW |
7 |
49,420,328 (GRCm38) |
missense |
probably benign |
0.01 |
R7312:Nav2
|
UTSW |
7 |
49,461,924 (GRCm38) |
missense |
possibly damaging |
0.55 |
R7315:Nav2
|
UTSW |
7 |
49,548,289 (GRCm38) |
missense |
possibly damaging |
0.61 |
R7337:Nav2
|
UTSW |
7 |
49,551,773 (GRCm38) |
missense |
possibly damaging |
0.56 |
R7366:Nav2
|
UTSW |
7 |
49,554,203 (GRCm38) |
splice site |
probably null |
|
R7451:Nav2
|
UTSW |
7 |
49,552,829 (GRCm38) |
splice site |
probably null |
|
R7545:Nav2
|
UTSW |
7 |
49,582,857 (GRCm38) |
missense |
probably damaging |
1.00 |
R7706:Nav2
|
UTSW |
7 |
49,594,319 (GRCm38) |
missense |
probably benign |
0.35 |
R7730:Nav2
|
UTSW |
7 |
49,572,397 (GRCm38) |
missense |
probably damaging |
1.00 |
R7812:Nav2
|
UTSW |
7 |
49,597,173 (GRCm38) |
missense |
probably benign |
0.13 |
R8097:Nav2
|
UTSW |
7 |
49,587,777 (GRCm38) |
missense |
probably damaging |
1.00 |
R8119:Nav2
|
UTSW |
7 |
49,453,484 (GRCm38) |
missense |
probably damaging |
0.99 |
R8298:Nav2
|
UTSW |
7 |
49,554,261 (GRCm38) |
critical splice donor site |
probably null |
|
R8306:Nav2
|
UTSW |
7 |
49,546,017 (GRCm38) |
missense |
probably benign |
0.33 |
R8331:Nav2
|
UTSW |
7 |
49,452,623 (GRCm38) |
missense |
probably benign |
|
R8402:Nav2
|
UTSW |
7 |
49,453,437 (GRCm38) |
missense |
probably benign |
0.43 |
R8421:Nav2
|
UTSW |
7 |
49,452,521 (GRCm38) |
missense |
probably benign |
|
R8478:Nav2
|
UTSW |
7 |
49,461,985 (GRCm38) |
missense |
probably damaging |
0.99 |
R8724:Nav2
|
UTSW |
7 |
49,491,436 (GRCm38) |
missense |
possibly damaging |
0.82 |
R8753:Nav2
|
UTSW |
7 |
49,452,572 (GRCm38) |
missense |
probably benign |
|
R8835:Nav2
|
UTSW |
7 |
49,598,803 (GRCm38) |
missense |
possibly damaging |
0.83 |
R8933:Nav2
|
UTSW |
7 |
49,461,957 (GRCm38) |
missense |
probably damaging |
1.00 |
R8957:Nav2
|
UTSW |
7 |
49,571,216 (GRCm38) |
missense |
probably damaging |
1.00 |
R9069:Nav2
|
UTSW |
7 |
49,558,813 (GRCm38) |
missense |
probably damaging |
0.99 |
R9095:Nav2
|
UTSW |
7 |
49,604,545 (GRCm38) |
missense |
probably damaging |
1.00 |
R9223:Nav2
|
UTSW |
7 |
49,552,851 (GRCm38) |
missense |
probably damaging |
1.00 |
R9261:Nav2
|
UTSW |
7 |
49,597,156 (GRCm38) |
missense |
probably damaging |
1.00 |
X0023:Nav2
|
UTSW |
7 |
49,547,899 (GRCm38) |
missense |
possibly damaging |
0.47 |
Z1177:Nav2
|
UTSW |
7 |
49,594,223 (GRCm38) |
missense |
probably benign |
0.01 |
Z1177:Nav2
|
UTSW |
7 |
49,452,761 (GRCm38) |
missense |
possibly damaging |
0.47 |
|