Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc9 |
T |
C |
6: 142,617,333 (GRCm39) |
H577R |
probably damaging |
Het |
Acvr1 |
T |
C |
2: 58,337,661 (GRCm39) |
M474V |
probably damaging |
Het |
Adam1a |
A |
T |
5: 121,657,513 (GRCm39) |
C593* |
probably null |
Het |
Agap2 |
A |
G |
10: 126,926,744 (GRCm39) |
N927S |
probably damaging |
Het |
Ahctf1 |
T |
C |
1: 179,598,218 (GRCm39) |
H958R |
probably damaging |
Het |
Apaf1 |
A |
G |
10: 90,835,581 (GRCm39) |
V1088A |
probably damaging |
Het |
Brpf1 |
G |
T |
6: 113,296,891 (GRCm39) |
K958N |
probably damaging |
Het |
Cadps |
A |
G |
14: 12,705,726 (GRCm38) |
I223T |
probably damaging |
Het |
Catsperg2 |
T |
C |
7: 29,397,189 (GRCm39) |
M1105V |
probably benign |
Het |
Clasp2 |
T |
A |
9: 113,735,265 (GRCm39) |
F1033L |
possibly damaging |
Het |
Col4a3 |
T |
A |
1: 82,678,094 (GRCm39) |
I1232N |
unknown |
Het |
Col4a3 |
T |
G |
1: 82,689,595 (GRCm39) |
|
probably benign |
Het |
Comtd1 |
T |
G |
14: 21,897,731 (GRCm39) |
E134A |
probably damaging |
Het |
Cyp2c55 |
A |
T |
19: 39,022,821 (GRCm39) |
T320S |
probably benign |
Het |
Dlx2 |
T |
C |
2: 71,376,522 (GRCm39) |
N72S |
probably benign |
Het |
Dnhd1 |
T |
A |
7: 105,301,459 (GRCm39) |
V272E |
probably damaging |
Het |
Dnhd1 |
T |
A |
7: 105,323,061 (GRCm39) |
I523N |
probably damaging |
Het |
Dpysl3 |
T |
A |
18: 43,465,996 (GRCm39) |
I140F |
probably damaging |
Het |
Elmod2 |
G |
A |
8: 84,048,093 (GRCm39) |
A123V |
probably benign |
Het |
Etv4 |
T |
C |
11: 101,662,507 (GRCm39) |
|
probably benign |
Het |
F3 |
A |
T |
3: 121,523,032 (GRCm39) |
T81S |
probably damaging |
Het |
Faf2 |
C |
T |
13: 54,799,865 (GRCm39) |
A224V |
probably damaging |
Het |
Fbn1 |
A |
T |
2: 125,205,549 (GRCm39) |
M1109K |
probably damaging |
Het |
Fnbp4 |
A |
G |
2: 90,596,187 (GRCm39) |
E586G |
probably damaging |
Het |
Gm10428 |
G |
T |
11: 62,644,179 (GRCm39) |
|
probably benign |
Het |
Gm5884 |
A |
T |
6: 128,622,050 (GRCm39) |
|
noncoding transcript |
Het |
Gm6471 |
T |
A |
7: 142,385,319 (GRCm39) |
|
noncoding transcript |
Het |
Gtse1 |
T |
C |
15: 85,757,939 (GRCm39) |
V515A |
probably benign |
Het |
H2-M2 |
T |
C |
17: 37,793,391 (GRCm39) |
E205G |
probably damaging |
Het |
Ido1 |
T |
A |
8: 25,075,306 (GRCm39) |
T259S |
possibly damaging |
Het |
Il1r2 |
A |
G |
1: 40,154,308 (GRCm39) |
Y225C |
probably damaging |
Het |
Kcnq3 |
T |
G |
15: 65,876,658 (GRCm39) |
D495A |
possibly damaging |
Het |
Lrrc49 |
T |
C |
9: 60,556,773 (GRCm39) |
N321D |
probably benign |
Het |
Lztr1 |
G |
T |
16: 17,341,247 (GRCm39) |
R291L |
probably damaging |
Het |
Micu1 |
C |
T |
10: 59,568,983 (GRCm39) |
|
probably benign |
Het |
Msh5 |
C |
T |
17: 35,248,928 (GRCm39) |
V702I |
probably benign |
Het |
Myh1 |
T |
C |
11: 67,101,996 (GRCm39) |
I792T |
probably benign |
Het |
Ntn4 |
C |
T |
10: 93,543,215 (GRCm39) |
R314W |
probably damaging |
Het |
Or11i1 |
C |
T |
3: 106,729,688 (GRCm39) |
M62I |
probably damaging |
Het |
Or5ac22 |
A |
G |
16: 59,135,027 (GRCm39) |
S248P |
probably damaging |
Het |
Or8u9 |
T |
C |
2: 86,001,354 (GRCm39) |
D269G |
probably benign |
Het |
Otof |
G |
C |
5: 30,551,532 (GRCm39) |
N340K |
probably benign |
Het |
Pdlim2 |
C |
T |
14: 70,402,228 (GRCm39) |
R296H |
probably damaging |
Het |
Plek2 |
T |
A |
12: 78,941,664 (GRCm39) |
Y155F |
probably damaging |
Het |
Ppa1 |
T |
A |
10: 61,487,388 (GRCm39) |
Y38* |
probably null |
Het |
Pramel22 |
T |
A |
4: 143,381,025 (GRCm39) |
T333S |
probably damaging |
Het |
Prmt9 |
T |
A |
8: 78,303,968 (GRCm39) |
C684S |
possibly damaging |
Het |
Rasl10a |
A |
G |
11: 5,009,473 (GRCm39) |
D87G |
possibly damaging |
Het |
Rtn4rl1 |
C |
A |
11: 75,156,864 (GRCm39) |
P432Q |
probably benign |
Het |
Scd4 |
T |
G |
19: 44,329,823 (GRCm39) |
Y265D |
probably damaging |
Het |
Scn5a |
C |
T |
9: 119,358,085 (GRCm39) |
A719T |
probably benign |
Het |
Sdk1 |
T |
A |
5: 142,171,040 (GRCm39) |
F1968I |
probably benign |
Het |
Sh3bp5 |
T |
C |
14: 31,157,880 (GRCm39) |
E12G |
probably benign |
Het |
Slc6a12 |
T |
A |
6: 121,337,485 (GRCm39) |
F390I |
probably benign |
Het |
Snapin |
A |
T |
3: 90,397,539 (GRCm39) |
D77E |
possibly damaging |
Het |
Sox2 |
G |
T |
3: 34,704,820 (GRCm39) |
E86* |
probably null |
Het |
Sparcl1 |
A |
G |
5: 104,241,220 (GRCm39) |
L68P |
probably benign |
Het |
Sptb |
T |
A |
12: 76,669,027 (GRCm39) |
E562V |
probably damaging |
Het |
Taar3 |
A |
T |
10: 23,826,483 (GRCm39) |
H343L |
probably benign |
Het |
Tanc1 |
T |
A |
2: 59,555,095 (GRCm39) |
V51E |
possibly damaging |
Het |
Tbc1d22a |
T |
C |
15: 86,123,350 (GRCm39) |
S128P |
probably damaging |
Het |
Thada |
A |
G |
17: 84,751,927 (GRCm39) |
S350P |
probably benign |
Het |
Tmem161b |
T |
C |
13: 84,408,348 (GRCm39) |
V93A |
probably benign |
Het |
Tnn |
T |
C |
1: 159,924,799 (GRCm39) |
Y1185C |
probably damaging |
Het |
Trim43a |
T |
C |
9: 88,464,371 (GRCm39) |
V94A |
probably benign |
Het |
Ttll12 |
C |
T |
15: 83,465,976 (GRCm39) |
E407K |
probably benign |
Het |
Ttn |
T |
C |
2: 76,555,856 (GRCm39) |
E30383G |
probably damaging |
Het |
Vmn1r29 |
T |
A |
6: 58,285,087 (GRCm39) |
M269K |
possibly damaging |
Het |
Vmn2r117 |
A |
G |
17: 23,697,363 (GRCm39) |
S110P |
probably benign |
Het |
Vmn2r6 |
C |
A |
3: 64,463,698 (GRCm39) |
V290L |
possibly damaging |
Het |
Vmn2r8 |
A |
T |
5: 108,950,019 (GRCm39) |
L276Q |
probably damaging |
Het |
Zan |
C |
A |
5: 137,423,904 (GRCm39) |
C2665F |
unknown |
Het |
Zfp507 |
C |
T |
7: 35,493,150 (GRCm39) |
R631Q |
probably damaging |
Het |
Zfp983 |
A |
G |
17: 21,880,933 (GRCm39) |
H287R |
probably damaging |
Het |
|
Other mutations in Nav1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01061:Nav1
|
APN |
1 |
135,378,368 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01455:Nav1
|
APN |
1 |
135,397,373 (GRCm39) |
missense |
probably benign |
0.44 |
IGL01650:Nav1
|
APN |
1 |
135,382,498 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01872:Nav1
|
APN |
1 |
135,381,814 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01967:Nav1
|
APN |
1 |
135,464,983 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02167:Nav1
|
APN |
1 |
135,398,699 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02278:Nav1
|
APN |
1 |
135,391,452 (GRCm39) |
splice site |
probably benign |
|
IGL02343:Nav1
|
APN |
1 |
135,382,490 (GRCm39) |
nonsense |
probably null |
|
IGL02378:Nav1
|
APN |
1 |
135,397,716 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02554:Nav1
|
APN |
1 |
135,512,651 (GRCm39) |
synonymous |
silent |
|
IGL03148:Nav1
|
APN |
1 |
135,397,762 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03286:Nav1
|
APN |
1 |
135,382,274 (GRCm39) |
missense |
probably benign |
|
IGL03372:Nav1
|
APN |
1 |
135,378,641 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4802001:Nav1
|
UTSW |
1 |
135,380,671 (GRCm39) |
missense |
unknown |
|
R0388:Nav1
|
UTSW |
1 |
135,376,655 (GRCm39) |
splice site |
probably benign |
|
R0390:Nav1
|
UTSW |
1 |
135,377,704 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0395:Nav1
|
UTSW |
1 |
135,460,361 (GRCm39) |
missense |
probably damaging |
0.97 |
R0395:Nav1
|
UTSW |
1 |
135,460,359 (GRCm39) |
nonsense |
probably null |
|
R0416:Nav1
|
UTSW |
1 |
135,398,864 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0463:Nav1
|
UTSW |
1 |
135,379,945 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0538:Nav1
|
UTSW |
1 |
135,392,430 (GRCm39) |
splice site |
probably benign |
|
R0594:Nav1
|
UTSW |
1 |
135,395,381 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0696:Nav1
|
UTSW |
1 |
135,460,352 (GRCm39) |
missense |
probably damaging |
0.99 |
R0699:Nav1
|
UTSW |
1 |
135,380,687 (GRCm39) |
missense |
probably benign |
0.00 |
R0759:Nav1
|
UTSW |
1 |
135,382,998 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1164:Nav1
|
UTSW |
1 |
135,400,148 (GRCm39) |
missense |
probably benign |
|
R1169:Nav1
|
UTSW |
1 |
135,382,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R1401:Nav1
|
UTSW |
1 |
135,388,163 (GRCm39) |
missense |
probably benign |
0.20 |
R1421:Nav1
|
UTSW |
1 |
135,512,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R1642:Nav1
|
UTSW |
1 |
135,380,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R1705:Nav1
|
UTSW |
1 |
135,512,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R1713:Nav1
|
UTSW |
1 |
135,522,972 (GRCm39) |
intron |
probably benign |
|
R1728:Nav1
|
UTSW |
1 |
135,512,465 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1729:Nav1
|
UTSW |
1 |
135,512,465 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1730:Nav1
|
UTSW |
1 |
135,512,465 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1739:Nav1
|
UTSW |
1 |
135,512,465 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1740:Nav1
|
UTSW |
1 |
135,386,127 (GRCm39) |
critical splice donor site |
probably null |
|
R1762:Nav1
|
UTSW |
1 |
135,512,465 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1783:Nav1
|
UTSW |
1 |
135,512,465 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1784:Nav1
|
UTSW |
1 |
135,512,465 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1785:Nav1
|
UTSW |
1 |
135,512,465 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1895:Nav1
|
UTSW |
1 |
135,386,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R1896:Nav1
|
UTSW |
1 |
135,388,475 (GRCm39) |
missense |
probably benign |
0.00 |
R1901:Nav1
|
UTSW |
1 |
135,400,148 (GRCm39) |
missense |
probably benign |
0.03 |
R1902:Nav1
|
UTSW |
1 |
135,400,148 (GRCm39) |
missense |
probably benign |
0.03 |
R1939:Nav1
|
UTSW |
1 |
135,393,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R1971:Nav1
|
UTSW |
1 |
135,460,091 (GRCm39) |
missense |
probably benign |
0.06 |
R2063:Nav1
|
UTSW |
1 |
135,376,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R2066:Nav1
|
UTSW |
1 |
135,376,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R2084:Nav1
|
UTSW |
1 |
135,535,158 (GRCm39) |
unclassified |
probably benign |
|
R2090:Nav1
|
UTSW |
1 |
135,534,903 (GRCm39) |
utr 5 prime |
probably benign |
|
R2107:Nav1
|
UTSW |
1 |
135,376,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R2110:Nav1
|
UTSW |
1 |
135,376,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R2111:Nav1
|
UTSW |
1 |
135,376,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R2112:Nav1
|
UTSW |
1 |
135,376,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R2136:Nav1
|
UTSW |
1 |
135,382,174 (GRCm39) |
missense |
probably null |
0.18 |
R2268:Nav1
|
UTSW |
1 |
135,399,974 (GRCm39) |
nonsense |
probably null |
|
R2269:Nav1
|
UTSW |
1 |
135,399,974 (GRCm39) |
nonsense |
probably null |
|
R2847:Nav1
|
UTSW |
1 |
135,378,382 (GRCm39) |
splice site |
probably null |
|
R2869:Nav1
|
UTSW |
1 |
135,388,495 (GRCm39) |
synonymous |
silent |
|
R2871:Nav1
|
UTSW |
1 |
135,388,495 (GRCm39) |
synonymous |
silent |
|
R2872:Nav1
|
UTSW |
1 |
135,388,495 (GRCm39) |
synonymous |
silent |
|
R2904:Nav1
|
UTSW |
1 |
135,512,976 (GRCm39) |
missense |
probably benign |
|
R3690:Nav1
|
UTSW |
1 |
135,395,382 (GRCm39) |
missense |
probably benign |
0.11 |
R3716:Nav1
|
UTSW |
1 |
135,378,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R3717:Nav1
|
UTSW |
1 |
135,378,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R3718:Nav1
|
UTSW |
1 |
135,378,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R3815:Nav1
|
UTSW |
1 |
135,398,862 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4282:Nav1
|
UTSW |
1 |
135,385,651 (GRCm39) |
intron |
probably benign |
|
R4361:Nav1
|
UTSW |
1 |
135,535,175 (GRCm39) |
unclassified |
probably benign |
|
R4610:Nav1
|
UTSW |
1 |
135,520,186 (GRCm39) |
intron |
probably benign |
|
R4730:Nav1
|
UTSW |
1 |
135,535,049 (GRCm39) |
unclassified |
probably benign |
|
R4784:Nav1
|
UTSW |
1 |
135,386,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R4788:Nav1
|
UTSW |
1 |
135,397,461 (GRCm39) |
missense |
probably benign |
|
R4808:Nav1
|
UTSW |
1 |
135,382,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R4996:Nav1
|
UTSW |
1 |
135,393,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R5284:Nav1
|
UTSW |
1 |
135,377,701 (GRCm39) |
nonsense |
probably null |
|
R5514:Nav1
|
UTSW |
1 |
135,398,299 (GRCm39) |
missense |
probably benign |
0.04 |
R5769:Nav1
|
UTSW |
1 |
135,379,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R5834:Nav1
|
UTSW |
1 |
135,460,144 (GRCm39) |
missense |
probably benign |
0.07 |
R5898:Nav1
|
UTSW |
1 |
135,512,884 (GRCm39) |
missense |
probably benign |
|
R6081:Nav1
|
UTSW |
1 |
135,398,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R6344:Nav1
|
UTSW |
1 |
135,378,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R6378:Nav1
|
UTSW |
1 |
135,382,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R7001:Nav1
|
UTSW |
1 |
135,382,349 (GRCm39) |
splice site |
probably null |
|
R7185:Nav1
|
UTSW |
1 |
135,398,746 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7291:Nav1
|
UTSW |
1 |
135,393,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R7361:Nav1
|
UTSW |
1 |
135,380,591 (GRCm39) |
missense |
unknown |
|
R7390:Nav1
|
UTSW |
1 |
135,512,656 (GRCm39) |
missense |
probably benign |
0.01 |
R7464:Nav1
|
UTSW |
1 |
135,512,647 (GRCm39) |
missense |
probably benign |
0.03 |
R7502:Nav1
|
UTSW |
1 |
135,397,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R7601:Nav1
|
UTSW |
1 |
135,388,176 (GRCm39) |
missense |
unknown |
|
R7625:Nav1
|
UTSW |
1 |
135,395,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R7639:Nav1
|
UTSW |
1 |
135,398,860 (GRCm39) |
missense |
probably benign |
0.09 |
R7786:Nav1
|
UTSW |
1 |
135,397,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R7808:Nav1
|
UTSW |
1 |
135,379,986 (GRCm39) |
missense |
unknown |
|
R7815:Nav1
|
UTSW |
1 |
135,512,377 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7825:Nav1
|
UTSW |
1 |
135,377,782 (GRCm39) |
missense |
probably damaging |
0.98 |
R8030:Nav1
|
UTSW |
1 |
135,464,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R8370:Nav1
|
UTSW |
1 |
135,398,882 (GRCm39) |
nonsense |
probably null |
|
R8405:Nav1
|
UTSW |
1 |
135,382,508 (GRCm39) |
missense |
unknown |
|
R8720:Nav1
|
UTSW |
1 |
135,388,464 (GRCm39) |
missense |
unknown |
|
R8868:Nav1
|
UTSW |
1 |
135,512,943 (GRCm39) |
missense |
probably benign |
0.05 |
R8973:Nav1
|
UTSW |
1 |
135,512,463 (GRCm39) |
missense |
probably benign |
0.01 |
R9039:Nav1
|
UTSW |
1 |
135,371,487 (GRCm39) |
missense |
unknown |
|
R9261:Nav1
|
UTSW |
1 |
135,388,095 (GRCm39) |
missense |
unknown |
|
R9523:Nav1
|
UTSW |
1 |
135,379,929 (GRCm39) |
missense |
unknown |
|
Z1088:Nav1
|
UTSW |
1 |
135,398,462 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Nav1
|
UTSW |
1 |
135,400,158 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Nav1
|
UTSW |
1 |
135,380,624 (GRCm39) |
missense |
unknown |
|
Z1177:Nav1
|
UTSW |
1 |
135,397,469 (GRCm39) |
missense |
possibly damaging |
0.56 |
|